Four new podocarpane-type trinorditerpenes from the bark of Taiwania cryptomerioides

Chemical and Pharmaceutical Bulletin

Volumn 50, Issue 4, 2002, Pages 544-546

  Kuo, Yueh Hsiung ^a   Chien, Shih Chang ^a   Huang, Shou Ling ^a  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

Author keywords

1 hydroxy 2 oxodehydropodocarpane; Bark; Taiwania cryptomerioides; Taxodiaceae; Trinorditerpene

Indexed keywords

14,18 DIHYDROXY 13 METHOXY 8,11,13 PODOCARPATRIENE; 1BETA,13 DIHYDROXY 8,11,13 PODOCARPATRIENE; 1BETA,14 DIHYDROXY 13 METHOXY 8,11,13 PODOCARPATRIENE 2,7 DIONE; 3BETA,13,14 TRIHYDROXY 8,11,13 PODOCARPATRIEN 7 ONE; 3BETA,14 DIHYDROXY 13 METHOXY 8,11,13 PODOCARPATRIEN 7 ONE; DITERPENE; PODOCARPIC ACID DERIVATIVE; UNCLASSIFIED DRUG; HERBACEOUS AGENT;

ARTICLE; BARK; DRUG ISOLATION; DRUG STRUCTURE; NONHUMAN; SPECTROSCOPY; STRUCTURE ANALYSIS; TAIWANIA CRYPTOMERIOIDES; TAXODIACEAE; CHEMISTRY; CHINESE MEDICINE; CUPRESSACEAE; ISOLATION AND PURIFICATION; MEDICINAL PLANT; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; TAIWAN;

CUPRESSACEAE; DITERPENES; DRUGS, CHINESE HERBAL; MAGNETIC RESONANCE SPECTROSCOPY; MEDICINE, CHINESE TRADITIONAL; PLANT BARK; PLANTS, MEDICINAL; TAIWAN;

EID: 0036549925     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.50.544     Document Type: Article

References (24)

1. Cheng Y. S., Kuo Y. H., Lin Y. T., J. Chem. Soc. Chem. Commun., 1967, 565-566.
2. Lin Y. T., Cheng Y. S., Kuo Y. H., Tetrahedron Lett., 1968, 3881-3882.
3. Kuo Y. H., Cheng Y. S., Lin Y. T., Tetrahedron Lett., 1969, 2375-2377.
4. Kuo Y. H., Shih J. S., Lin Y. T., Lin Y. T., J. Chin. Chem. Soc., 26, 71-73 (1979).
5. Kuo Y. H., Lin Y. T., Lin Y. T., J. Chin. Chem. Soc., 32, 381-383 (1985).
6. Day S. H., Chiu N. Y., Won S. J., Lin C. N., J. Nat. Prod., 62, 1056-1058 (1999).
7. He K., Zeng L., Shi G., Zhao G. X., Kozlowski J. F., McLaughlin J. L., J. Nat. Prod., 60, 38-40 (1997).
8. Chang S. T., Wang D. S. Y., Wu C. L., Shiah S. G., Kuo Y. H., Chang C. J., Phytochemistry, 55, 227-232 (2000).
9. Chang S. T., Wang S. Y., Wu C. L., Chen P. F., Kuo Y. H., Holzforschung, 54, 241-245 (2000).
10. Majumder P. L., Maiti D. C., Kraus W., Bokel M., Phytochemistry, 26, 3021-3023 (1987).
11. Ara I., Siddiqui B. S., Faigi S., Siddiqui S., Phytochemistry, 27, 1801-1804 (1988).
12. Siddiqui S., Ara I., Faigi S., Mahmood T., Siddiqui B. S., Phytochemistry, 27, 3903-3907 (1988).
13. Ara I., Siddiqui B. S., Faigi S., Siddiqui S., J. Nat. Prod., 51, 1054-1061 (1988).
14. Ara I., Siddiqui B. S., Faigi S., Siddiqui S., J. Nat. Prod., 53, 816-820 (1990).
15. Zoghbl M. D. G. B., Roque N. F., Gottlieb H. E., Phytochemistry, 20, 1669-1673 (1981).
16. Alvarenga M. A. D., Silva J. D., Gottlieb H. E., Gottlieb O. R., Phytochemistry, 20, 1159-1163 (1981).
17. Cambie R. C., Mander L. M., Tetrahedron, 18, 465-475 (1962).
18. Lin W. H., Fang J. M., Cheng Y. S., Phytochemistry, 48, 1391-1397 (1998).
19. Lin W. H., Fang J. M., Cheng Y. S., Phytochemistry, 40, 871-873 (1995).
20. Lin W. H., Fang J. M., Cheng Y. S., Phytochemistry, 42, 1657-1663 (1996).
21. Lin W. H., Fang J. M., Cheng Y. S., Phytochemistry, 46, 169-173 (1997).
22. Kuo Y. H., Chang C. I., Lee C. K., Chem. Pharm. Bull., 48, 597-599 (2000).
23. Kuo Y. H., Chang C. I., J. Nat. Prod., 63, 650-652 (2000).
24. Kuo Y. H., Chien S. C., Chem. Pharm. Bull., 49, 1033-1035 (2001).