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For: Abu-Izneid T, Rauf A, Shariati MA, Khalil AA, Imran M, Rebezov M, Uddin MS, Mahomoodally MF, Rengasamy KRR. Sesquiterpenes and their derivatives-natural anticancer compounds: An update. Pharmacol Res 2020;161:105165. [PMID: 32835868 DOI: 10.1016/j.phrs.2020.105165] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 4.5] [Reference Citation Analysis]
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7 Balakrishnan V, Ganapathy S, Veerasamy V, Duraisamy R, Sathiavakoo VA, Krishnamoorthy V, Lakshmanan V. Anticancer and antioxidant profiling effects of Nerolidol against DMBA induced oral experimental carcinogenesis. J Biochem Mol Toxicol 2022;:e23029. [PMID: 35243731 DOI: 10.1002/jbt.23029] [Reference Citation Analysis]
8 Stepanova VA, Patrushev SS, Rybalova TV, Shults EE. Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent. Journal of Molecular Structure 2022;1247:131373. [DOI: 10.1016/j.molstruc.2021.131373] [Reference Citation Analysis]
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11 Luca SV, Gaweł-Bęben K, Strzępek-Gomółka M, Jumabayeva A, Sakipova Z, Xiao J, Marcourt L, Wolfender JL, Skalicka-Woźniak K. Liquid-Liquid Chromatography Separation of Guaiane-Type Sesquiterpene Lactones from Ferula penninervis Regel & Schmalh. and Evaluation of Their In Vitro Cytotoxic and Melanin Inhibitory Potential. Int J Mol Sci 2021;22:10717. [PMID: 34639057 DOI: 10.3390/ijms221910717] [Reference Citation Analysis]
12 Bimoussa A, Oubella A, Hachim ME, Fawzi M, Itto MYA, Mentre O, Ketatni EM, Bahsis L, Morjani H, Auhmani A. New enaminone sesquiterpenic: TiCl4-catalyzed synthesis, spectral characterization, crystal structure, Hirshfeld surface analysis, DFT studies and cytotoxic activity. Journal of Molecular Structure 2021;1241:130622. [DOI: 10.1016/j.molstruc.2021.130622] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 11.0] [Reference Citation Analysis]
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14 Mai J, Li W, Ledesma-Amaro R, Ji XJ. Engineering Plant Sesquiterpene Synthesis into Yeasts: A Review. J Agric Food Chem 2021;69:9498-510. [PMID: 34376044 DOI: 10.1021/acs.jafc.1c03864] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Ben Hassine D, Kammoun El Euch S, Rahmani R, Ghazouani N, Kane R, Abderrabba M, Bouajila J. Clove Buds Essential Oil: The Impact of Grinding on the Chemical Composition and Its Biological Activities Involved in Consumer's Health Security. Biomed Res Int 2021;2021:9940591. [PMID: 34381841 DOI: 10.1155/2021/9940591] [Reference Citation Analysis]
16 Zhang J, Zheng ZQ, Xu Q, Li Y, Gao K, Fang J. Onopordopicrin from the new genus Shangwua as a novel thioredoxin reductase inhibitor to induce oxidative stress-mediated tumor cell apoptosis. J Enzyme Inhib Med Chem 2021;36:790-801. [PMID: 33733960 DOI: 10.1080/14756366.2021.1899169] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Popović M, Jukić Špika M, Veršić Bratinčević M, Ninčević T, Matešković A, Mandušić M, Rošin J, Nazlić M, Dunkić V, Vitanović E. Essential Oil Volatile Fingerprint Differentiates Croatian cv. Oblica from Other Olea europaea L. Cultivars. Molecules 2021;26:3533. [PMID: 34207862 DOI: 10.3390/molecules26123533] [Reference Citation Analysis]
18 Zheng X, Wu Z, Xu J, Zhang X, Tu Y, Lei J, Yuan R, Cheng H, Wang Q, Yu J. Bioactive sesquiterpenes from Inula helenium. Bioorg Chem 2021;114:105066. [PMID: 34134031 DOI: 10.1016/j.bioorg.2021.105066] [Reference Citation Analysis]
19 Althagbi HI, Budiyanto F, Abdel-Lateff A, Al-Footy KO, Bawakid NO, Ghandourah MA, Alfaifi MY, Elbehairi SEI, Alarif WM. Antiproliferative Isoprenoid Derivatives from the Red Sea Alcyonacean Xenia umbellata. Molecules 2021;26:1311. [PMID: 33804495 DOI: 10.3390/molecules26051311] [Cited by in F6Publishing: 1] [Reference Citation Analysis]