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. 2000 Nov 21;97(24):12970-5.
doi: 10.1073/pnas.200346897.

Batrachotoxin alkaloids from passerine birds: a second toxic bird genus (Ifrita kowaldi) from New Guinea

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Batrachotoxin alkaloids from passerine birds: a second toxic bird genus (Ifrita kowaldi) from New Guinea

J P Dumbacher et al. Proc Natl Acad Sci U S A. .

Abstract

Batrachotoxins, including many congeners not previously described, were detected, and relative amounts were measured by using HPLC-mass spectrometry, in five species of New Guinean birds of the genus Pitohui as well as a species of a second toxic bird genus, Ifrita kowaldi. The alkaloids, identified in feathers and skin, were batrachotoxinin-A cis-crotonate (1), an allylically rearranged 16-acetate (2), which can form from 1 by sigmatropic rearrangement under basic conditions, batrachotoxinin-A and an isomer (3 and 3a, respectively), batrachotoxin (4), batrachotoxinin-A 3'-hydroxypentanoate (5), homobatrachotoxin (6), and mono- and dihydroxylated derivatives of homobatrachotoxin. The highest levels of batrachotoxins were generally present in the contour feathers of belly, breast, or legs in Pitohui dichrous, Pitohui kirhocephalus, and Ifrita kowaldi. Lesser amounts are found in head, back, tail, and wing feathers. Batrachotoxin (4) and homobatrachotoxin (6) were found only in feathers and not in skin. The levels of batrachotoxins varied widely for different populations of Pitohui and Ifrita, a result compatible with the hypothesis that these birds are sequestering toxins from a dietary source.

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Figures

Figure 1
Figure 1
Batrachotoxins found in feathers and/or skins of New Guinean passerine birds. The protonated parent ion (m/z = [molecular ion + 1]) and major fragment ion in chemical ionization mass spectrometry (CIMS) is indicated in brackets for each structure.
Figure 2
Figure 2
Base-catalyzed rearrangements of batrachotoxins 1 and/or 5 to the acetates 2 and 2a.

Comment in

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