CHEBI:15625 - S-adenosylmethioninamine

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ChEBI Name S-adenosylmethioninamine ChEBI ID CHEBI:15625 ChEBI ASCII Name S-adenosylmethioninamine Definition The S-adenosyl derivative of methioninamine. It acts as the aminopropyl donor in the biosynthesis of the polyamines, spermidine and spermine. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:12743, CHEBI:22035, CHEBI:10906, CHEBI:12762, CHEBI:8947 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C14H23N6O3S Net Charge +1 Average Mass 355.43706 Monoisotopic Mass 355.15469 InChI InChI=1S/C14H23N6O3S/c1-24(4-2-3-15)5-8-10(21)11(22)14(23-8)20-7-19-9-12(16)17-6-18-13(9)20/h6-8,10-11,14,21-22H,2-5,15H2,1H3,(H2,16,17,18)/q+1/t8-,10-,11-,14-,24?/m1/s1 InChIKey ZUNBITIXDCPNSD-LSRJEVITSA-N SMILES C[S+](CCCN)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 Metabolite of Species Details Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Escherichia coli (NCBI:txid562) See: PubMed Homo sapiens (NCBI:txid9606) Found in urine (BTO:0001419). See: PubMed Roles Classification Biological Role(s): Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). human urinary metabolite Any metabolite (endogenous or exogenous) found in human urine samples. rat metabolite Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus). View more via ChEBI Ontology ChEBI Ontology Outgoing S-adenosylmethioninamine (CHEBI:15625) has functional parent 3-methylthiopropylamine (CHEBI:16696) S-adenosylmethioninamine (CHEBI:15625) has role Escherichia coli metabolite (CHEBI:76971) S-adenosylmethioninamine (CHEBI:15625) has role human urinary metabolite (CHEBI:84087) S-adenosylmethioninamine (CHEBI:15625) has role mouse metabolite (CHEBI:75771) S-adenosylmethioninamine (CHEBI:15625) has role rat metabolite (CHEBI:86264) S-adenosylmethioninamine (CHEBI:15625) is a adenosines (CHEBI:22260) S-adenosylmethioninamine (CHEBI:15625) is a sulfonium compound (CHEBI:26830) S-adenosylmethioninamine (CHEBI:15625) is conjugate base of S-adenosylmethioninaminium (CHEBI:57443) Incoming S-adenosylmethioninaminium (CHEBI:57443) is conjugate acid of S-adenosylmethioninamine (CHEBI:15625) IUPAC Name (3-aminopropyl)(5'-deoxyadenosin-5'-yl)(methyl)sulfonium Synonyms Sources (5-Deoxy-5-adenosyl)(3-aminopropyl)methylsulfonium KEGG COMPOUND (5-Deoxy-5-adenosyl)(3-aminopropyl)methylsulfonium cation KEGG COMPOUND (5-Deoxy-5-adenosyl)(3-aminopropyl)methylsulfonium salt KEGG COMPOUND [1-(adenin-9-yl)-1,5-dideoxy-β-D-ribofuranos-5-yl](3-aminopropyl)(methyl)sulfonium IUPAC dAdoMet ChEBI dc-SAM ChEBI dcAdoMet ChEBI dcSAM MetaCyc decarboxylated AdoMet HMDB decarboxylated S-adenosylmethionine HMDB decarboxylated SAM HMDB S-adenosyl 3-(methylsulfanyl)propylamine MetaCyc S-adenosyl 3-(methylthio)propylamine ChEBI S-adenosyl-(5')-3-methylthiopropylamine KEGG COMPOUND S-adenosyl-3-methylthiopropylamine ChemIDplus S-adenosylmethionamine ChEBI S-Adenosylmethioninamine KEGG COMPOUND S-adenosylmethioninamine JCBN S-methyl-S-adenosyl homocysteamine MetaCyc S-methyl-S-adenosylhomocysteamine ChEBI S-methyladenosylhomocysteamine ChEBI Manual Xrefs Databases C01137 KEGG COMPOUND FDB022353 FooDB HMDB0000988 HMDB S-Adenosylmethioninamine Wikipedia View more database links Registry Numbers Types Sources 22365-13-5 CAS Registry Number ChemIDplus 4161053 Beilstein Registry Number Beilstein Citations Types Sources 15130560 PubMed citation Europe PMC 17822713 PubMed citation Europe PMC 20523031 PubMed citation Europe PMC 20950271 PubMed citation Europe PMC 3006760 PubMed citation Europe PMC 3409208 PubMed citation Europe PMC 3728970 PubMed citation Europe PMC 4084287 PubMed citation Europe PMC 6439194 PubMed citation Europe PMC 6621404 PubMed citation Europe PMC 6807294 PubMed citation Europe PMC 7391043 PubMed citation Europe PMC 7396502 PubMed citation Europe PMC 7448956 PubMed citation Europe PMC 869190 PubMed citation Europe PMC Last Modified 11 January 2023