ChemicalBook--->CAS DataBase List--->188640-63-3

188640-63-3

188640-63-3 Structure

188640-63-3 Structure
IdentificationBack Directory
[Name]

4-ETHYNYL-L-PHENYLALANINE HYDROCHLORIDE
[CAS]

188640-63-3
[Synonyms]

p-Ethynylphenylalanine hydrochloride
4-ETHYNYL-L-PHENYLALANINE HYDROCHLORIDE
[Molecular Formula]

C11H12ClNO2
[MDL Number]

MFCD20259693
[MOL File]

188640-63-3.mol
[Molecular Weight]

225.671
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Methanol: 125 mg/mL (553.91 mM); DMSO: 100 mg/mL (443.12 mM)
[form ]

Solid
[color ]

Off-white to light yellow
[Water Solubility ]

Water: < 0.1 mg/mL (insoluble)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Uses]

p-Ethynylphenylalanine hydrochloride (4-Ethynyl-L-phenylalanine hydrochloride) is a potent, selective, reversible and competitive inhibitor of tryptophan hydroxylase (TPH), with a Ki of 32.6 μM[1]. p-Ethynylphenylalanine (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
[in vivo]

p-Ethynylphenylalanine hydrochloride (30 mg/kg; i.p.) decreases in 5-HT and 5-HIAA levels in the rat midbrain but not in tissue[1].
? p-Ethynylphenylalanine hydrochloride does not inhibit the aromatic amino acid decarboxylase[1].

Animal Model:Male Sprague-Dawley rats (200 g)[1]
Dosage:30 mg/kg
Administration:Intraperitoneal injection
Result:Decreased in 5-HT and 5-HIAA levels in the rat midbrain.
[References]

[1] Stokes AH, et al. p-ethynylphenylalanine: a potent inhibitor of tryptophan hydroxylase. J Neurochem. 2000 May;74(5):2067-73. DOI:10.1046/j.1471-4159.2000.0742067.x
Spectrum DetailBack Directory
[Spectrum Detail]

4-ETHYNYL-L-PHENYLALANINE HYDROCHLORIDE(188640-63-3)1HNMR
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