Isolation of melanin biosynthesis inhibitory compounds from the flowers of Magnolia denudata

Korean Journal of Pharmacognosy

Volumn 35, Issue 2, 2004, Pages 152-156

  Hua, Xu Guang ^a   Ah, Kim Jeong ^a   Hee, Park Sung ^a   Ryang, Son Ae ^a   Soo, Chang Tae ^b   Wook, Chang Hyun ^a   Ryun, Chung See ^a   Ho, Lee Seung ^a  

^a Yeungnam University   (South Korea)

^b Sorabol College   (South Korea)

Author keywords

Fragesin; Lignan; Magnolia denudata; Melanogenesis inhibitor

Indexed keywords

3,4,3',4' TETRAMETHOXY 9,7' DIHYDROXY 3,3',7 O 9' LIGNAN; ASCHANTINE; FARGESIN; KOBUSIN; LIGNAN DERIVATIVE; MAGNOLIA DENUDATA EXTRACT; MAGNOLIN; MELANIN; METHANOL; OPLODIOL; PLANT EXTRACT; POLYMER; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BIOASSAY; CONTROLLED STUDY; DRUG INHIBITION; DRUG ISOLATION; DRUG POTENCY; DRUG SYNTHESIS; FLOWER; FRACTIONATION; HORMONAL REGULATION; IC 50; MAGNOLIA DENUDATA; MAGNOLIACEAE; MELANOGENESIS; MELANOMA; MELANOMA CELL; MOUSE; NONHUMAN; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 3042731844     PISSN: 02533073     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

1. Hearing, V. J. and Tsukamoto, K. (1991) Enzymatic control of pigmentation in mammals. FASEB J. 5: 2902-2909.
2. Naeyaert, J. M., Eller, M., Gordon, P. R., Park, H. Y., and Gilchrest B. A. (1991) Pigment content of cultured human melanocytes does not correlate with tyrosinase message level. British J. Derma. 125: 297-303.
3. Choi, J. Y., Kim, J. A., Cho, S. H., Xu, G. H., Park, S. H., Chung, S. R., and Lee, S. H. (2004) Isolation of melanogenesis inhibitors from Ponciri Fructus. Kor. J. Pharmacogn. 35.
4. Pharmacognosy Research Group. Modern Pharmacognosy. (Edited in 1992).
5. Kamikado, T., Chang, C. F., Murakoshi, S., Sakurai, A., and Tamura, S. (1975) Isolation and structure elucidation of growth inhibitors on silkworm larvae from Magnolia kobus DC. Agr. Biol. Chem. 39: 833-836.
6. Pelter, A., Ward, R. S., and Nishino, C. (1977) Revised structures for epiaschantin and epimagnolin. Tetrahedron 47: 4137-4140.
7. Pelter, A., Ward, R. S., Venkata Rao, E., and Sastry, K. V. (1976) Revised structures for pluviatilol, methylpluviatilol and xanthoxylol. Tetrahedron 32: 2783-2788.
8. Yoshida, S. I., Yamanaka, T., Miyake, T., Moritani, Y., Ohmizu, H., and Iwasaki, T. (1997) Asymmetric syntheses of lignans utilizing novel diastereoselective michael addition of cyanohydrin: Syntheses of (+)-fargesin and (-)-picropodophyllone. Tetrahedron 53: 9585-9598.
9. Latip, J., Hartley, T. G., and Waterman, P. G. (1999) Lignans and coumarins metabolites from Melicope hayesii. Phytochemistry 51: 107-110.
10. Ahmed, A. A., Mahmoud, A. A., Ali, E. T., Tzakou, O., Couladis, M., Mabry, T. J., Gati, T., and Toth, G. (2002) Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea. Phytochemistry 59: 851-856.
11. Miyazawa, M., Kasahara, H., and Kameoka, H. (1992) Phenolic lignans from flower buds of Magnolia fargesii. Phytochemistry 31: 3666-3668.
12. Tanaka, H., Nakamura, T., Ichino, K., and Ito, K. (1989) A lignan from Actinodaphne longifolia. Phytochemistry 28: 952-954.
13. Ma, Y. L., Huang, Q. L., and Han, G. Q. (1996) A neolignan and lignans from Magnolia biondii. Phytochemistry 41: 287-288.
14. Nyasse, B., Tih, R. G., Sondengam, B. L., Martin, M. T., and Bodo, B. (1988) Isolation of α-corymbolol, an eudesmane sesquiterpene diol from Cyperus articulatus. Phytochemistry 27: 179-181.
15. Tchuendem, M. H., Mbah, J. A., Tsopmo, A., Ayafor, J. F., Sterner, O., Okunjic, C. C., Iwu, M. M., and Schuster, B. M. (1999) Anti-plasmodial sesquiterpenoids from the African Reneilmia cincinnata. Phytochemistry 52: 1095-1099.
16. Li, G., Ju, H. K., Chang, H. W., Jahng, Y. D., Lee, S. H., and Son, J. K. (2003) Melanin biosynthesis inhibitors from the bark of Machilus thunbergii. Biol. Pharm. Bull. 26: 1039-1041.