JP2016527277A5 - - Google Patents
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- JP2016527277A5 JP2016527277A5 JP2016531936A JP2016531936A JP2016527277A5 JP 2016527277 A5 JP2016527277 A5 JP 2016527277A5 JP 2016531936 A JP2016531936 A JP 2016531936A JP 2016531936 A JP2016531936 A JP 2016531936A JP 2016527277 A5 JP2016527277 A5 JP 2016527277A5
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- JP
- Japan
- Prior art keywords
- compound
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- Prior art date
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- 150000001875 compounds Chemical class 0.000 claims 54
- 229910052739 hydrogen Inorganic materials 0.000 claims 31
- 239000001257 hydrogen Substances 0.000 claims 31
- 150000002431 hydrogen Chemical class 0.000 claims 25
- 125000000217 alkyl group Chemical group 0.000 claims 17
- 150000003839 salts Chemical class 0.000 claims 10
- 239000011780 sodium chloride Substances 0.000 claims 10
- 125000001475 halogen functional group Chemical group 0.000 claims 9
- XOAAWQZATWQOTB-UHFFFAOYSA-N Taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 claims 8
- DHMQDGOQFOQNFH-UHFFFAOYSA-N glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 8
- 229910052760 oxygen Inorganic materials 0.000 claims 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- -1 methyl aspartate Chemical compound 0.000 claims 6
- 229910052717 sulfur Inorganic materials 0.000 claims 6
- 239000004471 Glycine Substances 0.000 claims 4
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims 4
- 229960003080 Taurine Drugs 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- UCMIRNVEIXFBKS-UHFFFAOYSA-N β-Alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- YIQPUJZXAGQSKG-VKHMYHEASA-N (2R)-2-amino-2-chloropropanoic acid Chemical compound C[C@@](N)(Cl)C(O)=O YIQPUJZXAGQSKG-VKHMYHEASA-N 0.000 claims 2
- YARNOIDQQUOOES-VKHMYHEASA-N (2R)-2-amino-2-fluoropropanoic acid Chemical compound C[C@@](N)(F)C(O)=O YARNOIDQQUOOES-VKHMYHEASA-N 0.000 claims 2
- MVMQEZPNWYPJIX-VKHMYHEASA-N (2R)-2-amino-2-iodopropanoic acid Chemical compound C[C@@](N)(I)C(O)=O MVMQEZPNWYPJIX-VKHMYHEASA-N 0.000 claims 2
- ORQLXCMGAMWKMJ-REOHCLBHSA-N (2R)-2-amino-3-bromopropanoic acid Chemical compound BrC[C@H](N)C(O)=O ORQLXCMGAMWKMJ-REOHCLBHSA-N 0.000 claims 2
- DIZAJUVUZKMLQL-REOHCLBHSA-N (2R)-2-amino-3-iodopropanoic acid Chemical compound IC[C@H](N)C(O)=O DIZAJUVUZKMLQL-REOHCLBHSA-N 0.000 claims 2
- CWLQUGTUXBXTLF-YFKPBYRVSA-N (2S)-1-methylpyrrolidine-2-carboxylic acid Chemical compound CN1CCC[C@H]1C(O)=O CWLQUGTUXBXTLF-YFKPBYRVSA-N 0.000 claims 2
- PEMUHKUIQHFMTH-QMMMGPOBSA-N (2S)-2-amino-3-(4-bromophenyl)propanoic acid Chemical compound OC(=O)[C@@H](N)CC1=CC=C(Br)C=C1 PEMUHKUIQHFMTH-QMMMGPOBSA-N 0.000 claims 2
- ASBJGPTTYPEMLP-UHFFFAOYSA-N 2-azaniumyl-3-chloropropanoate Chemical compound ClCC(N)C(O)=O ASBJGPTTYPEMLP-UHFFFAOYSA-N 0.000 claims 2
- NIGWMJHCCYYCSF-UHFFFAOYSA-N 4-Chloro-3-phenyl-L-alanine Chemical compound OC(=O)C(N)CC1=CC=C(Cl)C=C1 NIGWMJHCCYYCSF-UHFFFAOYSA-N 0.000 claims 2
- XWHHYOYVRVGJJY-QMMMGPOBSA-N 4-fluorophenyl-L-alanine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(F)C=C1 XWHHYOYVRVGJJY-QMMMGPOBSA-N 0.000 claims 2
- 229940009098 Aspartate Drugs 0.000 claims 2
- 229960005261 Aspartic Acid Drugs 0.000 claims 2
- QIVBCDIJIAJPQS-SECBINFHSA-N D-tryptophane Chemical compound C1=CC=C2C(C[C@@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-SECBINFHSA-N 0.000 claims 2
- 229960002989 Glutamic Acid Drugs 0.000 claims 2
- 229960000310 ISOLEUCINE Drugs 0.000 claims 2
- PZNQZSRPDOEBMS-QMMMGPOBSA-N Iodo-Phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(I)C=C1 PZNQZSRPDOEBMS-QMMMGPOBSA-N 0.000 claims 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims 2
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 2
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 2
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims 2
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 claims 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 2
- 241000124008 Mammalia Species 0.000 claims 2
- XLBVNMSMFQMKEY-BYPYZUCNSA-N N-Methyl-L-glutamic acid Chemical compound CN[C@H](C(O)=O)CCC(O)=O XLBVNMSMFQMKEY-BYPYZUCNSA-N 0.000 claims 2
- 229960005190 Phenylalanine Drugs 0.000 claims 2
- 235000004279 alanine Nutrition 0.000 claims 2
- 235000003704 aspartic acid Nutrition 0.000 claims 2
- 229940000635 beta-Alanine Drugs 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- 235000013922 glutamic acid Nutrition 0.000 claims 2
- 239000004220 glutamic acid Substances 0.000 claims 2
- 239000003638 reducing agent Substances 0.000 claims 2
- 229910052711 selenium Inorganic materials 0.000 claims 2
- 230000002194 synthesizing Effects 0.000 claims 2
- 239000004474 valine Substances 0.000 claims 2
- 206010001627 Alcoholic liver disease Diseases 0.000 claims 1
- UFHFLCQGNIYNRP-VVKOMZTBSA-N Dideuterium Chemical compound [2H][2H] UFHFLCQGNIYNRP-VVKOMZTBSA-N 0.000 claims 1
- 206010022489 Insulin resistance Diseases 0.000 claims 1
- 208000008338 Non-alcoholic Fatty Liver Disease Diseases 0.000 claims 1
- 206010053219 Non-alcoholic steatohepatitis Diseases 0.000 claims 1
- 108009000135 Nonalcoholic fatty liver disease Proteins 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- 208000001072 Type 2 Diabetes Mellitus Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361861109P | 2013-08-01 | 2013-08-01 | |
US61/861,109 | 2013-08-01 | ||
US201462004436P | 2014-05-29 | 2014-05-29 | |
US62/004,436 | 2014-05-29 | ||
PCT/US2014/049460 WO2015017813A2 (en) | 2013-08-01 | 2014-08-01 | Inhibitors of the farnesoid x receptor and uses in medicine |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2016527277A JP2016527277A (ja) | 2016-09-08 |
JP2016527277A5 true JP2016527277A5 (US07794700-20100914-C00152.png) | 2017-09-07 |
JP6556129B2 JP6556129B2 (ja) | 2019-08-07 |
Family
ID=51358096
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016531936A Active JP6556129B2 (ja) | 2013-08-01 | 2014-08-01 | ファルネソイドx受容体の阻害剤及び医薬としての使用 |
Country Status (9)
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
SI3626725T1 (sl) * | 2014-05-29 | 2023-04-28 | Bar Pharmaceuticals S.R.L. | Derivati holana za uporabo pri zdravljenju in/ali preprečevanju bolezni, posredovanih s FXR in TGR5/GPBAR1 |
MX2017005935A (es) | 2014-11-06 | 2018-01-11 | Enanta Pharm Inc | Análogos de ácido biliar como agonistas fxr/tgr5 y métodos de uso de los mismos. |
AU2015353473A1 (en) | 2014-11-26 | 2017-06-08 | Enanta Pharmaceuticals, Inc. | Bile acid analogs as FXR/TGR5 agonists and methods of use thereof |
US10208081B2 (en) | 2014-11-26 | 2019-02-19 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as FXR/TGR5 agonists and methods of use thereof |
US11578097B2 (en) | 2014-11-26 | 2023-02-14 | Enanta Pharmaceuticals, Inc. | Tetrazole derivatives of bile acids as FXR/TGR5 agonists and methods of use thereof |
CA2975257A1 (en) | 2015-02-11 | 2016-08-18 | Enanta Pharmaceuticals, Inc. | Bile acid analogs as fxr/tgr5 agonists and methods of use thereof |
CN107427527B (zh) | 2015-03-31 | 2021-01-26 | 英安塔制药有限公司 | 作为fxr/tgr5激动剂的胆汁酸衍生物及其使用方法 |
CN107250150B (zh) * | 2015-04-28 | 2019-11-22 | 江苏豪森药业集团有限公司 | 胆酸衍生物及其制备方法和医药用途 |
US10323060B2 (en) | 2016-02-23 | 2019-06-18 | Enanta Pharmaceuticals, Inc. | Benzoic acid derivatives of bile acid as FXR/TGR5 agonists and methods of use thereof |
PL3730487T3 (pl) | 2016-06-13 | 2022-08-16 | Gilead Sciences, Inc. | Pochodne azetydyny jako modulatory fxr (nr1h4) |
CA2968836A1 (en) | 2016-06-13 | 2017-12-13 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
IT201600068742A1 (it) * | 2016-07-01 | 2018-01-01 | Bar Pharmaceuticals Soc A Responsabilita Limitata | Derivati dell'acido iodesossicolico e loro uso |
CN106237332A (zh) * | 2016-08-11 | 2016-12-21 | 河南大学 | 核受体fxr在肝癌干细胞靶向治疗中的应用 |
WO2018102418A1 (en) | 2016-11-29 | 2018-06-07 | Enanta Pharmaceuticals, Inc. | Process for preparation of sulfonylurea bile acid derivatives |
WO2018152171A1 (en) | 2017-02-14 | 2018-08-23 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as fxr agonists and methods of use thereof |
CN110461328A (zh) | 2017-03-28 | 2019-11-15 | 吉利德科学公司 | 治疗肝疾病的治疗组合 |
CA3058754A1 (en) | 2017-04-07 | 2018-10-11 | Enanta Pharmaceuticals, Inc. | Process for preparation of sulfonyl carbamate bile acid derivatives |
EP3730509A4 (en) * | 2017-12-19 | 2021-09-01 | Xi' An Biocare Pharma | COMPOUND FOR THE TREATMENT OF METABOLIC DISEASES, METHOD OF PREPARATION AND USE |
IT201800005598A1 (it) | 2018-05-22 | 2019-11-22 | Ossadiazoli come antagonisti del recettore fxr | |
PL3911647T3 (pl) | 2019-01-15 | 2024-05-20 | Gilead Sciences, Inc. | Związek izoksazolowy jako agonista fxr oraz zawierające go kompozycje farmaceutyczne |
CN118388474A (zh) | 2019-02-19 | 2024-07-26 | 吉利德科学公司 | Fxr激动剂的固体形式 |
CN112409435B (zh) * | 2019-08-23 | 2023-07-18 | 深圳云合医药科技合伙企业(有限合伙) | 胆汁酸衍生物及其组合物和应用 |
US20220378766A1 (en) * | 2021-05-25 | 2022-12-01 | Louis Habash | Modulating expression level of a gene encoding an uncoupling protein by treating a human subject with a nitroxide |
US20230128120A1 (en) * | 2021-10-21 | 2023-04-27 | University Of Washington | Omega muricholic acid as a pregnane x receptor ligand for treating hepato-intestinal diseases |
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US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
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IT1222395B (it) * | 1987-07-30 | 1990-09-05 | Pierrel Spa | Composizione farmaceutica per somministrazione intranasale comprendente l'ormone ghrh,un agonista colinergico e/o un sale biliare |
IT1219733B (it) | 1988-06-28 | 1990-05-24 | Istituto Chemioterapico Di Lod | Derivato dell' acido ursodesossicolico |
JPH0637392B2 (ja) * | 1988-11-25 | 1994-05-18 | 健二 片桐 | 胆汁うっ滞改善剤 |
IT1229570B (it) | 1989-04-17 | 1991-09-04 | Giuliani Spa | Derivati fluorurati di acidi biliari, loro preparazione e composizioni farmaceutiche che li contengono. |
IT1264131B1 (it) * | 1993-04-16 | 1996-09-16 | D R Drug Research Srl | Derivato dell'acido iodesossicolico |
US6551623B1 (en) * | 1993-09-09 | 2003-04-22 | Lorus Therapeutics Inc. | Immunomodulating compositions from bile |
GB9320597D0 (en) * | 1993-10-06 | 1993-11-24 | Proteus Molecular Design | Improvements in and realting to vaccines |
IT1299270B1 (it) * | 1998-05-15 | 2000-02-29 | Moreno Paolini | Acidi biliari come induttori del sistema citocromo p450-dipendente, in particolare ad attivita' anticolestatica |
EP1140079B1 (en) * | 1998-12-23 | 2009-06-03 | Glaxo Group Limited | Assays for ligands for nuclear receptors |
US20020132223A1 (en) * | 1999-03-26 | 2002-09-19 | City Of Hope | Methods for modulating activity of the FXR nuclear receptor |
EP1392725A1 (en) | 2001-05-24 | 2004-03-03 | SmithKline Beecham Corporation | Nonhuman pregnane x receptor sequences for use in comparative pharmacology |
US7595311B2 (en) | 2002-05-24 | 2009-09-29 | Exelixis, Inc. | Azepinoindole derivatives as pharmaceutical agents |
CN101010078A (zh) | 2004-08-10 | 2007-08-01 | 埃克塞里艾克西斯公司 | 作为药物的杂环化合物 |
AU2007215207A1 (en) * | 2006-02-14 | 2007-08-23 | Intercept Pharmaceuticals, Inc. | Bile acid derivatives as FXR ligands for the prevention or treatment of FXR-mediated diseases or conditions |
WO2008002573A2 (en) * | 2006-06-27 | 2008-01-03 | Intercept Pharmaceuticals, Inc. | Bile acid derivatives as fxr ligands for the prevention or treatment of fxr-mediated deseases or conditions |
CA2723440A1 (en) | 2008-05-05 | 2009-11-12 | Tiltan Pharma Ltd. | Sulfobetaines for therapy |
EA020310B1 (ru) * | 2008-07-30 | 2014-10-30 | Интерсепт Фармасьютикалз, Инк. | Модуляторы рецептора tgr5 и их применение |
CN101891791B (zh) | 2009-05-22 | 2012-10-03 | 中国科学院上海应用物理研究所 | 一种标记胆汁酸衍生物及其参照化合物、制备方法和应用 |
AU2010286253A1 (en) | 2009-08-25 | 2012-04-19 | Victor Ling | Polyhydroxylated bile acids for treatment of biliary disorders |
-
2014
- 2014-08-01 AU AU2014296023A patent/AU2014296023B2/en active Active
- 2014-08-01 CA CA2920017A patent/CA2920017C/en active Active
- 2014-08-01 EP EP14752716.2A patent/EP3027637B1/en active Active
- 2014-08-01 NZ NZ716568A patent/NZ716568A/en unknown
- 2014-08-01 JP JP2016531936A patent/JP6556129B2/ja active Active
- 2014-08-01 CN CN201480054322.2A patent/CN105593237B/zh active Active
- 2014-08-01 CN CN201910393592.0A patent/CN110437297B9/zh active Active
- 2014-08-01 US US14/909,263 patent/US9540415B2/en active Active
- 2014-08-01 WO PCT/US2014/049460 patent/WO2015017813A2/en active Application Filing
- 2014-08-01 BR BR112016002268-8A patent/BR112016002268B1/pt active IP Right Grant
-
2016
- 2016-12-06 US US15/371,032 patent/US10233209B2/en active Active
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