Results 1 to 10 of about 4,762 (102)

N‐benzhydryl quinuclidine compounds are a potent and Src kinase‐independent inhibitor of NALCN channels [PDF]

open access: yesBritish Journal of Pharmacology, 2020
Background and PurposeNALCN is a Na+ leak, GPCR‐activated channel that regulates the resting membrane potential and neuronal excitability. Despite numerous possible roles for NALCN in both normal physiology and disease processes, lack of specific blockers hampers further investigation.Experimental ApproachThe effect of N‐benzhydryl quinuclidine ...
Suyun Hahn   +4 more
openaire   +2 more sources

Enzymatic synthesis of novel pyrrole esters and their thermal stability

open access: yesBMC Chemistry, 2023
In the present work a simple enzymatic approach (Novozym 435) for transesterification to synthesize pyrrole esters was reported. To generate the best reaction conditions, which resulted in the optimum yield of 92%, the effects of lipase type, solvent ...
Jingyi Hu   +6 more
doaj   +1 more source

Hydantoin Derivatives of L- and D-amino acids: Synthesis and Evaluation of Their Antiviral and Antitumoral Activity

open access: yesMolecules, 2006
3,5-Disubstituted hydantoin (1,3-imidazolidinedione) derivatives 5a-h wereprepared by base induced cyclization of the corresponding N-(1-benzotriazolecarbonyl)-L-and D-amino acid amides 4a-h.
Mladen Mintas   +8 more
doaj   +1 more source

Design, Synthesis and Characterization of Novel Arylamides Containing 1,2,4-triazole Nuclei for Possible Antimicrobial Activity

open access: yesE-Journal of Chemistry, 2004
Diphenyl aceto hydrazide on reaction with carbon disulfide and potassium hydroxide gave potassium α,α-diphenyl acetamido dithiocarbamate, which on cyclisation with hydrazine hydrate yielded key intermediate 3-mercapto-4,N-amino-5-benzhydryl-1,2,4 ...
S. R. Dhol   +3 more
doaj   +1 more source

Synthesis of novel benzenesulfamide derivatives with inhibitory activity against human cytosolic carbonic anhydrase I and II and Vibrio cholerae α- and β-class enzymes

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2018
The synthesis of a new series of sulfamides incorporating ortho-, meta, and para-benzenesulfamide moieties is reported, which were investigated for the inhibition of two human (h) isoforms of the zinc enzyme carbonic anhydrase (CA, EC 4.2.1.1), hCA I and
Silvia Bua   +10 more
doaj   +1 more source

Proton Chemical Shifts in Some Benzhydryl Compounds. [PDF]

open access: yesActa Chemica Scandinavica, 1970
Leiv J. Stangeland   +6 more
openaire   +1 more source

Structural Exploitation of Cinnarizine Identified Novel Drug-Like Anthelmintic Agents Against <i>Angiostrongylus cantonensis</i>. [PDF]

open access: yesACS Infect Dis
Lemes BL   +7 more
europepmc   +1 more source

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