16 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
New arylalkanones from Horsfieldia macrobotrys, effective antidiabetic agents concomitantly inhibitinga-glucosidase and free radicals.
Chulalongkorn University
Quercitylcinnamates, a new series of antidiabetic bioconjugates possessinga-glucosidase inhibition and antioxidant.
Chulalongkorn University
(+)-Pinoresinol is a putative hypoglycemic agent in defatted sesame (Sesamum indicum) seeds though inhibitinga-glucosidase.
Chulalongkorn University
Specific inhibition of human immunodeficiency virus type 1 reverse transcriptase mediated by soulattrolide, a coumarin isolated from the latex of calophyllum teysmannii.
Chulalongkorn University
Concise synthesis of (+)-conduritol F and inositol analogues from naturally available (+)-proto-quercitol and their glucosidase inhibitory activity.
Chulalongkorn University
Receptor-based 3D-QSAR studies of checkpoint Wee1 kinase inhibitors.
Chulalongkorn University
A new dimeric stilbene with tyrosinase inhibitiory activity from Artocarpus gomezianus.
Chulalongkorn University
Structural modification of tanshinone IIA and their α-glucosidase inhibitory activity.
Chulalongkorn University
Design, synthesis, and optimization of novel PD-L1 inhibitors and the identification of a highly potent and orally bioavailable PD-L1 inhibitor.
Chulalongkorn University
Machine learning-based QSAR and LB-PaCS-MD guided design of SARS-CoV-2 main protease inhibitors.
Chulalongkorn University
Chemical transformations of oxyresveratrol (trans-2,4,3',5'-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent.
Chulalongkorn University
Synthesis and in vitro study of novel neuraminidase inhibitors against avian influenza virus.
Chulalongkorn University
Heterocyclic analogs of propargyl-linked inhibitors of dihydrofolate reductase
University of Connecticut