Cistamin je organski disulfid.[6] On se formira zagrevanjem cistina, što dovodi do dekarboksilacije. Cistamin je nestabilna tečnost i njime se generalno rukuje u obliku dihidrohloridne soli, C4H12N2S2·2HCl, koja je stabilna do 203-214 °C, na kojoj temparaturi se razlaže. Cistamin je toksičan ako se proguta ili udahne, i potencijalno je štetan pri dodiru.
Reference
- ↑ 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
- ↑ Susan Budavari, ur. (1996). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (12th izd.). Merck. str. 2846. ISBN 0-911910-12-3.
- ↑ McMurry John E. (1992). Fundamentals of Organic Chemistry (3rd izd.). Belmont: Wadsworth. ISBN 0-534-16218-5.
Literatura
Vanjske veze