e-Drug3D

1855

MAYTANSINE


INN
MAYTANSINE
ADO-TRASTUZUMAB EMTANSINE

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

ROUTE (list)

INJECTION

NATURAL MOLECULE (link)

ATC code

L01FD03

PK parameters

PPB 93 PERCENT

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