Pharmacology & Pharmacy

Pharmacology & Pharmacy

ISSN Print: 2157-9423
ISSN Online: 2157-9431
www.scirp.org/journal/pp
E-mail: pp@scirp.org
"Synthesis and Screening of New 5-Substituted-1,3,4-oxadiazole-2-thioglycosides as Potent Anticancer Agents"
written by Mamdouh A .Z. Abu-Zaied, Galal A. M. Nawwar, Randa H. Swellem, Shahinaz H. El-Sayed,
published by Pharmacology & Pharmacy, Vol.3 No.2, 2012
has been cited by the following article(s):
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[2] Synthesis and Biological Activities Evaluation of Novel Spiroheterocycles Containing 1, 3, 4-Oxadiazoline Moiety
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[3] New syntheses of thiosaccharides utilizing substitution reactions
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[4] Naujų funkcionalizuotų pirazolo ar indolo žiedą turinčių heterociklinių junginių sintezė ir tyrimas
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[5] Synthesis and Anticancer Activity of New 1, 3, 4-Thiadiazolyl-1, 2, 4-Triazolyl and 1, 3, 4-Oxadiazolyl Hybrids, Their Thioglycosides, and Acyclic Analogs
Aal, ES Sharshar, HH Elganzory… - Russian Journal of …, 2021
[6] Synthesis of 5‐[(1H‐indol‐3‐yl)methyl]‐1,3,4‐oxadiazole‐2(3H)‐thiones and their protective activity against oxidative stress
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[7] Current Advancement in the Oxadiazole-Based Scaffolds as Anticancer Agents
2021
[8] Anti-Inflammatory and Analgesic Activities of Oxadiazoles Combined with the Nucleus of Benzothiazole.
International Journal of …, 2021
[9] Anticancer and Antiviral Activity of the Pyridine-Biphenyl Glycoside System
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[10] Anticancer activity of S-glycosylated quinazoline derivatives
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[11] Discovery of New S‐Glycosides and N‐Glycosides of Pyridine‐biphenyl System with Antiviral Activity and Induction of Apoptosis in MCF7 Cells
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[12] Synthesis, in vitro and in silico Anti-Proliferative Studies of Novel Piperiene-Oxadiazole and Thiadiazole Analogs
2019
[13] Synthesis, characterization, anticancer activity, and molecular docking of some new sugar hydrazone and arylidene derivatives
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[14] Design, synthesis, molecular docking and anti-hepatocellular carcinoma evaluation of novel acyclic pyridine thioglycosides
Nucleosides Nucleotides & Nucleic Acids, 2018
[15] Synthesis, Biological Evaluation and Docking Studies of 1, 3, 4-oxadiazole Fused Benzothiazole Derivatives for Anticancer Drugs
Letters in Drug Design & Discovery, 2018
[16] Synthesis of 1, 3, 4-Oxa (Thia) Diazole Derivatives of Amidomethylcytisine
Chemistry of Natural Compounds, 2018
[17] Synthesis, computational studies and antiproliferative activities of coumarin-tagged 1, 3, 4-oxadiazole conjugates against MDA-MB-231 and MCF-7 human breast …
Bioorganic & Medicinal Chemistry, 2018
[18] AN INTRODUCTION TO THE SYNTHETIC METHOD AND PHARAMCOLOGICAL ACITVITY OF OXADIAZOLE NUCLEUS: A
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[19] Design, Synthesis and Activities of Multiheterocyclic Modified Novel Molecules Using 1, 3-Selenazole as Template
Chinese Journal of Organic …, 2017
[20] Design, synthesis and in vitro anticancer activity of novel S-alkyl thieno[2,3-d]pyrimidinone derivatives
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[21] 1, 3-硒唑为模板多种杂环修饰的新型分子的设计合成及活性研究
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[22] 1, 3-硒唑为模板多种杂环修饰的新型分子的设计, 合成及活性研究
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[23] Synthesis, thymidine phosphorylase inhibition and molecular modeling studies of 1, 3, 4-oxadiazole-2-thione derivatives
Bioorganic chemistry, 2015
[24] Synthesis and in vivo Anti-inflammatory and Analgesic activities of Oxadiazoles clubbed with Benzothiazole nucleus
International Current Pharmaceutical Journal, 2015
[25] Synthesis characterization and biological Screening of new heterocycles containing oxadiazole thiadiazole indazole pyrazine and pyridine groups
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[26] Novel thiosemicarbazides induced apoptosis in human MCF-7 breast cancer cells via JNK signaling
Journal of enzyme inhibition and medicinal chemistry, 2014
[27] Synthesis and< i> in vitro antitumor activity of new series of benzothiazole and pyrimido [2, 1-< i> b] benzothiazole de
European journal of medicinal chemistry, 2014
[28] Synthesis and in vitro antitumor activity of new series of benzothiazole and pyrimido [2, 1-b] benzothiazole derivatives
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[29] Design, Synthesis and Cytotoxic Evaluation of Novel Heterocyclic Thioglycosides
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[30] Facile synthesis of 6-(heptadec-8-enyl) thiopyrimidines incorporating glycosyl moiety and their antitumor activity
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