HK1138567A1 - '- '- '- -叔丁基苯基 草氨酰基 丙氨酰基 氨基- '， '， '， '-四氟苯氧基 -氧代戊酸的結晶形式 - Google Patents

'- '- '- -叔丁基苯基 草氨酰基 丙氨酰基 氨基- '， '， '， '-四氟苯氧基 -氧代戊酸的結晶形式

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Publication number
HK1138567A1
HK1138567A1 HK10104322.9A HK10104322A HK1138567A1 HK 1138567 A1 HK1138567 A1 HK 1138567A1 HK 10104322 A HK10104322 A HK 10104322A HK 1138567 A1 HK1138567 A1 HK 1138567A1
Authority
HK
Hong Kong
Prior art keywords
alaniwyl
0x0penta
oxamyl
butylphenyl
tert
Prior art date
Application number
HK10104322.9A
Other languages
English (en)
Inventor
斯圖爾特‧蒂莫克
埃里克‧哈根
詹森‧漢科
Original Assignee
科內圖斯醫藥公司
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 科內圖斯醫藥公司 filed Critical 科內圖斯醫藥公司
Publication of HK1138567A1 publication Critical patent/HK1138567A1/zh

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/70—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/72—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atoms of the carboxamide groups bound to acyclic carbon atoms
    • C07C235/74—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of a saturated carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/52—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pain & Pain Management (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
HK10104322.9A 2006-12-06 2010-05-03 '- '- '- -叔丁基苯基 草氨酰基 丙氨酰基 氨基- '， '， '， '-四氟苯氧基 -氧代戊酸的結晶形式 HK1138567A1 (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US86874806P 2006-12-06 2006-12-06
PCT/IB2007/003900 WO2008068615A1 (en) 2006-12-06 2007-12-03 Crystalline forms of ( 3 s ) -3- [n- (n' - (2-tert-butylphenyl) oxamyl) alaninyl] amino-5- (2 ', 3 ', 5 ', 6 ' -tetrafluoro phenoxy) -4-0x0penta noic acid

Publications (1)

Publication Number Publication Date
HK1138567A1 true HK1138567A1 (zh) 2010-08-27

Family

ID=39205161

Family Applications (3)

Application Number Title Priority Date Filing Date
HK10104322.9A HK1138567A1 (zh) 2006-12-06 2010-05-03 '- '- '- -叔丁基苯基 草氨酰基 丙氨酰基 氨基- '， '， '， '-四氟苯氧基 -氧代戊酸的結晶形式
HK15100168.9A HK1199885A1 (zh) 2006-12-06 2015-01-07 '- '- '- -叔丁基苯基 草氨酰基 丙氨酰基 氨基- '， '， '， '-四氟苯氧基 -氧代戊酸的結晶形式
HK15100810.1A HK1200440A1 (zh) 2006-12-06 2015-01-23 種抑制劑的結晶形式

Family Applications After (2)

Application Number Title Priority Date Filing Date
HK15100168.9A HK1199885A1 (zh) 2006-12-06 2015-01-07 '- '- '- -叔丁基苯基 草氨酰基 丙氨酰基 氨基- '， '， '， '-四氟苯氧基 -氧代戊酸的結晶形式
HK15100810.1A HK1200440A1 (zh) 2006-12-06 2015-01-23 種抑制劑的結晶形式

Country Status (23)

Country Link
US (1) US7692038B2 (zh)
EP (1) EP2091910B1 (zh)
JP (1) JP5495787B2 (zh)
KR (1) KR101125932B1 (zh)
CN (3) CN101573328B (zh)
AR (1) AR064809A1 (zh)
AU (1) AU2007330478B2 (zh)
CA (1) CA2669849C (zh)
CL (1) CL2007003491A1 (zh)
DK (1) DK2091910T3 (zh)
ES (1) ES2524021T3 (zh)
HK (3) HK1138567A1 (zh)
HN (1) HN2007000536A (zh)
IL (1) IL198732A (zh)
MX (1) MX2009006055A (zh)
NO (1) NO338908B1 (zh)
PA (1) PA8759501A1 (zh)
PE (1) PE20081251A1 (zh)
PL (1) PL2091910T3 (zh)
PT (1) PT2091910E (zh)
TW (1) TWI345466B (zh)
UY (1) UY30758A1 (zh)
WO (1) WO2008068615A1 (zh)

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CA3024216C (en) * 2010-02-12 2021-03-30 Pfizer Inc. Salts and polymorphs of 8-fluoro-2-{4-[(methylamino)methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-cd]indol-6-one
CN103113405B (zh) * 2012-10-17 2016-03-02 上海日馨生物科技有限公司 苯磷硫胺多晶型体、制备方法及其应用
KR20220070066A (ko) * 2014-03-14 2022-05-27 아지오스 파마슈티컬스 아이엔씨. 치료적으로 활성인 화합물의 약제학적 조성물
EP3142649B1 (en) 2014-05-12 2019-07-24 Conatus Pharmaceuticals, Inc. Treatment of the complications of chronic liver disease with caspase inhibitor emricasan
LT3191461T (lt) * 2014-09-08 2021-12-10 Pfizer Inc. 6-karboksi-2-(3,5-dichlorfenil)-benzoksazolo kristalinės kietos formos
AU2016211246B2 (en) * 2015-01-30 2020-08-27 Biomed Valley Discoveries, Inc. Crystalline forms of C21H22CI2N4O2
WO2016144830A1 (en) 2015-03-06 2016-09-15 Concert Pharmaceuticals, Inc. Deuterated emricasan
CN105017061B (zh) * 2015-07-07 2017-03-29 苏州富士莱医药股份有限公司 一种恩利卡生的合成方法
WO2017079566A1 (en) 2015-11-05 2017-05-11 Conatus Pharmaceuticals, Inc. Caspase inhibitors for use in the treatment of liver cancer
SG11201805480TA (en) 2015-12-31 2018-07-30 Conatus Pharmaceuticals Inc Methods of using caspase inhibitors in treatment of liver disease
MX2019003889A (es) 2016-10-05 2019-08-12 Novartis Ag Composiciones de combinacion que comprenden agonistas de fxr para tratar o prevenir una enfermedad o trastorno fibrotico o cirrotico.
CA3050832A1 (en) * 2017-01-23 2018-07-26 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Bicyclic compounds as a capase inhibitor
WO2018172950A1 (en) * 2017-03-23 2018-09-27 Novartis Ag Anhydrous crystalline forms of sodium (s)-2-(diphenylacetyl)-1,2,3,4-tetrahydro-6-methoxy-5-(phenylmethoxy)-3-isoquinolinecarboxylate
US11103512B2 (en) * 2017-03-30 2021-08-31 Merck Patent Gmbh Crystalline form of (S)-[2-chloro-4-fluoro-5-(7-morpholin-4-yl-quinazolin-4-yl)phenyl]-(6-methoxy-pyridazin-3-yl)-methanol
AR114251A1 (es) * 2018-02-13 2020-08-12 Syngenta Participations Ag Formas cristalinas de n-[2-(2,4-diclorofenil)ciclobutil]-2-(trifluorometl)piridin-3-carboxamida
US11447497B2 (en) 2018-06-29 2022-09-20 Histogen, Inc. (S)-3-(2-(4-(benzyl)-3-oxopiperazin-1-yl)acetamido)-4-oxo-5-(2,3,5,6-tetrafluorophenoxy)pentanoic acid derivatives and related compounds as caspase inhibitors for treating cardiovascular diseases
CA3132613A1 (en) 2019-03-07 2020-09-10 Conatus Pharmaceuticals Inc. Caspase inhibitors and methods of use thereof
CN111351780A (zh) * 2019-12-29 2020-06-30 中船重工（邯郸）派瑞特种气体有限公司 一种三氟甲基磺酰氟电解槽中电解液成分的分析方法
WO2022123062A1 (en) 2020-12-11 2022-06-16 INSERM (Institut National de la Santé et de la Recherche Médicale) Blocking caspase and/or fasl for preventing fatal outcome in covid-19 patients
KR102670554B1 (ko) 2022-01-04 2024-05-30 주식회사 이노보테라퓨틱스 캐스파제 저해제로서의 신규한 이소인돌리논 유도체 화합물

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Publication number Priority date Publication date Assignee Title
ES2100291T3 (es) * 1991-07-30 1997-06-16 Ajinomoto Kk Cristales de n-(trans-4-isopropilciclohexilcarbonil)-d-fenilalanina y metodos para prepararlos.
DE59307210D1 (de) * 1993-05-12 1997-10-02 Heumann Pharma Gmbh & Co Stabile und kristalline Form von Bezafibrat
US7053056B2 (en) * 1998-07-02 2006-05-30 Idun Pharmaceuticals, Inc. C-terminal modified oxamyl dipeptides as inhibitors of the ICE/ced-3 family of cysteine proteases
US6544951B2 (en) * 1998-07-02 2003-04-08 Idun Pharmaceuticals, Inc. C-terminal modified oxamyl dipeptides as inhibitors of the ICE/ced-3 family of cysteine proteases
US6197750B1 (en) * 1998-07-02 2001-03-06 Idun Pharmaceuticals, Inc. C-terminal modified oxamyl dipeptides as inhibitors of the ICE/ced-3 family of cysteine proteases
GB9923933D0 (en) * 1999-10-08 1999-12-08 Smithkline Beecham Lab Novel pharmaceutical
DK1462439T3 (da) * 2001-12-11 2008-04-21 Kyorin Seiyaku Kk Hidtil ukendte stabile krystaller af substitueret phenylpropionsyrederivat og fremgangsmåder til fremstilling af den samme
US20090214527A1 (en) * 2005-07-11 2009-08-27 Gary Burgess Combination Of Anti-Madcam Antibody And Antifibrotic Caspase Inhibitor To Treat Liver Fibrosis

Also Published As

Publication number Publication date
AU2007330478A1 (en) 2008-06-12
NO338908B1 (no) 2016-10-31
AR064809A1 (es) 2009-04-29
CN103923169A (zh) 2014-07-16
CA2669849C (en) 2012-01-31
IL198732A0 (en) 2010-02-17
PE20081251A1 (es) 2008-09-17
CN103951583B (zh) 2016-01-06
CN101573328A (zh) 2009-11-04
HK1199885A1 (zh) 2015-07-24
IL198732A (en) 2014-02-27
NO20091892L (no) 2009-06-17
PL2091910T3 (pl) 2015-02-27
HK1200440A1 (zh) 2015-08-07
JP2010511689A (ja) 2010-04-15
KR20090080113A (ko) 2009-07-23
TW200833319A (en) 2008-08-16
TWI345466B (en) 2011-07-21
AU2007330478B2 (en) 2011-09-08
HN2007000536A (es) 2011-01-17
MX2009006055A (es) 2009-06-16
CN103951583A (zh) 2014-07-30
UY30758A1 (es) 2008-07-31
EP2091910B1 (en) 2014-08-20
PA8759501A1 (es) 2009-04-23
CN103923169B (zh) 2017-05-24
WO2008068615A8 (en) 2009-05-28
JP5495787B2 (ja) 2014-05-21
WO2008068615A1 (en) 2008-06-12
EP2091910A1 (en) 2009-08-26
DK2091910T3 (en) 2014-12-01
PT2091910E (pt) 2014-11-18
CN101573328B (zh) 2014-04-02
US20080249031A1 (en) 2008-10-09
CA2669849A1 (en) 2008-06-12
CL2007003491A1 (es) 2008-06-20
ES2524021T3 (es) 2014-12-03
US7692038B2 (en) 2010-04-06
KR101125932B1 (ko) 2012-03-22

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Legal Events

Date Code Title Description
PC Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee)

Effective date: 20191201