Nine new ent-labdane diterpenoids from the aerial parts of Andrographis paniculata

Helvetica Chimica Acta

Volumn 89, Issue 11, 2006, Pages 2654-2664

  Chen, Li Xia ^a   Qiu, Feng ^a   Wei, Hong ^b   Qu, Ge Xia ^a   Yao, Xin Sheng ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

^b Guangxi Institute of Traditional Medical & Pharmaceutical Sciences   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EXTRACTION; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STRUCTURE (COMPOSITION);

ANDROGRAPHIS PANICULATA; HIGH-RESOLUTION MASS SPECTROMETRY;

KETONES;

13,14,15,16 TETRANOR ENT LABDA 8(17) ENE 3,12,19 TRIOL; 14 DEOXYANDROGRAPHOLIDE; 19 [(BETA DEXTRO GLUCOPYRANOSYL)OXY] 19 OXO ENT LABDA 8(17),13 DIEN 16,15 OLIDE; 19 HYDROXY 3 OXO ENT LABDA 8(17),11,13 TRIEN 16,15 OLIDE; 3,15,19 TRIHYDROXY ENT LABDA 8(17),13 DIEN 16 OIC ACID; 3,18,19 TRIHYDROXY ENT LABDA 8(17),13 DIEN 16,15 OLIDE; 3,19 DIHYDROXY 14,15.16 TRINOR ENT LABDA 8(17),11 DIEN 13 OIC ACID; 3,19 DIHYDROXY 15 METHOXY ENT LABDA 8(17),13 DIEN 16,15 OLIDE; 3,19 DIHYDROXY ENT LABDA 8(17),12 DIEN 16,15 OLIDE; [10][12] ANDROGRAPHOLIDE; [10][12],14 DEOXY 11,12 DIDEHYDROANDROGRAPHISIDE; [7][10][12],3,14 DIDEOXYANDROGRAPHOLIDE; [8][10][12],19 HYDROXY ENT LABDA 8(17),13 DIEN 15,16 OLIDE; [9][10],14 DEOXY 11,12 DIDEHYDROANDROGRAPHOLIDE; ANDROGRAPHIS PANICULATA EXTRACT; ANDROGRAPHISIDE; DEOXYANDROGRAPHISIDE; DITERPENOID; ENT LABDA 8(17),13 DIEN 15,16,19 TRIOL; HERBACEOUS AGENT; LACTONE DERIVATIVE; NEOANDROGRAPHOLIDE; PLANT EXTRACT;

ANDROGRAPHIS PANICULATA; ARTICLE; CHEMICAL STRUCTURE; CONTROLLED STUDY; DRUG ISOLATION; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL;

EID: 33845369966     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200690237     Document Type: Article

References (21)

1. H. M. Chang, P. P. H. But, in 'Pharmacology and Application of Chinese Materia Medica', World Scientific, Singapore, 1987, Vol. 1, p. 918.
2. X. J. Yao, M. A. Wainberg, M. A. Parniak, Virology 1992, 187, 56.
3. M. George, K. M. Pandalai, Indian J. Med. Res. 1949, 37, 169.
4. A. Puri, R. Saxena, R. P. Saxena, V. Srivastava, J. S. Tandon, J. Nat. Prod. 1993, 56, 995.
5. P. T. Zeha, U. M. Rawal, Indian J. Exper. Biol. 2001, 39, 41.
6. M. P. Cava, W. R. Chan, R. P. Stein, C. R. Willis, Tetrahedron 1965, 21, 2617.
7. W. R. Chan, D. R. Taylor, C. R. Willis, R. L. Bodden, H. W. Fehlhaber, Tetrahedron 1971, 27, 5081.
8. A. Balmain, J. D. Connolly, J. Chem. Soc., Perkin Trans. 1 1973, 1247.
9. T. Fujita, R. Fujitani, Y. Takeda, Y. Takaishi, T. Yamada, M. Kido, I. Miura, Chem. Pharm. Bull. 1984, 32, 2117.
10. T. Matsuda, M. Kuroyanagi, S. Sugiyama, K. Umehara, A. Ueno, K. Nishi, Chem. Pharm. Bull. 1994, 42, 1216.
11. K. R. Muntha, V. B. Mopuru, D. Gunasekar, M. M. Madugula, C. Caux, B. Bodo, Phytochemistry 2003, 62, 1271.
12. Y. H. Shen, R. T. Li, W. L. Xiao, G. Xu, Z. W. Lin, Q. S. Zhao, H. D. Sun, J. Nat. Prod. 2006, 69, 319.
13. S. Pramanick, S. Banerjee, B. Achari, B. Das, K. S. S. Ashi, S. Mukhopadhyay, A. Neuman, T. Prange, J. Nat. Prod. 2006, 69, 403.
14. X. J. He, J. K. Li, H. Gao, F. Qiu, K. Hu, X. M. Cui, X. S.Yao, Tetrahedron 2003, 59, 6603.
15. X. J. He, J. K. Li, G. Hao, F. Qiu, X. M. Cui, X. S. Yao, Chem. Pharm. Bull. 2003, 51, 586.
16. L. Cui, F. Qiu, X. S. Yao, Drug Metab. Dispos. 2005, 33, 555.
17. B. H. Han, H. O. Yang, Y. H. Kang, D.-Y. Suh, H. J. Go, W.-J. Song, Y. C. Kim, M. K. Park, J. Med. Chem. 1998, 41, 2626.
18. 'Modern Methods in Plant Analysis', Eds. L. J. Haynes, K. I. Peach, M. V. Tracey, Springer-Verlag, Berlin, 1955, Vol. 2, p. 583.
19. P. Waridel, J.-L. Wolfender, J.-B. Lachavanne, K. Hostettmann, Phytochemistry 2004, 65, 945.
20. C. Zdero, F. Bohlmann, R. M. King, Phytochemistry 1991, 30, 1591.
21. G. Aranda, R. Azerad, M. Maurs, G. Bertho, D. Jiménez- González, E. Cabrera-Torres, A. F. Barrero, Phytochemistry 2000, 54, 23.