852527-09-4

Basic information

• Product Name: (S)-2-[2-((S)-2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-naphthalen-1-ylamino]-3-methyl-butyric acid benzyl ester
• Synonyms: (S)-2-[2-((S)-2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-naphthalen-1-ylamino]-3-methyl-butyric acid benzyl ester
• CAS NO: 852527-09-4
• Molecular Weight: 506.642
• Mol File: 852527-09-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-[2-((S)-2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-naphthalen-1-ylamino]-3-methyl-butyric acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-[2-((S)-2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-naphthalen-1-ylamino]-3-methyl-butyric acid benzyl ester(852527-09-4)
• EPA Substance Registry System: (S)-2-[2-((S)-2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-naphthalen-1-ylamino]-3-methyl-butyric acid benzyl ester(852527-09-4)

Safety Data

• Hazardous Substances Data: 852527-09-4(Hazardous Substances Data)

Upstream product

• 592478-91-6 2-(2,2-dimethoxy-ethyl)-1-nitro-naphthalene 
• 861354-92-9 (1-nitro-[2]naphthyl)-acetaldehyde 
• 881-03-8 1-nitro-2-methylnaphthalene 
• 852527-07-2 (S)-2-((R)-2-Hydroxy-1-phenyl-ethylamino)-3-(1-nitro-naphthalen-2-yl)-propan-1-ol 
• 852527-06-1 (S)-2-((R)-2-Hydroxy-1-phenyl-ethylamino)-3-(1-nitro-naphthalen-2-yl)-propionic acid methyl ester 
• 874620-07-2 (S)-2-((R)-2-Hydroxy-1-phenyl-ethylamino)-3-(1-nitro-naphthalen-2-yl)-propionitrile 
• 874620-08-3 (S)-3-(1-Amino-naphthalen-2-yl)-2-((R)-2-hydroxy-1-phenyl-ethylamino)-propan-1-ol 
• 339015-80-4 Dimethyl-[(E)-2-(1-nitro-naphthalen-2-yl)-vinyl]-amine 
• 852527-08-3 [2-(1-amino-naphthalen-2-yl)-1-hydroxymethyl-ethyl]-carbamic acid tert-butyl ester 
• 131423-64-8 benzyl (R)-4-methyl-2-(trifluoromethylsulfonyloxy)pentanoate 

Relevant articles and documents

Indolactam-V is involved in the CH/π interaction with Pro-11 of the PKCδ C1B domain: Application for the structural optimization of the PKCδ ligand

The CH/π interaction between the indole ring of indolactam-V (IL-V) and the hydrogen atom at position 4 of Pro-11 of the PKCδ C1B domain was evaluated using the mutant peptide of the PKCδ C1B domain, in which the CH/π interaction was inhibited by substitu