Hipotaurin

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.

Hipotaurin
IUPAC ime
Identifikacija
CAS registarski broj	300-84-5
PubChem[1][2]	107812
MeSH	Hypotaurine
Jmol-3D slike	Slika 1
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

Povezano

• Alanin
• Glicin
• Serin
• Taurin

Reference

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. 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]}
4. 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.
5. 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]}

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