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Substance Name: Brentuximab vedotin [USAN:INN]
RN: 914088-09-8
UNII: 7XL5ISS668

Notes

  • Consists of cAC10 conjugated to monomethylauristatin E.

    NCI: An antibody-drug conjugate (ADC) directed against the tumor necrosis factor (TNF) receptor CD30 with potential antineoplastic activity. Brentuximab vedotin is generated by conjugating the humanized anti-CD30 monoclonal antibody SGN-30 to the cytotoxic agent monomethyl auristatin E (MMAE) via a valine-citrulline peptide linker ... (NCI Thesaurus)
  • Immunoconjugate that consists of the chimeric monoclonal anti - CD30 ANTIGEN antibody cAC-10 conjugated to monomethyl auristatin E. It is used for the treatment of LYMPHOMA.

Molecular Formula

  • Unspecified

Molecular Weight

  • 1349.7134
 

Classification Codes

  • Antineoplastic Agents
  • Antineoplastic Agents, Immunological
  • Immunologic Factors
  • Immunotoxins
  • Noxae
  • Treatment of Hodgkin's Lymphoma, CD30-Positive Hematologic Malignancies

Names and Synonyms

Name of Substance

  • Brentuximab vedotin [USAN:INN]

MeSH Heading

  • Brentuximab vedotin

Synonyms

  • Adcetris
  • Anti-CD30 ADC SGN-35
  • Anti-CD30 antibody-drug conjugate SGN-35
  • Antibody-drug conjugate SGN-35
  • Brentuximab Vedotin
  • cAC10-vcMMAE
  • SGN 35
  • SGN-35
  • UNII-7XL5ISS668

Systematic Name

  • Immunoglobulin G1, anti-(human CD30 (antigen)) (human-mouse monoclonal cAC10 gamma1-chain), disulfide with human-mouse monoclonal cAC10 kappa-chain, dimer, complex with N-(((4-((N-(6-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-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-ethylpropyl)-4-oxobutyl)-N-methyl-L-valinamide

Registry Numbers

CAS Registry Number

  • 914088-09-8

FDA UNII

  • 7XL5ISS668

System Generated Number

  • 0914088098

Structure Descriptors

Smiles

[*]SC1CC(=O)N(CCCCCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCNC(=O)N)C(=O)Nc2ccc(COC(=O)N(C)[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N(C)[C@@H]([C@@H](C)CC)[C@@H](CC(=O)N3CCC[C@H]3[C@H](OC)[C@@H](C)C(=O)N[C@H](C)[C@@H](O)c4ccccc4)OC)cc2)C1=O