This study was aimed at examining the variations in the metabolite constituents of the different Ajwa grades and farm origins. It is also targeted at establishing the correlations between the metabolite contents and the grades and further to the nitric ...
Nur Ashikin Abdul-Hamid +6 more
doaj +1 more source
Inhibitory effect of catechin-related compounds on renin activity
Renin is a crucial enzyme in the renin-angiotensin system, and the inhibition of its activity is considered as a useful approach to the treatment of hypertension. The inhibitory effect of catechin-related compounds on renin was investigated in this work.
LI, Fengjuan +2 more
openaire +3 more sources
In-silico studies of inhibitory compounds against protease enzymes of SARS-CoV-2. [PDF]
Khan S +7 more
europepmc +1 more source
Ferroptosis Inhibitory Compounds from the Deep-Sea-Derived Fungus Penicillium sp. MCCC 3A00126. [PDF]
Hao YJ +7 more
europepmc +1 more source
Synthesis of curcumin derivatives for suppression of castration-resistant prostate cancer
In this work, 20 curcumin derivatives containing halogen atoms or nitrogen atoms were synthesized for suppression of castration-resistant prostate cancer.
Shunze Gong +3 more
doaj +1 more source
Novel Thiazolidin-4-ones as Potential Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase
Background: HIV is the causative agent of Acquired Immunodeficiency Syndrome (AIDS), an infectious disease with increasing incidence worldwide. Non-nucleoside reverse transcriptase inhibitors (NNRTIs) play an important role in the treatment of AIDS ...
Anthi Petrou +4 more
doaj +1 more source
Screening of MMV pandemic response and pathogen box compounds against pan-drug-resistant Klebsiella pneumoniae to identify potent inhibitory compounds. [PDF]
Sivasankar S +4 more
europepmc +1 more source
Indoleamine 2, 3-dioxygenase 1 inhibitory compounds from natural sources. [PDF]
Tan Y, Liu M, Li M, Chen Y, Ren M.
europepmc +1 more source
Thirteen novel 1,2,3-triazole linked nucleobases (5a-m) were designed and efficiently synthesized as potential human enzyme inhibitors. The target compounds were synthesized by using Copper (I)-catalysed Huisgen-Sharpless-Meldal 1,3-dipolar cycloaddition
Aditya Aggarwal +4 more
doaj +1 more source
In silico analysis of angiotensin-converting enzyme inhibitory compounds obtained from soybean [Glycine max (L.) Merr.]. [PDF]
Ramlal A +14 more
europepmc +1 more source

