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环长春新碱 | 101156-38-1

中文名称
环长春新碱
中文别名
——
英文名称
cyclovincristine
英文别名
methyl (1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-4-[(1R,10S,12R,14S,19S)-14-ethyl-14-hydroxy-10-methoxycarbonyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,8-tetraen-10-yl]-8-formyl-10-hydroxy-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate
环长春新碱化学式
CAS
101156-38-1
化学式
C46H54N4O10
mdl
——
分子量
822.956
InChiKey
FWCHYDZYHYJFEX-MRAFOVRVSA-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

  • 密度:
    1.47±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    60
  • 可旋转键数:
    10
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    168
  • 氢给体数:
    2
  • 氢受体数:
    13

SDS

SDS:fa04a42a91d9a9981adbeb6ffa051b10
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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

  • 作为反应物:
    描述:
    环长春新碱 在 sodium tetrahydroborate 作用下, 以 二氯甲烷溶剂黄146 为溶剂, 反应 2.0h, 以79%的产率得到长春新碱
    参考文献:
    名称:
    Synthesis of Vinca Alkaloids and Related Compounds. Part XCIII. Skeletal Rearrangement of Cyclovinblastine Derivatives: Formation of a Novel Bisindole System
    摘要:
    DOI:
    10.3987/com-98-s(h)25
  • 作为产物:
    描述:
    cyclovinblastine sulfate 在 chromium(VI) oxide乙酸酐 作用下, 以 二氯甲烷溶剂黄146 为溶剂, 反应 0.33h, 以29%的产率得到环长春新碱
    参考文献:
    名称:
    Synthesis of Vinca Alkaloids and Related Compounds. Part XCIII. Skeletal Rearrangement of Cyclovinblastine Derivatives: Formation of a Novel Bisindole System
    摘要:
    DOI:
    10.3987/com-98-s(h)25
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文献信息

  • Bisindole Alkaloids Condensed with a Cyclopropane Ring, Part 1. 14,15-Cyclopropanovinblastine and -vincristine
    作者:Csaba Szántay、Péter Keglevich、László Hazai、Zsófia Dubrovay、Csaba Szántay、György Kalaus
    DOI:10.3987/com-13-12918
    日期:——
    A new type of vinblastine and vincristine derivatives was synthesized. The carbon carbon double bond in position 14 and 15 of the vindoline ring was cyclopropanated. In the course of the synthetic work 14,15-cyclopropano-vindoline was coupled with catharanthine, resulting in the cyclopropanated anhydrovinblastine as a key intermediate to 14,15-cyclopropano-vinblastine and vincristine.
  • US4659816A
    申请人:——
    公开号:US4659816A
    公开(公告)日:1987-04-21
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同类化合物

长春立辛 长春新碱M1 脱乙酰基文多灵 罗西定碱 环长春新碱 温都罗新 文多灵 它波宁盐酸盐 它勃宁 Ervamycine; 11-甲氧基水甘草碱 4',5'-二去氢-4'-脱氧-2',19'-二氧代-2',19'-仲长春碱 16-O-乙酰文多灵 11-羟基他波宁 3-demethoxycarbonyl-3-(3'-methylbutyrylamino)methylvindoline 3-demethoxycarbonyl-3-(pivaloylamino)methylvindoline 10-acetylaminovindoline 10-methanesulfonylaminovindoline N(a)-Acetyl-20-oxo-aspido-fraktinin 3-demethoxycarbonyl-3-(propionylamino)methylvindoline (3aR,4R,5S,5aR,10bR,12bR)-4-Acetoxy-3a-ethyl-5-hydroxy-9-(hydroxy-methoxycarbonyl-methyl)-8-methoxy-6-methyl-3a,4,5,5a,6,11,12,12b-octahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester 3-demethoxycarbonyl-3-(butyrylamino)methylvindoline 3-demethoxycarbonyl-3-(isobutyrylamino)methylvindoline Na-Acetyl-7β-ethyl-5-desethylaspidospermidin-Nb-methiojodid (3aS,5aS,10bR,12bS)-3a-Ethyl-5-hydroxy-6-methyl-4-oxo-12a-oxy-3a,4,5,5a,6,11,12,12b-octahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester Neblinindiol 1-formyl-16-methoxy-8-oxo-aspidospermidine-3-carboxylic acid methyl ester 1-formyl-16-methoxy-8-oxo-3,4-didehydro-aspidospermidine-3-carboxylic acid methyl ester 1-acetoxy-13a-ethyl-11-methyl-2,3,5,6,6a,11,12,13,13a,13b-decahydro-1H-cyclopenta[ij]indolo[2,3-a]quinolizine Tetrahydrohaplophytin I 4-acetoxy-3-hydroxy-16-methoxy-1-methyl-6,7-didehydro-aspidospermidine-3-carboxylic acid methylamide Dihydrogeissovellin 15-formyl-16-methoxy-1-methyl-10-oxo-3,4-didehydro-aspidospermidine-3-carboxylic acid methyl ester 3,4-diacetoxy-8-acetyl-16-methoxy-1-methyl-7,8-didehydro-aspidospermidine-3-carboxylic acid methyl ester 4-acetoxy-1-formyl-3-hydroxy-16-methoxy-6,7-didehydro-aspidospermidine-3-carboxylic acid methyl ester (3a-ethyl-6-methyl-3a,4,5,5a,6,11,12,13a-octahydro-1H-indolizino[8,1-cd]carbazol-5-yl)-methanol (2R,3aS,4S,5R,5aS,10bS,12bS)-4-Acetoxy-3a-ethyl-2,5-dihydroxy-8-methoxy-6-methyl-2,3,3a,4,5,5a,6,11,12,12b-decahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester methyl (3aR,3a1S,4S,5R,5aS,10bR)-4-(benzyloxy)-3a-ethyl-8-methoxy-6-methyl-1-oxo-2,3,3a,4,5a,6,11,12-octahydro-3a1,5-epoxyindolizino[8,1-cd]carbazole-5(1H)-carboxylate Des-N(a)methyl-vindolin (3aR,10bR,13aS)-5-(methoxycarbonyl)-3a-ethyl-3a,4,6,11,12,13a-hexahydro-7,8-dimethoxy-1H-indolizino[8,1-cd]carbazol-9-yl methanesulfonate methyl (2R,3aR,3a1S,4S,5R,5aS,10bR)-4-(benzyloxy)-3a-ethyl-8-methoxy-6-methyl-1-oxo-2-((triisopropylsilyl)oxy)-2,3,3a,4,5a,6,11,12-octahydro-3a1,5-epoxyindolizino[8,1-cd]carbazole-5(1H)-carboxylate Acetylvindorosin 2,3,6,7-tetradehydro-16-methoxy-1-methyl-4-oxo-3-(methylthio)aspidospermidine 1,2-dehydro-19-carboethoxy-12-methoxy-19-demethylaspidospermidine aspidospermidin-3-one oxime Acetylvindolin-N-oxid rac-4,4-ethane-1,2-diylbissulfanyl-(5α)-20,21-dinor-aspidospermidin-10-one 3,4-diacetoxy-1-formyl-16-methoxy-9-oxy-6,7-didehydro-aspidospermidine-3-carboxylic acid methyl ester O-Methyl-tetrahydrohaplophytin I Methylester trans-15-Methoxyerythrinane