Our website is made possible by displaying online advertisements to our visitors.
Please consider supporting us by disabling your ad blocker.

Responsive image


Ibotenic acid

Ibotenic acid
Names
IUPAC name
(S)-2-Amino-2-(3-hydroxyisoxazol-5-yl)acetic acid
Other names
Ibotenic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.151.170 Edit this at Wikidata
EC Number
  • 622-405-7
KEGG
UNII
  • InChI=1S/C5H6N2O4/c6-4(5(9)10)2-1-3(8)7-11-2/h1,4H,6H2,(H,7,8)(H,9,10) checkY
    Key: IRJCBFDCFXCWGO-UHFFFAOYSA-N checkY
  • InChI=1/C5H6N2O4/c6-4(5(9)10)2-1-3(8)7-11-2/h1,4H,6H2,(H,7,8)(H,9,10)
    Key: IRJCBFDCFXCWGO-UHFFFAOYAQ
  • (S)-: Key: IRJCBFDCFXCWGO-BYPYZUCNSA-N
  • O=C1/C=C(\ON1)C(C(=O)O)N
Properties
C5H6N2O4
Molar mass 158.113 g·mol−1
Melting point 151-152 °C (anhydrous)
144-146 °C (monohydrate)
H2O: 1 mg/mL
0.1 M NaOH: 10.7 mg/mL
0.1 M HCl: 4.7 mg/mL
Hazards
GHS labelling:[1]
GHS06: Toxic
Danger
H301
P264, P270, P301+P316, P321, P330, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Ibotenic acid or (S)-2-amino-2-(3-hydroxyisoxazol-5-yl)acetic acid, also referred to as ibotenate, is a chemical compound and psychoactive drug which occurs naturally in Amanita muscaria and related species of mushrooms typically found in the temperate and boreal regions of the northern hemisphere. It is a prodrug of muscimol, broken down by the liver to that much more stable compound.[2] It is a conformationally-restricted analogue of the neurotransmitter glutamate, and due to its structural similarity to this neurotransmitter, acts as a non-selective glutamate receptor agonist.[3] Because of this, ibotenic acid can be a powerful neurotoxin in high doses, and is employed as a "brain-lesioning agent" through cranial injections in scientific research.[4][5] The neurotoxic effects appear to be dose-related and risks are unclear through consumption of ibotenic-acid containing fungi, although thought to be negligible in small doses.[6][better source needed]

  1. ^ "Ibotenic acid". pubchem.ncbi.nlm.nih.gov.
  2. ^ Stebelska, Katarzyna (August 2013). "Fungal Hallucinogens Psilocin, Ibotenic Acid, and Muscimol: Analytical Methods and Biologic Activities". Therapeutic Drug Monitoring. 35 (4): 420–442. doi:10.1097/FTD.0b013e31828741a5. ISSN 0163-4356. PMID 23851905. S2CID 44494685.
  3. ^ Tommy Liljefors; Povl Krogsgaard-Larsen; Ulf Madsen (25 July 2002). Textbook of Drug Design and Discovery, Third Edition. CRC Press. pp. 263–. ISBN 978-0-415-28288-8.
  4. ^ Becker, A; Grecksch, G; Bernstein, HG; Höllt, V; Bogerts, B (1999). "Social behaviour in rats lesioned with ibotenic acid in the hippocampus: quantitative and qualitative analysis". Psychopharmacology. 144 (4): 333–8. doi:10.1007/s002130051015. PMID 10435405. S2CID 25172395.
  5. ^ Isacson, O; Brundin, P; Kelly, PA; Gage, FH; Björklund, A (1984). "Functional neuronal replacement by grafted striatal neurones in the ibotenic acid-lesioned rat striatum". Nature. 311 (5985): 458–60. Bibcode:1984Natur.311..458I. doi:10.1038/311458a0. PMID 6482962. S2CID 4342937.
  6. ^ Filer, Crist N. (1 December 2018). "Ibotenic acid: on the mechanism of its conversion to [3H] muscimol". Journal of Radioanalytical and Nuclear Chemistry. 318 (3): 2033–2038. doi:10.1007/s10967-018-6203-8. ISSN 1588-2780. S2CID 91380050.

Previous Page Next Page