CN1424910A - Il－8受体拮抗剂 - Google Patents

Il－8受体拮抗剂 Download PDF

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Publication number
CN1424910A
CN1424910A CN01806605A CN01806605A CN1424910A CN 1424910 A CN1424910 A CN 1424910A CN 01806605 A CN01806605 A CN 01806605A CN 01806605 A CN01806605 A CN 01806605A CN 1424910 A CN1424910 A CN 1424910A
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alkyl
chloro
aryl
heteroaryl
group
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CN01806605A
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Chinese (zh)
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凯瑟琳·L·威多森
金琦
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SmithKline Beecham Corp
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SmithKline Beecham Corp
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/22—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
    • C07D295/26—Sulfur atoms
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/30—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by halogen atoms, or by nitro or nitroso groups
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    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/45—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
    • C07C311/47—Y being a hetero atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
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    • C—CHEMISTRY; METALLURGY
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
    • C07D309/14—Nitrogen atoms not forming part of a nitro radical
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
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    • C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
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    • C07C2603/58—Ring systems containing bridged rings containing three rings
    • C07C2603/70—Ring systems containing bridged rings containing three rings containing only six-membered rings
    • C07C2603/74—Adamantanes

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Virology (AREA)
  • Immunology (AREA)
  • Dermatology (AREA)
  • Oncology (AREA)
  • Pulmonology (AREA)
  • Communicable Diseases (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Biotechnology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Molecular Biology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Transplantation (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Toxicology (AREA)
CN01806605A 2000-03-16 2001-03-16 Il－8受体拮抗剂 Pending CN1424910A (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US18984800P 2000-03-16 2000-03-16
US60/189,848 2000-03-16

Publications (1)

Publication Number Publication Date
CN1424910A true CN1424910A (zh) 2003-06-18

Family

ID=22699008

Family Applications (1)

Application Number Title Priority Date Filing Date
CN01806605A Pending CN1424910A (zh) 2000-03-16 2001-03-16 Il－8受体拮抗剂

Country Status (23)

Country Link
EP (1) EP1263427A4 (enExample)
JP (1) JP2003526664A (enExample)
KR (1) KR20020091130A (enExample)
CN (1) CN1424910A (enExample)
AP (1) AP2002002606A0 (enExample)
AR (1) AR031098A1 (enExample)
AU (1) AU2001250873A1 (enExample)
BG (1) BG107013A (enExample)
BR (1) BR0108749A (enExample)
CA (1) CA2403062A1 (enExample)
CO (1) CO5280089A1 (enExample)
CZ (1) CZ20023075A3 (enExample)
DZ (1) DZ3317A1 (enExample)
EA (1) EA200200981A1 (enExample)
HU (1) HUP0300470A3 (enExample)
MA (1) MA25659A1 (enExample)
MX (1) MXPA02009094A (enExample)
NO (1) NO20024367L (enExample)
OA (1) OA12231A (enExample)
PL (1) PL366034A1 (enExample)
SK (1) SK13282002A3 (enExample)
WO (1) WO2001068084A1 (enExample)
ZA (1) ZA200207325B (enExample)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107027306A (zh) * 2014-05-29 2017-08-08 葛兰素史密斯克莱知识产权发展有限公司 1‑(环戊‑2‑烯‑1‑基)‑3‑(2‑羟基‑3‑(芳基磺酰基)苯基)脲衍生物作为cxcr2抑制剂
WO2019137484A1 (zh) * 2018-01-11 2019-07-18 南京明德新药研发股份有限公司 Cxcr2拮抗剂
WO2021004531A1 (zh) * 2019-07-11 2021-01-14 南京明德新药研发有限公司 一种cxcr2拮抗剂的晶型及其应用

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR030689A1 (es) * 2000-03-14 2003-09-03 Smithkline Beecham Corp Compuestos de 3-aminosulfonil-2-hidroxifenil urea, composiciones farmaceuticas que los comprenden, y uso de dichos compuestos en la manufactura de medicamentos para tratar enfermedades mediadas por quimioquinas
CN1984899B (zh) 2004-05-12 2011-07-27 先灵公司 Cxcr1和cxcr2趋化因子拮抗剂
CA2650007A1 (en) * 2006-04-21 2007-11-01 Smithkline Beecham Corporation Il-8 receptor antagonists
MX2008013600A (es) * 2006-04-21 2008-10-31 Smithkline Beechman Corp Antagonistas del receptor de interleuquina-8.
KR20170036753A (ko) * 2014-07-31 2017-04-03 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 화학요법 유도된 말초 신경병증 (cipn)의 예방 및/또는 치료를 위한 cxcr2 길항제의 용도

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11503110A (ja) * 1995-02-17 1999-03-23 スミスクライン・ビーチャム・コーポレイション Ｉｌ−８受容体拮抗剤
CZ425598A3 (cs) * 1996-06-27 1999-08-11 Smithkline Beecham Corporation Antagonista IL-8 receptoru
WO1998007418A1 (en) * 1996-08-21 1998-02-26 Smithkline Beecham Corporation Il-8 receptor antagonists
DK1115701T3 (da) * 1998-09-23 2003-06-23 Tularik Inc Arylsulfonanilidurinstoffer
UY25842A1 (es) * 1998-12-16 2001-04-30 Smithkline Beecham Corp Antagonistas de receptores de il-8

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107027306A (zh) * 2014-05-29 2017-08-08 葛兰素史密斯克莱知识产权发展有限公司 1‑(环戊‑2‑烯‑1‑基)‑3‑(2‑羟基‑3‑(芳基磺酰基)苯基)脲衍生物作为cxcr2抑制剂
CN107027306B (zh) * 2014-05-29 2020-05-05 葛兰素史密斯克莱知识产权发展有限公司 1-(环戊-2-烯-1-基)-3-(2-羟基-3-(芳基磺酰基)苯基)脲衍生物作为cxcr2抑制剂
WO2019137484A1 (zh) * 2018-01-11 2019-07-18 南京明德新药研发股份有限公司 Cxcr2拮抗剂
US11136315B2 (en) 2018-01-11 2021-10-05 Medshine Discovery Inc. CXCR2 antagonist
WO2021004531A1 (zh) * 2019-07-11 2021-01-14 南京明德新药研发有限公司 一种cxcr2拮抗剂的晶型及其应用
CN114286819A (zh) * 2019-07-11 2022-04-05 深圳嘉科生物科技有限公司 一种cxcr2拮抗剂的晶型及其应用
CN114286819B (zh) * 2019-07-11 2024-03-05 深圳嘉科生物科技有限公司 一种cxcr2拮抗剂的晶型及其应用
US12577235B2 (en) 2019-07-11 2026-03-17 Shenzhen Optimum Biological Technology Co., Ltd Crystalline form of CXCR2 antagonist and application thereof

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