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For: Biernacki K, Daśko M, Ciupak O, Kubiński K, Rachon J, Demkowicz S. Novel 1,2,4-Oxadiazole Derivatives in Drug Discovery. Pharmaceuticals (Basel) 2020;13:E111. [PMID: 32485996 DOI: 10.3390/ph13060111] [Cited by in Crossref: 19] [Cited by in F6Publishing: 12] [Article Influence: 9.5] [Reference Citation Analysis]
Number Citing Articles
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3 Shafiei I, Tavassoli SP, Rahmatollahi HR, Ghasemian R, Salehzadeh A. A Novel Copper Oxide Nanoparticle Conjugated by Thiosemicarbazone Promote Apoptosis in Human Breast Cancer Cell Line. J Clust Sci. [DOI: 10.1007/s10876-021-02187-1] [Reference Citation Analysis]
4 Wang C, Rui X, Si D, Dai R, Zhu Y, Wen H, Li W, Liu J. Copper‐Catalyzed Three‐Component Cascade Reaction of Benzaldehyde with Benzylamine and Hydroxylamine or Aniline: Synthesis of 1,2,4‐Oxadiazoles and Quinazolines. Adv Synth Catal 2021;363:2825-33. [DOI: 10.1002/adsc.202001535] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
5 Buommino E, De Marino S, Sciarretta M, Piccolo M, Festa C, D'Auria MV. Synergism of a Novel 1,2,4-oxadiazole-containing Derivative with Oxacillin against Methicillin-Resistant Staphylococcus aureus. Antibiotics (Basel) 2021;10:1258. [PMID: 34680838 DOI: 10.3390/antibiotics10101258] [Reference Citation Analysis]
6 Depa N, Erothu H. Design, synthesis, antibacterial evaluation and molecular docking studies of novel pyrazole/1,2,4-oxadiazole conjugate ester derivatives. Med Chem Res 2021;30:1087-98. [DOI: 10.1007/s00044-021-02710-z] [Reference Citation Analysis]
7 Bashir B, Shahid W, Ashraf M, Saleem M, Aziz-Ur-Rehman, Muzaffar S, Imran M, Amjad H, Bhattarai K, Riaz N. Identification of phenylcarbamoylazinane-1,3,4-oxadiazole amides as lipoxygenase inhibitors with expression analysis and in silico studies. Bioorg Chem 2021;115:105243. [PMID: 34403937 DOI: 10.1016/j.bioorg.2021.105243] [Reference Citation Analysis]
8 Banik BK, Sahoo BM, Kumar BVVR, Panda KC, Jena J, Mahapatra MK, Borah P. Green Synthetic Approach: An Efficient Eco-Friendly Tool for Synthesis of Biologically Active Oxadiazole Derivatives. Molecules 2021;26:1163. [PMID: 33671751 DOI: 10.3390/molecules26041163] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Jarocka-Karpowicz I, Markowska A. Jasmonate Compounds and Their Derivatives in the Regulation of the Neoplastic Processes. Molecules 2021;26:2901. [PMID: 34068337 DOI: 10.3390/molecules26102901] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Kulkarni PS, Sarda SR, Khandebharad AU, Farooqui M, Agrawal BR. Pyrazole Linked-1,2,4-Oxadiazole Derivatives as Potential Pharmacological Agent: Design, Synthesis and Antimicrobial Study. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2022.2072914] [Reference Citation Analysis]
11 Stankiewicz A, Kaczorowska K, Bugno R, Kozioł A, Paluchowska MH, Burnat G, Chruścicka B, Chorobik P, Brański P, Wierońska JM, Duszyńska B, Pilc A, Bojarski AJ. New 1,2,4-oxadiazole derivatives with positive mGlu4 receptor modulation activity and antipsychotic-like properties. J Enzyme Inhib Med Chem 2022;37:211-25. [PMID: 34894953 DOI: 10.1080/14756366.2021.1998022] [Reference Citation Analysis]
12 Benassi A, Doria F, Pirota V. Groundbreaking Anticancer Activity of Highly Diversified Oxadiazole Scaffolds. Int J Mol Sci 2020;21:E8692. [PMID: 33217987 DOI: 10.3390/ijms21228692] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
13 Shpigelman J, Lao FS, Yao S, Li C, Saito T, Sato-Kaneko F, Nolan JP, Shukla NM, Pu M, Messer K, Cottam HB, Carson DA, Corr M, Hayashi T. Generation and Application of a Reporter Cell Line for the Quantitative Screen of Extracellular Vesicle Release. Front Pharmacol 2021;12:668609. [PMID: 33935791 DOI: 10.3389/fphar.2021.668609] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Ticona LA, Sánchez ÁR, Bastante MH, Serban AM, Hernáiz MJ. Anti-inflammatory properties of Neowerdermannia vorwerkii Frič ‘Achacana’ used in treating stomach-related ailments. Journal of Ethnopharmacology 2022. [DOI: 10.1016/j.jep.2022.115198] [Reference Citation Analysis]
15 Dhameliya TM, Chudasma SJ, Patel TM, Dave BP. A review on synthetic account of 1,2,4-oxadiazoles as anti-infective agents. Mol Divers 2022. [PMID: 34984590 DOI: 10.1007/s11030-021-10375-4] [Reference Citation Analysis]
16 Kysil A, Biitseva A, Bugera O, Yegorova T, Voitenko Z. Synthesis of 2-(1,2,4-oxadiazol-5-yl)-2,3-dihydro-4H-chromen-4-ones. Fr Ukr J Chem 2020;8:176-82. [DOI: 10.17721/fujcv8i2p176-182] [Reference Citation Analysis]
17 Hendawy OM. A comprehensive review of recent advances in the biological activities of 1,2,4-oxadiazoles. Arch Pharm (Weinheim) 2022;:e2200045. [PMID: 35445430 DOI: 10.1002/ardp.202200045] [Reference Citation Analysis]
18 Baikov SV, Trukhanova YA, Tarasenko MV, Kinzhalov MA. Synthesis and Study of the Structure of Palladium(II) Acyclic Diaminocarbene Complexes Containing a 1,2,4-Oxadiazole Moiety. Russ J Gen Chem 2020;90:1892-900. [DOI: 10.1134/s1070363220100126] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
19 Baykov S, Semenov A, Tarasenko M, Boyarskiy VP. Application of amidoximes for the heterocycles synthesis. Tetrahedron Letters 2020;61:152403. [DOI: 10.1016/j.tetlet.2020.152403] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
20 Faheem M, Althobaiti YS, Khan AW, Ullah A, Ali SH, Ilyas U. Investigation of 1, 3, 4 Oxadiazole Derivative in PTZ-Induced Neurodegeneration: A Simulation and Molecular Approach. J Inflamm Res 2021;14:5659-79. [PMID: 34754213 DOI: 10.2147/JIR.S328609] [Reference Citation Analysis]
21 Baykov SV, Mikherdov AS, Novikov AS, Geyl KK, Tarasenko MV, Gureev MA, Boyarskiy VP. π-π Noncovalent Interaction Involving 1,2,4- and 1,3,4-Oxadiazole Systems: The Combined Experimental, Theoretical, and Database Study. Molecules 2021;26:5672. [PMID: 34577142 DOI: 10.3390/molecules26185672] [Reference Citation Analysis]
22 Wang X, Wang Y, Liu X, He T, Li L, Wu H, Zhou S, Li D, Liao S, Xu P, Huang X, Yuan J. Imidazole hydrochloride promoted synthesis of 3,5-disubstituted-1,2,4-oxadiazoles. Tetrahedron 2021;100:132496. [DOI: 10.1016/j.tet.2021.132496] [Reference Citation Analysis]
23 Apaza Ticona L, Rumbero Sánchez Á, Humanes Bastante M, Serban AM, Hernáiz MJ. Antitumoral activity of 1,2,4-oxadiazoles compounds isolated from the Neowerdermannia vorwerkii in liver and colon human cancer cells. Phytochemistry 2022;201:113259. [PMID: 35662550 DOI: 10.1016/j.phytochem.2022.113259] [Reference Citation Analysis]
24 Mancini RS, Barden CJ, Weaver DF, Reed MA. Furazans in Medicinal Chemistry. J Med Chem 2021;64:1786-815. [PMID: 33569941 DOI: 10.1021/acs.jmedchem.0c01901] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
25 Domingo LR, Acharjee N. Unveiling the Chemo‐ and Regioselectivity of the [3+2] Cycloaddition Reaction between 4‐Chlorobenzonitrile Oxide and β‐Aminocinnamonitrile with a MEDT Perspective**. ChemistrySelect 2021;6:4521-32. [DOI: 10.1002/slct.202100978] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
26 Nam S, Na HG, Oh EH, Jung E, Lee YH, Jeong EJ, Ou YD, Zhou B, Ahn S, Shin JS, Han SB, Go YY. Discovery and synthesis of 1,2,4-oxadiazole derivatives as novel inhibitors of Zika, dengue, Japanese encephalitis, and classical swine fever virus infections. Arch Pharm Res 2022. [PMID: 35441964 DOI: 10.1007/s12272-022-01380-8] [Reference Citation Analysis]
27 Ibrahim TS, Almalki AJ, Moustafa AH, Allam RM, Abuo-Rahma GEA, El Subbagh HI, Mohamed MFA. Novel 1,2,4-oxadiazole-chalcone/oxime hybrids as potential antibacterial DNA gyrase inhibitors: Design, synthesis, ADMET prediction and molecular docking study. Bioorg Chem 2021;111:104885. [PMID: 33838559 DOI: 10.1016/j.bioorg.2021.104885] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Ibrahim TS, Hawwas MM, Malebari AM, Taher ES, Omar AM, Neamatallah T, Abdel-Samii ZK, Safo MK, Elshaier YAMM. Discovery of novel quinoline-based analogues of combretastatin A-4 as tubulin polymerisation inhibitors with apoptosis inducing activity and potent anticancer effect. J Enzyme Inhib Med Chem 2021;36:802-18. [PMID: 33730937 DOI: 10.1080/14756366.2021.1899168] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
29 Chang M, Mahasenan KV, Hermoso JA, Mobashery S. Unconventional Antibacterials and Adjuvants. Acc Chem Res 2021;54:917-29. [PMID: 33512995 DOI: 10.1021/acs.accounts.0c00776] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
30 Deb PK, Al-Shar'i NA, Venugopala KN, Pillay M, Borah P. In vitro anti-TB properties, in silico target validation, molecular docking and dynamics studies of substituted 1,2,4-oxadiazole analogues against Mycobacterium tuberculosis. J Enzyme Inhib Med Chem 2021;36:869-84. [PMID: 34060396 DOI: 10.1080/14756366.2021.1900162] [Reference Citation Analysis]
31 Dai Z, An L, Chen X, Yang F, Zhao N, Li C, Ren R, Li B, Tao W, Li P, Jiang C, Yan F, Jiang Z, You Q, Di B, Xu L. Target Fishing Reveals a Novel Mechanism of 1,2,4-Oxadiazole Derivatives Targeting Rpn6, a Subunit of 26S Proteasome. J Med Chem . [DOI: 10.1021/acs.jmedchem.1c02210] [Reference Citation Analysis]