Structural manipulation of aporphines via C10 nitrogenation leads to the identification of new 5-HT


Journal

Bioorganic & medicinal chemistry
ISSN: 1464-3391
Titre abrégé: Bioorg Med Chem
Pays: England
ID NLM: 9413298

Informations de publication

Date de publication:
01 08 2020
Historique:
received: 29 04 2020
revised: 26 05 2020
accepted: 28 05 2020
entrez: 8 7 2020
pubmed: 8 7 2020
medline: 12 6 2021
Statut: ppublish

Résumé

Aporphine alkaloids containing a C10 nitrogen motif were synthesized and evaluated for affinity at 5-HT

Identifiants

pubmed: 32631561
pii: S0968-0896(20)30408-9
doi: 10.1016/j.bmc.2020.115578
pmc: PMC7340851
mid: NIHMS1603561
pii:
doi:

Substances chimiques

Aporphines 0
Ligands 0
Receptors, Serotonin 0
Serotonin Antagonists 0
serotonin 7 receptor 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

115578

Subventions

Organisme : NIDA NIH HHS
ID : SC1 DA049961
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Références

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Auteurs

Anupam Karki (A)

Department of Chemistry, Hunter College, City University of New York, 695 Park Avenue, NY 10065, USA; Program in Biochemistry, CUNY Graduate Center, 365 5(th) Avenue, New York, NY 10016, USA.

Hari K Namballa (HK)

Department of Chemistry, Hunter College, City University of New York, 695 Park Avenue, NY 10065, USA.

Ian Alberts (I)

LaGuardia Community College, Department of Chemistry, 31-10 Thompson Avenue, LIC, NY 11104, USA.

Wayne W Harding (WW)

Department of Chemistry, Hunter College, City University of New York, 695 Park Avenue, NY 10065, USA; Program in Biochemistry, CUNY Graduate Center, 365 5(th) Avenue, New York, NY 10016, USA; Program in Chemistry, CUNY Graduate Center, 365 5(th) Avenue, New York, NY 10016, USA. Electronic address: whardi@hunter.cuny.edu.

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Classifications MeSH