PL1776377T3 - Nowy steroid, agonista FXR - Google Patents

Nowy steroid, agonista FXR

Info

Publication number
PL1776377T3
PL1776377T3 PL05715596T PL05715596T PL1776377T3 PL 1776377 T3 PL1776377 T3 PL 1776377T3 PL 05715596 T PL05715596 T PL 05715596T PL 05715596 T PL05715596 T PL 05715596T PL 1776377 T3 PL1776377 T3 PL 1776377T3
Authority
PL
Poland
Prior art keywords
fxr
novel steroid
steroid agonist
agonist
novel
Prior art date
Application number
PL05715596T
Other languages
English (en)
Inventor
Roberto Pellicciari
Original Assignee
Intercept Pharmaceuticals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Intercept Pharmaceuticals Inc filed Critical Intercept Pharmaceuticals Inc
Publication of PL1776377T3 publication Critical patent/PL1776377T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J9/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
    • C07J9/005Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane containing a carboxylic function directly attached or attached by a chain containing only carbon atoms to the cyclopenta[a]hydrophenanthrene skeleton
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Steroid Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
PL05715596T 2004-02-26 2005-02-28 Nowy steroid, agonista FXR PL1776377T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04004408A EP1568706A1 (en) 2004-02-26 2004-02-26 Novel steroid agonist for FXR
EP05715596A EP1776377B1 (en) 2004-02-26 2005-02-28 Novel steroid agonist for fxr
PCT/EP2005/002086 WO2005082925A2 (en) 2004-02-26 2005-02-28 Novel steroid agonist for fxr

Publications (1)

Publication Number Publication Date
PL1776377T3 true PL1776377T3 (pl) 2009-02-27

Family

ID=34745911

Family Applications (1)

Application Number Title Priority Date Filing Date
PL05715596T PL1776377T3 (pl) 2004-02-26 2005-02-28 Nowy steroid, agonista FXR

Country Status (11)

Country Link
US (1) US7812011B2 (pl)
EP (2) EP1568706A1 (pl)
AT (1) ATE402945T1 (pl)
CY (1) CY1108455T1 (pl)
DE (1) DE602005008611D1 (pl)
DK (1) DK1776377T3 (pl)
ES (1) ES2313305T3 (pl)
PL (1) PL1776377T3 (pl)
PT (1) PT1776377E (pl)
SI (1) SI1776377T1 (pl)
WO (1) WO2005082925A2 (pl)

Families Citing this family (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2248581T3 (es) 2001-03-12 2006-03-16 Intercept Pharmaceuticals, Inc. Esteroides como agonistas de fxr.
US10987362B2 (en) 2004-03-12 2021-04-27 Intercept Pharmaceuticals, Inc. Treatment of fibrosis using FXR ligands
US9498484B2 (en) 2004-03-12 2016-11-22 Intercept Pharmaceuticals, Inc. Treatment of fibrosis using FXR ligands
ITMI20050912A1 (it) * 2005-05-19 2006-11-20 Erregierre Spa Processo di preparazione di acidi 3-a-ya(b)-diidrossi-6-a(b)-alchil-5b-colanici
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
EP1886685A1 (en) 2006-08-11 2008-02-13 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods, uses and compositions for modulating replication of hcv through the farnesoid x receptor (fxr) activation or inhibition
WO2008091540A2 (en) 2007-01-19 2008-07-31 Intercept Pharmaceuticals, Inc. 23-substituted bile acids as tgr5 modulators and methods of use thereof
US8338628B2 (en) * 2007-08-28 2012-12-25 City Of Hope Method of synthesizing alkylated bile acid derivatives
US8796249B2 (en) 2008-07-30 2014-08-05 Intercept Pharmaceuticals, Inc. TGR5 modulators and methods of use thereof
KR101667436B1 (ko) 2008-11-19 2016-10-18 인터셉트 파마슈티컬즈, 인크. Tgr5 조절제 및 그의 사용 방법
WO2010069604A1 (en) 2008-12-19 2010-06-24 Royal College Of Surgeons In Ireland Treatment of diarrhoea
EP2255813A1 (en) * 2009-05-29 2010-12-01 The Royal College of Surgeons in Ireland Derivatives of ursodeoxycholic acid for the treatment of diarrhoea
US8258485B2 (en) * 2010-08-30 2012-09-04 Media Lario Srl Source-collector module with GIC mirror and xenon liquid EUV LPP target system
US9982008B2 (en) 2012-06-19 2018-05-29 Intercept Pharmaceuticals, Inc. Preparation and uses of obeticholic acid
EA032347B1 (ru) * 2012-06-19 2019-05-31 Интерсепт Фармасьютикалз, Инк. Получение, применение и твердые формы обетихолевой кислоты
AU2013334122B2 (en) * 2012-10-26 2017-11-02 Intercept Pharmaceuticals, Inc. Process for preparing bile acid derivatives
JP6326131B2 (ja) * 2013-05-14 2018-05-16 インターセプト ファーマシューティカルズ, インコーポレイテッド ファルネソイドx受容体調節物質としての、胆汁酸の11−ヒドロキシル誘導体およびそのアミノ酸抱合体
MX2015017035A (es) 2013-06-13 2016-04-25 Fast Forward Pharmaceuticals B V Inhibidor de la señalizacion de cd40 y un compuesto adicional, en donde el compuesto adicional es un acido labil, un derivado de acido labil, un agonista del receptor tgr5, un agonista del fxr o una combinacion de los mismos, para el tratamiento de inflamacion cronica, y la prevencion de cancer gastrointestinal o fibrosis.
AU2014320463B2 (en) 2013-09-11 2018-08-02 Centre National De La Recherche Scientifique (Cnrs) Methods and pharmaceutical compositions for the treatment of hepatitis B virus infection
CN107075515B (zh) 2013-11-22 2020-10-30 米纳治疗有限公司 C/EBPα组合物和使用方法
MX2020004024A (es) 2014-05-29 2021-12-10 Bar Pharmaceuticals S R L Derivados del colano para uso en el tratamiento y/o prevencion de enfermedades en las que intervienen el fxr y el tgr5/gpbar1.
RU2017118569A (ru) 2014-11-06 2018-12-06 Энанта Фармасьютикалс, Инк. Аналоги желчных кислот как агонисты fxr/tgr5 и способы их применения
TWI686401B (zh) * 2014-11-19 2020-03-01 英商Nzp英國有限公司 化合物(三)
DK3221332T3 (da) 2014-11-19 2019-07-29 Nzp Uk Ltd Fremstilling af steroide fxr-modulatorer
CA2968309A1 (en) 2014-11-19 2016-05-26 NZP UK Limited 6-alkyl-7-hydroxy-4-en-3-one steroids as intermediates for the production of steroidal fxr modulators
MX2017006567A (es) 2014-11-19 2018-01-26 Nzp Uk Ltd Esteroides 6.alfa.-alquil-6,7-diona como intermedios para la produccion de moduladores esteroides del receptor x farnesoide (fxr).
BR112017010893A2 (pt) 2014-11-26 2018-02-06 Enanta Pharm Inc análogos de ácidos biliares como agonistas de fxr/tgr5 e métodos de uso dos mesmos
US10208081B2 (en) 2014-11-26 2019-02-19 Enanta Pharmaceuticals, Inc. Bile acid derivatives as FXR/TGR5 agonists and methods of use thereof
WO2016086115A1 (en) 2014-11-26 2016-06-02 Enanta Pharmaceuticals, Inc. Tetrazole derivatives of bile acids as fxr/tgr5 agonists and methods of use thereof
KR20170115071A (ko) 2015-02-06 2017-10-16 인터셉트 파마슈티컬즈, 인크. 병용 요법을 위한 약제학적 조성물
BR112017017238A2 (pt) 2015-02-11 2018-04-10 Enanta Pharm Inc análogos de ácidos biliares como agonistas de fxr/tgr5 e métodos de uso dos mesmos
CN105985396A (zh) * 2015-02-16 2016-10-05 苏州泽璟生物制药有限公司 氘代鹅去氧胆酸衍生物以及包含该化合物的药物组合物
RS62110B1 (sr) 2015-03-31 2021-08-31 Enanta Pharm Inc Derivati žučnih kiselina kao agonisti fxr/tgr5 i postupci njihove upotrebe
EA036757B1 (ru) 2015-04-07 2020-12-17 Интерсепт Фармасьютикалз, Инк. Фармацевтические композиции для комбинированной терапии
CN105777836A (zh) * 2015-04-09 2016-07-20 厦门蔚扬药业有限公司 奥贝胆酸的多晶型物及其制备方法
WO2016173524A1 (zh) * 2015-04-29 2016-11-03 正大天晴药业集团股份有限公司 鹅去氧胆酸衍生物
EP3124080A1 (en) 2015-07-28 2017-02-01 Merz Pharma GmbH & Co. KGaA Semisynthetic bile acids for injection lipolysis
CN105175473B (zh) * 2015-08-19 2018-12-21 丽珠医药集团股份有限公司 一种奥贝胆酸晶型i及其制备方法、药物组合物和用途
CN106632564B (zh) * 2015-10-30 2021-04-13 苏州泽璟生物制药股份有限公司 奥贝胆酸盐及其无定形物和药物组合物
CN106749466B (zh) * 2015-11-23 2019-05-21 南京济群医药科技股份有限公司 一种高纯度奥贝胆酸的制备方法
CN105315320B (zh) * 2015-11-30 2017-03-08 山东省药学科学院 一种制备奥贝胆酸的方法
CN106810587A (zh) * 2015-12-01 2017-06-09 中美华世通生物医药科技(武汉)有限公司 制备无定型奥贝胆酸的方法
CN106810586A (zh) * 2015-12-01 2017-06-09 中美华世通生物医药科技(武汉)有限公司 奥贝胆酸晶型ⅱ及其制备方法和用途
EP3409684B1 (en) * 2016-01-28 2024-01-03 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Steroid derivative fxr agonist
US20170233431A1 (en) 2016-02-17 2017-08-17 City Of Hope Bile acid derivatives and methods for synthesis and use
WO2017147159A1 (en) 2016-02-23 2017-08-31 Enanta Pharmaceuticals, Inc. Deuterated bile acid derivatives as fxr/tgr5 agonists and methods of use thereof
US10323061B2 (en) 2016-02-23 2019-06-18 Enanta Pharmaceuticals, Inc. Heteroaryl containing bile acid analogs as FXR/TGR5 agonists and methods of use thereof
WO2017147137A1 (en) 2016-02-23 2017-08-31 Enanta Pharmaceuticals, Inc. Benzoic acid derivatives of bile acid as fxr/tgr5 agonists and methods of use thereof
TWI740922B (zh) * 2016-03-31 2021-10-01 大陸商江蘇恆瑞醫藥股份有限公司 一種奧貝膽酸的新結晶形式及其製備方法
TW201738254A (zh) * 2016-04-19 2017-11-01 英特賽普醫藥品公司 奧貝膽酸及其衍生物之製備方法
GB201608776D0 (en) 2016-05-18 2016-06-29 Dextra Lab Ltd Methods and compounds
GB201608777D0 (en) 2016-05-18 2016-06-29 Dextra Lab Ltd Compounds
EA038580B9 (ru) * 2016-05-18 2021-10-05 Чиа Тай Тяньцин Фармасьютикал Груп Ко., Лтд. Агонист fxr, представляющий собой производное стероидов
WO2017207648A1 (en) 2016-05-31 2017-12-07 Bionice, S.L.U Process and intermediates for the preparation of obeticholic acid and derivatives thereof
WO2018010651A1 (zh) * 2016-07-13 2018-01-18 江苏恒瑞医药股份有限公司 一种奥贝胆酸及其中间体的制备方法
AU2017368069B2 (en) 2016-11-29 2021-07-08 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
WO2018153933A1 (en) 2017-02-21 2018-08-30 Genfit Combination of a ppar agonist with a fxr agonist
JP2020514337A (ja) * 2017-03-08 2020-05-21 インターセプト ファーマシューティカルズ, インコーポレイテッド オベチコール酸の結晶形態
CN110944635A (zh) 2017-03-30 2020-03-31 国家医疗保健研究所 用于减少附加体病毒的持久性和表达的方法和药物组合物
BR112019020780A2 (pt) 2017-04-07 2020-04-28 Enanta Pharm Inc processo para preparação de derivados de ácido biliar de carbamato de sulfonila
KR20200010483A (ko) 2017-05-26 2020-01-30 메드샤인 디스커버리 아이엔씨. Fxr 수용체 작용제로서 락탐 화합물
CN109021056B (zh) * 2017-06-09 2021-03-09 博瑞生物医药(苏州)股份有限公司 法尼酯x受体激动剂
EP3679138B1 (en) 2017-09-08 2023-03-22 MiNA Therapeutics Limited Hnf4a sarna compositions and methods of use
GB201812382D0 (en) 2018-07-30 2018-09-12 Nzp Uk Ltd Compounds
WO2020039449A1 (en) 2018-08-24 2020-02-27 Solara Active Pharma Sciences Limited An improved process for the preparation of obeticholic acid and intermediates used in the process thereof
CA3121020A1 (en) * 2018-11-26 2020-06-04 Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. Solid form, crystalline form, and crystal form a of fxr agonist, and preparation method therefor and application thereof
EA202193334A1 (ru) 2019-05-30 2022-03-14 Интерсепт Фармасьютикалз, Инк. Фармацевтические композиции, содержащие агонист fxr и фибрат, для применения при лечении холестатического заболевания печени
EP3999101A1 (en) 2019-07-18 2022-05-25 ENYO Pharma Method for decreasing adverse-effects of interferon
US20230146782A1 (en) * 2019-08-06 2023-05-11 Du Jessica Xinyun Deoxycholic acid compounds, pharmaceutical compositions and uses thereof
IL293892A (en) 2020-01-15 2022-08-01 Inserm Institut National De La Sant? Et De La Rech M?Dicale Use of fxr agonists to treat hepatitis d virus infection
US20240100125A1 (en) 2021-01-14 2024-03-28 Enyo Pharma Synergistic effect of a fxr agonist and ifn for the treatment of hbv infection
TW202308629A (zh) 2021-04-28 2023-03-01 法商Enyo製藥公司 使用fxr激動劑作為組合治療以增強tlr3激動劑之療效

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1223313B (it) * 1987-10-20 1990-09-19 Gipharmex Spa Derivati di acidi biliari loro preparazione e composizioni farmaceutiche che li contengono
WO2003080803A2 (en) * 2002-03-21 2003-10-02 Smithkline Beecham Corporation Methods of using farnesoid x receptor (fxr) agonists
ITMI20021532A1 (it) 2002-07-12 2004-01-12 Roberto Pellicciari Composti chimici

Also Published As

Publication number Publication date
EP1568706A1 (en) 2005-08-31
DE602005008611D1 (de) 2008-09-11
WO2005082925A2 (en) 2005-09-09
US7812011B2 (en) 2010-10-12
ATE402945T1 (de) 2008-08-15
US20080039435A1 (en) 2008-02-14
DK1776377T3 (da) 2008-11-24
SI1776377T1 (sl) 2009-04-30
CY1108455T1 (el) 2014-04-09
ES2313305T3 (es) 2009-03-01
EP1776377B1 (en) 2008-07-30
WO2005082925A3 (en) 2005-11-24
PT1776377E (pt) 2008-11-11
EP1776377A2 (en) 2007-04-25

Similar Documents

Publication Publication Date Title
SI1776377T1 (sl) Novi steroidni agonist za FXR
BE2017C018I2 (pl)
ZA200700765B (en) Nebivolol and its pharmaceutically acceptable salts, process for preparation and pharmaceutical compositions of nebivolol
HK1119699A1 (en) Pyridopyrimidinone inhibitors of pi3kalpha
ATE388958T1 (de) 4'-c-substituierte 2-haloadenosinderivate
MY141194A (en) Process for the synthesis of ivabradine and its pharmaceutically acceptable acid addition salts
HK1135703A1 (en) Piperidine gpcr agonists
TW200728307A (en) Novel spirochromanone derivatives
TW200833370A (en) Pharmaceutical composition containing low substituted hydroxypropylcellulose
UA96759C2 (en) 2-ARYLINDOLE DERIVATIVES AS mPGES-I INHIBITORS
GEP20084494B (en) New heterocyclic carboxylic acid amide derivatives
WO2004007521A3 (en) Bile acid derivatives as agonists of the farnesoid x receptor
NO20080033L (no) Kinolinderivater som NK3-antagonister
WO2004111008A3 (en) Use of a compound of formula i for making a pharmaceutical composition
WO2006026034A3 (en) Processes for the preparation of isothiazole derivatives
MXPA05006889A (es) Compuestos aromaticos como agentes anti-inflamatorios, inmunomoduladores y anti-proliferativos.
MY136288A (en) New process for the synthesis of perindopril and its pharmaceutically acceptable salts
WO2006109146A3 (en) Novel heterocyclic derivatives
WO2006123229A3 (en) Novel heterocyclic derivatives
UA80905C2 (en) Method for synthesis of perindopril and its pharmaceutically acceptable salts
WO2009019719A3 (en) Process for the preparation of 3-aryloxy-3-arylpropanamines
TW200740442A (en) Therapeutic agent for hypertension
WO2008005955A3 (en) Synthesis of heterocyclic compounds
UA100002C2 (en) Normal;heading 1;heading 2;heading 3;PYRIDOPYRIMIDINONE INHIBITORS OF PI3Kα