22907-68-2

Upstream product

• 67-56-1 methanol 
• 528-45-0 3,4-dinitrobenzoic acid 
• 24376-18-9 3,4-dinitrobenzoyl chloride 

Downstream Products

• 36692-49-6 Methyl 3,4-diaminobenzoate 
• 126824-22-4 2-(4-methoxyphenyl)-1H-benzo[d]imidazole-6-carbaldehyde 
• 126824-21-3 5-(Hydroxymethyl)-2-(4-methoxyphenyl)-1H-benzimidazole 
• 138969-09-2 methyl 2-(4-methoxyphenyl)-1H-benzo[d]imidazole-6-carboxylate 
• 138969-08-1 8-[2-(4-Methoxy-phenyl)-3H-benzoimidazol-5-yl]-2-(4-methyl-piperazin-1-yl)-9H-purine 
• 413577-28-3 methyl 2-(4-(N,N-diethyl)aminophenyl)benzimidazole-6-carboxylate 
• 66315-16-0 methyl 3-amino-4-(methylamino)benzoate 
• 26663-77-4 methyl 1H-benzo[d]imidazole-5-carboxylate 

Relevant academic research and scientific papers

Compositions and methods of the use thereof achiral analogues of CC-1065 and the duocarmycins

The present invention relates to novel achiral seco-analogues of the DNA minor groove and sequence-selective alkylating agents (+)-CC1065 and the duocarmycins, depicted as general class I, II III, IV and V: wherein X is a good leaving group, such as a chl

Compositions and methods of the use thereof achiral analogues of CC-1065 and the duocarmycins

The present invention relates to novel achiral seco-analogues of DNA minor groove and sequence-selective alkylating agents (+)-CC1065 and the duocarmycins, depicted as general class I, II, III, IV and V: wherein X is a good leaving group, such as a chlori

SYNTHESIS AND DNA BINDING PROPERTIES OF A PURINE ANALOGUE OF BISBENZIMIDE

The synthesis of a purine containing analogue (1) of bisbenzimide (2) and its DNA binding properties are described.Analogue 1 is found to have increased tolerance for binding to GC sites implying the formation of the new hydrogen bonds between guanine-2-N