For research use only. Not for therapeutic Use.
Glycine (Cat.No:R010916) is the simplest amino acid, a building block of proteins and an essential neurotransmitter in the central nervous system. It plays a vital role in various physiological processes, including neurotransmission and the synthesis of other amino acids and bioactive compounds. Glycine is used in medicine and the food industry.
Catalog Number | R010916 |
CAS Number | 56-40-6 |
Synonyms | 2-Aminoacetic Acid; Aciport; Aminoethanoic Acid; Glicoamin; Glycocoll; Glycolixir; Glycosthene; Gyn-Hydralin; H 1; NSC 25936; NSC 2916; NSC 54188; Padil; |
Molecular Formula | C2H5NO2 |
Purity | ≥95% |
Target | Neuronal Signaling |
Storage | Store at 4°C |
IUPAC Name | 2-aminoacetic acid |
InChI | InChI=1S/C2H5NO2/c3-1-2(4)5/h1,3H2,(H,4,5) |
InChIKey | DHMQDGOQFOQNFH-UHFFFAOYSA-N |
SMILES | C(C(=O)O)N |
Reference | </br>1:Presence of ethanol sensitive glycine receptors in medium spiny neurons in the mouse nucleus accumbens. Förstera B, Muñoz B, Lobo MK, Chandra R, Lovinger DM, Aguayo LG.J Physiol. 2017 May 19. doi: 10.1113/JP273767. [Epub ahead of print] PMID: 28524260 </br>2:Synthesis and Pharmacological Properties of Novel Esters Based on Monoterpenoids and Glycine. Nesterkina M, Kravchenko I.Pharmaceuticals (Basel). 2017 May 18;10(2). pii: E47. doi: 10.3390/ph10020047. PMID: 28524111 </br>3:Structural analysis of the dual function thioesterase SAV606 unravels the mechanism of Michael addition of glycine to an α,β-unsaturated thioester. Chisuga T, Miyanaga A, Kudo F, Eguchi T.J Biol Chem. 2017 May 18. pii: jbc.M117.792549. doi: 10.1074/jbc.M117.792549. [Epub ahead of print] PMID: 28522606 </br>4:Glycine Substitution at Helix-to-Coil Transitions Facilitates the Structural Determination of a Stabilized Subtype C HIV Envelope Glycoprotein. Guenaga J, Garces F, de Val N, Stanfield RL, Dubrovskaya V, Higgins B, Carrette B, Ward AB, Wilson IA, Wyatt RT.Immunity. 2017 May 16;46(5):792-803.e3. doi: 10.1016/j.immuni.2017.04.014. PMID: 28514686 </br>5:Subtype-specific agonists for NMDA receptor glycine binding sites. Maolanon A, Risgaard R, Wang SY, Snoep Y, Papangelis A, Yi F, Holley D, Barslund AF, Svenstrup N, Hansen KB, Clausen RP.ACS Chem Neurosci. 2017 May 17. doi: 10.1021/acschemneuro.7b00117. [Epub ahead of print] PMID: 28514141 </br>6:Variations in osmotic adjustment and water relations of Sphaerophysa kotschyana: Glycine betaine, proline and choline accumulation in response to salinity. Yildiztugay E, Ozfidan-Konakci C, Kucukoduk M, Duran Y.Bot Stud. 2014 Dec;55(1):6. doi: 10.1186/1999-3110-55-6. Epub 2014 Jan 17. PMID: 28510909 Free Article</br>7:Distribution of new satellites and simple sequence repeats in annual and perennial Glycine species. Chen H, Chung MC, Tsai YC, Wei FJ, Hsieh JS, Hsing YC.Bot Stud. 2015 Dec;56(1):22. doi: 10.1186/s40529-015-0103-9. Epub 2015 Sep 16. PMID: 28510831 Free Article</br>8:U(IV) Aqueous Speciation from the Monomer to UO<sub>2</sub> Nanoparticles: Two Levels of Control from Zwitterionic Glycine Ligands. Falaise C, Neal HA, Nyman M.Inorg Chem. 2017 May 16. doi: 10.1021/acs.inorgchem.7b00616. [Epub ahead of print] PMID: 28509548 </br>9:Effects of Maternal Zinc Glycine on Mortality, Zinc Concentration, and Antioxidant Status in a Developing Embryo and 1-Day-Old Chick. Zhang L, Wang JS, Wang Q, Li KX, Guo TY, Xiao X, Wang YX, Zhan XA.Biol Trace Elem Res. 2017 May 15. doi: 10.1007/s12011-017-1028-9. [Epub ahead of print] PMID: 28508186 </br>10:Poly(N-methacryloyl glycine)/nanocellulose composites as pH-sensitive systems for controlled release of diclofenac. Saïdi L, Vilela C, Oliveira H, Silvestre AJD, Freire CSR.Carbohydr Polym. 2017 Aug 1;169:357-365. doi: 10.1016/j.carbpol.2017.04.030. Epub 2017 Apr 17. PMID: 28504156 |