Synthesis of Chiral Melatonin Salts of Dithiophosphoric Acids Using Monoterpenyl Alcohol

Autor:	Ilnar D. Nizamov, Ramazan Z. Salikhov, Elvira S. Batyeva, G. G. Sergeenko, Il'yas S. Nizamov, R. A. Cherkasov, Oscar K. Pozdeev, Yevgeniy N. Nikitin, R. R. Davletshin, Marina P. Shulaeva
Rok vydání:	2020
Předmět:	0303 health sciences 010405 organic chemistry Chemistry Alcohol General Chemistry 01 natural sciences 0104 chemical sciences Melatonin 03 medical and health sciences chemistry.chemical_compound medicine Organic chemistry 030304 developmental biology medicine.drug
Zdroj:	Asian Journal of Chemistry. 32:1511-1514
ISSN:	0975-427X 0970-7077
DOI:	10.14233/ajchem.2020.22509
Popis:	Dithiophosphoric acids in the terms of (S)-(–)-menthol, (1S)-endo-(–)-borneol,(1R)-endo-(+)-fenchyl alcohol and (1S,2S,3S,5R)-(+)-isopinocampheol react with melatonin to form chiral N-acetyl 5-methoxytryptammonium dithiophosphates. The interations proceed via increase in the coordination of indole nitrogen of melatonin. The antibacterial and antifungal activity of N-acetyl 5-methoxytryptammonium dithiophosphate containing (+)-fenchyl substituent was established
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::c12d291b788a58bd457609e58290cc79 https://doi.org/10.14233/ajchem.2020.22509 Zobrazit plný text záznamu