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For: Devipriya D, Roopan SM. UV-light intervened synthesis of imidazo fused quinazoline and its solvatochromism, antioxidant, antifungal and luminescence properties. J Photochem Photobiol B 2019;190:42-9. [PMID: 30472613 DOI: 10.1016/j.jphotobiol.2018.11.003] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Lakshman C, Hari Prakash S, Mohana Roopan S. Materials based on molybdenum disulfide as a catalyst in organic transformations: An overview. Synthetic Communications. [DOI: 10.1080/00397911.2022.2048859] [Reference Citation Analysis]
2 Cheke RS, Shinde SD, Ambhore JP, Chaudhari SR, Bari SB. Quinazoline: An update on current status against convulsions. Journal of Molecular Structure 2022;1248:131384. [DOI: 10.1016/j.molstruc.2021.131384] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
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4 Abdelghany A, Soliman HA, Khatab TK. Biosynthesized Selenium nanoparticles as a new catalyst in the synthesis of quinazoline derivatives in pentacyclic system with docking validation as (TRPV1) inhibitor. Journal of Organometallic Chemistry 2021;944:121847. [DOI: 10.1016/j.jorganchem.2021.121847] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
5 Tian PP, Lv YY, Lv A, Yuan WJ, Zhang SB, Li N, Hu YS. Antifungal Effects of Fusion Puroindoline B on the Surface and Intracellular Environment of Aspergillus flavus. Probiotics Antimicrob Proteins 2021;13:249-60. [PMID: 32488675 DOI: 10.1007/s12602-020-09667-2] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
6 Tian P, Lv Y, Wei S, Zhang S, Li N, Hu Y. Antifungal properties of recombinant Puroindoline B protein against aflatoxigenic Aspergillus flavus. LWT 2021;144:111130. [DOI: 10.1016/j.lwt.2021.111130] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
7 Fedotov VV, Rusinov VL, Ulomsky EN, Mukhin EM, Gorbunov EB, Chupakhin ON. Pyrimido[1,2-a]benzimidazoles: synthesis and perspective of their pharmacological use. Chem Heterocycl Compd (N Y) 2021;:1-27. [PMID: 34024913 DOI: 10.1007/s10593-021-02916-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
8 Desai N, Shihory N, Khasiya A, Pandit U, Khedkar V. Quinazoline clubbed thiazole and 1,3,4-oxadiazole heterocycles: synthesis, characterization, antibacterial evaluation, and molecular docking studies. Phosphorus, Sulfur, and Silicon and the Related Elements 2021;196:569-77. [DOI: 10.1080/10426507.2021.1871732] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]
9 Devi Priya D, Mohana Roopan S. Effective catalytic approach of NiTiO 3 photosonocatalyst for the synthesis of indazolo[3,2‐ b ]quinazoline and its photophysical property. Appl Organomet Chem 2021;35. [DOI: 10.1002/aoc.6109] [Reference Citation Analysis]
10 Devi Priya D, Mohana Roopan S. Claisen-Schmidt, aza-Michael, cyclization via cascade strategy toward microwave promoted synthesis of imidazo[2,1-b]quinazolines. Synthetic Communications 2020;50:1813-34. [DOI: 10.1080/00397911.2020.1757112] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
11 Zhao Y, Liu F, He G, Li K, Zhu C, Yu W, Zhang C, Xie M, Lin J, Zhang J, Jin Y. Discovery of arylamide-5-anilinoquinazoline-8-nitro derivatives as VEGFR-2 kinase inhibitors: Synthesis, in vitro biological evaluation and molecular docking. Bioorg Med Chem Lett 2019;29:126711. [PMID: 31668972 DOI: 10.1016/j.bmcl.2019.126711] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 4.0] [Reference Citation Analysis]
12 Zi M, Liu F, Wu D, Li K, Zhang D, Zhu C, Zhang Z, Li L, Zhang C, Xie M, Lin J, Zhang J, Jin Y. Discovery of 6-Arylurea-2-arylbenzoxazole and 6-Arylurea-2-arylbenzimidazole Derivatives as Angiogenesis Inhibitors: Design, Synthesis and in vitro Biological Evaluation. ChemMedChem 2019;14:1291-302. [PMID: 31131561 DOI: 10.1002/cmdc.201900216] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]