CHEBI:131602 - CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid

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ChEBI Name CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid ChEBI ID CHEBI:131602 ChEBI ASCII Name CMP-8-amino-3,8-dideoxy-alpha-D-manno-oct-2-ulosonic acid Definition A CMP-sugar having 8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid as the sugar component. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C17H27N4O14P Net Charge 0 Average Mass 542.389 Monoisotopic Mass 542.12614 InChI InChI=1S/C17H27N4O14P/c18-4-7(23)13-10(24)6(22)3-17(34-13,15(27)28)35-36(30,31)32-5-8-11(25)12(26)14(33-8)21-2-1-9(19)20-16(21)29/h1-2,6-8,10-14,22-26H,3-5,18H2,(H,27,28)(H,30,31)(H2,19,20,29)/t6-,7-,8-,10-,11-,12-,13-,14-,17+/m1/s1 InChIKey DRAKZHNWGXXUTP-XKKDATLGSA-N SMILES C1=CC(=NC(N1[C@@H]2O[C@H](COP(O[C@@]3(C[C@@H](O)[C@@H](O)[C@](O3)([C@H](O)CN)[H])C(=O)O)(=O)O)[C@H]([C@H]2O)O)=O)N Metabolite of Species Details Shewanella oneidensis (NCBI:txid70863) See: PubMed Roles Classification Biological Role(s): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. View more via ChEBI Ontology ChEBI Ontology Outgoing CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid (CHEBI:131602) has functional parent 8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid (CHEBI:87313) CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid (CHEBI:131602) has role bacterial metabolite (CHEBI:76969) CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid (CHEBI:131602) is a CMP-sugar (CHEBI:20878) CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid (CHEBI:131602) is conjugate acid of CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonate(1−) (CHEBI:91089) Incoming CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonate(1−) (CHEBI:91089) is conjugate base of CMP-8-amino-3,8-dideoxy-α-D-manno-oct-2-ulosonic acid (CHEBI:131602) IUPAC Name cytidine 5'-[(8-amino-3,8-dideoxy-α-D-manno-oct-2-ulopyranosonyl) hydrogen phosphate] Synonym Source CMP-Kdo8N MetaCyc Manual Xref Database CPD-18062 MetaCyc View more database links Citation Type Source 23413030 PubMed citation Europe PMC Last Modified 22 March 2016