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2-benzenesulfonylamino-5,6,7,8-tetrahydronaphthalene-1-carboxylic acid methyl ester | 900492-91-3

中文名称
——
中文别名
——
英文名称
2-benzenesulfonylamino-5,6,7,8-tetrahydronaphthalene-1-carboxylic acid methyl ester
英文别名
methyl 2-(benzenesulfonamido)-5,6,7,8-tetrahydronaphthalene-1-carboxylate
2-benzenesulfonylamino-5,6,7,8-tetrahydronaphthalene-1-carboxylic acid methyl ester化学式
CAS
900492-91-3
化学式
C18H19NO4S
mdl
——
分子量
345.419
InChiKey
SJPPKQRMCMYLME-UHFFFAOYSA-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):
    4.2
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    80.8
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • TETRAZOLE COMPOUNDS AND METHODS OF MAKING AND USING SAME
    申请人:Dyke Hazel Joan
    公开号:US20130331420A1
    公开(公告)日:2013-12-12
    Described herein are tetrazole compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various tetrazole compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.
    本文描述了四唑化合物及其在治疗医学疾病(如肥胖症)方面的应用。提供了制备各种四唑化合物的制药组合物和方法。这些化合物被认为具有对甲酰基肽酶2的活性。
  • Tetrazole compounds and methods of making and using same
    申请人:Dyke Hazel Joan
    公开号:US09321740B2
    公开(公告)日:2016-04-26
    Described herein are tetrazole compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various tetrazole compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2.
    本文描述了四唑化合物及其在治疗医学疾病(如肥胖症)中的应用。提供了制备各种四唑化合物的药物组合物和方法。这些化合物被认为具有针对甲肽酶2的活性。
  • Development of sulfonamide compounds as potent methionine aminopeptidase type II inhibitors with antiproliferative properties
    作者:Megumi Kawai、Nwe Y. BaMaung、Steve D. Fidanze、Scott A. Erickson、Jason S. Tedrow、William J. Sanders、Anil Vasudevan、Chang Park、Charles Hutchins、Kenneth M. Comess、Douglas Kalvin、Jieyi Wang、Qian Zhang、Pingping Lou、Lora Tucker-Garcia、Jennifer Bouska、Randy L. Bell、Richard Lesniewski、Jack Henkin、George S. Sheppard
    DOI:10.1016/j.bmcl.2006.03.085
    日期:2006.7
    We have screened molecules for inhibition of MetAP2 as a novel approach toward antiangiogenesis and anticancer therapy using affinity selection/mass spectrometry (ASMS) employing MetAP2 loaded with Mn(2+) as the active site metal. After a series of anthranilic acid sulfonamides with micromolar affinities was identified, chemistry efforts were initiated. The micromolar hits were quickly improved to potent nanomolar inhibitors by chemical modifications guided by insights from X-ray crystallography.
  • US9321740B2
    申请人:——
    公开号:US9321740B2
    公开(公告)日:2016-04-26
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