1513888-73-7

Basic information

• Product Name: (S)-15-hydroxy-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)pentadecanamide
• Synonyms: (S)-15-hydroxy-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)pentadecanamide
• CAS NO: 1513888-73-7
• Molecular Weight: 407.594
• Mol File: 1513888-73-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-15-hydroxy-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)pentadecanamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-15-hydroxy-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)pentadecanamide(1513888-73-7)
• EPA Substance Registry System: (S)-15-hydroxy-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)pentadecanamide(1513888-73-7)

Safety Data

• Hazardous Substances Data: 1513888-73-7(Hazardous Substances Data)

Upstream product

• 4617-33-8 15-hydroxylpentadecanoic acid 
• 87745-27-5 (S)-tyrosinol hydrochloride 

Downstream Products

• 1513888-69-1 (S)-4-(3-hydroxy-2-((15-hydroxypentadecyl)amino)propyl)phenol 

Relevant articles and documents

Functionally optimized neuritogenic farinosone C analogs: SAR-study and investigations on their mode of action

Several natural products derived from entomopathogenic fungi have been shown to initiate neuronal differentiation in the rat pheochromocytoma PC12 cell line. After the successful completion of the total synthesis program, the reduction of structural complexity while retaining biological activity was targeted. In this study, farinosone C served as a lead structure and inspired the preparation of small molecules with reduced complexity, of which several were able to induce neurite outgrowth. This allowed for the elaboration of a detailed structure-activity relationship. Investigations on the mode of action utilizing a computational similarity ensemble approach suggested the involvement of the endocannabinoid system as potential target for our analogs and also led to the discovery of four potent new endocannabinoid transport inhibitors.