27 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis, screening and docking of fused pyrano[3,2-d]pyrimidine derivatives as xanthine oxidase inhibitor.

Guru Nanak Dev University
Benzoflavones as cholesterol esterase inhibitors: Synthesis, biological evaluation and docking studies.

Guru Nanak Dev University
Rational Design of Small Peptides for Optimal Inhibition of Cyclooxygenase-2: Development of a Highly Effective Anti-Inflammatory Agent.

Guru Nanak Dev University
Triazole tethered C5-curcuminoid-coumarin based molecular hybrids as novel antitubulin agents: Design, synthesis, biological investigation and docking studies.

Guru Nanak Dev University
Rational modification of the lead molecule: Enhancement in the anticancer and dihydrofolate reductase inhibitory activity.

Guru Nanak Dev University
Indole based peptidomimetics as anti-inflammatory and anti-hyperalgesic agents: Dual inhibition of 5-LOX and COX-2 enzymes.

Guru Nanak Dev University
Rational design, synthesis and evaluation of chromone-indole and chromone-pyrazole based conjugates: identification of a lead for anti-inflammatory drug.

Guru Nanak Dev University
Lead modification: amino acid appended indoles as highly effective 5-LOX inhibitors.

Guru Nanak Dev University
Microwave assisted synthesis of naphthopyrans catalysed by silica supported fluoroboric acid as a new class of non purine xanthine oxidase inhibitors.

Guru Nanak Dev University
N-1, C-3 substituted indoles as 5-LOX inhibitors--in vitro enzyme immunoaasay, mass spectral and molecular docking investigations.

Guru Nanak Dev University
Synthesis and evaluation of indole, pyrazole, chromone and pyrimidine based conjugates for tumor growth inhibitory activities--development of highly efficacious cytotoxic agents.

Guru Nanak Dev University
Mono-, di-, and triaryl substituted tetrahydropyrans as cyclooxygenase-2 and tumor growth inhibitors. Synthesis and biological evaluation.

Guru Nanak Dev University
Design, synthesis and evaluation of tetrahydropyran based COX-1/-2 inhibitors.

Guru Nanak Dev University
2,3,5-Substituted tetrahydrofurans: COX-2 inhibitory activities of 5-hydroxymethyl-/carboxyl-2,3-diaryl-tetrahydro-furan-3-ols.

Guru Nanak Dev University
1-Toluene-sulfonyl-3-[(3'-hydroxy-5'-substituted)-gamma-butyrolactone]-indoles: synthesis, COX-2 inhibition and anti-cancer activities.

Guru Nanak Dev University
Structure and ligand based design for identification of highly potent molecules against 5-LOX.

Guru Nanak Dev University
The development of thymol-isatin hybrids as broad-spectrum antibacterial agents with potent anti-MRSA activity.

Guru Nanak Dev University
Past, present and future of xanthine oxidase inhibitors: design strategies, structural and pharmacological insights, patents and clinical trials.

Guru Nanak Dev University
Hybrid molecules: The privileged scaffolds for various pharmaceuticals.

Guru Nanak Dev University
Design strategies, structure activity relationship and mechanistic insights for purines as kinase inhibitors.

Guru Nanak Dev University
Proline based rationally designed peptide esters against dipeptidyl peptidase-4: Highly potent anti-diabetic agents.

Guru Nanak Dev University
Rationally designed TNF-α inhibitors: Identification of promising cytotoxic agents.

Guru Nanak Dev University
New coumarin-benzotriazole based hybrid molecules as inhibitors of acetylcholinesterase and amyloid aggregation.

Guru Nanak Dev University
Modification of the lead molecule: Tryptophan and piperidine appended triazines reversing inflammation and hyeperalgesia in rats.

Guru Nanak Dev University
Rational approaches, design strategies, structure activity relationship and mechanistic insights for therapeutic coumarin hybrids.

Guru Nanak Dev University
Structural tuning of acridones for developing anticancer agents targeting dihydrofolate reductase.

Guru Nanak Dev University