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S-adenosil L-homocisteína

De Wikipedia, la enciclopedia libre

 
S-adenosil L-homocisteína
Nombre IUPAC
5'-S-(3-Amino-3-carboxipropil)-5'-tioadenosina
General
Otros nombres

AdoHcy, 2-S-adenosil-L-homocisteína,

S-adenosilhomocisteína, SAH
Fórmula molecular C14H20N6O5S
Identificadores
Número CAS 979-92-0[1]​
ChEBI 16680
ChEMBL CHEMBL418052
ChemSpider 388301
DrugBank 01752
PubChem 193
UNII 8K31Q2S66S
KEGG C00021
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)
[C@@H]1O)N2C=NC3=C2N=CN=C3N)C(O)=O
InChI=InChI=1S/C14H20N6O5S/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6-,7+,9+,10+,13+/m0/s1
Key: ZJUKTBDSGOFHSH-WFMPWKQPSA-N
Propiedades físicas
Masa molar 384,412 g/mol
Valores en el SI y en condiciones estándar
(25 ℃ y 1 atm), salvo que se indique lo contrario.
[editar datos en Wikidata]

La S-adenosil L-homocisteína (SAH) es un derivado de aminoácido que se utiliza en numerosas rutas metabólicas de la mayoría de los organismos. Es un intermediario de la síntesis de la cisteína. La SAH se forma por la desmetilación de S-adenosil metionina (SAM).

Enlaces externos



  1. ↑ Número CAS
Esta página se editó por última vez el 26 dic 2019 a las 02:30.
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