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Comparative molecular field analysis (CoMFA) of phthalazine derivatives as phosphodiesterase IV inhibitors.

National Institute of Pharmaceutical Education and Research
Design, synthesis and biological evaluation of 5-benzylidene-2-iminothiazolidin-4-ones as selective GSK-3ß inhibitors.

National Institute of Pharmaceutical Education and Research
Synthesis and biology of ring-modified l-Histidine containing thyrotropin-releasing hormone (TRH) analogues.

National Institute of Pharmaceutical Education and Research
Synthesis of CNS active thyrotropin-releasing hormone (TRH)-like peptides: Biological evaluation and effect on cognitive impairment induced by cerebral ischemia in mice.

National Institute of Pharmaceutical Education and Research
Synthesis, biological evaluation and docking analysis of 3-methyl-1-phenylchromeno[4,3-c]pyrazol-4(1H)-ones as potential cyclooxygenase-2 (COX-2) inhibitors.

National Institute of Pharmaceutical Education and Research
Synthesis, biological evaluation, molecular docking and theoretical evaluation of ADMET properties of nepodin and chrysophanol derivatives as potential cyclooxygenase (COX-1, COX-2) inhibitors.

National Institute of Pharmaceutical Education and Research
Probing the binding site of curcumin in Escherichia coli and Bacillus subtilis FtsZ--a structural insight to unveil antibacterial activity of curcumin.

National Institute of Pharmaceutical Education and Research
Quinolines and structurally related heterocycles as antimalarials.

National Institute of Pharmaceutical Education and Research
New PPARgamma ligands based on barbituric acid: virtual screening, synthesis and receptor binding studies.

National Institute of Pharmaceutical Education and Research
New PPARgamma ligands based on 2-hydroxy-1,4-naphthoquinone: computer-aided design, synthesis, and receptor-binding studies.

National Institute of Pharmaceutical Education and Research
CoMFA analysis of dual/multiple PPAR activators.

National Institute of Pharmaceutical Education and Research
Selectivity criterion for pyrazolo[3,4-b]pyrid[az]ine derivatives as GSK-3 inhibitors: CoMFA and molecular docking studies.

National Institute of Pharmaceutical Education and Research
Design and synthesis of 6-methyl-2-oxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid derivatives as PPARgamma activators.

National Institute of Pharmaceutical Education and Research
Benzophenone: a ubiquitous scaffold in medicinal chemistry.

National Institute of Pharmaceutical Education and Research
Synthetically-tailored and nature-derived dual COX-2/5-LOX inhibitors: Structural aspects and SAR.

National Institute of Pharmaceutical Education and Research
Modifications of the pyroglutamic acid and histidine residues in thyrotropin-releasing hormone (TRH) yield analogs with selectivity for TRH receptor type 2 over type 1.

National Institute of Pharmaceutical Education and Research
Thyrotropin-releasing hormone (TRH) analogues that exhibit selectivity to TRH receptor subtype 2.

National Institute of Pharmaceutical Education and Research
Synthesis and evaluation of S-4-(3-thienyl)phenyl-alpha-methylacetic acid.

National Institute of Pharmaceutical Education and Research
Synthesis of imine-pyrazolopyrimidinones and their mechanistic interventions on anticancer activity.

National Institute of Pharmaceutical Education and Research
Comparative 3D QSAR study on β(1)-, β(2)-, and β(3)-adrenoceptor agonists.

National Institute of Pharmaceutical Education and Research
Synthesis of 9-substituted derivatives of berberine as anti-HIV agents.

National Institute of Pharmaceutical Education and Research
Design and synthesis of caffeoyl-anilides as portmanteau inhibitors of HIV-1 integrase and CCR5.

National Institute of Pharmaceutical Education and Research
Antimalarials from nature.

National Institute of Pharmaceutical Education and Research
Biomimetic synthesis and anti-HIV activity of dimeric phloroglucinols.

National Institute of Pharmaceutical Education and Research
Tamarixetin 3-O-β-d-Glucopyranoside from Azadirachta indica Leaves: Gastroprotective Role through Inhibition of Matrix Metalloproteinase-9 Activity in Mice.

National Institute of Pharmaceutical Education and Research
Triazine carboxamides as sodium channel blockers

Purdue Pharma
Inhibitors of glucocorticoid receptor translocation

Sanford Burnham Prebys Medical Discovery Institute