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3,4-二氢-1H-异硫苯并吡喃-4-胺盐酸盐 | 123470-16-6

中文名称
3,4-二氢-1H-异硫苯并吡喃-4-胺盐酸盐
中文别名
3,4-二氢-1H-2-苯并噻喃-4-胺
英文名称
3,4-dihydro-1H-isothiochromen-4-amine hydrochloride
英文别名
3,4-dihydro-1H-isothiochromen-4-amine;hydrochloride
3,4-二氢-1H-异硫苯并吡喃-4-胺盐酸盐化学式
CAS
123470-16-6
化学式
C9H12ClNS
mdl
MFCD09999254
分子量
201.72
InChiKey
NZDWPPWVNMWXBR-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

物化性质

  • 熔点:
    153-155℃
  • 沸点:
    153-155 °C(Press: 14 Torr)
  • 密度:
    1.153

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    51.3
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:35ac97f66425113648e4235180f89b1c
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文献信息

  • HIV protease inhibitors having polyether substituents
    申请人:MERCK & CO. INC.
    公开号:EP0487270A2
    公开(公告)日:1992-05-27
    Polyether derivatives of the form,         A-G-B-B-J    wherein G is a dipeptide isostere substituted with a polyether, B an amino acid or analog thereof, and J a small terminal group are described. These compounds are useful in the inhibition of DIV protease, the prevention or treatment of infection by HIV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.
    描述了形式为A-G-B-B-J的聚醚衍生物,其中G是用聚醚取代的二肽同分异构体,B是氨基酸或其类似物,J是一个小的末端基团。这些化合物在抑制DIV蛋白酶、预防或治疗HIV感染以及治疗艾滋病方面具有用途,无论是作为化合物、药学上可接受的盐、药物组成成分,还是与其他抗病毒药物、免疫调节剂、抗生素或疫苗组合使用。还描述了治疗艾滋病的方法以及预防或治疗HIV感染的方法。
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同类化合物

6-溴-3,4-二氢-2H-异硫代色烯-4-胺盐酸盐 6-溴-3,4-二氢-1H-S,S-二氧代异硫色烯-4-氨基盐酸盐 4-氨基异硫代苯并二氢吡喃2,2-二氧化物盐酸盐 3,4-二氢-1H-异硫苯并吡喃-4-胺盐酸盐 3,4-二氢-1H-S,S-二-氧代-异硫基苯并吡喃-4-胺盐酸盐 3,4-二氢-1H-2-苯并噻喃 2-异硫代苯并二氢吡喃-4-酮 1H-2-苯并噻喃-4-醇,3,4-二氢- (9ci)-3,4-二氢-1H-2-苯并硫代吡喃-1-羰酰氯 (4r)-(9ci)-6-乙基-3,4-二氢-1H-2-苯并硫代吡喃-4-胺,2,2-二氧化物 4-amino-1-(3,3-dimethylisothiochroman-4-yl)-5-imidazolecarboxylic acid methyl ester methyl 5,8-dimethoxyisothiochroman-3-carboxylate 1-(2'-Dimethylaminopropyl)-1-ethylsulfonyl-isothiochroman-S,S-dioxid N-diethoxyphosphoryl-6,7-dimethyl-3,4-dihydro-1H-2-benzothiopyran-4-one-1-carboxamide 1-(3,3-dimethylisothiochroman-4-yl)-5-imidazolecarboxylic acid methyl ester 4-methyl-isothiochroman-2,2-dioxide 1-(α-methoxybenzylidene)-3,4-dihydro-1H-2-thianaphthalene 3-methyl-isothiochroman-4-one 1,3-dimethyl-1H-2-benzothiopyran-4-(3H)-one 8-Oxo-1,2,3,5,7,8-hexahydro-6-thia-cyclopenta[b]naphthalene-5-carboxylic acid ethyl isothiochroman-1-carboxylate 1-<(3,4-dihydro-1H-2-benzothiopyran-3-yl)acetyl>-1H-indole 7-Methoxy-3-phenyl-4-isothiochromanon 4-oxo-isothiochroman-3-carboxylic acid methyl ester 7-methoxy-isothiochroman-4-ol 8-methylisothiochroman-4-one 1-cyano-1-methylisothiochroman ethyl 6,7-dimethyl-3,4-dihydro-1H-2-benzothiopyran-4-one-1carboxylate 4-diazoisothiochroman-3-one 3,4-dihydro-3,3-dimethyl-1H-2-thianaphthalene 3,6-dithiaoctahydrophenanthrene-1,8-dione 3,6-dithia-3,4,5,6,7,8-hexahydrophenanthrene[1,2-d][1,2,3]selenadiazol-8-one (S)-(+)-4-ethyl-3,4-dihydro-1H-2-benzothiine 5-chloro-3,4-dihydro-1H-2-benzothiopyran 5-chloro-3,4-dihydro-1H-2-benzothiopyran 2,2-dioxide 8-oxo-5H-thiopyrano[4,3-f][1,3]benzodioxole-5-carboxylic acid 8-phenylisothiochroman-1-one N-<4-(diethoxyphosphorylmethyl)phenyl>-6-cyclohexyl-3,4-dihydro-4-oxo-1H-2-benzothiopyran-1-carboxamide 7-methoxy-isothiochroman-3-carbonyl chloride ethyl 3,4-dihydrospiro(1H-2-benzothiopyran-1,4'-piperidine)-1'-carboxylate 3,4-dihydrospiro(1H-2-benzothiopyran-1,4'-piperidine) 3,4-dihydrospiro(1H-2-benzothiopyran-1,4'-piperidine) 2-oxide 8-Chloroisothiochroman-4-one 1-(3-nitrophenyl)-3,4-dihydro-1H-isothiochromene 7-Chlor-isothiochroman-4-on 3-acetyl-5,8-dimethoxyisothiochroman isothiochroman-4-ylamine 5-methyl-3,4-dihydro-1H-2-benzothiopyran-1-one 2-ethyl-4-oxoisothiochromanium tetrafluoroborate 3,7-dithiaoctahydroanthracene-1,5-dione