Thiadiazole-a promising structure in medicinal chemistry. - Wikidata - awgldk - TriplyDB

Thiadiazole-a promising structure in medicinal chemistry.

Thiadiazole-a promising structure in medicinal chemistry.

http://www.wikidata.org/entity/Q38064804

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Comparison of carbon-sulfur and carbon-amine bond in therapeutic drug: 4β-S-aromatic heterocyclic podophyllum derivatives display antitumor activity.Palladium-catalyzed amination of unprotected five-membered heterocyclic bromides Synthesis and Evaluation of New Oxadiazole, Thiadiazole, and Triazole Derivatives as Potential Anticancer Agents Targeting MMP-9.Synthesis and Evaluation of New 1,3,4-Thiadiazole Derivatives as Antinociceptive Agents.Structural features of the carbon-sulfur chemical bond: a semi-experimental perspective.Design, Synthesis, and Biological Evaluation of Novel 1,3,4-Thiadiazole Derivatives as Potential Antitumor Agents against Chronic Myelogenous Leukemia: Striking Effect of Nitrothiazole Moiety.Realizing Over 13% Efficiency in Green-Solvent-Processed Nonfullerene Organic Solar Cells Enabled by 1,3,4-Thiadiazole-Based Wide-Bandgap Copolymers.Spectroscopic and Theoretical Studies of Fluorescence Effects in 2-Methylamino-5-(2,4-dihydroxyphenyl)-1,3,4-thiadiazole Induced by Molecular Aggregation.The structural analysis of MARK4 and the exploration of specific inhibitors for the MARK family: a computational approach to obstruct the role of MARK4 in prostate cancer progression.5-(Thiophen-2-yl)-1,3,4-thiadiazole derivatives: synthesis, molecular docking and in vitro cytotoxicity evaluation as potential anticancer agents.2-Amino-1,3,4-thiadiazole as a potential scaffold for promising antimicrobial agents.

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P2860

Thiadiazole-a promising structure in medicinal chemistry.

http://www.wikidata.org/entity/Q38064804

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Thiadiazole-a promising structure in medicinal chemistry.

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Thiadiazole-a promising structure in medicinal chemistry.

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Guisen Zhao

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Jingkun Geng

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Shenghui Yu

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Yang Liu

http://www.w3.org/2001/XMLSchema#string

Yijing Li

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P2860

Carbonic anhydrase inhibitors. The X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitors

Identification of a selective inverse agonist for the orphan nuclear receptor estrogen-related receptor alpha

Identification of a new class of steroid hormone receptors

The PPARs: from orphan receptors to drug discovery

Kinetics of novel competitive inhibitors of urease enzymes by a focused library of oxadiazoles/thiadiazoles and triazoles.

Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozymes IX and XII with a library of aromatic and heteroaromatic sulfonamides.

Discovery and SAR of 1,3,4-thiadiazole derivatives as potent Abl tyrosine kinase inhibitors and cytodifferentiating agents.

Synthesis and identification of [1,2,4]thiadiazole derivatives as a new series of potent and orally active dual agonists of peroxisome proliferator-activated receptors alpha and delta.

Pyrimidine metabolism in man. V. The measurement in vivo of the biochemical effect of antineoplastic agents in animal and human subjects.

The discovery of small molecule inhibitors of neutral endopeptidase. Structure-activity studies on functionalized glutaramides.

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27-41

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scholarly article

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10.1002/CMDC.201200355

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1

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8

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2012-12-03T00:00:00Z

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23208773

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