Synthesis of 2-chloropurine ribosides with chiral amino acid amides at C6 and their evaluation as A

Autor:	Maria Ya, Berzina, Barbara Z, Eletskaya, Alexei L, Kayushin, Elena V, Dorofeeva, Olga I, Lutonina, Ilya V, Fateev, Alexander S, Paramonov, Maria A, Kostromina, Evgeniy A, Zayats, Yulia A, Abramchik, Dmitriy V, Maltsev, Ludmila V, Naumenko, Alena S, Taran, Dmitry S, Yakovlev, Alexander A, Spasov, Anatoly I, Miroshnikov, Roman S, Esipov, Irina D, Konstantinova
Rok vydání:	2022
Předmět:	Molecular Docking Simulation Mice Receptor Adenosine A1 Purinergic P1 Receptor Agonists Animals Nucleosides Amino Acids Amides
Zdroj:	Bioorganic chemistry. 126
ISSN:	1090-2120
Popis:	A series of purine ribonucleosides bearing chiral amino acid amides at the C6 position of 2-chloropurine was synthesized. Molecular docking of the synthesized analogs of 2-chloroadenosine by their affinity for A
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::5569a050d6a85eb15cafb0a08fdce699 https://pubmed.ncbi.nlm.nih.gov/35660725 Zobrazit plný text záznamu Full Text from ScienceDirect