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	<title>Patents Archives - X-Chem</title>
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		<title>Inhibitors of P97 Protein and Methods of Use</title>
		<link>https://www.x-chemrx.com/fr/projects/inhibitors-of-p97-protein-and-methods-of-use/</link>
					<comments>https://www.x-chemrx.com/fr/projects/inhibitors-of-p97-protein-and-methods-of-use/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Wed, 19 Mar 2025 18:34:18 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3528</guid>

					<description><![CDATA[<p>Described herein are compounds and compositions useful for preventing and/or treating a disease or condition, e.g., a disease or condition associated with activity of p97 protein, e.g., cancer or a neurodegenerative disorder. In one aspect, the present disclosure provides a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein the variables R1, R2,  [...]</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/inhibitors-of-p97-protein-and-methods-of-use/">Inhibitors of P97 Protein and Methods of Use</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-1 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-0 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-1"><p>Sont décrits ici des composés et des compositions utiles pour prévenir et/ou traiter une maladie ou un état, par exemple une maladie ou un état associé à l'activité de la protéine p97, <em>par exemple.</em>, Dans un aspect, la présente divulgation fournit un composé de formule (I) ou un sel pharmaceutiquement acceptable de celui-ci. Dans un aspect, la présente divulgation fournit un composé de formule (I) ou un sel pharmaceutiquement acceptable de celui-ci, dans lequel les variables R<sup>1</sup>, R<sup>2</sup>, R<sup>3</sup>, R<sup>4</sup>, R<sup>5</sup>, R<sup>6</sup>, R<sup>7</sup>, m et n sont définis dans le présent document.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-1 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="sm-text-align-left" style="text-align:center;"><a class="fusion-button button-flat fusion-button-default-size button-custom fusion-button-default button-1 fusion-button-span-yes fusion-has-button-gradient" style="--button_accent_color:var(--awb-color1);--button_accent_hover_color:var(--awb-color1);--button_border_hover_color:var(--awb-color1);--button_border_width-top:0;--button_border_width-right:0;--button_border_width-bottom:0;--button_border_width-left:0;--button-border-radius-top-left:0;--button-border-radius-top-right:0;--button-border-radius-bottom-right:0;--button-border-radius-bottom-left:0;--button_gradient_start:89%;--button_gradient_end:0%;--button_gradient_top_color:var(--awb-color5);--button_gradient_bottom_color:hsla(var(--awb-color5-h),var(--awb-color5-s),calc(var(--awb-color5-l) - 8%),var(--awb-color5-a));--button_gradient_top_color_hover:hsla(var(--awb-color5-h),var(--awb-color5-s),calc(var(--awb-color5-l) - 8%),var(--awb-color5-a));--button_gradient_bottom_color_hover:hsla(var(--awb-color5-h),var(--awb-color5-s),calc(var(--awb-color5-l) - 8%),var(--awb-color5-a));--button_font_size:18px;--button_padding-top:24px;--button_padding-right:48px;--button_padding-bottom:26px;--button_padding-left:48px;--button_margin-top:0px;--button_margin-right:0px;--button_margin-bottom:0px;--button_margin-left:0px;width:calc(100% - 0px - 0px);" target="_blank" rel="noopener noreferrer" data-hover="bg_slide_left" href="https://patentscope.wipo.int/search/fr/WO2025014963"><span class="fusion-button-text awb-button__text awb-button__text--default">Voir la ressource</span><i class="awb-factoryarrow-right awb-button__icon awb-button__icon--default button-icon-right" aria-hidden="true"></i></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/inhibitors-of-p97-protein-and-methods-of-use/">Inhibitors of P97 Protein and Methods of Use</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
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					<wfw:commentrss>https://www.x-chemrx.com/fr/projects/inhibitors-of-p97-protein-and-methods-of-use/feed/</wfw:commentrss>
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		<title>Methods for identifying compounds binding to a target molecule using mirror-imaging of the target molecule</title>
		<link>https://www.x-chemrx.com/fr/projects/methods-for-identifying-compounds-binding-to-a-target-molecule-using-mirror-imaging-of-the-target-molecule/</link>
					<comments>https://www.x-chemrx.com/fr/projects/methods-for-identifying-compounds-binding-to-a-target-molecule-using-mirror-imaging-of-the-target-molecule/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Fri, 07 Mar 2025 20:55:53 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3538</guid>

					<description><![CDATA[<p>The present disclosure provides methods of screening DNA-encoded chemical libraries utilizing mirror-images of target molecules. These methods allow highly efficient selection of compounds that bind to a target molecule, even when the target molecule can bind the DNA tag of the encoded compounds.  View Resource</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/methods-for-identifying-compounds-binding-to-a-target-molecule-using-mirror-imaging-of-the-target-molecule/">Methods for identifying compounds binding to a target molecule using mirror-imaging of the target molecule</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-2 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-2 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-2"><p>La présente divulgation propose des méthodes de criblage de chimiothèques codées dans l'ADN utilisant des images miroir de molécules cibles. Ces méthodes permettent une sélection très efficace des composés qui se lient à une molécule cible, même lorsque la molécule cible peut lier l'étiquette d'ADN des composés codés.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-3 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-2 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://patents.google.com/patent/WO2025042899A2/fr"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Voir la ressource</span></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/methods-for-identifying-compounds-binding-to-a-target-molecule-using-mirror-imaging-of-the-target-molecule/">Methods for identifying compounds binding to a target molecule using mirror-imaging of the target molecule</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
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					<wfw:commentrss>https://www.x-chemrx.com/fr/projects/methods-for-identifying-compounds-binding-to-a-target-molecule-using-mirror-imaging-of-the-target-molecule/feed/</wfw:commentrss>
			<slash:comments>0</slash:comments>
		
		
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		<title>Crystalline and liquid crystalline 25-hydroxy-cholest-5-en-3-sulfate sodium and methods for preparing same</title>
		<link>https://www.x-chemrx.com/fr/projects/crystalline-and-liquid-crystalline-25-hydroxy-cholest-5-en-3-sulfate-sodium-and-methods-for-preparing-same/</link>
					<comments>https://www.x-chemrx.com/fr/projects/crystalline-and-liquid-crystalline-25-hydroxy-cholest-5-en-3-sulfate-sodium-and-methods-for-preparing-same/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Thu, 01 Jul 2021 15:36:17 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3715</guid>

					<description><![CDATA[<p>Crystalline and liquid crystalline forms of 25HC3S sodium are described herein. The disclosure includes Forms I, II, III, V, IX, XI, and XIII of 25HC3S sodium and combinations thereof. Pharmaceutical formulations of said forms, or combinations thereof, and methods of treating or preventing disease such as hypercholesterolemia, hypertriglyceridemia, and conditions related to fat accumulation  [...]</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/crystalline-and-liquid-crystalline-25-hydroxy-cholest-5-en-3-sulfate-sodium-and-methods-for-preparing-same/">Crystalline and liquid crystalline 25-hydroxy-cholest-5-en-3-sulfate sodium and methods for preparing same</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-3 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-4 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-3"><p>Les formes cristallines et cristallines liquides du 25HC3S sodium sont décrites dans le présent document. La divulgation comprend les formes I, II, III, V, IX, XI et XIII de 25HC3S sodium et leurs combinaisons. Des formulations pharmaceutiques de ces formes, ou des combinaisons de celles-ci, et des méthodes de traitement ou de prévention de maladies telles que l'hypercholestérolémie, l'hypertriglycéridémie et des conditions liées à l'accumulation de graisse et à l'inflammation (par exemple, la maladie du foie gras non alcoolique (NAFLD), la stéatohépatite non alcoolique (NASH), l'hépatite alcoolique, les lésions rénales aiguës (AKI), le psoriasis et l'athérosclérose) sont également divulguées dans le présent document. Des méthodes de préparation du 25HC3S sont également présentées.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-5 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-3 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://worldwide.espacenet.com/patent/search/family/076575692/publication/WO2021133976A1?q=WO2021133976A1"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Lire l'article complet</span></a></div><div class="fusion-text fusion-text-4" style="--awb-font-size:15px;--awb-margin-top:10px;">Veuillez noter que le contenu suivant est disponible uniquement en anglais.
</div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/crystalline-and-liquid-crystalline-25-hydroxy-cholest-5-en-3-sulfate-sodium-and-methods-for-preparing-same/">Crystalline and liquid crystalline 25-hydroxy-cholest-5-en-3-sulfate sodium and methods for preparing same</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
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			<slash:comments>0</slash:comments>
		
		
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		<title>Collaborative Medicinal Development, LLC, USA .; Preparation of heteroaromatic and heterobicyclic aromatic derivatives for the treatment of ferroptosis-related disorders</title>
		<link>https://www.x-chemrx.com/fr/projects/collaborative-medicinal-development-llc-usa-preparation-of-heteroaromatic-and-heterobicyclic-aromatic-derivatives-for-the-treatment-of-ferroptosis-related-disorders/</link>
					<comments>https://www.x-chemrx.com/fr/projects/collaborative-medicinal-development-llc-usa-preparation-of-heteroaromatic-and-heterobicyclic-aromatic-derivatives-for-the-treatment-of-ferroptosis-related-disorders/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Thu, 17 Sep 2020 16:15:58 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3744</guid>

					<description><![CDATA[<p>The present application discloses heteroaromatic and heterobicyclic aromatic derivative compounds and compositions, and methods for treating ferroptosis-related disorders and diseases in patients using the compounds and compositions as disclosed herein.  Read Full Article</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/collaborative-medicinal-development-llc-usa-preparation-of-heteroaromatic-and-heterobicyclic-aromatic-derivatives-for-the-treatment-of-ferroptosis-related-disorders/">Collaborative Medicinal Development, LLC, USA .; Preparation of heteroaromatic and heterobicyclic aromatic derivatives for the treatment of ferroptosis-related disorders</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-4 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-6 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-5"><p>La présente demande concerne des composés et des compositions de dérivés aromatiques hétéroaromatiques et hétérobicycliques, ainsi que des méthodes de traitement des troubles et des maladies liés à la ferroptose chez les patients à l'aide des composés et des compositions décrits dans la présente demande.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-7 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-4 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://patents.google.com/patent/WO2020185738A1/fr?oq=WO2020185738A1"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Lire l'article complet</span></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/collaborative-medicinal-development-llc-usa-preparation-of-heteroaromatic-and-heterobicyclic-aromatic-derivatives-for-the-treatment-of-ferroptosis-related-disorders/">Collaborative Medicinal Development, LLC, USA .; Preparation of heteroaromatic and heterobicyclic aromatic derivatives for the treatment of ferroptosis-related disorders</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
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		<title>Mitokinin, Inc., USA .; Preparation of purinamines and pyrrolopyrimidinamines, compositions and methods of using the same for treatment of neurodegenerative and mitochondrial disease</title>
		<link>https://www.x-chemrx.com/fr/projects/mitokinin-inc-usa-preparation-of-purinamines-and-pyrrolopyrimidinamines-compositions-and-methods-of-using-the-same-for-treatment-of-neurodegenerative-and-mitochondrial-disease/</link>
					<comments>https://www.x-chemrx.com/fr/projects/mitokinin-inc-usa-preparation-of-purinamines-and-pyrrolopyrimidinamines-compositions-and-methods-of-using-the-same-for-treatment-of-neurodegenerative-and-mitochondrial-disease/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Mon, 10 Aug 2020 16:16:34 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3746</guid>

					<description><![CDATA[<p>The present disclosure is directed to nitrogen-containing heteroaryl analogs, methods of making nitrogen-containing analogs, and methods of treating disorders associated with PINK1 kinase activity including, but not limited to, neurodegenerative diseases, mitochondrial diseases, fibrosis, and/or cardiomyopathy using these analogs. This abstract is intended as a scanning tool for purposes of searching in the particular  [...]</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/mitokinin-inc-usa-preparation-of-purinamines-and-pyrrolopyrimidinamines-compositions-and-methods-of-using-the-same-for-treatment-of-neurodegenerative-and-mitochondrial-disease/">Mitokinin, Inc., USA .; Preparation of purinamines and pyrrolopyrimidinamines, compositions and methods of using the same for treatment of neurodegenerative and mitochondrial disease</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-5 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-8 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-6"><p>La présente divulgation concerne des analogues hétéroaryles contenant de l'azote, des méthodes de fabrication d'analogues contenant de l'azote et des méthodes de traitement des troubles associés à l'activité de la kinase PINK1, y compris, mais sans s'y limiter, les maladies neurodégénératives, les maladies mitochondriales, la fibrose et/ou la cardiomyopathie, à l'aide de ces analogues. Cet abrégé est destiné à servir d'outil de recherche dans l'art particulier et n'est pas censé être limitatif de la présente invention.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-9 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-5 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://patentscope.wipo.int/search/fr/detail.jsf?docId=WO2020206363"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Lire l'article complet</span></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/mitokinin-inc-usa-preparation-of-purinamines-and-pyrrolopyrimidinamines-compositions-and-methods-of-using-the-same-for-treatment-of-neurodegenerative-and-mitochondrial-disease/">Mitokinin, Inc., USA .; Preparation of purinamines and pyrrolopyrimidinamines, compositions and methods of using the same for treatment of neurodegenerative and mitochondrial disease</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
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					<wfw:commentrss>https://www.x-chemrx.com/fr/projects/mitokinin-inc-usa-preparation-of-purinamines-and-pyrrolopyrimidinamines-compositions-and-methods-of-using-the-same-for-treatment-of-neurodegenerative-and-mitochondrial-disease/feed/</wfw:commentrss>
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		<title>Fulcrum Therapeutics, Inc., USA .; Macrocyclic azolopyridine derivatives as EED and PRC2 modulators and their preparation</title>
		<link>https://www.x-chemrx.com/fr/projects/fulcrum-therapeutics-inc-usa-macrocyclic-azolopyridine-derivatives-as-eed-and-prc2-modulators-and-their-preparation/</link>
					<comments>https://www.x-chemrx.com/fr/projects/fulcrum-therapeutics-inc-usa-macrocyclic-azolopyridine-derivatives-as-eed-and-prc2-modulators-and-their-preparation/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Fri, 13 Mar 2020 16:18:17 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3752</guid>

					<description><![CDATA[<p>The invention relates to modulators of Embryonic Ectoderm Development (EED) and/or Polycomb Repressive Complex 2 (PRC2) useful in the treatment of disorders and diseases associated with EEC and PRC2, being macrocyclic azolopyridine derivatives and compositions thereof of Formula (I), or a pharmaceutically acceptable salt, prodrug, solvate, hydrate, enantiomer, isomer, or tautomer thereof, wherein X1,  [...]</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/fulcrum-therapeutics-inc-usa-macrocyclic-azolopyridine-derivatives-as-eed-and-prc2-modulators-and-their-preparation/">Fulcrum Therapeutics, Inc., USA .; Macrocyclic azolopyridine derivatives as EED and PRC2 modulators and their preparation</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-6 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-10 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-7"><p>L'invention concerne des modulateurs du développement de l'ectoderme embryonnaire (EED) et/ou du complexe répressif de Polycomb 2 (PRC2) utiles dans le traitement de troubles et de maladies associés à l'EED et au PRC2, à savoir des dérivés azolopyridiniques macrocycliques et leurs compositions de formule (I), ou un sel, un promédicament, un solvate, un hydrate, un énantiomère, un isomère ou un tautomère pharmaceutiquement acceptable de ceux-ci, dans lesquels X<sub>1</sub>, X<sub>2</sub>, X<sub>3</sub>, A<sub>1</sub>, A<sub>2</sub>, Y, R<sub>1</sub>, R<sub>2</sub>, R<sub>3</sub>, et R<sub>4</sub> sont tels que décrits dans le présent document.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-11 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-6 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://patentscope.wipo.int/search/fr/detail.jsf?docId=WO2020190754"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Lire l'article complet</span></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/fulcrum-therapeutics-inc-usa-macrocyclic-azolopyridine-derivatives-as-eed-and-prc2-modulators-and-their-preparation/">Fulcrum Therapeutics, Inc., USA .; Macrocyclic azolopyridine derivatives as EED and PRC2 modulators and their preparation</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
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					<wfw:commentrss>https://www.x-chemrx.com/fr/projects/fulcrum-therapeutics-inc-usa-macrocyclic-azolopyridine-derivatives-as-eed-and-prc2-modulators-and-their-preparation/feed/</wfw:commentrss>
			<slash:comments>0</slash:comments>
		
		
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		<title>Achaogen, Inc., USA .; Modular synthesis of aminoglycosides as antibacterial agents</title>
		<link>https://www.x-chemrx.com/fr/projects/achaogen-inc-usa-modular-synthesis-of-aminoglycosides-as-antibacterial-agents/</link>
					<comments>https://www.x-chemrx.com/fr/projects/achaogen-inc-usa-modular-synthesis-of-aminoglycosides-as-antibacterial-agents/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Thu, 10 Oct 2019 16:18:48 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3754</guid>

					<description><![CDATA[<p>The present disclosure relates to novel methods for preparing antibacterial aminoglycoside compounds and the compounds used in such preparations.  Read Full Article</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/achaogen-inc-usa-modular-synthesis-of-aminoglycosides-as-antibacterial-agents/">Achaogen, Inc., USA .; Modular synthesis of aminoglycosides as antibacterial agents</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-7 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-12 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-8"><p>La présente divulgation concerne de nouvelles méthodes de préparation de composés aminoglycosides antibactériens et les composés utilisés dans ces préparations.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-13 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-7 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://patents.google.com/patent/WO2019194858A1/fr"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Lire l'article complet</span></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/achaogen-inc-usa-modular-synthesis-of-aminoglycosides-as-antibacterial-agents/">Achaogen, Inc., USA .; Modular synthesis of aminoglycosides as antibacterial agents</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></content:encoded>
					
					<wfw:commentrss>https://www.x-chemrx.com/fr/projects/achaogen-inc-usa-modular-synthesis-of-aminoglycosides-as-antibacterial-agents/feed/</wfw:commentrss>
			<slash:comments>0</slash:comments>
		
		
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		<title>Medimmune Limited, UK .; Cyclohexenone derivatives as small molecule modulators of the BTB domain of KEAP1 and their preparation, pharmaceutical compositions and use in the treatment of diseases</title>
		<link>https://www.x-chemrx.com/fr/projects/medimmune-limited-uk-cyclohexenone-derivatives-as-small-molecule-modulators-of-the-btb-domain-of-keap1-and-their-preparation-pharmaceutical-compositions-and-use-in-the-treatment-of-diseases/</link>
					<comments>https://www.x-chemrx.com/fr/projects/medimmune-limited-uk-cyclohexenone-derivatives-as-small-molecule-modulators-of-the-btb-domain-of-keap1-and-their-preparation-pharmaceutical-compositions-and-use-in-the-treatment-of-diseases/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Thu, 27 Jun 2019 16:20:01 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3756</guid>

					<description><![CDATA[<p>The present application relates to compounds of formula (I’) or formula (I), such as formula (Ia), and their pharmaceutical compositions/preparations. This application further relates to methods of treating or preventing neurodegenerative disorders, such as Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington disease (HD) and other CAG-triplet repeat (or polyglutamine) diseases, amyotrophic lateral sclerosis (ALS;  [...]</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/medimmune-limited-uk-cyclohexenone-derivatives-as-small-molecule-modulators-of-the-btb-domain-of-keap1-and-their-preparation-pharmaceutical-compositions-and-use-in-the-treatment-of-diseases/">Medimmune Limited, UK .; Cyclohexenone derivatives as small molecule modulators of the BTB domain of KEAP1 and their preparation, pharmaceutical compositions and use in the treatment of diseases</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-8 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-14 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-9"><p>La présente demande concerne des composés de la formule (I’) ou de la formule (I), tels que la formule (Ia), et leurs compositions/préparations pharmaceutiques. La présente demande concerne également des méthodes de traitement ou de prévention des troubles neurodégénératifs, tels que la maladie d'Alzheimer (MA), la maladie de Parkinson (MP), la maladie de Huntington (MH) et d'autres maladies à répétition de triplets CAG (ou polyglutamine), la sclérose latérale amyotrophique (SLA ; Lou Gehrig), la maladie diffuse à corps de Lewy, la chorée-acanthocytose, la sclérose latérale primaire, la sclérose en plaques (SEP), la démence frontotemporale, l'ataxie de Friedreich, les traumatismes crâniens aigus et l'épilepsie (répression de l'activation de la microglie).</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-15 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-8 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://patents.google.com/patent/WO2019122265A1/fr"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Lire l'article complet</span></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/medimmune-limited-uk-cyclohexenone-derivatives-as-small-molecule-modulators-of-the-btb-domain-of-keap1-and-their-preparation-pharmaceutical-compositions-and-use-in-the-treatment-of-diseases/">Medimmune Limited, UK .; Cyclohexenone derivatives as small molecule modulators of the BTB domain of KEAP1 and their preparation, pharmaceutical compositions and use in the treatment of diseases</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></content:encoded>
					
					<wfw:commentrss>https://www.x-chemrx.com/fr/projects/medimmune-limited-uk-cyclohexenone-derivatives-as-small-molecule-modulators-of-the-btb-domain-of-keap1-and-their-preparation-pharmaceutical-compositions-and-use-in-the-treatment-of-diseases/feed/</wfw:commentrss>
			<slash:comments>0</slash:comments>
		
		
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		<title>Geneyus LLC, USA .; Preparation of substituted quinolines as Rac inhibitors useful for treating cancer</title>
		<link>https://www.x-chemrx.com/fr/projects/geneyus-llc-usa-preparation-of-substituted-quinolines-as-rac-inhibitors-useful-for-treating-cancer/</link>
					<comments>https://www.x-chemrx.com/fr/projects/geneyus-llc-usa-preparation-of-substituted-quinolines-as-rac-inhibitors-useful-for-treating-cancer/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Thu, 07 Mar 2019 17:22:07 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3760</guid>

					<description><![CDATA[<p>The present invention relates to compounds that act as pan-Rac inhibitors, compositions including the compounds, and methods of using the compounds. In particular, the compounds are useful for treating certain cancers such as breast cancer.  Read Full Article</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/geneyus-llc-usa-preparation-of-substituted-quinolines-as-rac-inhibitors-useful-for-treating-cancer/">Geneyus LLC, USA .; Preparation of substituted quinolines as Rac inhibitors useful for treating cancer</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-9 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-16 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-10"><p>La présente invention concerne des composés qui agissent en tant qu'inhibiteurs pan-Rac, des compositions comprenant les composés et des méthodes d'utilisation des composés. En particulier, les composés sont utiles pour traiter certains cancers tels que le cancer du sein.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-17 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-9 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://patents.google.com/patent/WO2019023315A2/fr"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Lire l'article complet</span></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/geneyus-llc-usa-preparation-of-substituted-quinolines-as-rac-inhibitors-useful-for-treating-cancer/">Geneyus LLC, USA .; Preparation of substituted quinolines as Rac inhibitors useful for treating cancer</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
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		<title>AstraZeneca AB, Swed. .; Preparation of substituted imidazole and triazole compounds as inhibitors of protease-activated receptor-2</title>
		<link>https://www.x-chemrx.com/fr/projects/astrazeneca-ab-swed-preparation-of-substituted-imidazole-and-triazole-compounds-as-inhibitors-of-protease-activated-receptor-2/</link>
					<comments>https://www.x-chemrx.com/fr/projects/astrazeneca-ab-swed-preparation-of-substituted-imidazole-and-triazole-compounds-as-inhibitors-of-protease-activated-receptor-2/#respond</comments>
		
		<dc:creator><![CDATA[AdminGG]]></dc:creator>
		<pubdate>Sat, 11 Nov 2017 17:23:55 +0000</pubdate>
				<guid ispermalink="false">https://ggdev9.com/?post_type=avada_portfolio&#038;p=3766</guid>

					<description><![CDATA[<p>The present application relates to certain substituted imidazole and triazole compounds, pharmaceutical compositions containing them, and methods of using them, including methods for treating pain, musculoskeletal inflammation, neuroinflammatory disorders, airway inflammation, itch, dermatitis, colitis and related conditions. The compounds are of Formula (I) where X is N or CH, Z and Y are N  [...]</p>
<p>The post <a href="https://www.x-chemrx.com/fr/projects/astrazeneca-ab-swed-preparation-of-substituted-imidazole-and-triazole-compounds-as-inhibitors-of-protease-activated-receptor-2/">AstraZeneca AB, Swed. .; Preparation of substituted imidazole and triazole compounds as inhibitors of protease-activated receptor-2</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
]]></description>
										<content:encoded><![CDATA[<div class="fusion-fullwidth fullwidth-box fusion-builder-row-10 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling" style="--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;" ><div class="fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap" style="max-width:1248px;margin-left: calc(-4% / 2 );margin-right: calc(-4% / 2 );"><div class="fusion-layout-column fusion_builder_column fusion-builder-column-18 fusion_builder_column_2_3 2_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:66.666666666667%;--awb-spacing-right-large:2.88%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:2.88%;--awb-width-medium:66.666666666667%;--awb-order-medium:0;--awb-spacing-right-medium:2.88%;--awb-spacing-left-medium:2.88%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div class="fusion-text fusion-text-11"><p>La présente demande concerne certains composés imidazoles et triazoles substitués, des compositions pharmaceutiques les contenant et des méthodes pour les utiliser, y compris des méthodes pour traiter la douleur, l'inflammation musculo-squelettique, les troubles neuro-inflammatoires, l'inflammation des voies respiratoires, les démangeaisons, la dermatite, la colite et des conditions connexes. Les composés sont de formule (I) où X est N ou CH, Z et Y sont N ou C (mais pas N tous les deux) et R<sup>1</sup>-R<sup>3</sup> sont définis dans le présent document.</p>
</div></div></div><div class="fusion-layout-column fusion_builder_column fusion-builder-column-19 fusion_builder_column_1_3 1_3 fusion-flex-column" style="--awb-bg-size:cover;--awb-width-large:33.333333333333%;--awb-spacing-right-large:5.76%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:5.76%;--awb-width-medium:33.333333333333%;--awb-order-medium:0;--awb-spacing-right-medium:5.76%;--awb-spacing-left-medium:5.76%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;"><div class="fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column"><div ><a class="fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-10 fusion-button-span-yes fusion-button-default-type" target="_blank" rel="noopener noreferrer" href="https://patents.google.com/patent/WO2017194716A1/fr"><i class="fa-file-alt fas awb-button__icon awb-button__icon--default button-icon-left" aria-hidden="true"></i><span class="fusion-button-text awb-button__text awb-button__text--default">Lire l'article complet</span></a></div></div></div></div></div><p>The post <a href="https://www.x-chemrx.com/fr/projects/astrazeneca-ab-swed-preparation-of-substituted-imidazole-and-triazole-compounds-as-inhibitors-of-protease-activated-receptor-2/">AstraZeneca AB, Swed. .; Preparation of substituted imidazole and triazole compounds as inhibitors of protease-activated receptor-2</a> appeared first on <a href="https://www.x-chemrx.com/fr">X-Chem</a>.</p>
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