摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

异三尖杉酯碱 | 26833-86-3

中文名称
异三尖杉酯碱
中文别名
——
英文名称
isoharringtonine
英文别名
1-O-[(2S,3S,6R)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl] 4-O-methyl (2R,3S)-2,3-dihydroxy-2-(3-methylbutyl)butanedioate
异三尖杉酯碱化学式
CAS
26833-86-3
化学式
C28H37NO9
mdl
——
分子量
531.603
InChiKey
CAOHZEUEVKYHPF-XWHOPEMDSA-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:
    70.75°C
  • 沸点:
    610.6°C (rough estimate)
  • 密度:
    1.2566 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    38
  • 可旋转键数:
    10
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    124
  • 氢给体数:
    2
  • 氢受体数:
    10

反应信息

  • 作为反应物:
    描述:
    异三尖杉酯碱盐酸 作用下, 以 为溶剂, 反应 96.0h, 生成 2,3-Dihydroxy-2-isopentylbutan-1,4-dicarbonsaeure
    参考文献:
    名称:
    来自 Cephalotaxus harringtonia var. 的酯型三尖杉生物碱。核果
    摘要:
    从 Cephalotaxus harringtonia var. 的叶子和茎中分离出三种生物碱,新三尖杉酯碱、高三尖杉酯碱和 3'S-羟基新三尖杉酯碱。核果。它们的结构是通过光谱方法建立的,包括二维核磁共振和 CD 光谱,并使用 P-388 白血病细胞评估它们的抗白血病活性。
    DOI:
    10.1016/s0031-9422(96)00574-2
点击查看最新优质反应信息

文献信息

  • Alkaloids from Cephalotaxus harringtonia
    作者:Ichiro Takano、Ichiro Yasuda、Motohiro Nishijima、Yukio Hitotsuyanagi、Koichi Takeya、Hideji Itokawa
    DOI:10.1016/0031-9422(96)00217-8
    日期:1996.9
    Four alkaloids, 5′-des- O -methylharringtonine, 3′ S -hydroxy-5′-des- O -methylharringtonine, 5′-des- O -methylhomoharringtonine and 5′-des- O -methylisoharringtonine, were isolated from the leaves and stems of C. harringtonia var. drupacea. Their structures were established by 1 H and 13 C NMR spectroscopic studies, chemical conversions to known alkaloids and applying the advanced Mosher's method for
    摘要 从 5'-des-O-methylharringtonine、3'S-hydroxy-5'-des-O-methylharringtonine、5'-des-O-methylhomharringtonine 和 5'-des-O-methylisoharringtonine 中分离出四种生物碱。 C. harringtonia var. 的叶子和茎。核果。它们的结构是通过 1 H 和 13 C NMR 光谱研究、化学转化为已知生物碱以及对仲醇部分应用先进的 Mosher 方法确定的。
  • ACYLATED DERIVATIVE OF HOMOHARRINGTONINE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF
    申请人:Xu Rongzhen
    公开号:US20140303147A1
    公开(公告)日:2014-10-09
    The present invention belongs to the field of natural medicine and pharmaceutical chemistry, and relates to novel homoharringtonine acylated derivatives of formula (I) and formula (II) and a pharmaceutically acceptable salt thereof, to a process for the preparation of these compounds, compositions containing such compounds and their use in preparing antineoplastic medicaments.
    本发明属于天然药物和制药化学领域,涉及公式(I)和公式(II)的新型羟基哈林汀酰化衍生物及其药学上可接受的盐,以及制备这些化合物的方法,含有这些化合物的组合物以及它们在制备抗肿瘤药物中的应用。
  • AMINATED DERIVATIVE OF HOMOHARRINGTONINE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF
    申请人:Rong Frank
    公开号:US20140206669A1
    公开(公告)日:2014-07-24
    The present invention belongs to the field of natural medicine and pharmaceutical chemistry and specifically relates to novel aminated homoharringtonine derivatives of formula (I) and a pharmaceutically acceptable salt thereof, to a process for the preparation of these compounds, compositions containing such compounds and their use in preparing antineoplastic medicaments.
    本发明属于天然药物和药学化学领域,具体涉及公式(I)的新型基化的同蒿芦丁生物及其药学上可接受的盐,制备这些化合物的方法,含有这些化合物的组合物以及它们在制备抗肿瘤药物方面的用途。
  • [EN] AMINATED DERIVATIVE OF HOMOHARRINGTONINE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF<br/>[FR] DÉRIVÉ AMINÉ D'HOMOHARRINGTONINE, PROCÉDÉ DE PRÉPARATION ET APPLICATION ASSOCIÉS
    申请人:HANGZHOU BENSHENG PHARMACEUTICAL CO LTD
    公开号:WO2013023620A1
    公开(公告)日:2013-02-21
    本发明属于天然药物及药物化学领域,具体涉及通式I的新型高三尖杉酯碱的胺化衍生物或其药学上可接受的盐,制备这些化合物的方法、包含该化合物的药物组合物及其在制备抗肿瘤药物中的用途。
  • [EN] ACYLATED DERIVATIVE OF HOMOHARRINGTONINE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF<br/>[FR] DÉRIVÉ ACYLÉ D'HOMOHARRINGTONINE, PROCÉDÉ DE PRÉPARATION ET APPLICATION ASSOCIÉS
    申请人:HANGZHOU BENSHENG PHARMACEUTICAL CO LTD
    公开号:WO2013023622A1
    公开(公告)日:2013-02-21
    本发明属于天然药物及药物化学领域并涉及通式I和通式II的新型高三尖杉酯碱的酰化衍生物或其药学上可接受的盐,制备这些化合物的方法、包含该化合物的药物组合物及其在制备抗肿瘤药物中的用途。
查看更多

同类化合物

高三尖杉酯碱酰胺 高三尖杉酯碱 氧桥三尖杉碱 异三尖杉酯碱 双(去甲基)-脱氧三尖杉酯碱 去甲基三尖杉酮碱 去氧哈林通碱 乙酰三尖杉碱 三尖杉酯碱 三尖杉酯碱 三尖杉碱 4-羟基三尖杉碱 4'-去甲基高三尖杉酯碱 (1S,3aR)-1,5,6,8,9,14bbeta-六氢-2-甲氧基-4H-环戊并[a][1,3]二氧杂环戊并[4,5-H]吡咯并[2,1-b][3]苯并氮杂卓-1alpha,9alpha-二醇 (-)-脱水三尖杉酯碱 (2S,3R,4S,5S,7R)-2,3-dihydroxy-7-methyl-cephalotaxan-8-one (2R,3S,4S,5S)-2,3-dihydroxy-8-oxocephalotaxane (+/-)-D-homocephalotaxine Desmethyldiacetyl-cephalotaxin (3aα,4S*,10β,15bβ,15cα)-(+/-)-10-acetoxy-3a,4,6,7,9,10,15b,15c-octahydro-2,2-dimethyl-5H-<1,3>dioxolo<4,5-h>-1,3-dioxolo<4,5>cyclopenta<1,2-a>pyrrolo<2,1-b><3>benzazepine Cephalotaxyl 6,6-dimethyl-5,6-dihydropyran-1-carboxylate 3t-phenyl-acrylic acid (3aR)-2-methoxy-(3arC4,14bc)-1,5,6,8,9,14b-hexahydro-4H-cyclopenta[b][1,3]dioxolo[4',5':4,5]benzo[1,2-d]pyrrolo[1,2-a]azepin-1t-yl ester 6-O-(4-methylimidazole-3-carbonyl)2,6-diacetylhomoharringtonine 6-O-(2-chloropyridin-3-carbonyl)2,6-diacetylhomoharringtonine (Ξ)-methylsuccinic acid 1-((3aR)-2-methoxy-(3arC4,14bc)-1,5,6,8,9,14b-hexahydro-4H-cyclopenta[b][1,3]dioxolo[4',5':4,5]benzo[1,2-d]pyrrolo[1,2-a]azepin-1t-yl) ester 4-methyl ester 6-O-(phenylacetyl)2,6-diacetylhomoharringtonine 6-O-(furan-2-carbonyl)2,6-diacetylhomoharringtonine succinic acid (3aR)-2-methoxy-(3arC4,14bc)-1,5,6,8,9,14b-hexahydro-4H-cyclopenta[b][1,3]dioxolo[4',5':4,5]benzo[1,2-d]pyrrolo[1,2-a]azepin-1t-yl ester methyl ester O-3-[(2R)-2,6-dihydroxy-2-(2'-cyclohexaneamino-2'-oxoethyl)-6-methylheptanoyl]cephalotaxine (2R,7R)-17,19-dioxa-11-azapentacyclo[12.7.0.02,7.07,11.016,20]henicosa-1(21),4,12,14,16(20)-pentaen-10-one Acetic acid 6-((1aR,2aS,5aR,6S,6aS)-5-methyl-4-oxo-octahydro-1-oxa-5-aza-cyclopropa[f]inden-6-yl)-benzo[1,3]dioxol-5-ylmethyl ester (Ξ)-(3-methyl-butyl)-succinic acid 1-((3aR)-2-methoxy-(3arC4,14bc)-1,5,6,8,9,14b-hexahydro-4H-cyclopenta[b][1,3]dioxolo[4',5':4,5]benzo[1,2-d]pyrrolo[1,2-a]azepin-1t-yl) ester 4-methyl ester 1-O-[(2S,3S,6R)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl] 4-O-methyl (2R)-2-[4-methyl-4-(4-methyl-1,3-thiazole-5-carbonyl)oxypentyl]-2-(4-methyl-1,3-thiazole-5-carbonyl)oxybutanedioate 3,8-dioxocephalotax-1-ene furan-3,4-dicarboxylic acid (3aR)-2-methoxy-(3arC4,14bc)-1,5,6,8,9,14b-hexahydro-4H-cyclopenta[b][1,3]dioxolo[4',5':4,5]benzo[1,2-d]pyrrolo[1,2-a]azepin-1t-yl ester methyl ester 2α,3α-dihydroxycephalotaxan-8-one 2,3-dehydrocephalotaxan-8-one 1-O-[(2S,3S,6R)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl] 4-O-methyl (2R)-2-[4-(cyclohexanecarbonyloxy)-4-methylpentyl]-2-hydroxybutanedioate 2α,3α-epoxycephalotaxan-8-one [(2S,3R,4S,6S)-3-acetyloxy-9-oxo-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),13,15(19)-trien-4-yl] acetate (3-methyl-butyl)-butenedioic acid 1-((3aR)-2-methoxy-(3arC4,14bc)-1,5,6,8,9,14b-hexahydro-4H-cyclopenta[b][1,3]dioxolo[4',5':4,5]benzo[1,2-d]pyrrolo[1,2-a]azepin-1t-yl) ester 4-methyl ester benzyl ((2S,3S,3aR)-2,3-dihydroxy-2,3,5,6,8,9-hexahydro-4H-[1,3]dioxolo[4',5':4,5]benzo[1,2-d]cyclopenta[b]pyrrolo[1,2-a]azepin-1-yl) carbonate 3t-(4-nitro-phenyl)-acrylic acid (3aR)-2-methoxy-(3arC4,14bc)-1,5,6,8,9,14b-hexahydro-4H-cyclopenta[b][1,3]dioxolo[4',5':4,5]benzo[1,2-d]pyrrolo[1,2-a]azepin-1t-yl ester (2R,3S,4S,5S)-2-(tert-butyldimethylsililoxy)-3-hydroxy-8-oxocephalotaxane