NO20091892L - Krystallinsk form av (3S)-3-(N-(N`-(2-tert-butylfenyl)oksamyl) alaninyl)amino-5-(2`,3`,5`,6`-tetrafluorfenoksy)-4 oksopentanoisk syre - Google Patents

Krystallinsk form av (3S)-3-(N-(N`-(2-tert-butylfenyl)oksamyl) alaninyl)amino-5-(2`,3`,5`,6`-tetrafluorfenoksy)-4 oksopentanoisk syre

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Publication number
NO20091892L
NO20091892L NO20091892A NO20091892A NO20091892L NO 20091892 L NO20091892 L NO 20091892L NO 20091892 A NO20091892 A NO 20091892A NO 20091892 A NO20091892 A NO 20091892A NO 20091892 L NO20091892 L NO 20091892L
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NO
Norway
Prior art keywords
tetrafluorophenoxy
alaninyl
oxamyl
butylphenyl
tert
Prior art date
Application number
NO20091892A
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English (en)
Other versions
NO338908B1 (no
Inventor
Stuart Dimock
Eric Hagen
Jason Hanko
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Conatus Pharmaceuticals Inc
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Filing date
Publication date
Application filed by Conatus Pharmaceuticals Inc filed Critical Conatus Pharmaceuticals Inc
Publication of NO20091892L publication Critical patent/NO20091892L/no
Publication of NO338908B1 publication Critical patent/NO338908B1/no

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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)

Abstract

Det beskrives krystallinske former av (3S)-3-[N-(N'-(2-tert-butylfenyl)oksamyl)-alaninyl]amino-5-(2',3',5',6'-tetrafluorfenoksy)-4-oksopentanoisk syre (se formel I). Oppfinnelsen beskriver videre farmasøytiske sammensetninger 5 omfattende slike krystallinske former og anvendelse av nevnte farmasøytiske sammensetninger og nevnte krystallinske former i behandling av forskjellige tilstander, fortrinnsvis for behandling av leverfibrose.
NO20091892A 2006-12-06 2009-05-14 Krystallinsk form av (3S)-3-(N-(N'-(2-tert-butylfenyl)oksamyl)alaninyl)amino-5-(2',3',5',6'`-tetrafluorfenoksy)-4 oksopentanoisk syre NO338908B1 (no)

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 (2)

Publication Number Publication Date
NO20091892L true NO20091892L (no) 2009-06-17
NO338908B1 NO338908B1 (no) 2016-10-31

Family

ID=39205161

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20091892A NO338908B1 (no) 2006-12-06 2009-05-14 Krystallinsk form av (3S)-3-(N-(N'-(2-tert-butylfenyl)oksamyl)alaninyl)amino-5-(2',3',5',6'`-tetrafluorfenoksy)-4 oksopentanoisk syre

Country Status (22)

Country Link
US (1) US7692038B2 (no)
EP (1) EP2091910B1 (no)
JP (1) JP5495787B2 (no)
KR (1) KR101125932B1 (no)
CN (3) CN103951583B (no)
AR (1) AR064809A1 (no)
AU (1) AU2007330478B2 (no)
CA (1) CA2669849C (no)
CL (1) CL2007003491A1 (no)
DK (1) DK2091910T3 (no)
ES (1) ES2524021T3 (no)
HN (1) HN2007000536A (no)
IL (1) IL198732A (no)
MX (1) MX2009006055A (no)
NO (1) NO338908B1 (no)
PA (1) PA8759501A1 (no)
PE (1) PE20081251A1 (no)
PL (1) PL2091910T3 (no)
PT (1) PT2091910E (no)
TW (1) TWI345466B (no)
UY (1) UY30758A1 (no)
WO (1) WO2008068615A1 (no)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4166558A1 (en) * 2010-02-12 2023-04-19 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
NZ723859A (en) * 2014-03-14 2023-01-27 Servier Lab Pharmaceutical compositions of therapeutically active compounds and their uses
JP2017515854A (ja) 2014-05-12 2017-06-15 クオナトウス ファーマシューティカルズ,インコーポレイテッド カスパーゼ阻害剤による慢性肝疾患の合併症の治療
PT4349406T (pt) * 2014-09-08 2026-02-04 Pfizer Formas sólidas cristalinas de 6-carboxi-2-(3,5-diclorofenil)-benzoxazol para utilização como medicamento
HK1244274A1 (zh) * 2015-01-30 2018-08-03 生物医学谷探索股份有限公司 C21h22ci2n4o2的晶型
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
CA3010286A1 (en) 2015-12-31 2017-07-06 Conatus Pharmaceuticals Inc. Methods of using caspase inhibitors in treatment of liver disease
RU2019113150A (ru) 2016-10-05 2020-11-06 Новартис Аг Комбинация композиций, содержащих агонисты fxr, предназначенная для лечения или предупреждения фиброзирующего, цирротического заболевания или нарушения
WO2018133870A1 (zh) * 2017-01-23 2018-07-26 正大天晴药业集团股份有限公司 作为Caspase抑制剂的联环化合物
JP2019514862A (ja) * 2017-03-23 2019-06-06 ノバルティス アーゲー (s)−2−(ジフェニルアセチル)−1,2,3,4−テトラヒドロ−6−メトキシ−5−(フェニルメトキシ)−3−イソキノリンカルボン酸ナトリウムの無水結晶形
CN110446706B (zh) * 2017-03-30 2023-05-16 默克专利股份公司 (s)-[2-氯-4-氟-5-(7-吗啉-4-基喹唑啉-4-基)苯基]-(6-甲氧基-哒嗪-3-基)甲醇的晶型
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
EP3814327A1 (en) 2018-06-29 2021-05-05 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
CN119264211A (zh) 2018-08-27 2025-01-07 瑞泽恩制药公司 拉曼光谱在下游纯化中的应用
ES2988904T3 (es) 2019-03-07 2024-11-22 Nobo Medicine Inc Inhibidores de caspasa y métodos de utilización de los mismos
JP2022546861A (ja) * 2019-09-10 2022-11-09 ミラティ セラピューティクス, インコーポレイテッド マルチチロシンキナーゼ阻害剤の結晶形、調製方法およびその使用
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
EP4138843A4 (en) 2020-04-23 2024-07-10 Southern Research Institute COMPOSITION FOR THE TREATMENT OF BLOOD CANCER USING 4'-THIO-5-AZA-2'-DEOXYCYTIDINE AND USES THEREOF
CA3186696A1 (en) * 2020-07-23 2022-01-27 Mark J. Suto Polymorphs of 5-aza-4'-thio-2-deoxycytidine
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

Family Cites Families (8)

* Cited by examiner, † Cited by third party
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
MX2008000659A (es) * 2005-07-11 2008-03-13 Pfizer Ltd Nueva combinacion de anticuerpo contra madcam y de inhibidor de caspasa antifibrotico.

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US7692038B2 (en) 2010-04-06
CA2669849A1 (en) 2008-06-12
HK1199885A1 (zh) 2015-07-24
NO338908B1 (no) 2016-10-31
CA2669849C (en) 2012-01-31
UY30758A1 (es) 2008-07-31
CN103951583A (zh) 2014-07-30
DK2091910T3 (en) 2014-12-01
MX2009006055A (es) 2009-06-16
PT2091910E (pt) 2014-11-18
CN103951583B (zh) 2016-01-06
IL198732A (en) 2014-02-27
AR064809A1 (es) 2009-04-29
CN103923169B (zh) 2017-05-24
AU2007330478B2 (en) 2011-09-08
CN101573328A (zh) 2009-11-04
TWI345466B (en) 2011-07-21
AU2007330478A1 (en) 2008-06-12
HK1200440A1 (zh) 2015-08-07
TW200833319A (en) 2008-08-16
PL2091910T3 (pl) 2015-02-27
IL198732A0 (en) 2010-02-17
PA8759501A1 (es) 2009-04-23
EP2091910B1 (en) 2014-08-20
HK1138567A1 (en) 2010-08-27
CL2007003491A1 (es) 2008-06-20
EP2091910A1 (en) 2009-08-26
HN2007000536A (es) 2011-01-17
JP2010511689A (ja) 2010-04-15
ES2524021T3 (es) 2014-12-03
WO2008068615A8 (en) 2009-05-28
JP5495787B2 (ja) 2014-05-21
CN103923169A (zh) 2014-07-16
PE20081251A1 (es) 2008-09-17
US20080249031A1 (en) 2008-10-09
KR20090080113A (ko) 2009-07-23
CN101573328B (zh) 2014-04-02
KR101125932B1 (ko) 2012-03-22
WO2008068615A1 (en) 2008-06-12

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Owner name: CONATUS PHARMACEUTICALS INC, US

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