Occurrence and significance of decahydroquinolines from dendrobatid poison frogs and a myrmicine ant:: Use of 1H and 13C NMR in their conformational analysis

被引:93
作者
Spande, TF
Jain, P
Garraffo, HM
Pannell, LK
Yeh, HJC
Daly, JW
Fukumoto, S
Imamura, K
Tokuyama, T
Torres, JA
Snelling, RR
Jones, TH
机构
[1] NIH, Bioorgan Chem Lab, NIDDK, Bethesda, MD 20892 USA
[2] Shimadzu Corp, Kanagawa 2591304, Japan
[3] Toyo Polymer Co Ltd, Osaka 5640044, Japan
[4] Osaka City Univ, Fac Sci, Osaka 585, Japan
[5] Univ Puerto Rico, Dept Biol, San Juan, PR 00931 USA
[6] USDA, Forest Serv, Int Inst Trop Forestry, Rio Piedras, PR 00928 USA
[7] Los Angeles Cty Museum Nat Hist, Los Angeles, CA 90007 USA
[8] Virginia Mil Inst, Dept Chem, Lexington, VA 24450 USA
来源
JOURNAL OF NATURAL PRODUCTS | 1999年 / 62卷 / 01期
关键词
D O I
10.1021/np980298v
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Structures for 2,5-disubstituted decahydroquinolines (DHQs) are reported for the two diastereomeric pairs cis-275B (14) and cis-275B' (15) and 5-epi-trans-269AB (18) and trans-269AB (19), all isolated from skin extracts of dendrobatid frogs, and for 5-epi-cis-275B' (16) and 5-epi-trans-275B (17) found in the extracts of virgin queens of a myrmicine ant [Solenopsis (Diplorhoptrum) azteca]. Detection of such DHQs in an ant, their first reported occurrence, strengthens a dietary hypothesis for the origin of the approximately 30 DHQs that have been detected in extracts of frog skin. NMR data on the two conformers of cis-decahydroquinoline permit assignment of ring conformations and stereochemistry to cis-DHQs of the "N-endo" type or the "N-exo" type. These conformations are also assigned on whether H-8a is equatorial or axial as determined with E-COSY or 1D-HOHAHA spectra.
引用
收藏
页码:5 / 21
页数:17
相关论文
共 31 条
[1]   A SYNTHESIS OF DL-PUMILIOTOXIN-C [J].
ABE, K ;
TSUGOSHI, T ;
NAKAMURA, N .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1984, 57 (11) :3351-3352
[2]   C-13 MAGNETIC-RESONANCE STUDIES OF CYCLIC-COMPOUNDS .2. C-13 CHEMICAL-SHIFT PARAMETERS FOR EQUATORIAL AND AXIAL SUBSTITUENTS IN CYCLOHEXANE - SUBSTITUENTS METHYL, ETHYL, ISOPROPYL, METHOXY AND PHTHALIMIDO [J].
BOOTH, H ;
EVERETT, JR ;
FLEMING, RA .
ORGANIC MAGNETIC RESONANCE, 1979, 12 (02) :63-66
[3]   FIRE ANT VENOMS - COMPARATIVE ANALYSES OF ALKALOIDAL COMPONENTS [J].
BRAND, JM ;
BLUM, MS ;
FALES, HM ;
MACCONNELL, JG .
TOXICON, 1972, 10 (03) :259-+
[4]   C-13 MAGNETIC-RESONANCE .21. STERIC INTERACTIONS IN METHYLCYCLOHEXANES [J].
DALLING, DK ;
GRANT, DM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (15) :5318-&
[5]  
DALY JW, 1977, HELV CHIM ACTA, V60, P1128, DOI 10.1002/hlca.19770600336
[6]   DIETARY SOURCE FOR SKIN ALKALOIDS OF POISON FROGS (DENDROBATIDAE) [J].
DALY, JW ;
GARRAFFO, HM ;
SPANDE, TF ;
JARAMILLO, C ;
RAND, AS .
JOURNAL OF CHEMICAL ECOLOGY, 1994, 20 (04) :943-955
[7]   AN UPTAKE SYSTEM FOR DIETARY ALKALOIDS IN POISON FROGS (DENDROBATIDAE) [J].
DALY, JW ;
SECUNDA, SI ;
GARRAFFO, HM ;
SPANDE, TF ;
WISNIESKI, A ;
COVER, JF .
TOXICON, 1994, 32 (06) :657-663
[8]   DECAHYDROQUINOLINE ALKALOIDS - NONCOMPETITIVE BLOCKERS FOR NICOTINIC ACETYLCHOLINE RECEPTOR-CHANNELS IN PHEOCHROMOCYTOMA CELLS AND TORPEDO ELECTROPLAX [J].
DALY, JW ;
NISHIZAWA, Y ;
PADGETT, WL ;
TOKUYAMA, T ;
MCCLOSKEY, PJ ;
WAYKOLE, L ;
SCHULTZ, AG ;
ARONSTAM, RS .
NEUROCHEMICAL RESEARCH, 1991, 16 (11) :1207-1212
[9]   FURTHER CLASSIFICATION OF SKIN ALKALOIDS FROM NEOTROPICAL POISON FROGS (DENDROBATIDAE), WITH A GENERAL SURVEY OF TOXIC NOXIOUS SUBSTANCES IN THE AMPHIBIA [J].
DALY, JW ;
MYERS, CW ;
WHITTAKER, N .
TOXICON, 1987, 25 (10) :1023-1095
[10]   VARIABILITY IN ALKALOID PROFILES IN NEOTROPICAL POISON FROGS (DENDROBATIDAE) - GENETIC VERSUS ENVIRONMENTAL DETERMINANTS [J].
DALY, JW ;
SECUNDA, SI ;
GARRAFFO, HM ;
SPANDE, TF ;
WISNIESKI, A ;
NISHIHIRA, C ;
COVER, JF .
TOXICON, 1992, 30 (08) :887-898