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Design and Structure–Activity Relationships of Isothiocyana..:

Michael S. Malamas (2148259) ; Spiro Pavlopoulos (2409385) ; Shakiru O. Alapafuja (2259457)...
https://figshare.com/articles/dataset/Design_and_Structure_Activity_Relationships_of_Isothiocyanates_as_Potent_and_Selective_i_N_i_Acylethanolamine-Hydrolyzing_Acid_Amidase_Inhibitors/14488956. , 2021

Link: https://doi.org/10.1021/acs.jmedchem.1c00076.s004

RT Journal
T1 <Title>Design and Structure–Activity Relationships of Isothiocyanates as Potent and Selective N ‑Acylethanolamine-Hydrolyzing Acid Amidase Inhibitors</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14488956&Exemplar=1&LAN=DE
				
A1 Michael S. Malamas (2148259)
A1 Spiro Pavlopoulos (2409385)
A1 Shakiru O. Alapafuja (2259457)
A1 Shrouq I. Farah (10702329)
A1 Alexander Zvonok (334031)
A1 Khadijah A. Mohammad (5775539)
A1 Jay West (3623987)
A1 Nicholas Thomas Perry (10702332)
A1 Dimitrios N. Pelekoudas (10702335)
A1 Girija Rajarshi (1350981)
A1 Christina Shields (10702338)
A1 Honrao Chandrashekhar (10702341)
A1 Jodi Wood (10702344)
A1 Alexandros Makriyannis (32548)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Physiology
K1 Pharmacology
K1 Biotechnology
K1 Immunology
K1 Science Policy
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 Information Systems not elsewhere classified
K1 Amidase Inhibitors N
K1 plasma stability
K1 lipid molecules
K1 NAAA
K1 structure-activity relationship studies
K1 hydrolyzes lipid palmitoylethanolamide
K1 2 h
K1 Acylethanolamine acid amidase
K1 drug addiction
K1 isothiocyanate pharmacophore
K1 role
K1 inflammation
K1 pain processes
K1 cysteine peptidases
K1 serine hydrolases
K1 pathophysiological conditions
K1 nanomolar inhibitors
K1 hNAAA
JF https://figshare.com/articles/dataset/Design_and_Structure_Activity_Relationships_of_Isothiocyanates_as_Potent_and_Selective_i_N_i_Acylethanolamine-Hydrolyzing_Acid_Amidase_Inhibitors/14488956
LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.1c00076.s004
DO https://doi.org/10.1021/acs.jmedchem.1c00076.s004
SF ELIB - SuUB Bremen

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