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2S-hydroxy-3R-[1S-(5-thiophen-2-yl-[1,2,4]oxadiazol-3-yl)-2,2-dimethyl-propylcarbamoyl]-5-methylhexanohydroxamic acid | 586972-97-6

中文名称
——
中文别名
——
英文名称
2S-hydroxy-3R-[1S-(5-thiophen-2-yl-[1,2,4]oxadiazol-3-yl)-2,2-dimethyl-propylcarbamoyl]-5-methylhexanohydroxamic acid
英文别名
V7CB4Hwx8B;(2R,3S)-N-[(1S)-2,2-dimethyl-1-(5-thiophen-2-yl-1,2,4-oxadiazol-3-yl)propyl]-N',3-dihydroxy-2-(2-methylpropyl)butanediamide
2S-hydroxy-3R-[1S-(5-thiophen-2-yl-[1,2,4]oxadiazol-3-yl)-2,2-dimethyl-propylcarbamoyl]-5-methylhexanohydroxamic acid化学式
CAS
586972-97-6
化学式
C19H28N4O5S
mdl
——
分子量
424.521
InChiKey
BLZRQJYPLPCJTR-KWCYVHTRSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    29
  • 可旋转键数:
    9
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    166
  • 氢给体数:
    4
  • 氢受体数:
    8

文献信息

  • [EN] METALLOPROTEINASE INHIBITORS<br/>[FR] INHIBITEURS DE METALLOPROTEINASES
    申请人:BRITISH BIOTECH PHARM
    公开号:WO2004101537A1
    公开(公告)日:2004-11-25
    Compounds formula (IA) or (IB); wherein W represents HO(C=0)-, HONH(C=0)- or H(C=O)N(OH)-; X represents -O- or -S-; and R1, R2, and R3 are as defined in the description and claims, are inhibitors of matrix metalloproteinases, in particular MMP9 and/or MMP12.
    化合物的结构式(IA)或(IB);其中,W代表HO(C=0)-,HONH(C=0)-或H(C=0)N(OH)-;X代表-O-或-S-;而R1、R2和R3如描述和权利要求中所定义的,是基质金属蛋白酶,特别是MMP9和/或MMP12的抑制剂。
  • Benzothiazole Formulations and Use Thereof
    申请人:Esposito Pierandrea
    公开号:US20080051397A1
    公开(公告)日:2008-02-28
    The present invention is related to macrogol glyceride pharmaceutical formulations containing benzothiazole derivatives. In particular, the invention is related to benzothiazole stearoyl macrogol pharmaceutical formulations, method of preparation and use thereof.
    本发明涉及含有苯并噻唑衍生物的大聚乙二醇甘油酯制剂。具体地,本发明涉及苯并噻唑硬脂酰大聚乙二醇制剂,其制备方法和用途。
  • Sulfonamide derivatives and use thereof for the modulation of metalloproteinases
    申请人:Gerber Patrick
    公开号:US20090221575A1
    公开(公告)日:2009-09-03
    The present invention is related to sulfonamide derivatives of Formula (Ia) where the groups are as defined in the description, and use thereof in particular for the treatment and/or prophylaxis of autoimmune disorders, inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, cancer, respiratory diseases and fibrosis, including multiple sclerosis, arthritis, emphysema, chronic obstructive pulmonary disease, liver and pulmonary fibrosis.
    本发明涉及公式(Ia)的磺酰胺衍生物,其中各基团如描述中所定义,并且其在治疗和/或预防自身免疫性疾病、炎症性疾病、心血管疾病、神经退行性疾病、癌症、呼吸道疾病和纤维化,包括多发性硬化症、关节炎、肺气肿、慢性阻塞性肺疾病、肝脏和肺部纤维化等方面的用途。
  • OXA- AND THIADIAZOLES AND THEIR USE AS METALLOPROTEINASE INHIBITORS
    申请人:AYSCOUGH Andrew Paul
    公开号:US20080227833A1
    公开(公告)日:2008-09-18
    Compounds formula (IA) or (IB), wherein W represents HO(C═O)—, HONH(C═O)— or H(C═O)N(OH)—; X represents —O— or —S—; and R 1 , R 2 , and R 3 are as defined in the description and claims, are inhibitors of matrix metal oproteinases, in particular MMP9 and/or MMP12.
    化合物公式(IA)或(IB),其中W代表HO(C═O)—、HONH(C═O)—或H(C═O)N(OH)—;X代表—O—或—S—;而R1、R2和R3如描述和权利要求所定义的那样,是基质金属蛋白酶的抑制剂,特别是MMP9和/或MMP12。
  • Oxa-and thiadiazoles and their use as metalloproteinase inhibitors
    申请人:Ayscough Andrew Paul
    公开号:US20100035943A1
    公开(公告)日:2010-02-11
    Compounds formula (IA) or (IB), wherein W represents HO(C═O)—, HONH(C═O)— or H(C═O)N(OH)—; X represents —O— or —S—; and R 1 , R 2 , and R 3 are as defined in the description and claims, are inhibitors of matrix metal oproteinases, in particular MMP9 and/or MMP12.
    化合物公式(IA)或(IB),其中W代表HO(C═O)—,HONH(C═O)—或H(C═O)N(OH)—; X代表—O—或—S—; R1、R2和R3如说明书和权利要求中所定义的,是基质金属蛋白酶的抑制剂,特别是MMP9和/或MMP12。
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