Structure and stereochemistry of pseudolarolide J, a novel nortriterpene lactone from Pseudolarix kaempferi

Journal of Natural Products

Volumn 59, Issue 12, 1996, Pages 1200-1202

  Chen, Ke ^a   Zhang, Yi Ling ^a   Li, Zhu Lian ^b   Shi, Qian ^a   Poon, Chi Duen ^c   Tang, Ren Jiu ^a   McPhail, Andrew T ^d   Lee, Kuo Hsiung ^a  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b FUDAN UNIVERSITY   (China)

^c The University of North Carolina at Chapel Hill   (United States)

^d DUKE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LACTONE DERIVATIVE; PLANT EXTRACT; PSEUDOLAROLIDE J; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; MYCOSIS; PLANT SEED; SKIN INFECTION; TRADITIONAL MEDICINE; X RAY CRYSTALLOGRAPHY;

CHINA; CRYSTALLOGRAPHY, X-RAY; MOLECULAR CONFORMATION; PLANTS, MEDICINAL; TRITERPENES;

EID: 0030470644     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np960523d     Document Type: Article

References (10)

1. Wu, J. X. R.; Hu, S.; Yang, G. L. J. Chin. Dermatol. 1960, 8, 18-25.
2. Chen, K.; Li, Z. L.; Pan, D. J.; Xu, G. Y. Acta Chim. Sin. 1990, 48, 591-595.
3. Pan, D. J.; Li, Z. L.; Hu, C. Q.; Chen, K.; Chang, J. J.; Lee, K. H. Planta Med. 1990, 56, 383-385.
4. Lee, K. H. Antineoplastic Agents from Chinese Traditional Medicine and Their Analogs; Am. Chem. Symp. Series 534; American Chemical Society: Washington, DC, 1993; Chapter 12, pp 170-190.
5. Chen, G. F.; Li, Z. L.; Chen, K.; Tang, C. M.; He, X.; Pan, D. J.; McPhail, D. R.; McPhail, A. T.; Lee, K. H. J. Chem. Soc., Chem. Commun. 1990, 1113-1114.
6. Chen, G. F.; Li, Z. L.; Chen, K.; Tang, C. M.; He, X.; Pan, D. J.; Hu, C. Q.; McPhail, D. R.; McPhail, A. T.; Lee, K. H. Tetrahedron Lett. 1990, 31, 3413-3416.
7. Chen, G. F.; Li, Z. L.; Tang, C. M.; He, X.; Chen, K.; Pan, D. J.; Hu, C. Q.; McPhail, D. R.; McPhail, A, T.; Lee, K. H. Heterocycles 1990, 31, 1903-1906.
8. Chen, G. F.; Li, Z. L.; Pan, D. J.; Tang, C. M.; He, X.; Xu, G. Y.; Chen, K.; Lee, K. H. J. Nat. Prod. 1993, 56, 1114-1122.
9. Atomic parameters, bond lengths, bond angles, torsion angles, and selected intermolecular distances have been deposited at the Cambridge Crystallographic Data Centre. The coordinates can be obtained, upon request, from Dr. Olga Kennard, University Chemical Laboratory, 12 Union Road, Cambridge CB2 1EZ, U.K.
10. Ibers, J. A., Hamilton, W. C., Eds. International Tables for X-Ray Crystallography; The Kynoch Press: Birmingham, U.K., 1974; Vol. IV.