Cys-McMMAF
目录号: PL07230 纯度: ≥99%
CAS No. :1160590-05-5
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中文名称
Cys-McMMAF
英文名称
Cys-McMMAF
英文别名
N-[6-[3-[[(2R)-2-Amino-2-carboxyethyl]thio]-2,5-dioxo-1-pyrrolidinyl]-1-oxohexyl]-N-methyl-L-valyl-L-valyl-(3R,4S,5S)-3-methoxy-5-methyl-4-(methylamino)heptanoyl-(αR,βR,2S)-β-methoxy-α-methyl-2-pyrrolidinepropanoyl-L-phenylalanine;Cys-McMMAF;SGN-75;1399672-02-6;1165741-01-4;UNII-F3R7A4P04N;H5324S1M7H;Immunoglobulin G1-kappa auristatin F conjugate, anti-(homosapiens CD19 (b lymphocyte surface antigen B4, leu-12)), humanized monoclonal antibody;MONOMETHYL AURISTATIN F CYSTEINYL-CONJUGATE;denintuzumab-mafodotin;CYSTEINYL-MAFODOTIN;Depatuxizumab mafodotin [USAN];SGN 75;MAFODOTIN-CYSTEINYL;F3R7A4P04N;699619YVTQ;Denintuzumab mafodotin;Depatuxizumab mafodotin;L-Valinamide, N-(6-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxohexyl)-N-methyl-L-valyl-N-((1S,2R)-4-((2S)-2-((1S,2R)-3-(((1S)-1-carboxy-2-phenylethyl)amino)-1-methoxy-2-methyl-3-oxopropyl)-1-pyrrolidi nyl)-2-methoxy-1-((1S)-1-methylpropyl)-4-oxobutyl;SGN-CD19A;UNII-699619YVTQ;1160590-05-5;MS-31894;B4S8ET206U;Abbv-221;Vorsetuzumab mafodotin;UNII-H5324S1M7H;Denintuzumab mafodotin [USAN:INN];CYSTEINYL-MFFA;ABT-414;Vorsetzumab Mafodotin [USAN];Depatux-m;Vorsetzumab Mafodotin;1585973-65-4;Vorsetuzumab mafodotin [USAN:INN];N-(6-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanoyl)-N-methyl-L-valyl-N-((3R,4S,5S)-1-((2S)-2-((1S,2R)-3-(((1S)-1-carboxy-2-phenylethyl)amino)-1-methoxy-2-methyl-3-oxopropyl)-1-pyrrolidinyl)-3-methoxy-5-methyl-1-oxo-4-heptanyl)-N-methyl-L-valinamide;SGN-CD 19A
Cas No.
1160590-05-5
分子式
C52H83N7O13S
分子量
1046.32
包装储存
-20°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
产品详情
Cys-McMMAF 是 AlMcMMAF 释放的有效载荷,AlMcMMAF 是一种抗 5T4 的人源化 A1 抗体,通过马来酰咪唑丙基连接物偶联到微管破坏 MMAF (HY-15579)。Cys-McMMAF 对两种肿瘤小鼠模型(H1975 和 MDA-MB-361-DYT2 模型) 均有抑癌效果。
生物活性
Cys-McMMAF is the released payload of AlMcMMAF, an anti-5T4 humanized A1 antibody conjugated to the microtubule disrupting MMAF (HY-15579) via a maleimidocaproyl linker. Cys-McMMAF has antitumor efficacy in two tumor mouse models (H1975 and MDA-MB-361-DYT2 models).
性状
Solid
体内研究(In Vivo)
Cys-McMMAF (0.3 mg/kg, 3 mg/kg; 静脉注射; 单剂量) 在食蟹猴体内的稳定性一般,衰退时间短。

在裸鼠 (nu/nu) 中的药代动力学分析
Model/IV Dose (mg/kg) C max (ng/mL) T max (hr)
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
-20°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Leal M, et al. Preclinical Development of an anti-5T4 Antibody-Drug Conjugate: Pharmacokinetics in Mice, Rats, and NHP and Tumor/Tissue Distribution in Mice. Bioconjug Chem. 2015 Nov 18;26(11):2223-32.
溶解度数据
In Vitro: DMSO : 200 mg/mL (191.15 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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