Bile acid derivatives as FXR/TGR5 agonists and methods of use thereof

US10968249B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10968249-B2
Application numberUS-202016878329-A
CountryUS
Kind codeB2
Filing dateMay 19, 2020
Priority dateNov 26, 2014
Publication dateApr 6, 2021
Grant dateApr 6, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention provides compounds of Formula I, pharmaceutical compositions comprising these compounds and methods of using these compounds to prevent or treat FXR-mediated or TGR5-mediated diseases or conditions.

First claim

Opening claim text (preview).

What is claimed is: 1. A compound represented by Formula V-A or Formula V-B, or a pharmaceutically acceptable salt thereof: wherein: R 1 is selected from the group consisting of: 1) Halogen; 2) Hydroxyl; 3) Substituted or unsubstituted —C 1 -C 8 alkyl; 4) Substituted or unsubstituted —C 2 -C 8 alkenyl; 5) Substituted or unsubstituted —C 2 -C 8 alkynyl; 6) Substituted or unsubstituted —C 3 -C 8 cycloalkyl; 7) Substituted or unsubstituted aryl; 8) Substituted or unsubstituted arylalkyl; 9) Substituted or unsubstituted heterocycloalkyl; 10) Substituted or unsubstituted heteroaryl; 11) Substituted or unsubstituted heteroarylalkyl; and 12) —NR 10 R 11 ; m is selected from 0, 1, 2 and 3; and R 10 and R 11 are each independently selected from hydrogen, substituted or unsubstituted —C 1 -C 8 alkyl, substituted or unsubstituted —C 2 -C 8 alkenyl, Substituted or unsubstituted —C 2 -C 8 alkynyl, substituted or unsubstituted —C 3 -C 8 cycloalkyl, or R 10 and R 11 are taken together with the nitrogen atom to which they are attached to form a heterocyclic ring. 2. The compound of claim 1 , wherein R 1 is C 1 -C 4 -alkyl, halogenated C 1 -C 4 -alkyl, C 1 -C 4 -alkenyl, phenyl-C 1 -C 4 -alkyl, substituted or unsubstituted C 3 -C 6 -cycloalkyl, C 1 -C 6 -cycloalkyl-C 1 -C 4 -alkyl, 5- or 6-membered heterocycloalkyl, amino, substituted or unsubstituted phenyl or halogen. 3. The compound of claim 1 , wherein R 1 is selected from the groups set forth in the table below: 4. The compound of claim 1 , wherein R 1 is ethyl, butyl, t-butyl, propyl, benzyl, vinyl, allyl, CF 3 , or fluoro. 5. The compound of claim 1 , wherein R 1 is dimethylamino or p-tert-butylphenyl. 6. The compound of claim 1 , selected from the compounds set forth in the table below, or a pharmaceutically acceptable salt thereof: 7. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier. 8. A method for ameliorating a disease or condition selected from the group consisting of primary biliary cirrhosis, cerebrotendinous xanthomatosis, primary sclerosing cholangitis, alcoholic liver disease, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, atherosclerosis, hypercholesterolemia, hypertriglyceridemia, Type II diabetes, and hepatocellular carcinoma in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound according to claim 1 . 9. The method according to claim 8 , wherein the disease or condition is primary biliary cirrhosis, nonalcoholic fatty liver disease, or nonalcoholic steatohepatitis. 10. A method for ameliorating nonalcoholic steatohepatitis in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of claim 6 . 11. A method for ameliorating nonalcoholic fatty liver disease in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of claim 6 . 12. A method for ameliorating primary biliary cirrhosis in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of claim 6 .

Assignees

Inventors

Classifications

  • Normal steroids with unmodified cyclopenta(a)hydrophenanthrene skeleton not provided for in groups C07J1/00 - C07J43/00 · CPC title

  • spiro-condensed · CPC title

  • not condensed · CPC title

  • containing nitrile radicals, including thiocyanide radicals · CPC title

  • containing unsubstituted amino radicals · CPC title

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Frequently asked questions

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What does patent US10968249B2 cover?
The present invention provides compounds of Formula I, pharmaceutical compositions comprising these compounds and methods of using these compounds to prevent or treat FXR-mediated or TGR5-mediated diseases or conditions.
Who is the assignee on this patent?
Enanta Pharm Inc
What technology area does this patent fall under?
Primary CPC classification C07J41/0066. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 06 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).