C65H75ClN12O17
1331.8 g/mol
Research ReagentDanger
Vc-seco-duba
CAS1345681-58-4
Category
Research Reagent
Compound Class
Other
Primary Use
Research Compound
Vc-seco-duba is a complex research compound with a high molecular weight and a large polar surface area, featuring multiple amide and ether linkages along with an aromatic ring system. Its structure includes a chlorinated alkyl side chain and a maleimide group, indicating potential utility as a building block for antibody-drug conjugate (ADC) research.
research compound for antibody-drug conjugate developmentlaboratory reagent
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
ReferenceSame Category
2-((1E,3E,5E)-5-(3,3-dimethyl-1-(6-oxo-6-(prop-2-yn-1-ylamino)hexyl)-5-sulfoindolin-2-ylidene)penta-1,3-dien-1-yl)-1-ethyl-3,3-dimethyl-3H-indol-1-ium-5-sulfonate
CAS1345823-20-2
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Safety Reference
Danger
H340May cause genetic defects
H351Suspected of causing cancer
H373May cause damage to organs through prolonged or repeated exposure
Identifiers
IUPAC Name
[(1S)-1-(chloromethyl)-3-[6-[(4-hydroxybenzoyl)amino]imidazo[1,2-a]pyridine-2-carbonyl]-9-methyl-1,2-dihydrobenzo[e]indol-5-yl] N-[2-[[4-[[(2S)-5-(carbamoylamino)-2-[[(2S)-2-[2-[2-(2,5-dioxopyrrol-1-yl)ethoxy]ethoxycarbonylamino]-3-methylbutanoyl]amino]pentanoyl]amino]phenyl]methoxycarbonyl-methylamino]ethyl]-N-[2-(2-hydroxyethoxy)ethyl]carbamate
InChIKey
RFQYSAASDBNNDZ-UCGHAGIGSA-N
SMILES
CC1=C2C(=CC=C1)C(=CC3=C2[C@@H](CN3C(=O)C4=CN5C=C(C=CC5=N4)NC(=O)C6=CC=C(C=C6)O)CCl)OC(=O)N(CCN(C)C(=O)OCC7=CC=C(C=C7)NC(=O)[C@H](CCCNC(=O)N)NC(=O)[C@H](C(C)C)NC(=O)OCCOCCN8C(=O)C=CC8=O)CCOCCO
Synonyms (8)
- Duocarmazine (USAN)
- Duocarmazine
- Vc-seco-duba
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