5-(Aminomethyl)-3(2H)isoxazolon

MUSCIMOL Struktur
2763-96-4
CAS-Nr.
2763-96-4
Bezeichnung:
5-(Aminomethyl)-3(2H)isoxazolon
Englisch Name:
MUSCIMOL
Synonyma:
AGARIN;agarine;MUSCIMOL;pantherin;NSC 333569;PANTHERINE;MUSCIMOL(P);MUSCIMOL (RG);Pyroibotenic acid;Arylex Impurity 8
CBNumber:
CB6231349
Summenformel:
C4H6N2O2
Molgewicht:
114.1
MOL-Datei:
2763-96-4.mol

5-(Aminomethyl)-3(2H)isoxazolon Eigenschaften

Schmelzpunkt:
175-176°C
Siedepunkt:
213.59°C (rough estimate)
Dichte
1.291
Brechungsindex
1.4487 (estimate)
storage temp. 
2-8°C
Löslichkeit
ethanol: 1 mg/mL
Aggregatzustand
powder
pka
12.19±0.40(Predicted)
Farbe
white to off-white
Wasserlöslichkeit
Soluble in water (10 mg/ml), methanol, ethanol, 0.05 M HCl (20 mg/ml), DMSO (sparingly soluble), DMF (sparingly soluble), and PBS (pH 7.2) (10 mg/ml).
Merck 
13,6336
BRN 
1618960
Stabilität:
Hygroscopic, Store in Freezer at -20°C
EPA chemische Informationen
5-(Aminomethyl)-3-isoxazolol (2763-96-4)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher T
R-Sätze: 25
S-Sätze: 22-36/37/39-45
RIDADR  UN 1544 6.1/PG 2
WGK Germany  3
RTECS-Nr. NY3345000
3-10
TSCA  Yes
HazardClass  6.1(a)
PackingGroup  II
HS Code  29349990
Giftige Stoffe Daten 2763-96-4(Hazardous Substances Data)
Toxizität LD50 in mice (mg/kg): 3.8 s.c., 2.5 i.p.; in rats (mg/kg): 4.5 i.v., 45 orally (Theobald)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H300 Lebensgefahr bei Verschlucken. Akute Toxizität oral Kategorie 2 Achtung GHS hazard pictogramssrc="/GHS06.jpg" width="20" height="20" /> P264, P270, P301+P310, P321, P330,P405, P501
H336 Kann Schläfrigkeit und Benommenheit verursachen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Schläfrigkeit und Benommenheit) Warnung P261, P271, P304+P340, P312,P403+P233, P405, P501
Sicherheit
P261 Einatmen von Staub vermeiden.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P271 Nur im Freien oder in gut belüfteten Räumen verwenden.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.

5-(Aminomethyl)-3(2H)isoxazolon Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R25:Giftig beim Verschlucken.

S-Sätze Betriebsanweisung:

S22:Staub nicht einatmen.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).

Beschreibung

The amino acid γ-aminobutyric acid (GABA) is an inhibitory neurotransmitter that acts through two families of heteromeric ligand-gated ion channels, GABAA and GABAC and a G protein-coupled receptor, GABAB. Muscimol is a full GABAA agonist and partial GABAC agonist. It binds GABAA on both high- and low-affinity sites (Kd = 10 and 270 nM, respectively), stimulating chloride efflux with an EC50 value of 200 nM. Benzodiazepines enhance the effects of muscimol via GABAA without altering its binding. Muscimol activates GABAC receptors with an EC50 value of 1.3 μM. It also acts as an inhibitor of GABAA uptake and a substrate for the GABA-metabolizing enzyme GABA transaminase. Muscimol impairs memory formation and retrieval in mice and attenuates airway constriction in guinea pigs in vivo.

Chemische Eigenschaften

Tan Solid

Verwenden

A potent but toxic structural analogue of g-aminobutyric acid (GABA), with a zwitterionic structure that can cross the blood-brain barrier

Definition

ChEBI: A member of the class of isoxazoles that is 1,2-oxazol-3(2H)-one substituted by an aminomethyl group at position 5. It has been isolated from mushrooms of the genus Amanita.

Allgemeine Beschreibung

Crystals. Formerly used as a sedative and an anti-emetic.

Reaktivität anzeigen

MUSCIMOL is a ketone and an amine. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides

Health Hazard

MUSCIMOL is a natural constituent of amanita mushrooms and is extremely toxic. It is a potent central nervous system depressant, and is believed to be responsible for most of the nervous system effects that result from eating this mushroom. The lowest toxic dose in humans has been reported at 109 mg/kg.

Brandgefahr

When heated to decomposition, MUSCIMOL emits toxic fumes of nitrogen oxides.

Biologische Aktivität

Potent GABA A receptor agonist and partial GABA C receptor agonist. Inhibits memory retention and attenuates airway constriction in vivo .

läuterung methode

Recrystallise muscimol from MeOH/tetrahydrofuran or EtOH and sublime it at 110-140o (bath) at 10-4 mm to give a yellow spot with ninhydrin which slowly turns purple [NMR: Bowden et al. J Chem Soc (C) 172 1968]. It can also be purified by dissolving in the minimum volume of hot H2O and adding EtOH dropwise until cloudy, cool, and colourless crystals separate; IR: max 3445w, 3000-2560w br, 2156w, 1635s and 1475s cm-1. [NMR: Jager & Frey Justus Liebigs Ann Chem 817 1982.] Alternatively it has been purified by two successive chromatographic treatments on Dowex-1 x 8, with the first elution with 2M AcOH and a second with a linear gradient between 0—2M AcOH, evaporating the desired fractions and recrystallising the residue from MeOH. [McCarry & Savard Tetrahedron Lett 22 5153 1981, Nakamura Chem Pharm Bull Jpn 19 46 1971.]

5-(Aminomethyl)-3(2H)isoxazolon Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

2763-96-4(5-(Aminomethyl)-3(2H)isoxazolon)Verwandte Suche:


  • 5-(aminomethyl)isoxazol-3-ol hydrate
  • MUSCIMOL CRYSTALLINE
  • Containsupto10%Ethanol
  • 5-Aminomethyl-3-hydroxyisoxazole, 5-(Aminomethyl)-3(2H)-isoxazolone
  • Muscimol: (5-Aminomethyl-3-isoxyzole)
  • 5-Aminomethylisoxazol-3(2H)-one
  • Muscimol hydrate,98%
  • Muscimol hydrate5-(Aminomethyl)-3-isoxazolol
  • AGARIN
  • 3-HYDROXY-5-AMINOMETHYL-ISOXAZOLE
  • 3-HYDROXY-5-AMINOMETHYLISOXAZOLE HYDROBROMIDE
  • 5-(AMINOMETHYL)-3(2H)-ISOXAZOLONE
  • 5-(AMINOMETHYL)-3(2H)-ISOXAZOLONE, HYDROBROMIDE
  • 5-AMINOMETHYL-3-ISOXAZOLOL
  • 5-AMINOMETHYL-3-HYDROXYISOAZOLE, HBR
  • 5-AMINOMETHYL-3-HYDROXYISOOXAZOLE
  • 5-AMINOMETHYL-3-HYDROXYISOXAZOLE
  • 3-Hydroxy-5-aminomethyl-isoxazole, 5-Aminomethyl-3-hydroxy-isoxazole, 5-Aminomethyl-3-isoxazolol
  • MUSCIMOL (RG)
  • NSC 333569
  • Agarin, Pantherine
  • pantherin
  • rcrawastenumberp007
  • PANTHERINE
  • MUSCIMOL
  • MUSCIMOL HYDROBROMIDE
  • 5-Aminomethylisoxazol-3-one
  • MUSCIMOL(P)
  • Pyroibotenic acid
  • 5-(aminomethyl)isoxazol-3-ol
  • 3(2h)isoxazoione,5-(aminomethyl)-
  • 3-hydroxy-5-aminomethylisoxazole-agarin
  • 5-(aminomethyl)-3(2h)-isoxazolon
  • 5-(aminomethyl)-3-isoxazolo
  • 5-aminomethyl-3-isoxyzole
  • agarine
  • Arylex Impurity 8
  • 2763-96-4
  • C4H7BrN2O2
  • C4H6N2O2xH2O
  • Building Blocks
  • BioChemical
  • Cell Signaling and Neuroscience
  • Cell Biology
  • Ligand-Gated Ion Channels
  • Isoxazoles
  • Ion Channels
  • GABA and Glycine Receptor Modulators
  • Heterocyclic Building Blocks
  • Heterocycles
  • GABA/Glycine receptor
  • Bioactive Small Molecules
  • Building Blocks
  • Cell Biology
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Enzyme substrates
  • Neurochemicals
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