135257-17-9

Basic information

• Product Name: (S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-ureido-hexanoylamino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid
• CAS NO: 135257-17-9
• Molecular Weight: 736.825
• Mol File: 135257-17-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-ureido-hexanoylamino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-ureido-hexanoylamino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid(135257-17-9)
• EPA Substance Registry System: (S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-ureido-hexanoylamino}-N-((S)-1-carbamoyl-2-phenyl-ethyl)-succinamic acid(135257-17-9)

Safety Data

• Hazardous Substances Data: 135257-17-9(Hazardous Substances Data)

Upstream product

• 75-13-8 isocyanic acid 
• 131450-42-5 Boc-Trp-Lys-Asp-Phe-NH₂ acetic acid salt 

Relevant articles and documents

Boc-CCK-4 derivatives containing side-chain ureas as potent and selective CCK-A receptor agonists

Novel Boc-CCK-4 derivatives were communicated recently as having high potency and selectivity for the CCK-A receptor (Shiosaki et al. J. Med. Chem. 1990, 33, 2950-2952). While Boc-CCK-4 binds selectively to the CCK-B receptor, replacement of the methionin