SG11202005703TA - Cyclohexyl acid triazole azoles as lpa antagonists - Google Patents

Cyclohexyl acid triazole azoles as lpa antagonists

Info

Publication number
SG11202005703TA
SG11202005703TA SG11202005703TA SG11202005703TA SG11202005703TA SG 11202005703T A SG11202005703T A SG 11202005703TA SG 11202005703T A SG11202005703T A SG 11202005703TA SG 11202005703T A SG11202005703T A SG 11202005703TA SG 11202005703T A SG11202005703T A SG 11202005703TA
Authority
SG
Singapore
Prior art keywords
cyclohexyl acid
azoles
lpa antagonists
acid triazole
lpa
Prior art date
Application number
SG11202005703TA
Other languages
English (en)
Inventor
Yan Shi
Peter Tai Wah Cheng
Ying Wang
Jun Li
Tianan Fang
James R Corte
Jun Shi
Hao Zhang
Lawrence J Kennedy
Shiwei Tao
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of SG11202005703TA publication Critical patent/SG11202005703TA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
SG11202005703TA 2017-12-19 2018-12-18 Cyclohexyl acid triazole azoles as lpa antagonists SG11202005703TA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201762607488P 2017-12-19 2017-12-19
PCT/US2018/066123 WO2019126094A1 (en) 2017-12-19 2018-12-18 Cyclohexyl acid triazole azoles as lpa antagonists

Publications (1)

Publication Number Publication Date
SG11202005703TA true SG11202005703TA (en) 2020-07-29

Family

ID=65003581

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202005703TA SG11202005703TA (en) 2017-12-19 2018-12-18 Cyclohexyl acid triazole azoles as lpa antagonists

Country Status (16)

Country Link
US (1) US11319315B2 (enExample)
EP (1) EP3728224B1 (enExample)
JP (1) JP7280881B2 (enExample)
KR (1) KR20200100713A (enExample)
CN (1) CN111712492B (enExample)
AR (1) AR113965A1 (enExample)
AU (1) AU2018392325A1 (enExample)
BR (1) BR112020012177A2 (enExample)
CA (1) CA3085938A1 (enExample)
EA (1) EA202091505A1 (enExample)
ES (1) ES2938863T3 (enExample)
IL (1) IL275363A (enExample)
MX (1) MX2020005818A (enExample)
SG (1) SG11202005703TA (enExample)
TW (1) TW201927778A (enExample)
WO (1) WO2019126094A1 (enExample)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11202005699QA (en) 2017-12-19 2020-07-29 Bristol Myers Squibb Co Triazole n-linked carbamoyl cyclohexyl acids as lpa antagonists
CN112055710B (zh) * 2017-12-19 2025-01-28 百时美施贵宝公司 作为lpa拮抗剂的环己基酸吡唑吖嗪
US20210379210A1 (en) * 2018-10-15 2021-12-09 Bristol-Myers Squibb Company Radioligands for imaging the lpa1 receptor
CN111434653A (zh) 2019-01-15 2020-07-21 武汉朗来科技发展有限公司 三氮唑类化合物及其制备方法与用途
JP7465899B2 (ja) 2019-06-18 2024-04-11 ブリストル-マイヤーズ スクイブ カンパニー Lpaアンタゴニストとしてのシクロブチルカルボン酸
JP7431961B2 (ja) 2019-11-15 2024-02-15 ギリアード サイエンシーズ, インコーポレイテッド Lpa受容体アンタゴニストとしてのトリアゾールカルバメートピリジルスルホンアミド及びその使用
TWI838626B (zh) 2020-06-03 2024-04-11 美商基利科學股份有限公司 Lpa受體拮抗劑及其用途
CA3185689A1 (en) 2020-06-03 2021-12-09 Gilead Sciences, Inc. Lpa receptor antagonists and uses thereof
KR20240068583A (ko) * 2020-08-11 2024-05-17 비바 스타 바이오사이언시스 리미티드 Lpa 수용체 길항제로서의 트리아졸-피리디닐 치환된 아자시클로헥실 아세트산 화합물
US20240018102A1 (en) * 2020-10-22 2024-01-18 Lhotse Bio, Inc Compounds and compositions for treating conditions associated with lpa receptor activity
CN114621135B (zh) * 2020-12-11 2024-01-30 上海拓界生物医药科技有限公司 一种lpa1小分子拮抗剂
CN117295717A (zh) 2021-05-11 2023-12-26 吉利德科学公司 Lpa受体拮抗剂及其用途
KR20240109975A (ko) * 2021-08-12 2024-07-12 상하이 에스아이엠알 바이오테크놀로지 컴퍼니 리미티드 치환된 트리아졸 유도체, 이의 제조 방법, 이의 약제학적 조성물, 및 이의 용도
JP7709612B2 (ja) 2021-12-08 2025-07-16 ギリアード サイエンシーズ, インコーポレイテッド Lpa受容体アンタゴニスト及びそれらの使用
AR128613A1 (es) 2022-02-25 2024-05-29 Lhotse Bio Inc Compuestos y composiciones para el tratamiento de afecciones asociadas con la actividad del receptor de lpa
CN115785014B (zh) * 2022-12-27 2025-01-24 瑞石生物医药有限公司 四唑衍生物及其用途
WO2025029733A1 (en) 2023-08-01 2025-02-06 Discovery Energy, Llc Convertible silencer

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE447970T1 (de) 2001-02-08 2009-11-15 Ono Pharmaceutical Co Mittel zur behandlung von harnwegserkrankungen, umfassend mittel zur kontrolle des lpa-rezeptors
DE102004038403B4 (de) 2004-08-07 2006-08-31 Sanofi-Aventis Deutschland Gmbh Verfahren zur Herstellung der enantiomeren Formen von cis-konfigurierten 3-Hydroxycyclohexancarbonsäure-Derivaten
US20080186971A1 (en) 2007-02-02 2008-08-07 Tarari, Inc. Systems and methods for processing access control lists (acls) in network switches using regular expression matching logic
WO2009123948A2 (en) 2008-04-04 2009-10-08 Irm Llc Compounds and compositions as itpkb inhibitors
JP2013501064A (ja) * 2009-08-04 2013-01-10 アミラ ファーマシューティカルス,インコーポレーテッド リゾホスファチジン酸受容体アンタゴニストとしての化合物
GB2474120B (en) 2009-10-01 2011-12-21 Amira Pharmaceuticals Inc Compounds as Lysophosphatidic acid receptor antagonists
GB2474748B (en) 2009-10-01 2011-10-12 Amira Pharmaceuticals Inc Polycyclic compounds as lysophosphatidic acid receptor antagonists
EA201390821A1 (ru) 2010-12-07 2013-10-30 Амира Фармасьютикалс, Инк. Антагонисты рецепторов лизофосфатидной кислоты и их применение
US8785442B2 (en) 2011-01-30 2014-07-22 Curegenix, Inc. Compound as antagonist of lysophosphatidic acid receptor, composition, and use thereof
EP2694472B1 (en) 2011-04-05 2020-03-11 Takeda Pharmaceutical Company Limited Sulfonamide derivative and use thereof
WO2012138648A1 (en) * 2011-04-06 2012-10-11 Irm Llc Compositions and methods for modulating lpa receptors
MX356683B (es) 2011-09-27 2018-06-08 Genfit Derivados de triazolpiridazinas 6-sustituidas como agonistas rev-erb.
WO2013070879A1 (en) 2011-11-10 2013-05-16 Bristol-Myers Squibb Company Methods for treating spinal cord injury with lpa receptor antagonists
WO2013085824A1 (en) 2011-12-04 2013-06-13 Angion Biomedica Corp. Small molecule anti-fibrotic compounds and uses thereof
WO2013134298A1 (en) 2012-03-07 2013-09-12 Deciphera Pharmaceuticals, Llc Raf inhibitor compounds
MA37762B1 (fr) 2012-06-20 2018-04-30 Hoffmann La Roche Composés n-aryltriazole utilisés comme antagonistes de lpar
CA2869541A1 (en) 2012-06-20 2013-12-27 F. Hoffmann-La Roche Ag N-alkyltriazole compounds as lpar antagonists
JP6853619B2 (ja) 2015-01-16 2021-03-31 大塚製薬株式会社 シアノトリアゾール化合物の医薬用途
AR108838A1 (es) * 2016-06-21 2018-10-03 Bristol Myers Squibb Co Ácidos de carbamoiloximetil triazol ciclohexilo como antagonistas de lpa
SG11202005699QA (en) 2017-12-19 2020-07-29 Bristol Myers Squibb Co Triazole n-linked carbamoyl cyclohexyl acids as lpa antagonists

Also Published As

Publication number Publication date
US11319315B2 (en) 2022-05-03
IL275363A (en) 2020-07-30
EP3728224B1 (en) 2023-01-11
EP3728224A1 (en) 2020-10-28
JP2021507900A (ja) 2021-02-25
BR112020012177A2 (pt) 2020-11-24
AR113965A1 (es) 2020-07-01
CA3085938A1 (en) 2019-06-27
JP7280881B2 (ja) 2023-05-24
EA202091505A1 (ru) 2020-09-22
CN111712492A (zh) 2020-09-25
ES2938863T3 (es) 2023-04-17
CN111712492B (zh) 2024-05-31
WO2019126094A1 (en) 2019-06-27
US20210163470A1 (en) 2021-06-03
MX2020005818A (es) 2020-08-20
AU2018392325A1 (en) 2020-07-30
TW201927778A (zh) 2019-07-16
KR20200100713A (ko) 2020-08-26

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