[1]
Helfenstein, A.; Vahermo, M.; Nawrot, D.A.; Demirci, F.; İşcan, G.; Krogerus, S.; Yli-Kauhaluoma, J.; Moreira, V.M.; Tammela, P. Antibacterial profiling of abietane-type diterpenoids. Bioorg. Med. Chem., 2017, 25(1), 132-137.
[2]
AbdelMonem, A.R.; Abdelrahman, E.H. New abietane diterpenes from Euphorbia Pseudocactus Berger (Euphorbiaceae) and their antimicrobial activity. Pharmacogn. Mag., 2016, 12(Suppl. 3), S346-S349.
[3]
Subash-Babu, P.; Alshammari, G.M.; Ignacimuthu, S.; Alshatwi, A.A. Epoxy clerodane diterpene inhibits MCF-7 human breast cancer cell growth by regulating the expression of the functional apoptotic genes Cdkn2A, Rb1, mdm2 and p53. Biomed. Pharmacother., 2017, 87, 388-396.
[4]
Shrestha, S.; Song, Y.W.; Kim, H.; Lee, D.S.; Cho, S.K. Sageone, a diterpene from Rosmarinus officinalis, synergizes with cisplatin cytotoxicity in SNU-1 human gastric cancer cells. Phytomedicine, 2016, 23(13), 1671-1679.
[5]
Erharuyi, O.; Adhikari, A.; Falodun, A.; Jabeen, A.; Imad, R.; Ammad, M.; Choudhary, M.I.; Gören, N. Cytotoxic, antiinflammatory,
and leishmanicidal activities of diterpenes isolated
from the roots of Caesalpinia pulcherrima. Planta Med, 2017, 83(1-02), 104-110.
[6]
Jiménez-García, L.; Través, P.G.; López-Fontal, R.; Herranz, S.; Higueras, M.A.; de Las Heras, B.; Hortelano, S.; Luque, A. 8,9-Dehydrohispanolone-15,16-lactol diterpene prevents LPS-triggered inflammatory responses by inhibiting endothelial activation. Biochem. J., 2016, 473(14), 2061-2071.
[7]
Han, B.S.; Kim, K.S.; Kim, Y.J.; Jung, H.Y.; Kang, Y.M.; Lee, K.S.; Sohn, M.J.; Kim, C.H.; Kim, K.S.; Kim, W.G. Daphnane diterpenes from Daphne genkwa activate Nurr1 and have a neuroprotective effect in an animal model of Parkinson’s disease. J. Nat. Prod., 2016, 79(6), 1604-1609.
[8]
Costa, J.P.; Ferreira, P.B.; De Sousa, D.P.; Jordan, J.; Freitas, R.M. Anticonvulsant effect of phytol in a pilocarpine model in mice. Neurosci. Lett., 2012, 523(2), 115-118.
[9]
He, F.; Lindqvist, C.; Harding, W.W. Leonurenones A-C: labdane diterpenes from Leonotis leonurus. Phytochemistry, 2012, 83, 168-172.
[10]
Farkhondeh, T.; Samarghandian, S.; Borji, A. Evaluation of antidiabetic activity of carnosol (phenolic diterpene in rosemary) in streptozotocin-induced diabetic rats. Cardiovasc. Hematol. Disord. Drug Targets, 2016, in press
[11]
Ebrahimi, A.; Schluesener, H. Natural polyphenols against neurodegenerative disorders: potentials and pitfalls. Ageing Res. Rev., 2012, 11(2), 329-345.
[12]
Lu, X.Z.; Luo, H.W.; Ji, J.; Cai, H. The structure of trijuganone C from Salvia trijuga. Acta. Pharmaceutica. Sinica., 1991, 26(3), 193-196.
[13]
Zhao, M.Z.; Li, J.Q.; Zhang, Y.; Zhang, X.J.; Jiang, B. Study on chemical constituents from rhizome of Rabdosia flavida. Zhong Yao Cai, 2014, 37(7), 1193-1196.
[14]
Yao, F.; Zhang, D.W.; Qu, G.W.; Li, G.S.; Dai, S.J. New abietane norditerpenoid from Salvia miltiorrhiza with cytotoxic activities. J. Asian Nat. Prod. Res., 2012, 14(9), 913-917.
[15]
Roa-Linares, V.C.; Brand, Y.M.; Agudelo-Gomez, L.S.; Tangarife-Castaño, V.; Betancur-Galvis, L.A.; Gallego-Gomez, J.C.; González, M.A. Anti-herpetic and anti-dengue activity of abietane ferruginol analogues synthesized from (+)-dehydroabietylamine. Eur. J. Med. Chem., 2016, 108, 79-88.
[16]
Búfalo, J.; Cantrell, C.L.; Jacob, M.R.; Schrader, K.K.; Tekwani, B.L.; Kustova, T.S.; Ali, A.; Boaro, C.S. Antimicrobial and antileishmanial activities of diterpenoids isolated from the roots of Salvia deserta. Planta Med., 2016, 82(1-2), 131-137.
[17]
Saijo, H.; Kofujita, H.; Takahashi, K.; Ashitani, T. Antioxidant activity and mechanism of the abietane-type diterpene ferruginol. Nat. Prod. Res., 2015, 29(18), 1739-1743.
[18]
Ho, S.T.; Tung, Y.T.; Kuo, Y.H.; Lin, C.C.; Wu, J.H. Ferruginol inhibits non-small cell lung cancer growth by inducing caspase-associated apoptosis. Integr. Cancer Ther., 2015, 14(1), 86-97.
[19]
González, M.A.; Clark, J.; Connelly, M.; Rivas, F. Antimalarial activity of abietane ferruginol analogues possessing a phthalimide group. Bioorg. Med. Chem. Lett., 2014, 24(22), 5234-5237.
[20]
Alqasoumi, S.I.; Abdel-Kader, M.S. Terpenoids from Juniperus procera with hepatoprotective activity. Pak. J. Pharm. Sci., 2012, 25(2), 315-322.
[21]
Areche, C.; Theoduloz, C.; Yáñez, T.; Souza-Brito, A.R.; Barbastefano, V.; de Paula, D.; Ferreira, A.L.; Schmeda-Hirschmann, G.; Rodríguez, J.A. Gastroprotective activity of ferruginol in mice and rats: effects on gastric secretion, endogenous prostaglandins and non-protein sulfhydryls. J. Pharm. Pharmacol., 2008, 60(2), 245-251.
[22]
Wei, Y.H.; He, J.Q.; Qin, H.Y.; Wu, X.A.; Yao, X.J. Determination of ferruginol in rat plasma via high-performance liquid chromatography and its application in pharmacokinetics study. Biomed. Chromatogr., 2009, 23(10), 1116-1120.
[23]
Zhang, Z.W.; Liu, X.X.; Cao, W.; Xiao, X.; Qu, J.G.; Zhao, M.G.; Li, X.Q. Pharmacokinetics and tissue distribution of fargesin after oral administration in rats by high performance liquid chromatography. Curr. Pharm. Anal., 2016, 12(4), 379-385.
[24]
Je, W.P.; Nguyen, H.H.; Nguyen, L.H. Analysis of ursodeoxycholic acid using ultra-performance liquid chromatography with tandem mass spectrometry. Curr. Pharm. Anal., 2016, 12(3), 185-191.
[25]
Alves, E.A.; Agonia, A.S.; Cravo, S.M. GC-MS method for the analysis of thirteen opioids, cocaine and cocaethylene in whole blood based on a modified quechers extraction. Curr. Pharm. Anal., 2017, 13(3), 215-223.
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