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

cis-α-(N2-Deoxyguanosinyl)-N-desmethyltamoxifen

中文名称
——
中文别名
——
英文名称
cis-α-(N2-Deoxyguanosinyl)-N-desmethyltamoxifen
英文别名
9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-[[(Z)-4-[4-[2-(methylamino)ethoxy]phenyl]-3,4-diphenylbut-3-en-2-yl]amino]-1H-purin-6-one
cis-α-(N<sup>2</sup>-Deoxyguanosinyl)-N-desmethyltamoxifen化学式
CAS
——
化学式
C35H38N6O5
mdl
——
分子量
622.724
InChiKey
NRPRRGFWSXQYLN-LCBQWNOESA-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):
    4.5
  • 重原子数:
    46
  • 可旋转键数:
    12
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    142
  • 氢给体数:
    5
  • 氢受体数:
    8

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

反应信息

  • 作为产物:
    描述:
    (E)-4-{4-[2-(N-Ethoxycarbonyl-N-methylamino)ethoxy]phenyl}-3,4-diphenyl-3-buten-2-ol 在 palladium on activated charcoal 吡啶氢氧化钾 、 Tris-HCl buffer 、 氢气一水合肼三乙胺 作用下, 以 甲醇乙二醇乙酸乙酯乙腈 为溶剂, 反应 40.0h, 生成 cis-α-(N2-Deoxyguanosinyl)-N-desmethyltamoxifen
    参考文献:
    名称:
    Identification of Tamoxifen−DNA Adducts Induced by α-Acetoxy-N-desmethyltamoxifen
    摘要:
    Treatment with tamoxifen increased the risk of endometrial cancers in breast cancer patients and women participating in the chemoprevention study. In our laboratory, tamoxifen-DNA adducts, including alpha-(N-2-deoxyguanosinyl)tamoxifen (dG-N-2-TAM), were detected in the endometrium of women taking tamoxifen [Shibutani, S., et al. (1999) Chem. Res. Toxicol. 12, 646-653]. On the basis of recent animal studies, deoxyguanosinyl-N-desmethyltamoxifen (dG-N-desmethylTAM) adducts are also suspected to be formed in the liver. In the study presented here, we synthesized alpha-acetoxy-N-desmethyltamoxifen as a model activated metabolite of N-desmethyltamoxifen. The overall yield of alpha-acetoxy-N-desmethyltamoxifen from alpha-hydroxytamoxifen was approximately 42%. alpha-Acetoxy-N-desmethyltamoxifen was highly reactive to 2'-deoxyguanosine, as was similarly observed for tamoxifen alpha-sulfate. The two reaction products were identified as a mixture of epimers of the trans form or cis form of alpha-(N-2-deoxyguanosinyl)N-desmethyltamoxifen (dG-N-2-N-desmethylTAM) by mass and proton magnetic resonance spectres copy. In addition, the trans and cis forms of dG 3'-monophosphate-N-2-N-desmethylTAM were prepared as standard markers for P-32-postlabeling/HPLC analysis. Using this technique, dG-N-2-N-desmethylTAM adducts were detected in calf thymus DNA reacted with alpha-acetoxy-N-desmethyltamoxifen.
    DOI:
    10.1021/tx000074o
点击查看最新优质反应信息