SG11201500236SA - Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid - Google Patents

Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid

Info

Publication number
SG11201500236SA
SG11201500236SA SG11201500236SA SG11201500236SA SG11201500236SA SG 11201500236S A SG11201500236S A SG 11201500236SA SG 11201500236S A SG11201500236S A SG 11201500236SA SG 11201500236S A SG11201500236S A SG 11201500236SA SG 11201500236S A SG11201500236S A SG 11201500236SA
Authority
SG
Singapore
Prior art keywords
isoquinoline
phenoxy
carbonyl
hydroxy
amino
Prior art date
Application number
SG11201500236SA
Inventor
Claudia Witschi
Jung Min Park
Michael D Thompson
Michael John Martinelli
David A Yeowell
Michael P Arend
Original Assignee
Fibrogen 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=48857025&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201500236S(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Fibrogen Inc filed Critical Fibrogen Inc
Publication of SG11201500236SA publication Critical patent/SG11201500236SA/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
    • C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/472—Non-condensed isoquinolines, e.g. papaverine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • 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
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
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    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
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    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06—Antianaemics
    • A—HUMAN NECESSITIES
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    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
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  • Veterinary Medicine (AREA)
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  • General Health & Medical Sciences (AREA)
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  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
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SG11201500236SA 2012-07-16 2013-07-15 Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid SG11201500236SA (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201261672191P 2012-07-16 2012-07-16
US201361768297P 2013-02-22 2013-02-22
US201361832566P 2013-06-07 2013-06-07
PCT/US2013/050539 WO2014014835A2 (en) 2012-07-16 2013-07-15 Crystalline forms of a prolyl hydroxylase inhibitor

Publications (1)

Publication Number Publication Date
SG11201500236SA true SG11201500236SA (en) 2015-02-27

Family

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SG10201700873UA SG10201700873UA (en) 2012-07-16 2013-07-15 Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid
SG10202111314YA SG10202111314YA (en) 2012-07-16 2013-07-15 Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid
SG11201500236SA SG11201500236SA (en) 2012-07-16 2013-07-15 Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid

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SG10201700873UA SG10201700873UA (en) 2012-07-16 2013-07-15 Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid
SG10202111314YA SG10202111314YA (en) 2012-07-16 2013-07-15 Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid

Country Status (27)

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US (5) US9115085B2 (en)
EP (3) EP2872488B1 (en)
JP (2) JP6491093B2 (en)
KR (4) KR20210130849A (en)
CN (9) CN109369524A (en)
AU (1) AU2013290438C1 (en)
BR (1) BR112015001101A2 (en)
CA (1) CA2879242C (en)
CY (2) CY1120805T1 (en)
DK (2) DK2872488T3 (en)
ES (2) ES2689430T3 (en)
FR (1) FR22C1030I2 (en)
HK (1) HK1243409A1 (en)
HR (2) HRP20220182T1 (en)
HU (2) HUE057925T2 (en)
IL (1) IL236626B (en)
IN (1) IN2015KN00262A (en)
LT (3) LT2872488T (en)
MX (1) MX355428B (en)
MY (1) MY182428A (en)
NZ (1) NZ704662A (en)
PL (2) PL3470397T3 (en)
PT (2) PT2872488T (en)
RS (2) RS57795B1 (en)
SG (3) SG10201700873UA (en)
SI (2) SI3470397T1 (en)
WO (1) WO2014014835A2 (en)

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CN106187888A (en) * 2016-07-18 2016-12-07 江苏德源药业股份有限公司 FG 4592 monocrystalline and preparation method thereof
CN108017583B (en) * 2016-11-01 2021-04-06 徐州万邦金桥制药有限公司 Preparation method of kebomei
CN107382986B (en) * 2017-08-02 2022-09-20 江苏艾立康医药科技有限公司 4-hydroxy-1-methylisoquinoline derivatives and their use in increasing endogenous erythropoietin
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JP7144510B2 (en) * 2017-09-04 2022-09-29 サンド・アクチエンゲゼルシヤフト Co-crystals of orally administrable HIF prolyl hydroxylase inhibitors
CN111978226B (en) 2018-06-05 2022-03-04 沈阳化工大学 Trifluoroethyl sulfide (sulfoxide) substituted benzene compound and application thereof
CN111320583A (en) * 2018-12-14 2020-06-23 广东东阳光药业有限公司 New crystal form of nodestat and preparation method thereof
CN109369525A (en) * 2018-12-29 2019-02-22 安礼特（上海）医药科技有限公司 Its novel crystal forms and preparation method thereof of Luo Shasi
WO2020217190A1 (en) * 2019-04-26 2020-10-29 Dr. Reddy’S Laboratories Limited Process for the purification of roxadustat
CN112679428A (en) * 2019-10-17 2021-04-20 罗欣药业(上海)有限公司 New crystal form of roxasistat and preparation method thereof
CN114344301B (en) * 2019-10-22 2023-06-23 苏州科睿思制药有限公司 Crystal form of hypoxia inducible factor prolyl hydroxylase inhibitor
CN110721185B (en) * 2019-11-13 2022-04-12 南京市儿童医院 Use of Rosxastat for myocardial protection
CN112961107B (en) * 2019-12-13 2024-06-25 罗欣药业(上海)有限公司 Luo Shasi his crystal form and preparation method thereof
US20230190731A1 (en) * 2020-03-17 2023-06-22 Zydus Lifesciences Limited Formulation comprising hif prolyl hydroxylase inhibitors
CN111205224B (en) * 2020-04-22 2020-08-25 南京佰麦生物技术有限公司 Crystal form of roxasistat hydrate, and preparation method and application thereof
CN113754569B (en) * 2020-06-04 2024-07-02 四川国为制药有限公司 Intermediate compound and preparation method and application thereof
CN111533691A (en) * 2020-06-08 2020-08-14 重庆三圣实业股份有限公司 Preparation method of Rosxastat
CN114057643B (en) * 2020-08-04 2023-02-28 成都苑东生物制药股份有限公司 Rosemastat eutectic crystal and preparation method thereof
CN112500344B (en) * 2020-11-18 2022-07-01 江苏豪森药业集团有限公司 Crystalline form of roxasistat and preparation method thereof
CN112194624A (en) * 2020-11-18 2021-01-08 江苏豪森药业集团有限公司 Crystal form of isoquinoline compound and preparation method thereof
CN115724796A (en) * 2021-08-26 2023-03-03 成都苑东生物制药股份有限公司 New crystal form of roxasistat and preparation method thereof
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