Structural Formula Vector Image
Title: Histrionicotoxin
CAS Registry Number: 34272-51-0
CAS Name: (2S,6R,7S,8S)-7-(1Z)-1-Buten-3-ynyl-2-(2Z)-2-penten-4-ynyl-1-azaspiro[5.5]undecan-8-ol
Additional Names: HTX; (-)-HTX 1; (-)-histrionicotoxin
Molecular Formula: C19H25NO
Molecular Weight: 283.41
Percent Composition: C 80.52%, H 8.89%, N 4.94%, O 5.65%
Literature References: One of a family of piperidine alkaloids isolated from the skin of the poison arrow frog Dendrobates histrionicus. Noncompetitive inhibitor of nicotinic acetylcholine receptors characterized by an unusual spirocyclic cis-enyne structure. Virtually nontoxic, the family was originally misnamed because of the source. Isoln: J. W. Daly et al., Proc. Natl. Acad. Sci. USA 68, 1870 (1971). Isoforms: idem et al., Helv. Chim. Acta 60, 1128 (1977). Acetylcholine antagonism: M. Glavinovic et al., Can. J. Physiol. Pharmacol. 52, 1220 (1974); as allosteric inhibitor: S. M. Sine, P. Taylor, J. Biol. Chem. 257, 8106 (1982). Total synthesis: S. C. Carey et al., Tetrahedron Lett. 26, 5887 (1985); stereospecific synthesis: G. M. Williams et al., J. Am. Chem. Soc. 121, 4900 (1999). Review: J. W. Daly, J. Nat. Prod. 61, 162-172 (1997).
Properties: Viscous oil; on storage at -15°C crystals slowly form, mp 75-76°. uv max: 224 nm (e 15500). [a]D20 -112° (c = 0.34 in ethanol).
Melting point: mp 75-76°
Optical Rotation: [a]D20 -112° (c = 0.34 in ethanol)
Absorption maximum: uv max: 224 nm (e 15500)
Use: Biochemical probe for neuromuscular transmission.

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