New oplopane and eremophilane derivatives from Robinsonecio gerberifolius

Journal of Natural Products

Volumn 66, Issue 2, 2003, Pages 225-229

  Arciniegas, Amira ^a   Pérez Castorena, Ana L ^a   Reyes, Sibet ^a   Contreras, José Luis ^b   De Vivar, Alfonso Romo ^a  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b BENEMÉRITA UNIVERSIDAD AUTÓNOMA DE PUEBLA   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

3BETA ANGELOYLOXY 1,10 EPOXYFURANOEREMOPHILANE; DOXORUBICIN; EREMOPHILANE DERIVATIVE; OPLOPANE; PLANT EXTRACT; SESQUITERPENOID; UNCLASSIFIED DRUG;

ARTICLE; CANCER CELL CULTURE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; HUMAN; HUMAN CELL; MEDICINAL PLANT; NONHUMAN; PHYTOCHEMISTRY; PROTON NUCLEAR MAGNETIC RESONANCE; ROBINSONECIO GERBERIFOLIUS; STEREOCHEMISTRY;

ANTINEOPLASTIC AGENTS, PHYTOGENIC; ASTERACEAE; DRUG SCREENING ASSAYS, ANTITUMOR; HUMANS; INHIBITORY CONCENTRATION 50; MEXICO; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PLANTS, MEDICINAL; SESQUITERPENES; STEREOISOMERISM; TUMOR CELLS, CULTURED; X-RAY DIFFRACTION;

ROBINSONECIO GERBERIFOLIUS;

EID: 0346035901     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np0203739     Document Type: Article

References (12)

1. Barkley, T. M.; Javonec J. P. Sida 1996, 17, 77-81.
2. Robins, D. J. In The Biology and Chemistry of the Compositae; Heywood, J. H., Harborne, J. B., Turner, B. L., Eds.; Academic Press: London, 1977; Chapter 30, pp 831-850.
3. Joseph-Nathan, P.; Villagómez, J. R.; Román, L. U.; Hernández, J. D. Phytochemistry 1990, 29, 977-979.
4. Marco, A.; Sanz-Cervera, J. F.; Sancenon, F.; Jakupovic, J.; Rustaiyan, A.; Mohamadi, F. Phytochemistry 1993, 34, 1061-1065.
5. Takeda, K.; Minato, H.; Ishikawa, M. Tetrahedron 1966, Suppl. 7, 219-225.
6. Reynolds, W. F.; McLean, S.; Perpick-Dumont, M.; Enriquez, R. Magn. Reson. Chem. 1989, 21, 162-169.
7. Naya, K.; Takagi, I. Tetrahedron Lett. 1968, 629-632.
8. Bohlmann, F.; Zdero, C. Phytochemistry 1978, 17, 1135-1153.
9. Wang, W.; Gao, K.; Jia, Z. J. Nat. Prod. 2002, 65, 714-717.
10. Monks, A.; Scudiero, D.; Skehan, P.; Shoemaker, R.; Paul, K.; Vistica, D.; Hose, C.; Langley, J.; Cronise, P.; Vaigro-Wolff, A.; Gray-Goodrich, M.; Campbell, H.; Mayp, J.; Boyd, M. J. Natl. Cancer Inst. 1991, 38, 757-766.
11. 1H NMR spectrum No. 10590. The Sadtler Standard Spectra; Sadtler Research Laboratories, Inc.: Philadelphia, 1971.
12. X-ray data for compounds 1, 4, and 7 have been deposited in the Cambridge Crystallographic Data Centre (CCDC 197755, 197756, and 197757, respectively). Copies of the data can be obtained free of charge on application to the Director, CCDC, 12 Union Rd., Cambridge CB2 1EZ, UK (fax: +44-(1223-336033; e-mail: deposit@ccdc.cam.ac.uk).