99745-88-7Relevant articles and documents
Synthesis of Mitomycin C and Decarbamoylmitomycin C N2 deoxyguanosine-adducts
Champeil, Elise,Cheng, Shu-Yuan,Huang, Bik Tzu,Conchero-Guisan, Marta,Martinez, Thibaut,Paz, Manuel M.,Sapse, Anne-Marie
, p. 90 - 99 (2016/03/01)
Mitomycin C (MC) and Decarbamoylmitomycin C (DMC) - a derivative of MC lacking the carbamate on C10 - are DNA alkylating agents. Their cytotoxicity is attributed to their ability to generate DNA monoadducts as well as intrastrand and interstrand cross-lin
Studies on the reactivity of reductively activated mitomycin C
Schiltz, Pascal,Kohn, Harold
, p. 10510 - 10518 (2007/10/02)
Mitomycin C (1a), a clinically significant antineoplastic antiobiotic, is considered to be the prototype of bioreductive alkylating agents. It has been reported that, in the absence of DNA, reductive activation of 1a furnished both solvolytic C(1) electro
Comparative reactivities of mitomycin C, 7-(N-piperidino)mitomycin, and mitomycin A. The role of the C(7)substituent
Subramaniam,Kohn
, p. 10519 - 10526 (2007/10/02)
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