Chemistry:S-Adenosylmethioninamine
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Names | |
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IUPAC name
S-(3-Aminopropyl)-S-methyl-5′-thioadenosin-5′-ium
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Systematic IUPAC name
(3-Aminopropyl){[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}methylsulfanium | |
Other names
S-Adenosyl-(5′)-3-methylthiopropylamine
decarboxylated S-adenosyl methionine decarboxy-S-adenosyl methionine (5-Deoxy-5-adenosyl)(3-aminopropyl)methylsulfonium cation | |
Identifiers | |
3D model (JSmol)
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Abbreviations | dAdoMet, dc-SAM |
ChEBI | |
ChemSpider | |
KEGG | |
PubChem CID
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UNII | |
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Properties | |
C14H23N6O3S+ | |
Molar mass | 355.43582 g/mol |
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 | |
S-Adenosylmethioninamine is a substrate that is required for the biosynthesis of polyamines including spermidine, spermine, and thermospermine.[1] It is produced by decarboxylation of S-adenosyl methionine.
See also
- Adenosylmethionine decarboxylase (AMD1)
- Spermidine synthase
- Spermine synthase
- Thermospermine synthase (ACAULIS5)
References
- ↑ Takahashi, Taku; Kakehi, Jun-Ichi (2009-10-13). "Polyamines: Ubiquitous polycations with unique roles in growth and stress responses". Annals of Botany 105 (1): 1–6. doi:10.1093/aob/mcp259. PMID 19828463.
Original source: https://en.wikipedia.org/wiki/S-Adenosylmethioninamine.
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