Published April 30, 2021
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Abietane diterpenoids from Dracocephalum moldavica L. and their anti-inflammatory activities in vitro
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- 1. ** & * & State Key Lab. of New Drug and Pharmaceutical Process, Shanghai Institute of Pharmaceutical Industry, China State Institute of Pharmaceutical Industry, Shanghai,
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Nie, Lanlan, Li, Rui, Huang, Jie, Wang, Lingling, Ma, Mengjie, Huang, Chunyue, Wu, Tong, Yan, Renjie, Hu, Xiao (2021): Abietane diterpenoids from Dracocephalum moldavica L. and their anti-inflammatory activities in vitro. Phytochemistry (112680) 184: 1-8, DOI: 10.1016/j.phytochem.2021.112680, URL: http://dx.doi.org/10.1016/j.phytochem.2021.112680
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- urn:lsid:plazi.org:pub:FFC9FFC2A472FFB8FFBF9735CB7AFFF7
References
- Adilamu, Abilimiti, 2014. Study on Promoting Blood Circulation and Chemical Constituents of Dracocerhalum Moldavica L. Xin Jiang. XinJiang Medical University.
- Amani Machiani, M., Rezaei-Chiyaneh, E., Javanmard, A., Maggi, F., Morshedloo, M.R., 2019. Evaluation of common bean (Phaseolus vulgaris L.) seed yield and qualiquantitative production of the essential oils from fennel (Foeniculum vulgare Mill.) and dragonhead (Dracocephalum moldavica L.) in intercropping system under humic acid application. J. Clean. Prod. 235, 112-122. https://doi.org/10.1016/j. jclepro.2019.06.241.
- Dorsaz, A.C., Marston, A., Stoeckli-Evans, H., Jerome, D.M., Kurt, Hostettmann, 1985. Uncinatone, a new antifungal hydroquinone diterpenoid from Clerodendrum uncinatum Schinz. Helv. Chim. Acta 68, 1605-1610. https://doi.org/10.1002/ hlca.19850680612.
- Gwag, J.E., Lee, Y.G., Kim, H.G., Lee, D.S., Lee, D.Y., Beak, N.I., 2020. Syringoleosides A- H, secoiridoids from syringa dilatata flowers and their inhibition of NO production in LPS-induced RAW 264.7 cells. J. Nat. Prod. 83, 2655-2663. https://doi.org/ 10.1021/acs.jnatprod.0c00490.
- Hu, H.J., Zhou, Y., Han, Z.Z., Shi, Y.H., Zhang, S.S., Wang, Z.T., Yang, L., 2018. Abietane diterpenoidsfrom the roots of clerodendrum trichotomum and their nitric Oxide inhibitory activities. J. Nat. Prod. 81 (7), 1508-1516. https://doi.org/10.1021/acs. jnatprod.7b00814.
- Jia, J.X., Zhang, Y., Wang, Z.L., Yan, X.S., Jin, M., Huo, D.S., Yang, Z.J., 2017. The inhibitory effects of Dracocephalum moldavica L. (DML) on rat cerebral ischemia reperfusion injury. J. Toxicol. Environ. Health 80 (22), 1206-1211. https://doi.org/ 10.1080/15287394. 2017.1367139.
- Liu, Z.G., Li, Z.L., Bai, J., Meng, D.L., Li, N., Pei, Y.H., Zhao, F., Hua, H.M., 2014. Anti-inflammatory diterpenoids from the roots of Euphorbia ebracteolata. J. Nat. Prod. 77, 792-799. https://doi.org/10.1021/np400873v.
- Liu, Z.G., Li, Z.L., Li, D.H., Li, N., Bai, J., Zhao, F., Meng, D.L., Hua, H.M., 2016. ent- Abietane-type diterpenoids from the roots of Euphorbia ebracteolata with their inhibitory activities on LPS-induced NO production in RAW 264.7 macrophages. Bioorg. Med. Chem. Lett 26, 1-5. https://doi.org/10.1016/j. bmcl. 2015.11.080.
- Luo, G.Y., Ye, Q., Du, B., Wang, F., Zhang, G.L., Luo, Y., 2016. Iridoid glucosides and diterpenoids from Caryopteris glutinosa. J. Nat. Prod. 79 (4), 886-893. https://doi. org/10.1021/acs.jnatprod. 5b00946.
- Khan, Shabana I., Walker, Larry A., Muhammad, Ilias, 2010. Antimicrobial and antiparasitic abietane diterpenoids from the roots of clerodendrum eriophyllum. Natural Product Communications 5, 853-858. https://doi.org/10.1177/ 1934578x1000500605.
- Mora-Ramiro, B., Jimenez-Estrada, M., Zentella-Dehesa, A., Ventura-Gallegos, J.L., Gomez-Quiroz, L.E., Rosiles-Alanis, W., Almanza-Perez, J.C., 2020. Cacalol acetate, a sesquiterpene from psacalium decompositum, exerts an anti-inflammatory effect through LPS/NF-KB signaling in raw 264.7 macrophages. J. Nat. Prod. 83 (8), 2447-2455. https://doi.org/10.1021/acs.jnatprod.0c00300.
- Morshedloo, M.R., Amani Machiani, M., Mohammadi, A., Maggi, F., Aghdam, M.S., Mumivand, H., Javanmard, A., 2020. Comparison of drying methods for the extraction of essential oil from dragonhead (Dracocephalum moldavica L., Lamiaceae). J. Essent. Oil Res. 1-9. https://doi.org/10.1080/ 10412905.2020.1848652.
- Murata, T., Ishikawa, Y., Saruul, E., Selenge, E., Sasaki, K., Umehara, K., Batkhuu, J., 2016. Abietane-type diterpenoids from the roots of Caryopteris mongolica and their cholinesterase inhibitory activities. Phytochemistry 130, 152-158. https://doi.org/ 10.1016/j.phytochem.2016.05.011.
- Rodriguez, B., 2002. Complete assignments of the1H and13C NMR spectra of five rearranged abietane diterpenoids. Magn. Reson. Chem. 40 (11), 752-754. https:// doi.org/10.1002/mrc.1070.
- Tan, M.E., He, C.H., Jiang, W., Zeng, C., Yu, N., Huang, W., Xing, J.G., 2017. Development of solid lipid nanoparticles containing total flavonoid extract from Dracocephalum moldavica L. and their therapeutic effect against myocardial ischemia-reperfusion injury in rats. Int. J. Nanomed. 12, 3253-3265. https://doi. org/10.2147/IJN.S131893.
- Wang, W.X., Xiong, J., Tang, Y., Zhu, J.J., Li, M., Zhao, Y., Hu, J.F., 2013. Rearranged abietane diterpenoids from the roots of Clerodendrum trichotomum and their cytotoxicities against human tumor cells. Phytochemistry 89, 89-95. https://doi. org/10.1016/j.phytochem.2013.01.008.
- Xu, M.F., Bai, X.L., Shi, L.E., Liu, Q., 2016. Abietane-type Diterpene Compound, Preparation Method and Application Thereof. Faming Zhuanli Shenqing. CN 2016- 11005614.
- Zhang, J.L., Yan, R. J Yu N., Zhang, X., Chen, D.J., Wu, T., Xin, J.G., 2018. A new caffeic acid tetramer from the Dracocephalum moldavica L. Nat. Prod. Res. 32, 370-373. https://doi.org/10.1080/14786419.2017.1359168.
- Zhao, S.M., Chou, G.X., Yang, Q.S., Wang, W., Zhou, J.L., 2013. Abietane diterpenoids from Caryopteris incana (thunb.) miq. Org. Biomol. Chem. 14, 3510-3520. https:// doi.org/10.1039/C6OB00139D.