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5-formyl-furan-2-carbothionic acid-S-2,4,6-trichlorophenyl ester | 685903-55-3

中文名称
——
中文别名
——
英文名称
5-formyl-furan-2-carbothionic acid-S-2,4,6-trichlorophenyl ester
英文别名
S-(2,4,6-trichlorophenyl) 5-formylfuran-2-carbothioate
5-formyl-furan-2-carbothionic acid-S-2,4,6-trichlorophenyl ester化学式
CAS
685903-55-3
化学式
C12H5Cl3O3S
mdl
——
分子量
335.595
InChiKey
MVIGJFSIXDUHKY-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):
    5
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    72.6
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • [EN] 2 - SUBSTITUTED HETEROCYCLIC COMPOUNDS AND ANTITUMOR COMPOSITION COMPRISING THE SAME<br/>[FR] COMPOSES HETEROCYCLIQUES SUBSTITUES EN POSITION 2 ET COMPOSITION ANTITUMORALE RENFERMANT LESDITS COMPOSES
    申请人:CHONG KUN DANG PHARM CORP
    公开号:WO2004037808A1
    公开(公告)日:2004-05-06
    The present invention relates with 2-substituted heterocyclic compounds and antitumor composition comprising the same. The compound according to the present invention exhibits superior effect as telomerase inhibitor based on new mechanism (terlomere-terlomerase) which can resolve the problems occurring at the time of using chemotherapeutics, i.e side effects and cross resistance between related mechanism on using chemotherapeutics. In addition, the antitumor composition comprising the compound of the present invention exhibits superior effect in inhibiting the growth of cancer cell.
    本发明涉及2-取代杂环化合物和包括其在内的抗肿瘤组合物。根据本发明的化合物基于新机制(端粒酶-端粒酶)表现出优越的端粒酶抑制剂效果,可以解决在使用化疗药物时出现的问题,即副作用和化疗药物之间相关机制的交叉耐药性。此外,包括本发明化合物的抗肿瘤组合物表现出优越的抑制癌细胞生长的效果。
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同类化合物

硬脂酸对甲苯硫酯 硫基丙酸苯酯 硫代乙酸S-[4-[二(2-氯乙基)氨基]苯基]酯 硫代乙酸 S-(2-乙基苯基)酯 乙硫酸,[[(1,1-二甲基乙基)二甲基甲硅烷基]氧代]-,S-苯基酯 丙硫酸,S-(2-甲氧苯基)酯 S1,S2-二(4-氯苯基)乙烷二(硫代ate) S-苯基硫代异丁酸酯 S-苯基3-羟基硫代丁酸酯 S-苯基2-氟硫代乙酸酯 S-硫代乙酸苯酯 S-氯乙酰基-P-巯基甲苯 S-丙酰基-p-疏基甲苯 S-[4-[2-[4-(2-苯乙炔基)苯基]乙炔基]苯基]硫代乙酸酯 S-(三氟乙酰基)-4-疏基甲苯 S-(4-甲基苯基)硫代乙酸酯 S,S′-[1,4-亚苯基二(2,1-乙炔二基-4,1-亚苯基)]双(硫代乙酸酯) O-乙基S-(4-甲基苯基)单硫代草酸酯 4-溴苯基硫代乙酸酯 4-(S-乙酰基硫代)苯甲醛 4,4-二甲基-1-氧代-1-(苯基硫基)-2-戊烷基乙酸酯 3-氧代-3-(4-甲氧基苯氧基)丙酸 2-甲基苯硫酚乙酸酯 2-(氯甲酰基)-1-环戊烯-1-基硫氰酸酯 1-乙酰巯基-4-碘苯 S-(p-tolyl) cyclohexanecarbothioate 4-(2,5-Dioxo-pyrrolidin-1-yl)-thiobutyric acid S-phenyl ester S-phenyl 2-[(S)-[(2-methylpropan-2-yl)oxycarbonylamino]-phenylmethyl]-3-oxobutanethioate Tribromthioessigsaeure-phenylester Thiocrotonsaeure-S-<4-chlor>-phenylester (4S)-4-<(Z)-3-Acetoxy-2-phenylthio-2-propenoyl>-2,2-dimethyl-1,3-dioxolane (Z)-2,3,4,5,5-Pentachloro-penta-2,4-dienethioic acid S-(4-tert-butyl-phenyl) ester trans-dichlorobis(thio-L-leucine-S-phenylester-N)platinum(II) 2,3,4,5,5-Pentachlor-2,4-pentadienthiosaeure-S-(4-tolyl)ester (2Z)-2,3,4,5-tetrachloro-5-(p-tolylthio)penta-2,4-dienoyl chloride (Z)-1,3-bis(phenylthio)-5-hydroxy-2-penten-1-one (2Z,4E)-2,3,4,5-Tetrachloro-5-(4-chloro-phenylsulfanyl)-penta-2,4-dienoyl chloride S-phenyl 2-diazoethanethioate (Z)-2,3,4,5,5-Pentachloro-penta-2,4-dienethioic acid S-(4-chloro-phenyl) ester Dithiocarbonic acid S-pentachlorophenyl ester S-phenyl ester Phenyl-α-phenylacetothiol-acetat S-(2,3,4,5,6-pentachlorophenyl) (2Z)-2,3,4,5,5-pentachloropenta-2,4-dienethioate tert-butyl 2-methyl-3-oxo-3-(phenylthio)propanoate (2Z,4E)-2,3,4,5-tetrachloro-5-(phenylthio)penta-2,4-dienoyl chloride (Z)-2,3,5,5-Tetrachlor-4-phenylthio-2,4-pentadienthiosaeure-S-phenylester (Z)-2,3,4,5-Tetrachlor-5-methylthio-2,4-pentadienthiosaeure-S-pentachlorphenylester tridecanethioic acid S-phenyl ester 1,4-bis[4-(acetylsulfanyl)phenylethynyl]-2,6-di-t-butylbenzene phenyl 2,3,4,6-tetradeoxy-4-(acetylthio)-1-thio-α-D-erythro-hex-2-enopyranoside