Occurrence and Significance of Decahydroquinolines from Dendrobatid Poison Frogs and a Myrmicine Ant:  Use of 1H and 13C NMR in Their Conformational Analysis

Author:

Spande Thomas F.1,Jain Poonam1,Garraffo H. Martin1,Pannell Lewis K.1,Yeh Herman J. C.1,Daly John W.1,Fukumoto Sinji2,Imamura Kohji3,Tokuyama Takashi4,Torres Juan A.5,Snelling Roy R.6,Jones Tappey H.7

Affiliation:

1. Laboratory of Bioorganic Chemistry, National Institute of Diabetes, and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0820

2. Shimadzu Corporation, Hadano, Kanagawa 2591304, Japan

3. Toyo Polymer Co., Ltd., Suita, Osaka 5640044, Japan

4. Faculty of Science, Osaka City University, Osaka, 585, Japan

5. University of Puerto Rico, Department of Biology, P.O. Box 23360, San Juan, Puerto Rico 00931-3360, and International Institute of Tropical Forestry, USDA Forest Service, Call Box 25000, Río Piedras 00928-2500, Puerto Rico

6. Los Angeles County Museum of Natural History, 900 Exposition Boulevard, Los Angeles, California 90007

7. Department of Chemistry, Virginia Military Institute, Lexington, Virginia 24450-0304

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Reference32 articles.

1. Daly, J. W.; Garraffo, H. M.; Spande, T. F. InThe Alkaloids; Cordell, G. A., Ed.; Academic Press:  New York, 1993; Vol. 43, Chapter 3, pp 186−288.

2. Alkaloids from dendrobatid poison frogs: trans-decahydroquinolines and indolizidines

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