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1H-2-Benzothiopyran-4-on-oxim | 41231-28-1

中文名称
——
中文别名
——
英文名称
1H-2-Benzothiopyran-4-on-oxim
英文别名
1H-isothiochromen-4(3H)-one oxime;(NZ)-N-(1H-isothiochromen-4-ylidene)hydroxylamine
1H-2-Benzothiopyran-4-on-oxim化学式
CAS
41231-28-1
化学式
C9H9NOS
mdl
——
分子量
179.243
InChiKey
AXHKOOVWXLLLFD-MDZDMXLPSA-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):
    2.2
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    57.9
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

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文献信息

  • HIV protease inhibitors useful for the treatment of aids
    申请人:MERCK & CO. INC.
    公开号:EP0534511A1
    公开(公告)日:1993-03-31
    Compounds of the form,         A-G-J    wherein A is an amine protecting group or urethane, G a dipeptide isostere and J a small terminal group are described. They are distinguished by tetrahydrofuryl or tetrahydropyranyl substituents, and the like. These compounds are useful in the inhibition of HIV 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.
    形式为A-G-J的化合物被描述,其中A是胺保护基或醚,G是二肽同分异构体,J是小的末端基团。它们以四氢呋喃基或四氢吡喃基取代等方式进行区分。这些化合物在抑制HIV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、药用组合成分,还是与其他抗病毒药物、免疫调节剂、抗生素或疫苗结合使用。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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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 isothiochroman-1-yl-methyl-amine Isothiochroman-carbonsaeure-(1)-methylester 1-methyl-1H-2-benzothiopyran-1-carbonitrile 1-Methylenisothiochroman-2,2-dioxid 3,4-dihydro-1-vinyl-1H-2-benzothiopyran N-(2,4-Dinitro-phenyl)-N'-[(S)-1-methyl-isothiochroman-(4Z)-ylidene]-hydrazine 1,1'-Bis-(4,5-dihydro-1-oxy-2H-3-benzothiepin-3,3-dioxid)thiokohlensaeure-O,O-diester pyrrolidine-1-carboxylic acid isothiochroman-1-ylamide 1-(Chlormethyl)-isothiochroman-2,2-dioxid 4,5-Dihydro-2H-3-benzothiepin-1-on-2-thiocarbonsaeure-S-methylester isothiochroman-1-yl-carbamic acid ethyl ester piperidine-1-carbothioic acid isothiochroman-1-ylamide piperidine-1-carboxylic acid isothiochroman-1-ylamide 4,5-dihydro-benzo[d]thiepin-1-one semicarbazone 1-ethyl-3-isothiochroman-1-yl-thiourea 1-isothiochroman-1-yl-3-methyl-thiourea 2-(Methylen-dithiomethylen)-4,5-dihydro-2H-3-benzothiepin-1-on-3,3-dioxid 2-Benzyliden-4,5-dihydro-2H-3-benzothiepin-1-on methyl spiro[benzo[c]thiophene-1(3H),4'-piperidine]-1'-carboxylate 2,2-dioxide 1-hydroxy-3-isothiochroman-1-yl-urea 2-(N-p-Chlorphenyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on 1-isothiochroman-1-yl-3-methyl-urea di-isothiochroman-1-yl-amine 2-(N-Cyclohexyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on isothiochroman-1-yl-carbamic acid methyl ester 3-isothiochroman-1-yl-1,1-dimethyl-urea N-Isothiochroman-1-yl-N-methyl-formamide 2-(N-Phenyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on 4-isothiochroman-1-yl-semicarbazide 4,5-Dihydro-2H-3-benzothiepin-1-on-2-dithiocarbonsaeuremethylester 2-[2-Isothiochroman-(4Z)-ylidene-ethyl]-2-methyl-cyclopentane-1,3-dione 4-Hydroxy-4-vinylthiochroman 2-Methyl-2-{2-[6-methyl-isothiochroman-(4Z)-ylidene]-ethyl}-cyclopentane-1,3-dione 1-Methyl-1-carbamoyl-isothiochroman-2,2-dioxid 1-Deutero-1-cyano-isothiochroman morpholine-4-carbothioic acid isothiochroman-1-ylamide Dimethylaminomethyl-1-cyan-isothiochroman 1-Diethylaminomethyl-1-cyan-isothiochroman 2-Methyl-2-{2-[7-methyl-isothiochroman-(4Z)-ylidene]-ethyl}-cyclopentane-1,3-dione 55-((trimethylsilyl)ethynyl)-3,7-dithia-1(1,3),5(1,4)-dibenzenacyclooctaphane-12,15-dicarbonitrile