Glycine
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| Names | |||
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| IUPAC name Glycine | |||
| Systematic IUPAC name Aminoacetic acid | |||
| Other names 
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| Identifiers | |||
| 3D model (JSmol) | |||
| Abbreviations | Gly, G | ||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| DrugBank | |||
| ECHA InfoCard | 100.000.248 | ||
| EC Number | 
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| E number | E640 (flavour enhancer) | ||
| KEGG | |||
| PubChem CID | |||
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| 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. Glycine is one of the proteinogenic amino acids. It is encoded by all the codons starting with GG (GGU, GGC, GGA, GGG). Glycine disrupts the formation of alpha-helices in secondary protein structure. Its small side chain causes it to favor random coils instead. 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 both hydrophilic and hydrophobic environments, due to its minimal side chain of only one hydrogen atom.