Hipotaurin

Hipotaurin
	2-Aminoethanesulfinic acid
Identifikacija
CAS registarski broj	300-84-5
PubChem	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) ; Kod: VVIUBCNYACGLLV-UHFFFAOYSA-N
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.

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↑ 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. 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. http://www.springerlink.com/content/jm48380677232738/.
↑ 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" (PDF). J Reprod Fert 66: 87–3.

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