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| | PICROTOXININ Basic information |
| Product Name: | PICROTOXININ | | Synonyms: | 6a-beta,8as*,8b-beta,9r*))-6-beta;ahydro-2a-hydroxy-8b-methyl-9-(1-methylethenyl)-,(1ar-(1a-alpha,2a-beta,3-bet;PICROTOXININ;Yellowmouth Dutchmanspipe Root;Picrotoxinin CRS;3,6-Methano-8H-1,5,7-trioxacyclopenta[ij]cycloprop[a]azulene-4,8(3H)-dione, hexahydro-2a-hydroxy-8b-methyl-9-(1-methylethenyl)-, (1aR,2aR,3S,6R,6aS,8aS,8bR,9R)-;PICROTOXININ USP/EP/BP | | CAS: | 17617-45-7 | | MF: | C15H16O6 | | MW: | 292.28 | | EINECS: | | | Product Categories: | Miscellaneous Natural Products;AntagonistsIon Channels;GABA and Glycine Receptor Modulators;GABAergics;Ligand-Gated Ion Channels;Neurotransmitters | | Mol File: | 17617-45-7.mol |  |
| | PICROTOXININ Chemical Properties |
| Melting point | 203-205°C | | alpha | D17 +4.4° (c = 4.28 in abs alc), +3.49° (c = 7.57 in acetone) | | Boiling point | 354.22°C (rough estimate) | | density | 1.2207 (rough estimate) | | refractive index | 1.4359 (estimate) | | storage temp. | 2-8°C | | pka | 13.18±0.60(Predicted) | | form | neat | | LogP | -0.130 (est) | | EPA Substance Registry System | Picrotoxinin (17617-45-7) |
| Hazard Codes | T+ | | Risk Statements | 25-28 | | Safety Statements | 13-20-45-36/37-28 | | RIDADR | 3172 | | WGK Germany | 3 | | RTECS | PC5150000 | | HazardClass | 6.1(a) | | PackingGroup | I | | Toxicity | LD50 i.p. in mice: 3 mg/kg (Jarboe) |
| | PICROTOXININ Usage And Synthesis |
| Uses | Picrotoxinin is a L-glutamate and channel blockers. | | Definition | ChEBI: Picrotoxinin is a picrotoxane sesquiterpenoid that is 3a,4,5,6,7,7a-hexahydro-1H-indene-3,7-dicarboxylic acid which is substituted at positions 3a, 6, and 7a by methyl, isopropenyl, and hydroxy groups, respectively; in which the double bond at position 2-3 has been epoxidised; and in which the carboxy groups at positions 3 and 7 have undergone gamma-lactone formation by O-alkylation to positions 4 and 5, respectively. A component of picrotoxin. It has a role as a plant metabolite, a GABA antagonist and a serotonergic antagonist. It is an organic heteropentacyclic compound, an epoxide, a tertiary alcohol, a gamma-lactone and a picrotoxane sesquiterpenoid. | | Biochem/physiol Actions | GABAA receptor antagonist; binds to the GABA receptor-linked Cl? channel. | | Enzyme inhibitor | These neurotoxic GABAA receptor antagonists, consisting of a nearly 1:1
mixture of picrotoxinin, (FW = 292.29 g/mol; CAS 17617-45-7) and
picrotin (FW = 310.30 g/mol; CAS 124-87-8), is a bitter-tasting (hence the
Greek prefix picros) principle, also known as cocculin, from fishberry seeds
(Anamirta cocculus) and the Philippine bayating (Tinomiscium
philippinense). Picrotoxin binds to the chloride channel of the receptor
without displacing g-aminobutyric acid. Picrotoxin is highly toxic,
exerting both stimulant and convulsant effects, and care must be exercised
when handling this agent. |
| | PICROTOXININ Preparation Products And Raw materials |
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