CHEBI:68255 - platensin A4

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name platensin A4 ChEBI ID CHEBI:68255 Definition A polycyclic cage that is the 3-hydroxy derivative of platencin. It is isolated from Streptomyces platensis. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information ChemicalBook:CB5855401, ZINC000005854633 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C24H29NO7 Net Charge 0 Average Mass 443.48960 Monoisotopic Mass 443.19440 InChI InChI=1S/C24H29NO7/c1-22(8-7-18(28)25-19-15(26)4-3-14(20(19)29)21(30)31)16-11-13-5-9-24(16,10-6-17(22)27)12-23(13,2)32/h3-4,6,10,13,16,26,29,32H,5,7-9,11-12H2,1-2H3,(H,25,28)(H,30,31)/t13-,16-,22-,23+,24+/m0/s1 InChIKey PNAZDWJMYGFNNJ-NAXDPANMSA-N SMILES [H][C@@]12CC[C@]3(C[C@@]1(C)O)C=CC(=O)[C@@](C)(CCC(=O)Nc1c(O)ccc(C(O)=O)c1O)[C@]3([H])C2 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 platensin A4 (CHEBI:68255) has functional parent platencin (CHEBI:68241) platensin A4 (CHEBI:68255) has role bacterial metabolite (CHEBI:76969) platensin A4 (CHEBI:68255) is a aromatic amide (CHEBI:62733) platensin A4 (CHEBI:68255) is a cyclic ketone (CHEBI:3992) platensin A4 (CHEBI:68255) is a dihydroxybenzoic acid (CHEBI:23778) platensin A4 (CHEBI:68255) is a monocarboxylic acid amide (CHEBI:29347) platensin A4 (CHEBI:68255) is a polycyclic cage (CHEBI:33640) platensin A4 (CHEBI:68255) is a tertiary alcohol (CHEBI:26878) IUPAC Name 2,4-dihydroxy-3-({3-[(2S,3R,4aS,8S,8aR)-3-hydroxy-3,8-dimethyl-7-oxo-1,3,4,7,8,8a-hexahydro-2H-2,4a-ethanonaphthalen-8-yl]propanoyl}amino)benzoic acid Registry Number Type Source 20323714 Reaxys Registry Number Reaxys Citation Type Source 21214253 PubMed citation Europe PMC Last Modified 06 March 2014