S-Adenosyl-L-homocysteine: Difference between revisions

S-Adenosyl-L-homocysteine
Names
	IUPAC name S-(5'-Deoxyadenos-5'-yl)-L-homocysteine
	Other names AdoHcy, 2-S-adenosyl-L-homocysteine,; 5'-S-(3-Amino-3-carboxypropyl)-5'-thioadenosine S-adenosylhomocysteine, SAH
Identifiers
CAS Number	979-92-0 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:16680 ;
ChEMBL	ChEMBL418052 ;
ChemSpider	388301 ;
ECHA InfoCard	100.012.328
IUPHAR/BPS	5265;
KEGG	C00021 ;
MeSH	S-Adenosylhomocysteine
PubChem CID	439155;
CompTox Dashboard (EPA)	DTXSID30895860 ;
	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 ; InChI=1/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-WFMPWKQPBX;
	SMILES O=C(O)[C@@H](N)CCSC[C@H]3O[C@@H](n2cnc1c(ncnc12)N)[C@H](O)[C@@H]3O;
Properties
Chemical formula	C14H20N6O5S
Molar mass	384.412
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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Revision as of 18:02, 31 March 2017

S-Adenosyl-L-homocysteine (SAH) is an amino acid derivative used in several metabolic pathways in most organisms. It is an intermediate in the synthesis of cysteine and adenosine.

SAH is formed by the demethylation of S-adenosyl-L-methionine (aka SAM, SAMe, AdoMet).

External links

BioCYC E.Coli K-12 Compound: S-adenosyl-L-homocysteine

This biochemistry article is a stub. You can help Wikipedia by expanding it.

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 '''''S''-Adenosyl-<small>L</small>-homocysteine''' ('''SAH''') is an [[amino acid]] derivative used in several metabolic pathways in most organisms. It is an intermediate in the synthesis of [[cysteine]] and [[adenosine]].
-SAH is formed by the [[demethylation]] of [[S-Adenosyl-L-methionine|''S''-adenosyl-<small>L</small>-methionine]] (SAM).
+SAH is formed by the [[demethylation]] of [[S-Adenosyl-L-methionine|''S''-adenosyl-<small>L</small>-methionine]] ([[aka]] SAM, SAMe, AdoMet).
 ==External links==