Veratridine
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Names | |
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Other names
(3β,4β,16β)-4,12,14,16,17,20-Hexahydroxy-4,9-epoxycevan-3yl 3,4-dimethoxybenzoate
3-Veratroylveracevine |
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Identifiers | |
71-62-5 ![]() |
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ChEMBL | ChEMBL451227 ![]() |
ChemSpider | 5290571 ![]() |
2626 | |
Jmol 3D model | Interactive image |
PubChem | 6914694 |
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Properties | |
C36H51NO11 | |
Molar mass | 673.80 g·mol−1 |
Melting point | 160 to 180 °C (320 to 356 °F; 433 to 453 K) |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Veratridine is a steroid-derived alkaloid from plants in the Liliaceae family that functions as a neurotoxin by abolishing inactivation of sodium ion channels.[1] It is primarily obtained from the herb Veratrum and sabadilla seeds. It binds to intramembrane receptor site 2 and increases intracellular Ca2+ concentration. It acts by preferentially binding to activated Na+ channels causing persistent activation that leads to increased nerve excitability.
Contents
Isolation
Isolated from seeds of Schoenocaulon officinale, and from rhizomes of Veratrum album.[2]
Chemistry
Veratridine is a derivative, the 3-veratroate ester, of veracevine, which belongs to the class of C-nor-D-homosteroidal alkaloids. The molecular structure and stereochemistry of this and related alkaloids were only established after decades of chemical investigations.[3] The structure of veratridine has been confirmed by NMR spectroscopy[4] and X-ray crystallography.[5]
Obsolete use
It is used in ointments for the treatment of neuralgia and rheumatoid pain.[citation needed]
References
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- Neurotoxins
- Alkaloids
- Steroids
- Ion channel toxins
- Benzoates