252289-06-8

Upstream product

• 319921-87-4 Phenylmethyl (S,S)-2-{4-[1-(Phenylmethyloxycarbonyl)-2-phenylethylamino]-1H-indol-3-yl}-1-(hydroxymethyl)ethylcarbamate 
• 319921-01-2 Bis(allyl) [4-(N-tert-butyloxycarbonyl)amino-1H-indol-3yl]methylphenylacetamidomalonate 
• 252288-59-8 2-benzyloxycarbonylamino-3-(4-tert-butoxycarbonylamino-1H-indol-3-yl)-propionic acid 
• 252289-08-0 (S)-N-Benzyloxycarbonyl-4-(N-tert-butyloxycarbonyl)aminotryptophan methyl ester 
• 252288-57-6 4-(N-tert-Butyloxycarbonyl)amino-N-phenylacetyltryptophan 
• 252288-55-4 3-Dimethylaminomethyl-4-(N-tert-butyloxycarbonyl)amino-1-triisopropylsilylindole 
• 252289-09-1 (S)-N-Benzyloxycarbonyl-4-aminotryptophan methyl ester 
• 252292-65-2 (-)-N¹³-Desmethyl-C¹²-desisopropyl-C¹²-phenylmethylindolactam V 
• 252288-58-7 (S)-4-(N-tert-Butyloxycarbonyl)aminotryptophan 
• 146886-61-5 3-Dimethylaminomethyl-4-amino-1-triisopropylsilylindole 
• 146886-51-3 1-(N-triisopropylsilyl-1H-indol-3-yl)-N,N-dimethylmethanamine 
• 110815-32-2 (S)-(2-(4-amino-1H-indol-3-yl)-1-(hydroxymethyl)ethyl)carbamic acid, phenylmethyl ester 

Relevant academic research and scientific papers

Natural product synthesis on polymeric supports - Synthesis and biological evaluation of an indolactam library

Potent activators of protein kinase C in fibroblasts: This property was determined for several indolactam V analogues (1) with a new cell-based assay system. This tumor-promoting indole alkaloid and analogues thereof can be synthesized efficiently on the solid phase. The key steps of the combinatorial approach are a regioselective amination of the indole ring and an enantioselective enzymatic reaction.