Mycobacterium tuberculosis Growth Inhibition by Constituents of Sapium haematospermum

Journal of Natural Products

Volumn 67, Issue 4, 2004, Pages 598-603

  Woldemichael, Girma M ^a,d   Gutierrez Lugo, Maria Teresa ^a   Franzblau, Scott G ^b   Wang, Yuehong ^b   Suarez, Enrique ^c   Timmermann, Barbara N ^a  

^a UNIVERSITY OF ARIZONA   (United States)

^b UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^c INSTITUTO NACIONAL DE TECNOLOGÍA AGROPECUARIA INTA   (Argentina)

^d NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2ALPHA,3BETA,23 TRIHYDROXYOLEAN 12 EN 28 OIC ACID; 3 O BETA LAUROYLCYCLOARTEN 25 OL; 3ALPHA HYDROXYLUP 20(29)ENE; 3ALPHA HYDROXYOLEAN 12 ENE; 3ALPHA HYDROXYURS 12 ENE; 3BETA HYDROXYLUP 20(29)ENE; 3BETA HYDROXYOLEAN 12 ENE; ALPHA,BETA,3,4,5,2',4',6' OCTAHYDROXYDIHYDROCHALCONE; ASTRAGALIN; CHALCONE DERIVATIVE; CYCLOARTANOL; FLAVONOL DERIVATIVE; GLUCOSIDE; HERBACEOUS AGENT; ISOQUERCETIN; LECHERONOL A; LECHERONOL B; METHANOL; METHYL CHLORIDE; PLANT EXTRACT; SAPIUM HAEMATOSPERMUM EXTRACT; SITOGLUSIDE; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTIBACTERIAL ACTIVITY; ARTICLE; BACTERIAL GROWTH; CARBON NUCLEAR MAGNETIC RESONANCE; CELL ASSAY; CHEMICAL REACTION; CONTROLLED STUDY; CYTOPATHOGENIC EFFECT; DRUG ISOLATION; DRUG STRUCTURE; GROWTH INHIBITION; HERBAL MEDICINE; IC 50; INFRARED SPECTROSCOPY; MEDICINAL PLANT; MINIMUM INHIBITORY CONCENTRATION; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; SAPIUM; SAPIUM HAEMATOSPERMUM; STRUCTURE ANALYSIS; VERO CELL;

ANIMALS; ANTITUBERCULAR AGENTS; ARGENTINA; CERCOPITHECUS AETHIOPS; DITERPENES; DITERPENES, ABIETANE; INHIBITORY CONCENTRATION 50; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; MYCOBACTERIUM TUBERCULOSIS; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PLANTS, MEDICINAL; SAPIUM; VERO CELLS;

ACTINOBACTERIA (CLASS); ANIMALIA; BACTERIA (MICROORGANISMS); MYCOBACTERIUM; MYCOBACTERIUM TUBERCULOSIS; SAPIUM; UNCULTURED ACTINOMYCETE;

EID: 2042519320     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np0303411     Document Type: Article

References (29)

1. Quyang, J.; Zhang, H.; Shen, S.; Shi, J. Nanjing Huagong Daxue Xuebo 1997, 19, 37-41.
2. Panthong, A.; Kanjanapothi, D.; Thitiponpunt, Y.; Taesotikul, T.; Arbain, D. Planta Med. 1998, 64, 530-535.
3. Hsu, F. L.; Lee, Y. Y.; Cheng, J. T. J. Nat. Prod. 1994, 57, 308-312.
4. Brooks, G.; Morrice, N. A.; Ellis, C.; Aitken, A.; Evans, A. T.; Evans, F. J. Toxicon 1987, 25, 1229-1233.
5. Tessier, A. M.; Paris, R. R. Tox. Eur. Res. 1978, 1, 329-336.
6. Ahn, Y.-J.; Lee, S.-H.; Kang, S.-J.; Hwang, B. Y.; Park, W. Y.; Ahn, B. T.; Ro, J.-S.; Lee, K. S. Yakhak Hoechi 1996, 40, 183-192.
7. (a) Ahmad, V. U.; Atta-ur-Rahman. Handbook of Natural Products Data: Pentacyclic Triterpenoids; Elsevier: Amsterdam, 1994; Vol. 2, p 25; (b) p 21; (c) p 716; (d) p 320; (e) p 1033; (f) p 1038.
8. (a) Ahmad, V. U.; Atta-ur-Rahman. Handbook of Natural Products Data: Pentacyclic Triterpenoids; Elsevier: Amsterdam, 1994; Vol. 2, p 25; (b) p 21; (c) p 716; (d) p 320; (e) p 1033; (f) p 1038.
9. (a) Ahmad, V. U.; Atta-ur-Rahman. Handbook of Natural Products Data: Pentacyclic Triterpenoids; Elsevier: Amsterdam, 1994; Vol. 2, p 25; (b) p 21; (c) p 716; (d) p 320; (e) p 1033; (f) p 1038.
10. (a) Ahmad, V. U.; Atta-ur-Rahman. Handbook of Natural Products Data: Pentacyclic Triterpenoids; Elsevier: Amsterdam, 1994; Vol. 2, p 25; (b) p 21; (c) p 716; (d) p 320; (e) p 1033; (f) p 1038.
11. (a) Ahmad, V. U.; Atta-ur-Rahman. Handbook of Natural Products Data: Pentacyclic Triterpenoids; Elsevier: Amsterdam, 1994; Vol. 2, p 25; (b) p 21; (c) p 716; (d) p 320; (e) p 1033; (f) p 1038.
12. (a) Ahmad, V. U.; Atta-ur-Rahman. Handbook of Natural Products Data: Pentacyclic Triterpenoids; Elsevier: Amsterdam, 1994; Vol. 2, p 25; (b) p 21; (c) p 716; (d) p 320; (e) p 1033; (f) p 1038.
13. Kamisako, W.; Honda, C.; Suwa, K.; Isoi, K. Magn. Reson. Chem. 1987, 25, 683-687.
14. Woldemichael, G. M.; Singh, M. P.; Maiese, W. M.; Timmermann, B. N. Z. Naturforsh. C 2003, 58c, 70-75.
15. Agrawal, P. K. Carbon-13 NMR of Flavonoids; Elsevier: Amsterdam, 1989; pp 336-339.
16. Kuraishi, T.; Ninomiya, K.; Murakami, T.; Tanaka, N.; Saiki, Y.; Chen, C.-M. Chem. Pharm Bull. 1988, 27 (12), 3769-3779.
17. Sakai, T.; Nakagawa, Y. Phytochemistry 1988, 27 (12), 3769-3779.
18. Wenkert, E.; Afonso, A.; Beak, P.; Carney, R. W. J.; Jeffs, P. W.; McChesney, J. D. J. Org. Chem. 1965, 30, 713-722.
19. Bégué, J. P. J. Org. Chem. 1982, 47, 8-4271.
20. Gutierrez-Lugo, M.-T.; Singh, M. P.; Maiese, W. M.; Timmermann, B. N. J. Nat. Prod. 2002, 65, 872-875.
21. Weber, S.; Puripattanavong, J.; Brecht, V.; Frahm, A. W. J. Nat. Prod. 2000, 63, 636-642.
22. Mabry, T. J.; Markham, T. R.; Thomas, M. B. The Systematic Identification of Flavonoids; Springer: Berlin, 1970; p 25.
23. Hauteville, M.; Favre-Bonvin, J. Pharmazie 1984, 711-712.
24. Takahashi, H.; Kubota, Y.; Fang, L.; Li, S.; Onda, M. Chem. Pharm. Bull. 1986, 34, 4597-4604.
25. Seco, J. M.; Martino, M.; Quiñoá, E.; Riguera, R. Org. Lett. 2000, 2, 3261-3264.
26. Kelly, D. R. Tetrahedron: Asymmetry 1999, 10, 2917-2934.
27. Cantrell, C. L.; Franzblau, S. G.; Fischer, N. H. Planta Med. 2001, 67, 685-694.
28. Cantrell, C. L.; Lu, T.; Fronczek, F. R.; Fischer, N. H.; Adams, L. B.; Franzblau, S. G. J. Nat. Prod. 1996, 59, 1131-1136.
29. Collins, L.; Franzblau, S. G. Antimicrob. Agents Chemother. 1997, 41, 1004-1009.