Hipotaurin : Vidi još, Reference, Literatura, Spoljašnje veze Wikipedia, slobodna enciklopedija

Hipotaurin

IUPAC ime


2-Aminoethanesulfinic acid

Identifikacija

CAS registarski broj

300-84-5

PubChem^[1]^[2]

107812

MeSH

Hypotaurine

Jmol-3D slike

Slika 1

SMILES

C(CS(=O)O)N

InChI
InChI=1S/C2H7NO2S/c3-1-2-6(4)5/h1-3H2,(H,4,5)^Y Kod: VVIUBCNYACGLLV-UHFFFAOYSA-N^Y

Svojstva

Molekulska formula

C₂H₇NO₂S

Molarna masa

109.15 g/mol

Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala

Infobox references

Hipotaurin je derivat sulfinske kiseline koji je intermedijar u biosintezi taurina^[3]^[4]. Poput taurina, ova kiselina takođe dejstvuje kao endogeni neurotransmiter ^[5] putem akcije na glicin receptore.

Vidi još

Alanin
Glicin
Serin
Taurin

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.
↑ Mario Fontana, Silvestro Duprè and Laura Pecci (2006). Advances in Experimental Medicine and Biology: The Reactivity of Hypotaurine and Cysteine Sulfinic Acid with Peroxynitrite. str. 15-24. DOI:10.1007/978-0-387-33504-9_2. ISBN 978-0-387-32356-5. ^{[mrtav link]}
↑ Brand A, Leibfritz D, Hamprecht B, Dringen R (1998). „Metabolism of cysteine in astroglial cells: synthesis of hypotaurine and taurine”. J Neurochem 71 (2): 827-32. PMID 9681475.
↑ M. Lorraine Leibfried and B. D. Bavister (1982). „Effects of epinephrine and hypotaurine on in-vitro fertilization in the golden hamster”. J Reprod Fert 66: 87-3.

Literatura

Mario Fontana, Silvestro Duprè and Laura Pecci (2006). Advances in Experimental Medicine and Biology: The Reactivity of Hypotaurine and Cysteine Sulfinic Acid with Peroxynitrite. str. 15-24. DOI:10.1007/978-0-387-33504-9_2. ISBN 978-0-387-32356-5. ^{[mrtav link]}