HK1138567A1 - Crystalline forms of (3s)-3-[n-(n-(2-tert- butylphenyl)oxamyl)alaniwyl]amino-5-(2,3,5,6-tetrafluoro phenoxy)-4- 0x0penta noic acid (3s)-3-[n-(n-(2-))]-5-(2356- )-4- - Google Patents

Crystalline forms of (3s)-3-[n-(n-(2-tert- butylphenyl)oxamyl)alaniwyl]amino-5-(2,3,5,6-tetrafluoro phenoxy)-4- 0x0penta noic acid (3s)-3-[n-(n-(2-))]-5-(2356- )-4-

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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)
Chinese (zh)
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
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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/xx

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/70Carboxylic 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
    • C07C235/72Carboxylic 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
    • C07C235/74Carboxylic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic 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
    • C07C237/22Carboxylic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167Amides, 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42Carboxylic 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
    • C07C235/44Carboxylic 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
    • C07C235/52Carboxylic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

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  • 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)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pain & Pain Management (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)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
HK10104322.9A 2006-12-06 2010-05-03 Crystalline forms of (3s)-3-[n-(n-(2-tert- butylphenyl)oxamyl)alaniwyl]amino-5-(2,3,5,6-tetrafluoro phenoxy)-4- 0x0penta noic acid (3s)-3-[n-(n-(2-))]-5-(2356- )-4- HK1138567A1 (en)

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 (en) 2010-08-27

Family

ID=39205161

Family Applications (3)

Application Number Title Priority Date Filing Date
HK10104322.9A HK1138567A1 (en) 2006-12-06 2010-05-03 Crystalline forms of (3s)-3-[n-(n-(2-tert- butylphenyl)oxamyl)alaniwyl]amino-5-(2,3,5,6-tetrafluoro phenoxy)-4- 0x0penta noic acid (3s)-3-[n-(n-(2-))]-5-(2356- )-4-
HK15100168.9A HK1199885A1 (en) 2006-12-06 2015-01-07 Crystalline forms of (3s)-3-[n-(n-(2-tert- butylphenyl)oxamyl)alaniwyl]amino-5-(2,3,5,6-tetrafluoro phenoxy)-4-0x0penta noic acid (3s)-3-[n-(n-(2-))]-5-(2356- )-4-
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 (en) 2006-12-06 2015-01-07 Crystalline forms of (3s)-3-[n-(n-(2-tert- butylphenyl)oxamyl)alaniwyl]amino-5-(2,3,5,6-tetrafluoro phenoxy)-4-0x0penta noic acid (3s)-3-[n-(n-(2-))]-5-(2356- )-4-
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 (es)
EP (1) EP2091910B1 (es)
JP (1) JP5495787B2 (es)
KR (1) KR101125932B1 (es)
CN (3) CN101573328B (es)
AR (1) AR064809A1 (es)
AU (1) AU2007330478B2 (es)
CA (1) CA2669849C (es)
CL (1) CL2007003491A1 (es)
DK (1) DK2091910T3 (es)
ES (1) ES2524021T3 (es)
HK (3) HK1138567A1 (es)
HN (1) HN2007000536A (es)
IL (1) IL198732A (es)
MX (1) MX2009006055A (es)
NO (1) NO338908B1 (es)
PA (1) PA8759501A1 (es)
PE (1) PE20081251A1 (es)
PL (1) PL2091910T3 (es)
PT (1) PT2091910E (es)
TW (1) TWI345466B (es)
UY (1) UY30758A1 (es)
WO (1) WO2008068615A1 (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL3150610T3 (pl) * 2010-02-12 2020-02-28 Pfizer Inc. Sole i polimorfy 8-fluoro-2-{4-[(metyloamino}metylo]fenylo}-1,3,4,5-tetrahydro-6Hazepino[5,4,3-cd]indol-6-onu
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
EA036325B1 (ru) * 2014-03-14 2020-10-27 Аджиос Фармасьютикалз, Инк. Фармацевтическая композиция на основе твердой дисперсии ингибитора idh1
MX2016014731A (es) 2014-05-12 2017-05-04 Conatus Pharmaceuticals Inc Tratamiento de las complicaciones de la enfermedad cronica del higado con enfermedades de caspasa.
WO2016038500A1 (en) * 2014-09-08 2016-03-17 Pfizer Inc. Crystalline solid forms of 6-carboxy-2-(3,5-dichlorophenyl)-benzoxazole
CA2975048C (en) 2015-01-30 2024-01-02 Biomed Valley Discoveries, Inc. Crystalline forms of c21h22ci2n4o2
US20180044375A1 (en) 2015-03-06 2018-02-15 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
EP3397251A1 (en) 2015-12-31 2018-11-07 Conatus Pharmaceuticals, Inc. Methods of using caspase inhibitors in treatment of liver disease
JP2019530696A (ja) 2016-10-05 2019-10-24 ノバルティス アーゲー 線維性、硬変性の疾患もしくは障害を治療または予防するためのfxrアゴニストを含む組合せ組成物
JP7113831B2 (ja) * 2017-01-23 2022-08-05 チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッド カスパーゼ阻害薬としての二環式化合物
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
CA3058280C (en) * 2017-03-30 2023-11-28 Merck Patent Gmbh Crystalline form of (s)-[2-chloro-4-fluoro-5-(7-morpholin-4-ylquinazolin-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
CA3105352A1 (en) 2018-06-29 2020-01-02 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
MX2021010603A (es) 2019-03-07 2022-01-31 Conatus Pharmaceuticals Inc Inhibidores de caspasa y metodos de uso de los mismos.
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

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69217762T2 (de) * 1991-07-30 1997-10-09 Ajinomoto Kk Kristalle von N-(Trans-4-isopropylcyclohexylcarbonyl)-D-phenylalanin und Verfahren zu ihrer Herstellung
DE59307210D1 (de) * 1993-05-12 1997-10-02 Heumann Pharma Gmbh & Co Stabile und kristalline Form von Bezafibrat
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
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
GB9923933D0 (en) * 1999-10-08 1999-12-08 Smithkline Beecham Lab Novel pharmaceutical
CA2469882C (en) * 2001-12-11 2009-09-29 Kazuo Orita Novel stable crystals of substituted phenylpropionic acid derivative and process for producing the same
CN101217980A (zh) * 2005-07-11 2008-07-09 辉瑞有限公司 治疗肝纤维化的抗madcam抗体和抗纤维化半胱天冬蛋白酶抑制剂的新组合

Also Published As

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

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

Effective date: 20191201