1 |
Agrawal, P.K. 1989. Carbon-13 NMR of Flavonoids. Elsevier, Amsterdam.
|
2 |
Bergeron, C., Marston, A., Antus, S., Gauthier, R., Hostettmann, K. 1998. Flavonoids from Pyrola elliptica. Phytochemistry 49(1): 233-236.
DOI
|
3 |
Dubeler, A., Volmer, G., Gora, J., Lunderstadt, J., Zeeck, A. 1997. Phenols from Fagus sylvatica and their role in defence against Cryptococcus fagisuga. Phytochemistry 45(1): 51-57.
DOI
|
4 |
Farnsworth, N.R., Akerele, O., Bingel, A.S. 1985. Medicinal plants in therapy. Bulletin of the World Health Organization 63(6): 965-981.
|
5 |
Foo, L.Y., McGraw, G.W., Hemingway, R.W. 1983. Condensed tannins: Preferential substitution at the interflavanoid bond by sulphite ion. Journal of the Chemical Society, Chemical Communications 12: 672-673.
|
6 |
Harborne, J.B., Mabry, T.J. 1982. The flavonoid : advances in research, Chapman and Hall Ltd.
|
7 |
Isimaru, K., Omoto, T., Asai, K.E., Shimonura, K. 1995. Taxifolin-3-arabinoside from Fragaria X Ananassa. Phytochemistry 40(1): 345-347.
DOI
|
8 |
Kador, P.F., Robison, W.G., Kinoshita, J.H. 1985a. The pharmacology of aldose reductase inhibitors. Annual Review Pharmacology, Toxicology 25: 691-714.
DOI
|
9 |
Kim, H.Y., Oh, J.H. 1999. Screening of Korean forest plants for rat lens aldose reductase inhibition. Bioscience, Biotechnology and Biochemistry 63: 184-188.
DOI
|
10 |
Kador, P.J., Konishita, J.H., Sharpless, N.E. 1985b. Aldose reductase inhibitors: a potential new class of agents for the pharmacological control of certain diabetic complications. Journal of Medicinal Chemistry 28: 841-849.
DOI
|
11 |
Kim, H.Y., Kim, K. 2003. Protein glycation inhibitory and antioxidative activities of some plant extracts in vitro. Journal of Agricultural and Food Chemeistry 51: 1586-1591.
DOI
|
12 |
Kim, H.Y., Kang, M.H. 2005. Screening of Korean medicinal plants for lipase inhibitory activity. Phytotherapy Research 19: 359-361.
DOI
|
13 |
Pyo, M.K., Koo, Y.K., Yun-Choi, H.S. 2002. Anti-platelet effect of the phenolic constituents isolated from the leaves of Magnolia obovata. Natural Product Sciences 8(4): 147-151.
|
14 |
Ko, E.K., Choi, S.E. 2015. Inhibitory effects of phenolic compounds from stems of Acer ginnala on nitric oxide production. Journal of Chemical and Pharmaceutical Research 7(2): 395-402.
|
15 |
Ko, R.K., Kim, G.O., Hyun, C.G., Jung, D.S., Lee, N.H. 2011. Compounds with tyrosinase inhibition, elastase inhibition and DPPH radical scavenging activities from the branches of Distylium racemosum Sieb. et Zucc. Phytotherapy research 25: 1451-1456.
DOI
|
16 |
Lee, J.H., Chung, H.K., Baek, N.I., Kim, S.H., Hee, W.P., Dae, K.K. 2004. Phytochemical constituents from Diodia teres. Archives of Pharmacal Research 27(1): 40-43.
DOI
|
17 |
Shibuya, M., Abe, K., Nakahahsi, Y., Kubota S. 1978. Phenolic components from leaf oil of Illicium anisatum L. Chemical and Pharmaceutical Bulletin 26(9): 2671-2673.
DOI
|
18 |
Yamada, K., Takada, S., Nakamura, S., Hirata, Y. 1968. Structures of anisatin and neoanisatin toxic sesquiterpenes from Illicium anisatum. Tetrahedron 24(1): 199-229.
DOI
|
19 |
Yang, Z.G., Jia, L.N., Shen, Y., Ohmura, A., Kitanaka, S. 2011. Inhibitory effects of constituents from Euphorbia lunulata on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 Cells. Molecules 16: 8305-8318.
DOI
|