Trimetilglicin

Trimetilglicin
	2-trimetilamonioacetat
Drugi nazivi	Betain, TMG, glicinski betain, anhidrat betaina, N,N,N-trimetilglicin
Identifikacija
CAS registarski broj	107-43-7
PubChem	247
ChemSpider	242
UNII	3SCV180C9W
MeSH	Betaine
ChEBI	17750
ChEMBL	CHEMBL1182
ATC code	A16AA06
Jmol-3D slike	Slika 1
SMILES
	C[N+](C)(C)CC(=O)[O-]
InChI
	InChI=1S/C5H11NO2/c1-6(2,3)4-5(7)8/h4H2,1-3H3 ; Kod: KWIUHFFTVRNATP-UHFFFAOYSA-N InChI=1/C5H11NO2/c1-6(2,3)4-5(7)8/h4H2,1-3H3; Kod: KWIUHFFTVRNATP-UHFFFAOYAI
Svojstva
Molekulska formula	C5H11NO2
Molarna masa	117,146
Srodna jedinjenja
Srodna amino kiselina	Glicin; Metilglicin; Dimetilglicin
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Trimetilglicin (TMG) je organsko jedinjenje koje se javlja u biljkama u obliku glicin betaina i njegovih holinskih derivata. Trimetilglicin je bio prvi otkriveni betain. Originalno je nazivan jednostavno betain, jer je u 19. veku oktriven u šećernoj repi.^[5] Od tog vremena, mnogi drugi betaini su otkriveni, te se koristi specifičnije ime, glicin betain.

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ Hubert Schiweck, Margaret Clarke, Günter Pollach "Sugar” in Ullmann’s Encyclopedia of Industrial Chemistry 2007, Wiley-VCH, Weinheim.}{DOI|10.1002/14356007.a25_345.pub2}}

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[Ullmann-5] Hubert Schiweck, Margaret Clarke, Günter Pollach "Sugar” in Ullmann’s Encyclopedia of Industrial Chemistry 2007, Wiley-VCH, Weinheim.}{DOI|10.1002/14356007.a25_345.pub2}}

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