Cistamin

Cistamin
	2,2'-Dithiobis(ethylamine)
Drugi nazivi	2,2'-Ditiobisetanamin; 2-Aminoetil disulfid; Dekarboksicistin
Identifikacija
Abrevijacija	AED
CAS registarski broj	51-85-4
PubChem	2915
ChemSpider	2812
UNII	R110LV8L02
ChEMBL	CHEMBL61350
Jmol-3D slike	Slika 1
SMILES
	S(SCCN)CCN
InChI
	InChI=1S/C4H12N2S2/c5-1-3-7-8-4-2-6/h1-6H2 ; Kod: APQPRKLAWCIJEK-UHFFFAOYSA-N InChI=1/C4H12N2S2/c5-1-3-7-8-4-2-6/h1-6H2; Kod: APQPRKLAWCIJEK-UHFFFAOYAQ
Svojstva
Molekulska formula	C4H12N2S2
Molarna masa	152.28 g/mol
Agregatno stanje	Viscozno ulje
Tačka ključanja	Razlaže se
Rastvorljivost u vodi	meša se
Rastvorljivost u Etanol	rastvoran je
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

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[uredi | uredi kod]

↑ 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[uredi | uredi kod]

Spoljašnje veze[uredi | uredi kod]

Portal Hemija

[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

[5] Susan Budavari, ur. (1996). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (12th izd.). Merck. str. 2846. ISBN 0-911910-12-3.

[6] McMurry John E. (1992). Fundamentals of Organic Chemistry (3rd izd.). Belmont: Wadsworth. ISBN 0-534-16218-5.

[1]

[2]

[3]

[4]

[5]

[6]

Cistamin

Reference[uredi | uredi kod]

Literatura[uredi | uredi kod]

Spoljašnje veze[uredi | uredi kod]

Navigacija

Pretraga