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DISITAMAB VEDOTIN

UNII:RB3U3A1S27
Type:INGREDIENT SUBSTANCE
Formula:
Preferred Substance Name:DISITAMAB VEDOTIN
GSRS Full Record:
RB3U3A1S27
i

  • 2136633-23-1
  • DISITAMAB VEDOTIN [USAN]
  • Disitamab Vedotin
  • Disitamab Vedotin [WHO-DD]
  • Immunoglobulin G1, anti-(human tyrosine kinase receptor ErbB2) (human-Mus musculus monoclonal RC48-270A4023 γ1-chain), disulfide with human-Mus musculus monoclonal RC48-270A4023 κ-chain, dimer, thioether with N-[[[4-[[N-[6-(3-mercapto-2,5-dioxo-1-pyrrolidinyl)-1-oxohexyl]-L-valyl-N5-(aminocarbonyl)-L-ornithyl]amino]phenyl]methoxy]carbonyl]-N-methyl-L-valyl-N-[(1S,2R)-4-[(2S)-2-[(1R,2R)-3-[[(1R,2S)-2-hydroxy-1-methyl-2-phenylethyl]amino]-1-methoxy-2-methyl-3-oxopropyl]-1-pyrrolidinyl]-2-methoxy-1-[(1S)-1-methylpropyl]-4-oxobutyl]-N-methyl-L-valinamide
  • Immunoglobulin G1-kappa, anti-[Homo sapiens ERBB2 (epidermal growth factor receptor 2, receptor tyrosine-protein kinase erbB-2, EGFR2, HER2, HER-2, p185c-erbB2, NEU, CD340)], humanized monoclonal antibody conjugated to auristatin E; gamma1 heavy chain humanized (1-445) [VH (Homo sapiens IGHV1-69-2*01 (83.5%) -(IGHD) -IGHJ1*01 (92.9%)) [8.8.8] (1-115) -Homo sapiens IGHG1*03v, G1m3>G1m17, nG1m1 (CH1 R120>K (212) (116-213), hinge (214-228), CH2 (229-338), CH3 E12 (354), M14 (357) (339-443), CHS (444-445)) (116-445)] (218-212')-disulfide with kappa light chain humanized (1'-212') [V-KAPPA (Homo sapiens IGKV1-39*01 (83.3%) -IGKJ4*01 (100%))[6.3.7] (1'-105') -Homo sapiens IGKC*01 (100%) Km3 A45.1 (151), V101 (189) (106'-212')]; dimer (224-224'':227-227'')-bisdisulfide; conjugated on an average of 4 cysteinyl to monomethylauristatin E (MMAE), via a cleavable maleimidocaproyl-valyl-citrullinyl-paminobenzyloxycarbonyl (mc-val-cit-PABC) type linker
  • RC48-ADC
  • disitamab vedotin [INN]




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