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Journal Abstract Search

131 related items for PubMed ID: 33312212

  • 1.
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  • 2. Synthesis and cytotoxicity evaluation of novel cyclic/non-cyclic N-aryl enamino amides against human cancer cell lines.
    Bohlooli S, Nejatkhah N, Sepehri S, Doostkamel D, Razzaghi-Asl N.
    Res Pharm Sci; 2020 Dec; 15(6):563-570. PubMed ID: 33828599
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  • 3. Synthesis, antileishmanial activity and molecular modeling of new 1-aryl/alkyl-3-benzoyl/cyclopropanoyl thiourea derivatives.
    Mohammadi-Ghalehbin B, Shiran JA, Gholizadeh N, Razzaghi-Asl N.
    Mol Divers; 2023 Aug; 27(4):1531-1545. PubMed ID: 36001225
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  • 5. Synthesis and cytotoxic effect of a few N-heteroaryl enamino amides and dihydropyrimidinethiones on AGS and MCF-7 human cancer cell lines.
    Tavangar S, Bohlooli S, Razzaghi-Asl N.
    Res Pharm Sci; 2020 Apr; 15(2):154-163. PubMed ID: 32582355
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  • 7. Novel 5-(nitrothiophene-2-yl)-1,3,4-Thiadiazole Derivatives: Synthesis and Antileishmanial Activity against promastigote stage of Leishmania major.
    Sadat-Ebrahimi SE, Mirmohammadi M, Mojallal Tabatabaei Z, Azimzadeh Arani M, Jafari-Ashtiani S, Hashemian M, Foroumadi P, Yahya-Meymandi A, Moghimi S, Moshafi MH, Norouzi P, Kabudanian Ardestani S, Foroumadi A.
    Iran J Pharm Res; 2019 Apr; 18(4):1816-1822. PubMed ID: 32184848
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  • 13. Antidiabetic Activity of Dihydropyrimidine Scaffolds and Structural Insight by Single Crystal X-ray Studies.
    Bairagi KM, Younis NS, Emeka PM, Sangtani E, Gonnade RG, Venugopala KN, Alwassil OI, Khalil HE, Nayak SK.
    Med Chem; 2020 Apr; 16(7):996-1003. PubMed ID: 31880253
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  • 14. Aryl/heteroaryl Substituted Celecoxib Derivatives as COX-2 Inhibitors: Synthesis, Anti-inflammatory Activity and Molecular Docking Studies.
    Madhava G, Ramana KV, Sudhana SM, Rao DS, Kumar KH, Lokanatha V, Rani AU, Raju CN.
    Med Chem; 2017 Apr; 13(5):484-497. PubMed ID: 28228088
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  • 16. Design, synthesis, in vitro antiproliferative activity and apoptosis-inducing studies of 1-(3',4',5'-trimethoxyphenyl)-3-(2'-alkoxycarbonylindolyl)-2-propen-1-one derivatives obtained by a molecular hybridisation approach.
    Preti D, Romagnoli R, Rondanin R, Cacciari B, Hamel E, Balzarini J, Liekens S, Schols D, Estévez-Sarmiento F, Quintana J, Estévez F.
    J Enzyme Inhib Med Chem; 2018 Dec; 33(1):1225-1238. PubMed ID: 30141353
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  • 18. Repurposing Glyburide as Antileishmanial Agent to Fight Against Leishmaniasis.
    Rub A, Shaker K, Kashif M, Arish M, Dukhyil AAB, Alshehri BM, Alaidarous MA, Banawas S, Amir K.
    Protein Pept Lett; 2019 Dec; 26(5):371-376. PubMed ID: 30827222
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  • 19. In vitro activity of new N-benzyl-1H-benzimidazol-2-amine derivatives against cutaneous, mucocutaneous and visceral Leishmania species.
    Nieto-Meneses R, Castillo R, Hernández-Campos A, Maldonado-Rangel A, Matius-Ruiz JB, Trejo-Soto PJ, Nogueda-Torres B, Dea-Ayuela MA, Bolás-Fernández F, Méndez-Cuesta C, Yépez-Mulia L.
    Exp Parasitol; 2018 Jan; 184():82-89. PubMed ID: 29191699
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  • 20. β-Nitrostyrenes as Potential Anti-leishmanial Agents.
    Shafi S, Afrin F, Islamuddin M, Chouhan G, Ali I, Naaz F, Sharma K, Zaman MS.
    Front Microbiol; 2016 Jan; 7():1379. PubMed ID: 27635124
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