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912569-84-7

中文名稱 N2'-脫乙?;?N2'-[3-(甲硫基)-1-氧丙基]-五月氨酸
CAS 912569-84-7
912569-84-7 結(jié)構(gòu)式 912569-84-7 結(jié)構(gòu)式

基本信息

中文別名
N2'-脫乙?;?N2'-[3-(甲硫基)-1-氧丙基]-五月氨酸
英文別名
S-methyl DM1
N2'-Deacetyl-N2'-[3-(methylthio)-1-oxopropyl]-maytansine
N2'-Deacetyl-N2'-[3-(methylthio)-1-oxopropyl]-maytansine (>90%)

常見問題列表

生物活性
S-methyl DM1 是一種美登素 (Maytansine) 的硫代甲基衍生物。S-methyl DM1 以 Kd 為 0.93 μM 結(jié)合微管蛋白并抑制微管聚合。S-methyl DM1 可以有效抑制微管動態(tài)不穩(wěn)定性,并具有抗癌作用。
靶點

Maytansinoids

體外研究

S-methyl DM1 is the primary cellular or liver metabolite of antibody-maytansinoid conjugates prepared with thiol-containing maytansinoids DM1.
The half-maximal concentration for inhibition of microtubule assembly for for S-methyl DM1 is 4 μM. At 100 nM S-methyl-DM1 (84%) suppresses dynamic instability more strongly than Maytansine (45%). Tritiated S-methyl-DM1 bound to 37 high-affinity sites per microtubule (K d of 0.1 μM).
The concentration dependence curves for the inhibition of cell proliferation by S-methyl DM1 is sigmoidal in shape in MCF7 cells. Minimal inhibition occurred at 200 pM S-methyl DM1, and inhibition is maximal at 3 nM. S-methyl DM1 (IC 50 of 330 pM) is slightly more potent than Maytansine (IC 50 of 710 pM).
S-methyl DM1 induces maxima of 80% accumulation of cells in G2/M as compared with only 30% in controls in MCF7 cells.

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