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1-cyano-3-[4-(2-guanidino-thiazol-4-yl)-butyl]-2-methyl-isothiourea | 69014-73-9

中文名称
——
中文别名
——
英文名称
1-cyano-3-[4-(2-guanidino-thiazol-4-yl)-butyl]-2-methyl-isothiourea
英文别名
2-Guanidino-4-[4-(3-cyano-2-methylisothioureido)butyl]thiazole;methyl N-cyano-N'-[4-[2-(diaminomethylideneamino)-1,3-thiazol-4-yl]butyl]carbamimidothioate
1-cyano-3-[4-(2-guanidino-thiazol-4-yl)-butyl]-2-methyl-isothiourea化学式
CAS
69014-73-9
化学式
C11H17N7S2
mdl
——
分子量
311.435
InChiKey
RRNFEWMTOUNYAU-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):
    1.2
  • 重原子数:
    20
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    179
  • 氢给体数:
    3
  • 氢受体数:
    6

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

  • Guanidino imidazoles and thiazoles
    申请人:Imperial Chemical Industries Limited
    公开号:US04234735A1
    公开(公告)日:1980-11-18
    The invention relates to guanidine derivatives of imidazoles and thiazoles which are histamine H-2 antagonists and which inhibit the secretion of gastric acid, to methods for their manufacture, to pharmaceutical compositions containing them and to methods of using such guanidine derivatives and compositions. The guanidine derivatives are of the general formula I: ##STR1## in which X is S or NH, Y is CH.sub.2, a direct bond or a vinylene radical, m is 0 to 4 and n is 1 to 4, R.sup.1 is hydrogen, halogen or alkyl, R.sup.2 is hydrogen, alkyl, alkanoyl or aroyl, A is a 3,4-dioxocyclobuten-1,2-diyl radical or C.dbd.Z in which Z is O, S, NCN, NNO.sub.2, CHNO.sub.2, NCONH.sub.2, C(CN).sub.2, NCOR.sup.3, NCO.sub.2 R.sup.3, NSO.sub.2 R.sup.3 or NR.sup.4 in which R.sup.3 is alkyl or aryl and R.sup.4 is hydrogen or alkyl, B is alkoxy or alkylthio or NR.sup.5 R.sup.6 in which R.sup.5 and R.sup.6 are independently hydrogen, alkyl, alkenyl, cycloalkyl, hydroxyalkyl, alkoxyalkyl, alkylaminoalkyl or dialkylaminoalkyl; and the salts thereof.
    本发明涉及咪唑噻唑生物,它们是组胺H-2拮抗剂,可以抑制胃酸分泌,涉及其制备方法,含有它们的制药组合物以及使用这种生物和组合物的方法。该生物的一般式为I:##STR1## 其中X为S或NH,Y为CH.sub.2,直接键或乙烯基,m为0至4,n为1至4,R.sup.1为氢,卤素或烷基,R.sup.2为氢,烷基,烷酰基或芳酰基,A为3,4-二氧杂环丁-1,2-二基基团或C.dbd.Z,其中Z为O,S,NCN,NNO.sub.2,CHNO.sub.2,NCONH.sub.2,C(CN).sub.2,NCOR.sup.3,NCO.sub.2 R.sup.3,NSO.sub.2 R.sup.3或NR.sup.4,其中R.sup.3为烷基或芳基,R.sup.4为氢或烷基,B为烷氧基或烷基或NR.sup.5R.sup.6,其中R.sup.5和R.sup.6独立地为氢,烷基,烯基,环烷基,羟基烷基,烷氧基烷基,烷基基烷基或二烷基基烷基;以及它们的盐。
  • Novel Compound, Organic Cation Transporter 3 Detection Agent, And Organic Cation Transporter 3 Activity Inhibitor
    申请人:SHIN NIPPON BIOMEDICAL LABORATORIES, LTD.
    公开号:US20160318886A1
    公开(公告)日:2016-11-03
    [Problem] The present invention addresses the problem of providing a novel compound. The present invention also addresses the problem of providing an OCT3 detection agent or an OCT3 activity inhibitor, which comprises the novel compound. [Solution] A compound represented by formula (A), a pharmaceutically acceptable salt thereof, or a pharmaceutically acceptable solvate thereof. R 1 -R 2 -R 3 -R 4 (A)
  • US9745274B2
    申请人:——
    公开号:US9745274B2
    公开(公告)日:2017-08-29
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