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For: Roa-Linares VC, Brand YM, Agudelo-Gomez LS, Tangarife-Castaño V, Betancur-Galvis LA, Gallego-Gomez JC, González MA. Anti-herpetic and anti-dengue activity of abietane ferruginol analogues synthesized from (+)-dehydroabietylamine. Eur J Med Chem 2016;108:79-88. [PMID: 26638041 DOI: 10.1016/j.ejmech.2015.11.009] [Cited by in Crossref: 35] [Cited by in F6Publishing: 25] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Li FY, Huang L, Li Q, Wang X, Ma XL, Jiang CN, Zhou XQ, Duan WG, Lei FH. Synthesis and Antiproliferative Evaluation of Novel Hybrids of Dehydroabietic Acid Bearing 1,2,3-Triazole Moiety. Molecules 2019;24:E4191. [PMID: 31752282 DOI: 10.3390/molecules24224191] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
2 Roa-Linares VC, Miranda-Brand Y, Tangarife-Castaño V, Ochoa R, García PA, Castro MÁ, Betancur-Galvis L, San Feliciano A. Anti-Herpetic, Anti-Dengue and Antineoplastic Activities of Simple and Heterocycle-Fused Derivatives of Terpenyl-1,4-Naphthoquinone and 1,4-Anthraquinone. Molecules 2019;24:E1279. [PMID: 30986933 DOI: 10.3390/molecules24071279] [Cited by in Crossref: 10] [Cited by in F6Publishing: 3] [Article Influence: 3.3] [Reference Citation Analysis]
3 Yang YQ, Chen H, Liu QS, Sun Y, Gu W. Synthesis and anticancer evaluation of novel 1H-benzo[d]imidazole derivatives of dehydroabietic acid as PI3Kα inhibitors. Bioorg Chem 2020;100:103845. [PMID: 32344183 DOI: 10.1016/j.bioorg.2020.103845] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
4 Gu W, Wang S, Jin X, Zhang Y, Hua D, Miao T, Tao X, Wang S. Synthesis and Evaluation of New Quinoxaline Derivatives of Dehydroabietic Acid as Potential Antitumor Agents. Molecules 2017;22:E1154. [PMID: 28696365 DOI: 10.3390/molecules22071154] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
5 Li A, Wang Z, Wang W, Liu Q, Sun Y, Wang S, Gu W. A novel dehydroabietic acid-based fluorescent probe for detection of Fe3+ and Hg2+ ions and its application in live-cell imaging. Microchemical Journal 2021;160:105682. [DOI: 10.1016/j.microc.2020.105682] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 10.0] [Reference Citation Analysis]
6 Mori N, Kuzuya K, Watanabe H. Synthesis of (−)-Chamobtusin A from (+)-Dehydroabietylamine. J Org Chem 2016;81:11866-70. [DOI: 10.1021/acs.joc.6b02328] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
7 Gu W, Miao TT, Hua DW, Jin XY, Tao XB, Huang CB, Wang SF. Synthesis and in vitro cytotoxic evaluation of new 1H-benzo[d]imidazole derivatives of dehydroabietic acid. Bioorg Med Chem Lett 2017;27:1296-300. [PMID: 28169166 DOI: 10.1016/j.bmcl.2017.01.028] [Cited by in Crossref: 22] [Cited by in F6Publishing: 15] [Article Influence: 4.4] [Reference Citation Analysis]
8 Tavares WR, Seca AML. The Current Status of the Pharmaceutical Potential of Juniperus L. Metabolites. Medicines (Basel) 2018;5:E81. [PMID: 30065158 DOI: 10.3390/medicines5030081] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
9 Islam MT, Mubarak MS. Diterpenes and their derivatives as promising agents against dengue virus and dengue vectors: A literature‐based review. Phytotherapy Research 2020;34:674-84. [DOI: 10.1002/ptr.6562] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
10 Liu X, Li Z, Zhan G, Wu Y, Zhuang Q. Bio‐based benzoxazines based on sesamol: Synthesis and properties. J Appl Polym Sci 2019;136:48255. [DOI: 10.1002/app.48255] [Cited by in Crossref: 13] [Cited by in F6Publishing: 1] [Article Influence: 4.3] [Reference Citation Analysis]
11 Chen H, Qiao C, Miao TT, Li AL, Wang WY, Gu W. Synthesis and biological evaluation of novel N-(piperazin-1-yl)alkyl-1H-dibenzo[a,c]carbazole derivatives of dehydroabietic acid as potential MEK inhibitors. J Enzyme Inhib Med Chem 2019;34:1544-61. [PMID: 31448648 DOI: 10.1080/14756366.2019.1655407] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
12 Miao T, Tao X, Li D, Chen H, Jin X, Geng Y, Wang S, Gu W. Synthesis and biological evaluation of 2-aryl-benzimidazole derivatives of dehydroabietic acid as novel tubulin polymerization inhibitors. RSC Adv 2018;8:17511-26. [DOI: 10.1039/c8ra02078g] [Cited by in Crossref: 7] [Article Influence: 1.8] [Reference Citation Analysis]
13 Ghosh R, Chakraborty A, Biswas A, Chowdhuri S. Computer aided identification of potential SARS CoV-2 main protease inhibitors from diterpenoids and biflavonoids of Torreya nucifera leaves. J Biomol Struct Dyn 2020;:1-16. [PMID: 33140695 DOI: 10.1080/07391102.2020.1841680] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
14 Li A, Yang Y, Wang W, Liu Q, Sun Y, Gu W. Synthesis, cytotoxicity and apoptosis‐inducing activity of novel 1 H ‐benzo[ d ]imidazole derivatives of dehydroabietic acid. J Chin Chem Soc 2020;67:1668-78. [DOI: 10.1002/jccs.202000075] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
15 Bansal M, Upadhyay C, Poonam, Kumar S, Rathi B. Phthalimide analogs for antimalarial drug discovery. RSC Med Chem 2021;12:1854-67. [PMID: 34825184 DOI: 10.1039/d1md00244a] [Reference Citation Analysis]
16 Barros de Alencar MV, de Castro E Sousa JM, Rolim HM, de Medeiros MD, Cerqueira GS, de Castro Almeida FR, Citó AM, Ferreira PM, Lopes JA, de Carvalho Melo-Cavalcante AA, Islam MT. Diterpenes as lead molecules against neglected tropical diseases. Phytother Res 2017;31:175-201. [PMID: 27896890 DOI: 10.1002/ptr.5749] [Cited by in Crossref: 18] [Cited by in F6Publishing: 15] [Article Influence: 3.0] [Reference Citation Analysis]
17 Cao G, Han S, Li K, Shen L, Wang X, Zhang Y. Pharmacokinetics and Tissue Distribution Study of Ferruginol in Wistar Rat by High-performance Liquid Chromatography. CPA 2018;15:67-73. [DOI: 10.2174/1573412914666180508154147] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
18 Hanson JR. Diterpenoids of terrestrial origin. Nat Prod Rep 2017;34:1233-43. [DOI: 10.1039/c7np00040e] [Cited by in Crossref: 24] [Cited by in F6Publishing: 3] [Article Influence: 4.8] [Reference Citation Analysis]
19 Rajtar B, Skalicka-woźniak K, Świątek Ł, Stec A, Boguszewska A, Polz-dacewicz M. Antiviral effect of compounds derived from Angelica archangelica L. on Herpes simplex virus-1 and Coxsackievirus B3 infections. Food and Chemical Toxicology 2017;109:1026-31. [DOI: 10.1016/j.fct.2017.05.011] [Cited by in Crossref: 23] [Cited by in F6Publishing: 16] [Article Influence: 4.6] [Reference Citation Analysis]
20 Jin X, Zhang K, Chen H, Miao T, Wang S, Gu W. Synthesis, in vitro Antimicrobial, and Cytotoxic Activities of New 1,3,4-Oxadiazin-5( 6H )-one Derivatives from Dehydroabietic Acid: New Oxadiazine Derivatives of Dehydroabietic Acid. Journal of the Chinese Chemical Society 2018;65:538-47. [DOI: 10.1002/jccs.201700358] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
21 El Had MA, Guardia JJ, Ramos JM, Taourirte M, Chahboun R, Alvarez-manzaneda E. Bioinspired Synthesis of Pygmaeocins and Related Rearranged Abietane Diterpenes: Synthesis of Viridoquinone. Org Lett 2018;20:5666-70. [DOI: 10.1021/acs.orglett.8b02395] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
22 Roa Linares VC, Gallego Gómez JC. La pérdida de función de la quinasa dependiente de ciclina 5 (CDK5) altera el citoesqueleto y reduce la infección in vitro por el virus del dengue 2. Acta biol Colomb 2019;24:474-85. [DOI: 10.15446/abc.v24n3.79347] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
23 Chen Q, Tang K, Guo Y. Discovery of sclareol and sclareolide as filovirus entry inhibitors. J Asian Nat Prod Res 2020;22:464-73. [PMID: 31738086 DOI: 10.1080/10286020.2019.1681407] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
24 Dea-Ayuela MA, Bilbao-Ramos P, Bolás-Fernández F, González-Cardenete MA. Synthesis and antileishmanial activity of C7- and C12-functionalized dehydroabietylamine derivatives. Eur J Med Chem 2016;121:445-50. [PMID: 27318121 DOI: 10.1016/j.ejmech.2016.06.004] [Cited by in Crossref: 21] [Cited by in F6Publishing: 18] [Article Influence: 3.5] [Reference Citation Analysis]
25 Jia Y, Wu C, Zhang B, Zhang Y, Li J. Ferruginol induced apoptosis on SK-Mel-28 human malignant melanoma cells mediated through P-p38 and NF-κB. Hum Exp Toxicol 2019;38:227-38. [DOI: 10.1177/0960327118792050] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
26 Kovaleva KS, Yarovaya OI, Shernyukov AV, Zarubaev VV, Shtro AA, Orshanskaya YR, Salakhutdinov NF. Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity. Chem Heterocycl Comp 2017;53:364-70. [DOI: 10.1007/s10593-017-2058-0] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.4] [Reference Citation Analysis]
27 Sousa FTG, Nunes C, Romano CM, Sabino EC, González-Cardenete MA. Anti-Zika virus activity of several abietane-type ferruginol analogues. Rev Inst Med Trop Sao Paulo 2020;62:e97. [PMID: 33295481 DOI: 10.1590/S1678-9946202062097] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
28 Li J, Liu C. Synthesis, antitumor and DNA cleavage activities of a novel class of dehydroabietylamine derivatives. Heliyon 2020;6:e03390. [PMID: 32099921 DOI: 10.1016/j.heliyon.2020.e03390] [Reference Citation Analysis]
29 Zhang X, Li X, Wang C, Li H, Wang L, Chen Y, Feng J, Ali Alharbi S, Deng Y. Ameliorative effect of ferruginol on isoprenaline hydrochloride-induced myocardial infarction in rats. Environ Toxicol 2021;36:249-56. [PMID: 32946155 DOI: 10.1002/tox.23030] [Reference Citation Analysis]
30 Berezin V, Bogoyavlenskiy A, Alexyuk M, Alexyuk P. Plant Metabolites as Antiviral Preparations Against Coronaviruses. J Med Food 2021. [PMID: 33689397 DOI: 10.1089/jmf.2020.0190] [Reference Citation Analysis]
31 Jia P, Ma Y, Feng G, Hu L, Zhou Y. High-value utilization of forest resources: Dehydroabietic acid as a chemical platform for producing non-toxic and environment-friendly polymer materials. Journal of Cleaner Production 2019;227:662-74. [DOI: 10.1016/j.jclepro.2019.04.220] [Cited by in Crossref: 13] [Cited by in F6Publishing: 2] [Article Influence: 4.3] [Reference Citation Analysis]
32 Qin Y, Chen X, Wang L, Wei X, Mo H, Wei X, Liang J. Measurement and correlation of isothermal vapor-liquid equilibrium for (−)-β-caryophyllene + p-cymene with dehydroabietic acid at 313.15, 323.15, and 333.15K. Journal of the Taiwan Institute of Chemical Engineers 2022;138:104466. [DOI: 10.1016/j.jtice.2022.104466] [Reference Citation Analysis]