CHEBI:68253 - platencin A₃

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ChEBI Name platencin A3 ChEBI ID CHEBI:68253 ChEBI ASCII Name platencin A3 Definition A polycyclic cage that is the 4-hydroxy derivative of platencin. It is isolated from Streptomyces platensis. 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 C24H27NO7 Net Charge 0 Average Mass 441.47370 Monoisotopic Mass 441.17875 InChI InChI=1S/C24H27NO7/c1-12-13-5-9-24(21(12)30)10-6-17(27)23(2,16(24)11-13)8-7-18(28)25-19-15(26)4-3-14(20(19)29)22(31)32/h3-4,6,10,13,16,21,26,29-30H,1,5,7-9,11H2,2H3,(H,25,28)(H,31,32)/t13-,16-,21-,23-,24-/m0/s1 InChIKey FHLUNOXZZMCXBM-GFZIYMICSA-N SMILES [H][C@]12CC[C@@]3(C=CC(=O)[C@@](C)(CCC(=O)Nc4c(O)ccc(C(O)=O)c4O)[C@]3([H])C1)[C@@H](O)C2=C Metabolite of Species Details Streptomyces platensis (NCBI:txid58346) of strain MA7327 See: PubMed Roles Classification Chemical Role(s): Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) Biological Role(s): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. View more via ChEBI Ontology ChEBI Ontology Outgoing platencin A3 (CHEBI:68253) has functional parent platencin (CHEBI:68241) platencin A3 (CHEBI:68253) has role bacterial metabolite (CHEBI:76969) platencin A3 (CHEBI:68253) is a aromatic amide (CHEBI:62733) platencin A3 (CHEBI:68253) is a cyclic ketone (CHEBI:3992) platencin A3 (CHEBI:68253) is a dihydroxybenzoic acid (CHEBI:23778) platencin A3 (CHEBI:68253) is a monocarboxylic acid amide (CHEBI:29347) platencin A3 (CHEBI:68253) is a polycyclic cage (CHEBI:33640) platencin A3 (CHEBI:68253) is a secondary alcohol (CHEBI:35681) Incoming platencin A3 methyl ester (CHEBI:68254) has functional parent platencin A3 (CHEBI:68253) IUPAC Name 2,4-dihydroxy-3-({3-[(2S,4S,4aS,8S,8aR)-4-hydroxy-8-methyl-3-methylidene-7-oxo-1,3,4,7,8,8a-hexahydro-2H-2,4a-ethanonaphthalen-8-yl]propanoyl}amino)benzoic acid Registry Number Type Source 20323716 Reaxys Registry Number Reaxys Citation Type Source 21214253 PubMed citation Europe PMC Last Modified 06 March 2014