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HIT212667016
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HIT212667016
  • HIT ID:HIT212667016
  • Cas No:615538-51-7
  • 常用名:DC0-NH2
  • IUPAC:5-amino-N-{2-[(1S)-1-(chloromethyl)-5-hydroxy-1H,2H,3H-benzo[e]indole-3-carbonyl]-1H-indol-5-yl}-1H-indole-2-carboxamide
    IUPAC:5-amino-N-{2-[(1S)-1-(chloromethyl)-5-hydroxy-1H,2H,3H-benzo[e]indole-3-carbonyl]-1H-indol-5-yl}-1H-indole-2-carboxamide
  • InChI key:PANFWPQOVGEWSD-GOSISDBHSA-N
  • 分子式:C31H24ClN5O3
  • 分子量:550.02
  • 氢键供体数 (HBD):5
  • 氢键受体数 (HBA):4
  • LogP:4.2799244
  • SMILES:Nc1ccc2[nH]c(cc2c1)C(=O)Nc1ccc2[nH]c(cc2c1)C(=O)N1C[C@@H](CCl)c2c1cc(O)c1ccccc21
    SMILES:Nc1ccc2[nH]c(cc2c1)C(=O)Nc1ccc2[nH]c(cc2c1)C(=O)N1C[C@@H](CCl)c2c1cc(O)c1ccccc21
  • The cytotoxicity of DC0-NH2 is 1000 times that of commonly used anti-cancer drugs (such as doxorubicin). It is the effect part of ADC. It is a simplified simulation of DC1 and has better stability. DC0-NH2 can bind to the small groove of DNA, and then adenine residue is alkylated by its propabenzindole (CBI) component.
市场产品/服务共显示1个结果
  • 供应商
    TargetMolSC
    规格
    货期
    6-8周
    纯度
    -
    ¥ 10,600.00
    1

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