S-Methyl DM1 (S-Methyl Mertansine) Standard

S-Methyl DM1 (S-Methyl Mertansine) Standard

Catalog Number:
BRAK456787CEL
Mfr. No.:
CM11016-1MG
Price:
$482
  • Size:
    1mg
    Quantity:
    Add to Cart:
      • Overview
        • S-methyl DM1 is the primary cellular or liver metabolite of ADC or other conjugates prepared with DM1. DM1 (mertansine) is a thiol-containing derivative of maytansine. It binds to tubulin and inhibits the assembly of microtubules. DM1 is used to prepare antibody-drug conjugates, such as trastuzumab emtansine (abbreviated as T-DM1). DM1 is not very stable in aqueous solution and can be oxidized or dimerized.

          The S-methyl DM1 is a high purity product that can serve as a standard for HPLC and LC-MS/MS analysis. The product is formulated in DMSO solution, quantified by UV/HPLC using DM1 as standard/calibrator at 252 nm, and ready to use after dilution. Although S-methyl DM1 inhibits polymerization weaker than DM1, it can also be used as a stable control for ADC studies instead of DM1.

          The product is sold as 1 vial of 1 mg (133 uL x 10 mM).

          • Chemical Information
          Chemical name: S-Methyl DM1 (S-Methyl Mertansine) Synonym: N2'-deacetyl-N2'-(3-methylthio-1-oxopropyl)-maytansine
          Chemical formula: C36H50ClN3O10S
          Molecular weight: 752.32 Da; CAS number: 912569-84-7

          • Specifications
          Physical appearance: solution
          Storage temp.: -20 °C
          Purity: ≥ 98 % by C18 HPLC
          Concentration: 10 mM in DMSO (determined by UV/HPLC using DM1 as standard/calibrator at 252 nm)

          Please contact us at for specific academic pricing.

      • Properties
        • Categories
          Drug Intermediates and Metabolites

          * For Research Use Only. Not for Use in Diagnostic Procedures.

      • Reference
        • Lopus M. et al. (2010). Maytansine and Cellular Metabolites of Antibody-Maytansinoid Conjugates Strongly Suppress Microtubule Dynamics by Binding to Microtubules. Mol. Cancer. Ther. 9(1), 2689-2699.
          Oroudjev E. et al. (2010). Maytansinoid-Antibody Conjugates Induce Mitotic Arrest by Suppressing Microtubule Dynamic Instability. Cancer Ther. 9(10), 2700-2713.
          Davis J.A. et al. (2012) In Vitro Characterization of the Drug-Drug Interaction Potential of Catabolites of Antibody-Maytansinoid Conjugates. Drug Metabolism and Disposition 40(10), 1927-1934.

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