161646-54-4Relevant academic research and scientific papers
An efficient synthesis of 1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI): An enhanced and simplified analog of the CC-1065 and duocarmycin alkylation subunits
Boger,McKie
, p. 1271 - 1275 (1995)
An efficient synthesis of 4, the immediate precursor to N-BOC-CBI and related analogs of CC-1065 incorporating the 1,2,9,9a-tetrahydrocyclopropa[c]benz[c]indol-4-one alkylation subunit, is described based on a Tempo trap of a 5-exo-trig aryl radical-alken
ISOQUINOLIDINOBENZODIAZEPINE (IQB)-1(CHLOROMETHYL)-2,3-DIHYDRO-1H-BENZO[E]INDOLE (CBI) DIMERS
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Paragraph 0011; 00241; 00255-00258, (2018/04/27)
Provided herein are isoquinolidinobenzodiazepine (IQB)-1(chloromethyl)-2,3-dihydro-1H-benzo[e]indole (CBI) dimers, antibody-drug conjugates comprising them and methods of use for killing cells and treating disease.
