Literature DB >> 18667305

A facile regioselective synthesis of novel spiro-thioxanthene and spiro-xanthene-9',2-[1,3,4]thiadiazole derivatives as potential analgesic and anti-inflammatory agents.

H N Hafez1, M I Hegab, I S Ahmed-Farag, A B A el-Gazzar.   

Abstract

The 1,3-dipolar cycloaddition of nitrile imines to 9H-thioxanthone-9-thione and 9H-xanthone-9-thione afforded novel spiro-thioxanthene-9',2-[1,3,4]thiadiazoles 6a-g and spiro-xanthene-9',2-[1,3,4]thiadiazoles 7a-g in good yields. Some of the newly synthesized compounds were tested for anti-inflammatory and analgesic activities comparable to ibuprofen. Compounds 6a,d,e and 7a,d,e showed significant activity compared to standard drug. The toxicity studies revealed that neither death nor other behavioral or toxicological changes were observed on rats up to a dose as high as 200 mg/kg.

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Year:  2008        PMID: 18667305     DOI: 10.1016/j.bmcl.2008.07.042

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  21 in total

1.  Greener Route for Synthesis of aryl and alkyl-14H-dibenzo [a.j] xanthenes using Graphene Oxide-Copper Ferrite Nanocomposite as a Recyclable Heterogeneous Catalyst.

Authors:  Aniket Kumar; Lipeeka Rout; Lakkoji Satish Kumar Achary; Rajendra S Dhaka; Priyabrat Dash
Journal:  Sci Rep       Date:  2017-02-24       Impact factor: 4.379

2.  Facile, efficient and one-pot access to diverse new functionalized aminoalkyl and amidoalkyl naphthol scaffolds via green multicomponent reaction using triethylammonium hydrogen sulfate ([Et3NH][HSO4]) as an acidic ionic liquid under solvent-free conditions.

Authors:  Elahe Hadadianpour; Behjat Pouramiri
Journal:  Mol Divers       Date:  2019-04-05       Impact factor: 2.943

3.  Green and four-component cyclocondensation synthesis and in silico docking of new polyfunctionalized pyrrole derivatives as the potential anticholinesterase agents.

Authors:  Mohammad Hadi Meshkatalsadat; Ahmad Mahmoudi; Safa Lotfi; Behjat Pouramiri; Alireza Foroumadi
Journal:  Mol Divers       Date:  2022-01-16       Impact factor: 2.943

4.  Sulfamic acid catalyzed solvent-free synthesis of 10-aryl-7,7-dimethyl-6,7,8,10-tetrahydro-9H-[1,3]-dioxolo [4,5- b]xanthen-9-ones and 12-aryl-9,9-dimethyl-8,9,10,12-tetrahydro-11H-benzo[a]xanthen-11-ones.

Authors:  Majid M Heravi; Hamideh Alinejhad; Khadijeh Bakhtiari; Hossein A Oskooie
Journal:  Mol Divers       Date:  2009-09-30       Impact factor: 2.943

5.  Synthesis, Molecular Structure, DNA/Protein Binding, Cytotoxicity, Apoptosis, Reactive Oxygen Species, and Mitochondrial Membrane Potential of Dibenzoxanthenes Derivatives.

Authors:  Hui-Hui Yang; Bing-Jie Han; Wei Li; Yun-Jun Liu; Xiu-Zhen Wang
Journal:  J Membr Biol       Date:  2015-09-23       Impact factor: 1.843

6.  Novel domino procedures for the synthesis of chromene derivatives and their isomerization.

Authors:  Afsaneh Zonouzi; Zakieh Izakian; Seik Weng Ng
Journal:  Mol Divers       Date:  2016-03-22       Impact factor: 2.943

7.  Multicomponent synthesis of diverse pyrano-fused benzophenazines using bifunctional thiourea-based organocatalyst in aqueous medium.

Authors:  Ruchi Bharti; Tasneem Parvin
Journal:  Mol Divers       Date:  2016-06-17       Impact factor: 2.943

8.  9-(4-Hy-droxy-3-meth-oxy-phen-yl)-3,3,6,6-tetra-methyl-3,4,5,6-tetra-hydro-9H-xanthene-1,8(2H,7H)-dione.

Authors:  Noorhafizah Hasanudin; Aisyah Saad Abdul Rahim; Nornisah Mohamed; Ching Kheng Quah; Hoong-Kun Fun
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-06-05

9.  Ethyl 2-[(Z)-2-benzyl-hydrazin-1-yl-idene]-2-bromo-acetate.

Authors:  Qian-Jiao Yang; Dan Liu; Jian Zuo; Guo-Dong Hu; Lin-Xiang Zhao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-08-18

10.  ChCl: Gly (DESs) Promote Environmentally Benign Synthesis of Xanthene Derivatives and Their Antitubercular Activity.

Authors:  Mashooq A Bhat; Ahmed M Naglah; Siddique Akber Ansari; Hanaa M Al-Tuwajiria; Abdullah Al-Dhfyan
Journal:  Molecules       Date:  2021-06-16       Impact factor: 4.411

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