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1 Ergebnisse
1
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/14488950. , 2021
Link:
https://doi.org/10.1021/acs.jmedchem.1c00076.s002
RT Journal T1
Design and Structure–Activity Relationships of Isothiocyanates as Potent and Selective N ‑Acylethanolamine-Hydrolyzing Acid Amidase Inhibitors
UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14488950&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/14488950 LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.1c00076.s002 DO https://doi.org/10.1021/acs.jmedchem.1c00076.s002 SF ELIB - SuUB Bremen
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