IBOTENIC ACID

Bezeichnung:IBOTENIC ACID

CAS-Nr2552-55-8

Englisch Name:IBOTENIC ACID

CBNumberCB0400501

SummenformelC5H6N2O4

Molgewicht158.11

MOL-Datei2552-55-8.mol

IBOTENIC ACID physikalisch-chemischer Eigenschaften

Schmelzpunkt	141-147 °C
Dichte	1.621±0.06 g/cm3 (20 ºC 760 Torr)
storage temp.	Keep in dark place,Inert atmosphere,Room temperature
Löslichkeit	H2O: soluble1mg/mL, clear, colorless (with sonication)
Aggregatzustand	White solid
pka	2.16±0.10(Predicted)
Farbe	white
Geruch (Odor)	Practically odorless. Faint, meat-like, mild and sweet taste in aqueous dilutions.
Wasserlöslichkeit	Soluble to 10 mM in water and to 100 mM in 1.1eq. NaOH
Stabilität	Stable for 1 year from date of purchase as supplied. Solutions in distilled water may be stored at -20°C for up to 1 month.
InChIKey	IRJCBFDCFXCWGO-UHFFFAOYSA-N
LogP	-1.070 (est)
CAS Datenbank	2552-55-8(CAS DataBase Reference)

Sicherheit

Kennzeichnung gefährlicher	T,Xn
R-Sätze:	23/24/25-25-40
S-Sätze:	45-38-36/37/39-28A-22-36
RIDADR	1544
WGK Germany	3
RTECS-Nr.	NY2100000
HazardClass	6.1(b)
PackingGroup	III
Toxizität	LD50 in mice, rats (mg/kg): 15, 42 i.v.; 38, 129 orally (Theobald)

Gefahreninformationscode (GHS)

IBOTENIC ACID Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R25:Giftig beim Verschlucken.
R40:Verdacht auf krebserzeugende Wirkung.
S-Sätze Betriebsanweisung:
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S38:Bei unzureichender Belüftung Atemschutzgerät anlegen.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S22:Staub nicht einatmen.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Beschreibung
Ibotenic acid (60573-88-8) is a conformationally restricted analog of glutamate which occurs naturally in Amanita mascaria and related mushrooms.? It is a non-specific glutamate receptor (both NMDA and mGluR) agonist.1 May be used to induce hippocampal lesioning in rat neurodegeneration models.2,3 Induces lesions in the subiculum in a mouse model of Alzheimer’s disease.4
Chemische Eigenschaften
Crystalline solid; forms monohydrate; mp151°C (303.8°F) (anhydrous), 145°C (293°F)(monohydrate); soluble in water and alcohol.
Verwenden
Ibotenic acid is a neuroexcitatory amino acid originally isolated from Amanita species that functions as a NMDA and metabotropic glutamate receptor agonist. As a neurotoxin, ibotenic acid is often used to induce brain lesions in animals that model cognitive dysfunctions resulting from neurodegenerative diseases, traumatic brain injury, and stroke.
Verwenden
Ibotenic acid has been used to perform surgery in adult male zebra finches (Taeniopygia guttata) to study reversing reinforcement-induced vocal changes.
Verwenden
Neurobiological tool.
synthetische
Isolated from the Japanese fly mushroom. The acid can be produced synthetically.
Definition
A isoxazole which, together with muscimol, is largely responsible for the toxicities of a number of mushrooms including those of the genus Amanita. It is a potent excitatory amino acid.
Hazard
Neurotoxic; causes motor depression, ataxia, changes in mood, perceptions and feelings.
Health Hazard
Ibotenic acid is a potent neurologic aminoacid. It exhibits neuroexcitatory activity andcauses sedative actions on spinal neurons.High doses can cause sleep, hallucinations,distorted perceptions, and nausea. In humansthe symptoms above may be manifested fromingestion of 6–8 mg of ibotenic acid.
LD50 value, oral (mice): 38 mg/kg
LD50 value, intraperitoneal (mice): 15 mg/kg.
Biologische Aktivität
NMDA and metabotropic glutamate receptor agonist.
Biochem/physiol Actions
Non-selective agonist with preference for NMDA glutamate receptors; neurotoxin; neuroexcitatory amino acid originally isolated from Amanita species.
Lager
-20°C (desiccate)
läuterung methode
It has been converted to the ammonium salt (m 121-123o dec) dissolved in H2O, passed through an Amberlite IR 120 resin (H+ form) and eluted with H2O. The acidic fractions are collected, evaporated to dryness and the residue recrystallises from H2O as the monohydrate (m 144-146o). The anhydrous acid is obtained by making a slurry with MeOH, decanting and evaporating to dryness, and repeating the process twice more to give the anhydrous acid (m 151-152o). Recrystallisation from H2O gives the monohydrate. [Nakamura Chem Pharm Bull Jpn 19 46 1971.] The ethyl ester forms needles when crystallised from a small volume of Et2O and has m 78-79o and IR (CHCl3) with max 35002300 (OH), 1742 (ester C=O), 1628, 1528cm-1, and UV with λmax (EtOH) at 206nm (ε 7,080). The hydrazide has m 174-175o (from MeOH) with IR (KBr) 1656 (C=O)cm-1.
Einzelnachweise
1) Nakanishi (1992), Molecular diversity of glutamate receptors and implications for brain function; Science 258 597 2) Jarrard (1989), On the use of ibotenic acid to lesion selectively different components of the hippocampal formation; J. Neurosci. Methods 29 251 3) Isacson and Peschanski (1992), Is there capacity for anatomical and functional repair in the adult somatosensory thalamus?; Exp. Neurol. 115 173 4) George et al. (2014), Lesion of the subiculum reduces the spread of amyloid beta pathology to interconnected brain regions in a mouse model of Alzheimer’s disease; Acta Neuropathol. Commun. 2 17

IBOTENIC ACID Upstream-Materialien And Downstream Produkte

IBOTENIC ACID Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Send Inquriy