BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Shin SY, Yoon H, Hwang D, Ahn S, Kim D, Koh D, Lee YH, Lim Y. Benzochalcones bearing pyrazoline moieties show anti-colorectal cancer activities and selective inhibitory effects on aurora kinases. Bioorganic & Medicinal Chemistry 2013;21:7018-24. [DOI: 10.1016/j.bmc.2013.09.014] [Cited by in Crossref: 36] [Cited by in F6Publishing: 26] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Ahn S, Truong VN, Kim B, Yoo M, Lim Y, Cho SK, Koh D. Design, synthesis, and biological evaluation of chalcones for anticancer properties targeting glycogen synthase kinase 3 beta. Appl Biol Chem 2022;65. [DOI: 10.1186/s13765-022-00686-x] [Reference Citation Analysis]
2 Shin SY, Jung E, Yeo H, Ahn S, Lee Y, Park J, Kang H, Yeo WS, Koh D, Lim Y. Design, synthesis, and biological activities of 3-((4,6-diphenylpyrimidin-2-ylamino)methylene)-2,3-dihydrochromen-4-ones. Bioorg Chem 2022;120:105634. [PMID: 35114524 DOI: 10.1016/j.bioorg.2022.105634] [Reference Citation Analysis]
3 Yepes AF, Arias JD, Cardona-g W, Herrera-r A, Moreno G. New class of hybrids based on chalcone and melatonin: a promising therapeutic option for the treatment of colorectal cancer. Med Chem Res 2021;30:2240-55. [DOI: 10.1007/s00044-021-02805-7] [Reference Citation Analysis]
4 Shin SY, Lee J, Ahn S, Yoo M, Lee YH, Koh D, Lim Y. Design, synthesis, and evaluation of 4-chromenone derivatives combined with N-acylhydrazone for aurora kinase A inhibitor. Appl Biol Chem 2021;64. [DOI: 10.1186/s13765-021-00596-4] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Rasal NK, Sonawane RB, Jagtap SV. Synthesis, biological evaluation, and in silico study of pyrazoline-conjugated 2,4-dimethyl-1H-pyrrole-3-carboxylic acid derivatives. Arch Pharm (Weinheim) 2021;354:e2000267. [PMID: 33078449 DOI: 10.1002/ardp.202000267] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
6 Safaa I. Elewa, Mansour E, Nassar IF, Mekawey AAI. Synthesis of Some New Pyrazoline-Based Thiazole Derivatives and Evaluation of Their Antimicrobial, Antifungal, and Anticancer Activities. Russ J Bioorg Chem 2020;46:382-92. [DOI: 10.1134/s1068162020030061] [Cited by in Crossref: 5] [Article Influence: 2.5] [Reference Citation Analysis]
7 Al-Refai M, Ali BF, Geyer A, Harms K, Marsch M. Unexpected formation of a co-crystal containing the chalcone (E)-1-(5-chloro-thio-phen-2-yl)-3-(3-methyl-thio-phen-2-yl)prop-2-en-1-one and the keto-enol tautomer (Z)-1-(5-chloro-thio-phen-2-yl)-3-(3-methyl-thio-phen-2-yl)prop-1-en-1-ol. Acta Crystallogr E Crystallogr Commun 2020;76:477-80. [PMID: 32280487 DOI: 10.1107/S2056989020002583] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Lee YH, Park J, Ahn S, Lee Y, Lee J, Shin SY, Koh D, Lim Y. Design, synthesis, and biological evaluation of polyphenols with 4,6-diphenylpyrimidin-2-amine derivatives for inhibition of Aurora kinase A. Daru 2019;27:265-81. [PMID: 31154600 DOI: 10.1007/s40199-019-00272-5] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
9 Santosh R, Prabhu A, Selvam MK, Krishna PM, Nagaraja GK, Rekha PD. Design, synthesis, and pharmacology of some oxadiazole and hydroxypyrazoline hybrids bearing thiazoyl scaffold: antiproliferative activity, molecular docking and DNA binding studies. Heliyon 2019;5:e01255. [PMID: 30886919 DOI: 10.1016/j.heliyon.2019.e01255] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
10 Khamees HA, Jyothi M, Khanum SA, Madegowda M. Synthesis, crystal structure, spectroscopic characterization, docking simulation and density functional studies of 1-(3,4-dimethoxyphenyl) -3-(4-flurophenyl)-propan-1-one. Journal of Molecular Structure 2018;1161:199-217. [DOI: 10.1016/j.molstruc.2018.02.045] [Cited by in Crossref: 11] [Cited by in F6Publishing: 3] [Article Influence: 2.8] [Reference Citation Analysis]
11 Abd-rabou AA, Abdel-wahab BF, Bekheit MS. Synthesis, molecular docking, and evaluation of novel bivalent pyrazolinyl-1,2,3-triazoles as potential VEGFR TK inhibitors and anti-cancer agents. Chem Pap 2018;72:2225-37. [DOI: 10.1007/s11696-018-0451-5] [Cited by in Crossref: 14] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
12 Lee Y, Koh D, Ahn S, Lee YH, Shin SY, Lim Y. Clonogenic long-term survival assay of HCT 116 colorectal cancer cells after treatment with the synthesized diphenyl imidazoline derivatives. Appl Biol Chem 2018;61:303-12. [DOI: 10.1007/s13765-018-0355-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
13 Song YW, Lim Y, Cho SK. 2,4‑Di‑tert‑butylphenol, a potential HDAC6 inhibitor, induces senescence and mitotic catastrophe in human gastric adenocarcinoma AGS cells. Biochim Biophys Acta Mol Cell Res 2018;1865:675-83. [PMID: 29427610 DOI: 10.1016/j.bbamcr.2018.02.003] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
14 Borisa AC, Bhatt HG. A comprehensive review on Aurora kinase: Small molecule inhibitors and clinical trial studies. European Journal of Medicinal Chemistry 2017;140:1-19. [DOI: 10.1016/j.ejmech.2017.08.045] [Cited by in Crossref: 85] [Cited by in F6Publishing: 80] [Article Influence: 17.0] [Reference Citation Analysis]
15 Kim BS, Shin SY, Ahn S, Koh D, Lee YH, Lim Y. Biological evaluation of 2-pyrazolinyl-1-carbothioamide derivatives against HCT116 human colorectal cancer cell lines and elucidation on QSAR and molecular binding modes. Bioorg Med Chem 2017;25:5423-32. [PMID: 28811071 DOI: 10.1016/j.bmc.2017.07.062] [Cited by in Crossref: 14] [Cited by in F6Publishing: 8] [Article Influence: 2.8] [Reference Citation Analysis]
16 Tessmann JW, Buss J, Begnini KR, Berneira LM, Paula FR, de Pereira CMP, Collares T, Seixas FK. Antitumor potential of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-1H-pyrazoles in human bladder cancer cells. Biomed Pharmacother 2017;94:37-46. [PMID: 28750358 DOI: 10.1016/j.biopha.2017.07.060] [Cited by in Crossref: 21] [Cited by in F6Publishing: 15] [Article Influence: 4.2] [Reference Citation Analysis]
17 Koh D, Jung Y, Ahn S, Mok KH, Shin SY, Lim Y. Synthesis and structure elucidation of polyphenols containing the N ′-methyleneformohydrazide scaffold as aurora kinase inhibitors: Synthesis and structure elucidation of polyphenols. Magn Reson Chem 2017;55:864-76. [DOI: 10.1002/mrc.4611] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
18 Jung K, Park J, Han Y, Lee YH, Shin SY, Lim Y. Synthesis and biological evaluation of hesperetin derivatives as agents inducing apoptosis. Bioorganic & Medicinal Chemistry 2017;25:397-407. [DOI: 10.1016/j.bmc.2016.11.006] [Cited by in Crossref: 14] [Cited by in F6Publishing: 12] [Article Influence: 2.8] [Reference Citation Analysis]
19 Lee Y, Kim BS, Ahn S, Koh D, Lee YH, Shin SY, Lim Y. Anticancer and structure-activity relationship evaluation of 3-(naphthalen-2-yl)-N,5-diphenyl-pyrazoline-1-carbothioamide analogs of chalcone. Bioorg Chem 2016;68:166-76. [PMID: 27543822 DOI: 10.1016/j.bioorg.2016.08.003] [Cited by in Crossref: 23] [Cited by in F6Publishing: 13] [Article Influence: 3.8] [Reference Citation Analysis]
20 Shin SY, Ahn S, Yoon H, Jung H, Jung Y, Koh D, Lee YH, Lim Y. Colorectal anticancer activities of polymethoxylated 3-naphthyl-5-phenylpyrazoline-carbothioamides. Bioorg Med Chem Lett 2016;26:4301-9. [PMID: 27476140 DOI: 10.1016/j.bmcl.2016.07.037] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
21 Saleh AM, Aziz MA, Abdou IM, Taha MO, Al-qudah MA, Abadleh MM, Aljada A, Rizvi SA. Cytotoxic activity of the novel heterocyclic compound G-11 is primarily mediated through intrinsic apoptotic pathway. Apoptosis 2016;21:873-86. [DOI: 10.1007/s10495-016-1248-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
22 Jung Y, Ahn S, Jung H, Koh D, Lim Y. (1) H and (13) C NMR spectral assignments of 30 novel n-methoxylated polyphenols containing thiourea skeletons. Magn Reson Chem 2016;54:403-13. [PMID: 26891199 DOI: 10.1002/mrc.4405] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
23 Jung H, Ahn S, Kim BS, Shin SY, Lee YH, Lim Y. Isoflavones as modulators of adenosine monophosphate-activated protein kinase. Appl Biol Chem 2016;59:217-25. [DOI: 10.1007/s13765-016-0149-8] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
24 Karabacak M, Altıntop MD, İbrahim Çiftçi H, Koga R, Otsuka M, Fujita M, Özdemir A. Synthesis and Evaluation of New Pyrazoline Derivatives as Potential Anticancer Agents. Molecules 2015;20:19066-84. [PMID: 26492233 DOI: 10.3390/molecules201019066] [Cited by in Crossref: 39] [Cited by in F6Publishing: 28] [Article Influence: 5.6] [Reference Citation Analysis]
25 Naik VS, Yathirajan HS, Jasinski JP, Smolenski VA, Glidewell C. The crystal structures of six (2E)-3-aryl-1-(5-halogeno-thio-phen-2-yl)prop-2-en-1-ones. Acta Crystallogr E Crystallogr Commun 2015;71:1093-9. [PMID: 26396857 DOI: 10.1107/S2056989015015534] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
26 Jandial DD, Blair CA, Zhang S, Krill LS, Zhang YB, Zi X. Molecular targeted approaches to cancer therapy and prevention using chalcones. Curr Cancer Drug Targets 2014;14:181-200. [PMID: 24467530 DOI: 10.2174/1568009614666140122160515] [Cited by in Crossref: 59] [Cited by in F6Publishing: 55] [Article Influence: 8.4] [Reference Citation Analysis]
27 Jung H, Ahn S, Park M, Yoon H, Noh HJ, Kim SY, Yoo JS, Koh D, Lim Y. 1 H and 13 C NMR spectral assignments of 18 novel polymethoxylated naphthochalcones bearing pyrazoline-1-carbothioamide groups: 1 H and 13 C NMR spectral assignments of polymethoxylated naphthochalcones. Magn Reson Chem 2015;53:383-90. [DOI: 10.1002/mrc.4217] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 1.7] [Reference Citation Analysis]
28 Yong Y, Shin SY, Jung Y, Jung H, Ahn S, Chong Y, Lim Y. Flavonoids activating adenosine monophosphate-activated protein kinase. J Korean Soc Appl Biol Chem 2015;58:13-9. [DOI: 10.1007/s13765-015-0003-4] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.9] [Reference Citation Analysis]
29 Tran TA, Ahn KS, Song YW, Moon JY, Cho M, Lim Y, Cho SK. Mechanism of 2′,3′-dimethoxyflavanone-induced apoptosis in breast cancer stem cells: Role of ubiquitination of caspase-8 and LC3. Archives of Biochemistry and Biophysics 2014;562:92-102. [DOI: 10.1016/j.abb.2014.08.001] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 1.4] [Reference Citation Analysis]
30 Jung Y, Shin SY, Yong Y, Jung H, Ahn S, Lee YH, Lim Y. Plant-Derived Flavones as Inhibitors of Aurora B Kinase and Their Quantitative Structure-Activity Relationships. Chem Biol Drug Des 2015;85:574-85. [DOI: 10.1111/cbdd.12445] [Cited by in Crossref: 17] [Cited by in F6Publishing: 12] [Article Influence: 2.1] [Reference Citation Analysis]
31 Yong Y, Shin SY, Jung H, Ahn S, Lee YH, Koh D, Lim Y. Investigation of 2-hydroxy-4-methoxy-2′,3′-benzochalcone binding to tubulin by using NMR and in silico docking. J Korean Soc Appl Biol Chem 2014;57:693-8. [DOI: 10.1007/s13765-014-4181-2] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
32 Koh D. Crystal structure of (E)-3-(2,4-di-meth-oxy-phen-yl)-1-(1-hy-droxy-naphthalen-2-yl)prop-2-en-1-one. Acta Crystallogr Sect E Struct Rep Online 2014;70:o1034-5. [PMID: 25309211 DOI: 10.1107/S1600536814018704] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
33 Shin SY, Yong Y, Lee J, Ahn S, Jung K, Koh D, Lee YH, Lim Y. A novel hydroxymethoxynaphthochalcone induces apoptosis through the p53-dependent caspase-mediated pathway in HCT116 human colon cancer cells. J Korean Soc Appl Biol Chem 2014;57:413-8. [DOI: 10.1007/s13765-014-4043-y] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
34 Drutovic D, Chripkova M, Pilatova M, Kruzliak P, Perjesi P, Sarissky M, Lupi M, Damia G, Broggini M, Mojzis J. Benzylidenetetralones, cyclic chalcone analogues, induce cell cycle arrest and apoptosis in HCT116 colorectal cancer cells. Tumour Biol 2014;35:9967-75. [PMID: 25008568 DOI: 10.1007/s13277-014-2289-y] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 1.9] [Reference Citation Analysis]
35 Shin SY, Jung H, Ahn S, Hwang D, Yoon H, Hyun J, Yong Y, Cho HJ, Koh D, Lee YH, Lim Y. Polyphenols bearing cinnamaldehyde scaffold showing cell growth inhibitory effects on the cisplatin-resistant A2780/Cis ovarian cancer cells. Bioorganic & Medicinal Chemistry 2014;22:1809-20. [DOI: 10.1016/j.bmc.2014.01.058] [Cited by in Crossref: 39] [Cited by in F6Publishing: 32] [Article Influence: 4.9] [Reference Citation Analysis]
36 Koh D. (E)-1-(2-Hy-droxy-6-meth-oxy-phen-yl)-3-(2,4,6-tri-meth-oxy-phen-yl)prop-2-en-1-one. Acta Crystallogr Sect E Struct Rep Online 2013;69:o1809. [PMID: 24454240 DOI: 10.1107/S1600536813031498] [Reference Citation Analysis]