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MAYTANSINE
 INN MAYTANSINE ADO-TRASTUZUMAB EMTANSINE
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cas 139504-50-0 |
CLASS ANTINEOPLASTIC TREATMENT OF PATIENTS WITH HER2-POSITIVE, METASTATIC BREAST CANCER WHO PREVIOUSLY RECEIVED TRASTUZUMAB AND A TAXANE, SEPARATELY OR IN COMBINATION HER2-TARGETED ANTIBODY-DRUG CONJUGATE (ADC) EMTANSINE REFERS TO THE MCC-DM1 DM1 IS A MAYTANSINE DERIVATIVE AND MCC IS STABLE THIOETHER LINKER (4-[N-MALEIMIDOMETHYL] CYCLOHEXANE-1-CARBOXYLATE) LEAD TO THE RELEASE OF DM1 A MICROTUBULE INHIBITOR |
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NATURAL MOLECULE (link) ATC code
L01FD03 |
PK parameters PPB 93 PERCENT
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Target TARGET TUBULIN |
DrugCentral Receptor tyrosine-protein kinase erbB-2 UNIPROT P04626 ERBB2_HUMAN Tubulin beta UNIPROT P07437 TBB5_HUMAN |
Download SDF file |
Maytansine, N2'-deacetyl-N2'-(3-mercapto-1-oxopropyl)- Formula: C35H48ClN3O10S Calculated chemical properties: MW 738.28 NB_atoms 50 XLogP 3.83 PSA 146.757 NB_HD 2 NB_HA 13 fsp3 0.60 Lipinski(0=no;1=yes) 0 |
FDA NDA 125427 ( label) INN (ADO-TRASTUZUMAB EMTANSINE) KADCYLA (GENENTECH) APPROVAL= AP YEAR= 2013 |
Other links: PubChem ChemicalProbes U.S. repository of Clinical Trials VigiAccess SIDER side effects ChemSynthesis Patent@SureChEMBL |