CHEBI:75391 - hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester

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ChEBI Name hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester ChEBI ID CHEBI:75391 Definition An organic phosphonate that is the trisacetoxymethylester derivative of naphthalene substituted hydroxymethylphosphonic acid. It has been found to inhibit insulin receptor tyrosine kinase activity and insulin stimulated glucose oxidation. 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 C20H23O10P Net Charge 0 Average Mass 454.36440 Monoisotopic Mass 454.10288 InChI InChI=1S/C20H23O10P/c1-14(21)25-11-28-20(19-9-8-17-6-4-5-7-18(17)10-19)31(24,29-12-26-15(2)22)30-13-27-16(3)23/h4-10,20H,11-13H2,1-3H3 InChIKey UQODAZKXEREJLZ-UHFFFAOYSA-N SMILES CC(=O)OCOC(c1ccc2ccccc2c1)P(=O)(OCOC(C)=O)OCOC(C)=O Roles Classification Biological Role(s): tyrosine kinase inhibitor Any protein kinase inhibitor that interferes with the action of tyrosine kinase. View more via ChEBI Ontology ChEBI Ontology Outgoing hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester (CHEBI:75391) has functional parent hydroxymethylphosphonic acid (CHEBI:5810) hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester (CHEBI:75391) has role tyrosine kinase inhibitor (CHEBI:38637) hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester (CHEBI:75391) is a acetate ester (CHEBI:47622) hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester (CHEBI:75391) is a naphthalenes (CHEBI:25477) hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester (CHEBI:75391) is a organic phosphonate (CHEBI:37592) Synonyms Sources 3-[(acetyloxy)methoxy]-4-(naphthalen-2-yl)-3-oxido-8-oxo-2,5,7-trioxa-3λ5-phosphanon-1-yl acetate ChEBI HNMPA-(AM)3 ChEBI Manual Xref Database LSM-6443 LINCS View more database links Registry Number Type Source 11322049 Reaxys Registry Number Reaxys Citation Type Source 2550060 PubMed citation Europe PMC Last Modified 25 February 2016