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For: Prakash O, Aneja DK, Hussain K, Lohan P, Ranjan P, Arora S, Sharma C, Aneja KR. Synthesis and biological evaluation of dihydroindeno and indeno [1,2-e] [1,2,4]triazolo [3,4-b] [1,3,4]thiadiazines as antimicrobial agents. European Journal of Medicinal Chemistry 2011;46:5065-73. [DOI: 10.1016/j.ejmech.2011.08.019] [Cited by in Crossref: 34] [Cited by in F6Publishing: 20] [Article Influence: 3.1] [Reference Citation Analysis]
Number Citing Articles
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9 Arora L, Prakash R, Pundeer R. Developments in the synthesis of α,α-dibromoacetophenones and related compounds. Synthetic Communications 2019;49:1486-507. [DOI: 10.1080/00397911.2019.1579915] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
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11 Penta S, Gadidasu KK, Basavoju S, Rajeswar Rao V. An efficient one-pot synthesis of pyrazolyl-[1,2,4]triazolo[3,4-b][1,3,4] thiadiazin-6-yl)-2H-pyran-2-one derivatives via multicomponent approach and their potential antimicrobial and nematicidal activities. Tetrahedron Letters 2013;54:5663-6. [DOI: 10.1016/j.tetlet.2013.07.148] [Cited by in Crossref: 20] [Cited by in F6Publishing: 8] [Article Influence: 2.2] [Reference Citation Analysis]
12 Xiong P, Li J, Bu H, Wei Q, Zhang R, Chen S. Copper(II) complexes with 4-(1H-1, 2, 4-trizol-1-ylmethyl) benzoic acid: Syntheses, crystal structures and antifungal activities. Journal of Solid State Chemistry 2014;215:292-9. [DOI: 10.1016/j.jssc.2014.04.012] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
13 Abd El Salam HA, Yakout EMA, Nawwar GAM, El-hashash MA, Mossa AH. Synthesis of some new 1,2,4-triazoles containing olyl moiety and evaluation of their antimicrobial and antioxidant activities. Monatsh Chem 2017;148:291-304. [DOI: 10.1007/s00706-016-1751-5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
14 Ahmad A, Varshney H, Rauf A, Sherwani A, Owais M. Synthesis and anticancer activity of long chain substituted 1,3,4-oxadiazol-2-thione, 1,2,4-triazol-3-thione and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine derivatives. Arabian Journal of Chemistry 2017;10:S3347-57. [DOI: 10.1016/j.arabjc.2014.01.015] [Cited by in Crossref: 19] [Cited by in F6Publishing: 5] [Article Influence: 3.8] [Reference Citation Analysis]
15 Mohamady S, Galal M, Eldehna WM, Gutierrez DC, Ibrahim HS, Elmazar MM, Ali HI. Dual Targeting of VEGFR2 and C-Met Kinases via the Design and Synthesis of Substituted 3-(Triazolo-thiadiazin-3-yl)indolin-2-one Derivatives as Angiogenesis Inhibitors. ACS Omega 2020;5:18872-86. [PMID: 32775889 DOI: 10.1021/acsomega.0c02038] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
16 Faidallah HM, Rostom SAF, Badr MH, Ismail AE, Almohammadi AM. Synthesis of Some 1,4,6-Trisubstituted-2-oxo-1,2-dihydropyridine-3-carbonitriles and Their Biological Evaluation as Cytotoxic and Antimicrobial Agents: 1,4,6-Trisubstituted-2-oxo-1,2-dihydropyridine-3-carbonitriles as Antimicrobial Agents. Arch Pharm Chem Life Sci 2015;348:824-34. [DOI: 10.1002/ardp.201500175] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 1.1] [Reference Citation Analysis]
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18 Kamel MM, Megally Abdo NY. Synthesis of novel 1,2,4-triazoles, triazolothiadiazines and triazolothiadiazoles as potential anticancer agents. European Journal of Medicinal Chemistry 2014;86:75-80. [DOI: 10.1016/j.ejmech.2014.08.047] [Cited by in Crossref: 49] [Cited by in F6Publishing: 30] [Article Influence: 6.1] [Reference Citation Analysis]
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21 Kumar P, Bhatia R, Khanna R, Dalal A, Kumar D, Surain P, Kamboj RC. Synthesis of some benzothiazoles by developing a new protocol using urea nitrate as a catalyst and their antimicrobial activities. Journal of Sulfur Chemistry 2017. [DOI: 10.1080/17415993.2017.1334781] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
22 Ammar YA, Farag AA, Ali AM, Hessein SA, Askar AA, Fayed EA, Elsisi DM, Ragab A. Antimicrobial evaluation of thiadiazino and thiazolo quinoxaline hybrids as potential DNA gyrase inhibitors; design, synthesis, characterization and morphological studies. Bioorg Chem 2020;99:103841. [PMID: 32325335 DOI: 10.1016/j.bioorg.2020.103841] [Cited by in Crossref: 20] [Cited by in F6Publishing: 8] [Article Influence: 10.0] [Reference Citation Analysis]
23 Deng Q, Meng J, Liu Y, Guan Y, Xiao C. IMB-SD62, a triazolothiadiazoles derivative with promising action against tuberculosis. Tuberculosis (Edinb) 2018;112:37-44. [PMID: 30205967 DOI: 10.1016/j.tube.2018.07.006] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
24 Khan I, Ibrar A, Abbas N. Triazolothiadiazoles and triazolothiadiazines – Biologically attractive scaffolds. European Journal of Medicinal Chemistry 2013;63:854-68. [DOI: 10.1016/j.ejmech.2013.01.060] [Cited by in Crossref: 59] [Cited by in F6Publishing: 33] [Article Influence: 6.6] [Reference Citation Analysis]