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S-methyl DM1, a thiomethyl derivative of Maytansine, binds to tubulin (Kd of 0.93 μM) and inhibits microtubule polymerization.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
25 mg | $1,670 | 6-8 weeks | |
50 mg | $2,180 | 6-8 weeks | |
100 mg | $2,800 | 6-8 weeks |
Description | S-methyl DM1, a thiomethyl derivative of Maytansine, binds to tubulin (Kd of 0.93 μM) and inhibits microtubule polymerization. |
Targets&IC50 | Tubulin:(kd)0.93 μM |
In vitro | S-methyl DM1, the primary cellular or liver metabolite of antibody-maytansinoid conjugates prepared with thiol-containing maytansinoids DM1[1], inhibits microtubule assembly at a half-maximal concentration of 4 μM. At 100 nM, S-methyl-DM1 (84%) suppresses dynamic instability more effectively than Maytansine (45%). Tritiated S-methyl-DM1 binds to 37 high-affinity sites per microtubule (Kd of 0.1 μM)[1]. Minimal inhibition occurs at 200 pM and is maximal at 3 nM. S-methyl DM1 (IC50 of 330 pM) is slightly more potent than Maytansine (IC50 of 710 pM)[2]. In MCF7 cells, S-methyl DM1 induces up to 80% accumulation of cells in G2/M compared to 30% in controls[2]. |
Molecular Weight | 752.31 |
Formula | C36H50ClN3O10S |
Cas No. | 912569-84-7 |
Relative Density. | 1.32 g/cm3 (Predicted) |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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