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For: Xu D, Xu Z. Indole Alkaloids with Potential Anticancer Activity. CTMC 2020;20:1938-49. [DOI: 10.2174/1568026620666200622150325] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 6.7] [Reference Citation Analysis]
Number Citing Articles
1 Chen W, Li G, Wen F, Wang Q, Li Z. Concise Construction of 1‐Sulfonyl‐1 H ‐indoles Using Solid Calcium Carbide as a Surrogate of Gaseous Acetylene. ChemistrySelect 2023;8. [DOI: 10.1002/slct.202203855] [Reference Citation Analysis]
2 Jiang CX, Yu JX, Fei X, Pan XJ, Zhu NN, Lin CL, Zhou D, Zhu HR, Qi Y, Wu ZG. Gene coexpression networks allow the discovery of two strictosidine synthases underlying monoterpene indole alkaloid biosynthesis in Uncaria rhynchophylla. Int J Biol Macromol 2023;226:1360-73. [PMID: 36442554 DOI: 10.1016/j.ijbiomac.2022.11.249] [Reference Citation Analysis]
3 Rivera-Yañez N, Ruiz-Hurtado PA, Rivera-Yañez CR, Arciniega-Martínez IM, Yepez-Ortega M, Mendoza-Arroyo B, Rebollar-Ruíz XA, Méndez-Cruz AR, Reséndiz-Albor AA, Nieto-Yañez O. The Role of Propolis as a Natural Product with Potential Gastric Cancer Treatment Properties: A Systematic Review. Foods 2023;12. [PMID: 36673507 DOI: 10.3390/foods12020415] [Reference Citation Analysis]
4 Song J, Zhang B, Li M, Zhang J. The current scenario of naturally occurring indole alkaloids with anticancer potential. Fitoterapia 2023;165:105430. [PMID: 36634875 DOI: 10.1016/j.fitote.2023.105430] [Reference Citation Analysis]
5 Reddy TS, Rai S, Koppula SK. Synthesis of indole-tetrazole coupled aromatic amides; In vitro anticancer activity, in vitro tubulin polymerization inhibition assay and in silico studies. Journal of Molecular Structure 2022;1267:133556. [DOI: 10.1016/j.molstruc.2022.133556] [Reference Citation Analysis]
6 Zheng Y, Yuan D, Zhang F, Tang R. A systematic pan-cancer analysis of the gasdermin (GSDM) family of genes and their correlation with prognosis, the tumor microenvironment, and drug sensitivity. Front Genet 2022;13:926796. [DOI: 10.3389/fgene.2022.926796] [Reference Citation Analysis]
7 Abinaya R, Srinath S, Soundarya S, Sridhar R, Balasubramanian KK, Baskar B. Recent Developments on Synthesis Strategies, SAR Studies and Biological Activities of β-Carboline Derivatives – An Update. Journal of Molecular Structure 2022;1261:132750. [DOI: 10.1016/j.molstruc.2022.132750] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Trybus W, Trybus E, Król T. Emodin Sensitizes Cervical Cancer Cells to Vinblastine by Inducing Apoptosis and Mitotic Death. IJMS 2022;23:8510. [DOI: 10.3390/ijms23158510] [Reference Citation Analysis]
9 Xiao J, Zhou G, Ji C. Syntheses of Mersicarpine, a Monoterpenoid Indole Alkaloid with an Atypical Tetracyclic Structure. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201373] [Reference Citation Analysis]
10 Shamsiya A, Pathoor R, Bahulayan D. Indole/oxazolone functionalized coumarins as pH-sensitive fluorescent kinase inhibitors. Tetrahedron Letters 2022;101:153905. [DOI: 10.1016/j.tetlet.2022.153905] [Reference Citation Analysis]
11 Kadu VD, Patil AA, Shendage PR. Oxone-Promoted Synthesis of Bis(indolyl)methanes from Arylmethylamines and Indoles. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.133502] [Reference Citation Analysis]
12 Yu JH, Yu ZP, Capon RJ, Zhang H. Natural Enantiomers: Occurrence, Biogenesis and Biological Properties. Molecules 2022;27:1279. [PMID: 35209066 DOI: 10.3390/molecules27041279] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
13 Reis FL, Adolpho L, Ruiz ALTG, Simionatto E, Dalcol II, Mostardeiro MA, Morel AF. In vitro antiproliferative activity of alkaloids isolated from Tabernaemontana catharinensis A.DC (Apocynaceae). Nat Prod Res 2022;:1-5. [PMID: 35075954 DOI: 10.1080/14786419.2021.2017928] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Nancy, Chaudhary S, Kumar D, Archana. Synthesis and Anti-inflammatory Activity of Newer Indolyl Pyrazolines and Indolyl Isoxazolines. Asian J Org Med Chem 2022;7:79-83. [DOI: 10.14233/ajomc.2022.ajomc-p365] [Reference Citation Analysis]
15 Wang G, Sun S, Guo H. Current status of carbazole hybrids as anticancer agents. Eur J Med Chem 2021;:113999. [PMID: 34838335 DOI: 10.1016/j.ejmech.2021.113999] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
16 Santos AF, Santos Mota NSR, Schiefer EM, da Cunha RS, Junkert AM, Stinghen AEM, Pontarolo R, Crisma AR, Weffort-Santos AM, Pedrosa RC, de Souza WM, Felipe KB. The toxicity of Aspidosperma subincanum to MCF7 cells is related to modulation of oxidative status and proinflammatory pathways. J Ethnopharmacol 2021;281:114512. [PMID: 34384848 DOI: 10.1016/j.jep.2021.114512] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
17 Mitra S, Prova SR, Sultana SA, Das R, Nainu F, Emran TB, Tareq AM, Uddin MS, Alqahtani AM, Dhama K, Simal-Gandara J. Therapeutic potential of indole alkaloids in respiratory diseases: A comprehensive review. Phytomedicine 2021;90:153649. [PMID: 34325978 DOI: 10.1016/j.phymed.2021.153649] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 6.5] [Reference Citation Analysis]
18 Liang T, Sun X, Li W, Hou G, Gao F. 1,2,3-Triazole-Containing Compounds as Anti-Lung Cancer Agents: Current Developments, Mechanisms of Action, and Structure-Activity Relationship. Front Pharmacol 2021;12:661173. [PMID: 34177578 DOI: 10.3389/fphar.2021.661173] [Cited by in Crossref: 15] [Cited by in F6Publishing: 17] [Article Influence: 7.5] [Reference Citation Analysis]
19 Zhuravleva OI, Antonov AS, Trang VTD, Pivkin MV, Khudyakova YV, Denisenko VA, Popov RS, Kim NY, Yurchenko EA, Gerasimenko AV, Udovenko AA, Amsberg GV, Dyshlovoy SA, Afiyatullov SS. New Deoxyisoaustamide Derivatives from the Coral-Derived Fungus Penicillium dimorphosporum KMM 4689. Mar Drugs 2021;19:32. [PMID: 33445521 DOI: 10.3390/md19010032] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
20 Wei X, Liang X, Li Y, Liu Q, Liu X, Zhou Y, Liu H. I 2 -induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines. Green Chem 2021;23:9165-71. [DOI: 10.1039/d1gc02713a] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
21 Meng T, Hou Y, Shang C, Zhang J, Zhang B. Recent advances in indole dimers and hybrids with antibacterial activity against methicillin-resistant Staphylococcus aureus. Arch Pharm (Weinheim) 2021;354:e2000266. [PMID: 32986279 DOI: 10.1002/ardp.202000266] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]