Substance

ID:180520

Names and Identifiers
Synonyms
L-谷氨酸(S)-2-氨基戊二酸L-Glutamic acidGlu
IUPAC name
(2S)-2-aminopentanedioic acid
IUPAC Traditional name
L-glutamic acid
Registration numbers
EC Number
Beilstein Number
CAS Number
MDL Number
PubChem SID
Properties
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class
1
Pharmacology Properties
Gene Information
human ... CCR2(1231), GRIA1(2890), GRIA2(2891), GRIA4(2893), GRIK1(2897), GRIK2(2898), GRIK3(2899), GRIK5(2901), GRIN2B(2904), GRM2(2912), SLC1A1(6505), SLC1A2(6506)rat ... Gria1(50592), Grik1(29559), Grik2(54257), Grik4(24406), Grin2a(24409), Grm1(24414), Grm2(24415), Grm3(24416), Grm4(24417), Grm5(24418), Grm6(24419), Grm7(81672), Slc1a2(29482)
Product Information
Purity
98.5-100.5%
Biological Source
from non-animal source
Suitability
meets EP testing specifications
suitable for cell culture
Impurities
endotoxin, tested
Physical Property
Apperance
powder
Melting Point
205 °C (dec.)(lit.)
Solubility
1 M HCl: soluble100 mg/mL
Molecule Details
Biochem/physiol Actions
Glutamic acid, or glutamate, the salt form of glutamic acid, functions as a neurotransmitter. Glutamic acid also plays a key role in many metabolic pathways. It is converted to α-ketoglutarate, a key component of the TCA cycle, and a precursor for the biosynthesis of nucleic acids and certain amino acids. In cells, glutamine is converted to glutamate by the enzyme glutaminase.
一种兴奋性氨基酸神经递质,为谷氨酸盐受体所有亚型(代谢型红藻氨酸、NMDA 和 AMPA)的激动剂。
包装
10 mg in autosmp vl
Molecular Spectra
No Data Available
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References
No Data Available
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