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  • McMMAF (Maleimidocaproyl monomethylauristatin F)
McMMAF (Maleimidocaproyl monomethylauristatin F)的可视化放大

McMMAF (Maleimidocaproyl monomethylauristatin F)

McMMAF (Maleimidocaproyl monomethylauristatin F) 是一种保护基团缀合的 MMAF。 MMAF 是一种有效的微管蛋白聚合抑制剂。

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McMMAF (Maleimidocaproyl monomethylauristatin F)的二维码
  • 库存: 现货
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  • 包装
    价格
    促销价
    数量
  • 1mg
    ¥825.00
    660.00
    - +
  • 5mg
    ¥1462.00
    1170.00
    - +
  • 10mg
    ¥2437.00
    1950.00
    - +
已选 0 0
金额: ¥0.00
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  • 货号: ajce52378
  • CAS: 863971-19-1
  • 别名: Maleimidocaproyl monomethylauristatin F
  • 分子式: C49H76N6O11
  • 分子量: 925.16
  • 纯度: >98%
  • 溶解度: DMSO : ≥ 100 mg/mL (108.09 mM)
  • 储存: Store at -20°C,unstable in solution, ready to use.
  • 库存: 现货

Background

Mc-MMAF is a protective group-conjugated MMAF. MMAF is a more potent drug than Monomethyl auristatin E (MMAE), but is charged and relatively membrane-impermeable, is a potent tubulin inhibitor, is a toxin payload in antibody drug conjugate.Target:MMAF is a new auristatin derivative with a charged C-terminal phenylalanine that attenuates its cytotoxic activity compared to its uncharged counterpart, Monomethyl auristatin E (MMAE). Because of MMAF is highly toxic, it cannot be used as a drug itself. MMAF induces potent antitumor effects when conjugated via protease cleavable linkers to a monoclonal antibody targeting internalizing, tumor-specific cell surface antigens. The linker to the monoclonal antibody is stable in extracellular fluid, but is cleaved by cathepsin once the conjugate has entered a tumor cell, thus activating the anti-mitotic mechanism.



[1]. Polson AG, et al. Antibody-drug conjugates for the treatment of non-Hodgkin's lymphoma: target and linker-drug selection. Cancer Res. 2009 Mar 15;69(6):2358-2364. [2]. Jianmin Fang, et al. Anti-her2 antibody and conjugate thereof. US 20160304621 A1.

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