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Cacalol derivatives from Roldana angulifolia.
J Nat Prod. 2006 Dec; 69(12):1826-9.JN

Abstract

Four new modified eremophilanes, angulifolide (1) and angulifolins A-C (2-4), and two new triacetylglucosides (7 and 8) were isolated from Roldana angulifolia, together with several known compounds. The structures of the new compounds were elucidated by spectroscopic analysis and chemical reactions. The absolute configuration of compounds 2 and 3 was established by Mosher ester methodology. Cytotoxicity against selected human cancer cell lines was determined for the more abundant isolated metabolites.

Authors+Show Affiliations

Instituto de Química and Instituto de Biología, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Coyoacán 04510, D.F., México.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

17190472

Citation

Arciniegas, Amira, et al. "Cacalol Derivatives From Roldana Angulifolia." Journal of Natural Products, vol. 69, no. 12, 2006, pp. 1826-9.
Arciniegas A, Pérez-Castorena AL, Villaseñor JL, et al. Cacalol derivatives from Roldana angulifolia. J Nat Prod. 2006;69(12):1826-9.
Arciniegas, A., Pérez-Castorena, A. L., Villaseñor, J. L., & Romo de Vivar, A. (2006). Cacalol derivatives from Roldana angulifolia. Journal of Natural Products, 69(12), 1826-9.
Arciniegas A, et al. Cacalol Derivatives From Roldana Angulifolia. J Nat Prod. 2006;69(12):1826-9. PubMed PMID: 17190472.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Cacalol derivatives from Roldana angulifolia. AU - Arciniegas,Amira, AU - Pérez-Castorena,Ana-L, AU - Villaseñor,José Luis, AU - Romo de Vivar,Alfonso, PY - 2006/12/28/pubmed PY - 2007/2/1/medline PY - 2006/12/28/entrez SP - 1826 EP - 9 JF - Journal of natural products JO - J Nat Prod VL - 69 IS - 12 N2 - Four new modified eremophilanes, angulifolide (1) and angulifolins A-C (2-4), and two new triacetylglucosides (7 and 8) were isolated from Roldana angulifolia, together with several known compounds. The structures of the new compounds were elucidated by spectroscopic analysis and chemical reactions. The absolute configuration of compounds 2 and 3 was established by Mosher ester methodology. Cytotoxicity against selected human cancer cell lines was determined for the more abundant isolated metabolites. SN - 0163-3864 UR - https://www.unboundmedicine.com/medline/citation/17190472/Cacalol_derivatives_from_Roldana_angulifolia_ L2 - https://doi.org/10.1021/np0604073 DB - PRIME DP - Unbound Medicine ER -