Glycine
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Names | |||
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IUPAC name
Glycine | |||
Systematic IUPAC name
Aminoacetic acid | |||
Other names
2-Aminoethanoic acid Glycocol Glycic acid Dicarbamic acid | |||
Identifiers | |||
3D model (JSmol) |
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Abbreviations | Gly, G | ||
ChEBI | |||
ChEMBL | |||
ChemSpider | |||
DrugBank | |||
ECHA InfoCard | 100.000.248 | ||
EC Number |
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KEGG | |||
PubChem CID |
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UNII | |||
CompTox Dashboard (EPA) |
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Properties | |||
C2H5NO2 | |||
Molar mass | 75.067 g·mol−1 | ||
Appearance | White solid | ||
Density | 1.1607 g/cm3 | ||
Melting point | 233 °C (451 °F; 506 K) (decomposition) | ||
249.9 g/L (25 °C) | |||
Solubility | soluble in pyridine sparingly soluble in ethanol insoluble in ether | ||
Acidity (pKa) | 2.34 (carboxyl), 9.6 (amino) | ||
-40.3·10−6 cm3/mol | |||
Pharmacology | |||
B05CX03 (WHO) | |||
Hazards | |||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose) |
2600 mg/kg (mouse, oral) | ||
Supplementary data page | |||
Glycine (data page) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
Glycine (symbol Gly or G; /ˈɡlaɪsiːn/ ⓘ) is an amino acid that has a single hydrogen atom as its side chain. It is the simplest stable amino acid (carbamic acid is unstable), with the chemical formula NH2‐CH2‐COOH. Glycine is one of the proteinogenic amino acids. It is encoded by all the codons starting with GG (GGU, GGC, GGA, GGG). Glycine is integral to the formation of alpha-helices in secondary protein structure due to the "flexibility" caused by such a small R group. Glycine is also an inhibitory neurotransmitter – interference with its release within the spinal cord (such as during a Clostridium tetani infection) can cause spastic paralysis due to uninhibited muscle contraction.
It is the only achiral proteinogenic amino acid. It can fit into hydrophilic or hydrophobic environments, due to its minimal side chain of only one hydrogen atom.