Published April 30, 2023
| Version v1
Journal article
Restricted
Triterpenoids from the leaves of Abies koreana and their biological activities
Creators
- 1. ** & Natural Products Laboratory, School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea
Description
Lee, Dong Jun, Hong, Seong-Min, Yoon, Da Hye, Ham, Song Lim, Kim, Jonghwan, Kim, Sun Yeou, Choi, Sang Un, Kim, Chung Sub, Lee, Kang Ro (2023): Triterpenoids from the leaves of Abies koreana and their biological activities. Phytochemistry (113594) 208: 1-7, DOI: 10.1016/j.phytochem.2023.113594, URL: http://dx.doi.org/10.1016/j.phytochem.2023.113594
Files
Linked records
Additional details
Identifiers
- LSID
- urn:lsid:plazi.org:pub:FFC3FF9119166D2B3C195D46C73E177C
References
- Baek, S.W., Kim, E.R., Kim, J.W., Kim, Y.C., 2011. Chemical constituents of Abies koreana leaves with inhibitory activity against nitric oxide production in BV2 microglia cells. Nat. Prod. Sci. 17, 175-180.
- Baran, S., von Reuss, S.H., K¨onig, W.A., Kalemba, D., 2007. Composition of the essential oil of Abies koreana Wils. Flavour Fragrance J. 22, 78-83. https://doi.org/10.1002/ ffj.1762.
- Della Greca, M., Fiorention, A., Monaco, P., Previtera, L., 1994. Cycloartane triterpenes from Juncus effusus. Phytochemistry 35, 1017-1022. https://doi.org/10.1016/ S0031-9422(00)90659-9.
- Grimblat, N., Zanardi, M.M., Sarotti, A.M., 2015. Beyond DP4: an improved probability for the stereochemical assignment of isomeric compounds using quantum chemical calculations of NMR shifts. J. Org. Chem. 80, 12526-12534. https://doi.org/ 10.1021/acs.joc.5b02396.
- Inada, A., Murayta, H., Inatomi, Y., Nakanishi, T., Darnaedi, D., 1995. Cycloartane triterpenes from the leaves of Aglaia harmsiana. J. Nat. Prod. (Lloydia) 58, 1143-1146. https://doi.org/10.1021/np50121a030.
- Inada, A., Ohtsuki, S., Sorano, T., Murata, H., Inatomi, Y., Darnaedi, D., Nakanishi, T., 1997. Cycloartane triterpenoids from Aglaia harmsiana. Phytochemistry 46, 379-381. https://doi.org/10.1016/S0031-9422(97)00287-2.
- Jeong, S.I., Lim, J.P., Jeon, H., 2007. Chemical composition and antibacterial activities of the essential oil from Abies koreana. Phytother. Res. 21, 1246-1250. https://doi.org/ 10.1002/ptr.2229.
- Kim, C.S., Oh, J., Subedi, L., Kim, S.Y., Choi, S.U., Lee, K.R., 2017a. Holophyllane A: a triterpenoid possessing an unprecedented B-nor-3, 4-seco-17, 14-friedo-lanostane architecture from Abies holophylla. Sci. Rep. 7, 1-8. https://doi.org/10.1038/ srep43646.
- Kim, C.S., Oh, J., Subedi, L., Kim, S.Y., Choi, S.U., Lee, K.R., 2018. Structural characterization of terpenoids from Abies holophylla using computational and statistical methods and their biological activities. J. Nat. Prod. (Lloydia) 81, 1795-1802. https://doi.org/10.1021/acs.jnatprod.8b00245.
- Kim, C.S., Shin, B., Kwon, O.W., Kim, S.Y., Choi, S.U., Oh, D.-C., Kim, K.H., Lee, K.R., 2014. Holophyllin A, a rearranged abietane-type diterpenoid from the trunk of Abies holophylla. Tetrahedron Lett. 55, 6504-6507. https://doi.org/10.1016/j. tetlet.2014.10.030.
- Kim, C.S., Subedi, L., Oh, J., Kim, S.Y., Choi, S.U., Lee, K.R., 2017b. Bioactive triterpenoids from the twigs of Chaenomeles sinensis. J. Nat. Prod. (Lloydia) 80, 1134-1140. https://doi.org/10.1021/acs.jnatprod.7b00111.
- Kim, H.J., Choi, E.H., Lee, I.-S., 2004. Two lanostane triterpenoids from Abies koreana. Phytochemistry 65, 2545-2549. https://doi.org/10.1016/j. phytochem.2004.07.007.
- Kim, H.J., Le, Q.K., Lee, M.H., Kim, T.S., Lee, H.-K., Kim, Y.H., Bae, K., Lee, I.-S., 2001. A cytotoxic secocycloartenoid from Abies koreana. Arch. Pharm. Res. (Seoul) 24, 527-531. https://doi.org/10.1007/BF02975159.
- Kim, Y.-G., Lee, H., Ozawa, S., Sasaya, T., Moon, C.-K., 1994. Lignans of Abies koreana wilson. Mokuzai Gakkaishi 40, 414-418.
- Lavoie, S., Legault, J., Gauthier, C., Mshvildadze, V., Mercier, S., Pichette, A., 2012. Abibalsamins A and B, two new tetraterpenoids from Abies balsamea oleoresin. Org. Lett. 14, 1504-1507. https://doi.org/10.1021/ol300237f.
- Lee, J.-H., Hong, S.-K., 2009. Comparative analysis of chemical compositions and antimicrobial activities of essential oils from Abies holophylla and Abies koreana. J. Microbiol. Biotechnol. 19, 372-377. https://doi.org/10.4014/jmb.0811.630.
- Park, J.E., Lee, T.H., Ham, S.L., Subedi, L., Hong, S.M., Kim, S.Y., Choi, S.U., Kim, C.S., Lee, K.R., 2022. Anticancer and anti-neuroinflammatory constituents isolated from the roots of Wasabia japonica. Antioxidants 11, 482. https://doi.org/10.3390/ antiox11030482.
- Schicchi, R., Geraci, A., Rosselli, S., Spinella, A., Maggio, A., Bruno, M., 2020. Phytochemical investigation of the needles of Abies nebrodensis (lojac.) mattei. Nat. Prod. Res. 34, 2131-2136. https://doi.org/10.1080/14786419.2019.1576044.
- Wada, S.-i., Iida, A., Tanaka, R., 2002. Triterpenoid constituents isolated from the bark of Abies sachalinensis. J. Nat. Prod. (Lloydia) 65, 1657-1659. https://doi.org/10.1021/ np020282b.
- Wajs-Bonikowska, A., Olejnik, K., Bonikowski, R., Banaszczak, P., 2013. Composition of essential oils from seeds of Abies koreana. Nat. Prod. Commun. 8 https://doi.org/ 10.1177/1934578X1300800225, 1934578X1300800225.
- Wajs Bonikowska, A., Sienkiewicz, M., Stobiecka, A., Maciag, A., Szoka, L., Karna, E., 2015. Chemical composition and biological activity of Abies alba and A. koreana seed and cone essential oils and characterization of their seed hydrolates. Chem. Biodivers. 12, 407-418. https://doi.org/10.1002/cbdv.201400167.
- Yang, X.W., Ding, Y., Li, X.C., Ferreira, D., Shen, Y.H., Li, S.M., Wang, N., Zhang, W.D., 2009. Cycloabiesesquine A, a unique sesquiterpenoid from Abies delavayi. Chem. Commun. 3771-3773. https://doi.org/10.1039/B905710B.
- Zhao, Q.Q., Song, Q.Y., Jiang, K., Li, G.D., Wei, W.J., Li, Y., Gao, K., 2015. Spirochensilides A and B, two new rearranged triterpenoids from Abies chensiensis. Org. Lett. 17, 2760-2763. https://doi.org/10.1021/acs.orglett.5b01166.