{"ymdb_id":"YMDB02319","created_at":"2012-06-08T21:51:55.000Z","updated_at":"2016-09-11T18:50:41.000Z","name":"5-hydroxy furancarboxylic acid","cas":null,"state":null,"melting_point":null,"description":"5-Hydroxy furancarboxylic acid belongs to the class of chemical entities known as furoic acids. These are organic compounds containing a furoic acid moiety, with a structure characterized by a furan ring bearing a carboxylic acid group at the C2 or C3 carbon atom.","experimental_water_solubility":null,"experimental_logp_hydrophobicity":null,"location":null,"synthesis_reference":null,"chebi_id":"37125","hmdb_id":null,"kegg_id":null,"pubchem_id":null,"cs_id":"3373337","foodb_id":null,"wikipedia_link":null,"biocyc_id":null,"iupac":"5-hydroxyfuran-2-carboxylic acid","traditional_iupac":"5-hydroxyfuran-2-carboxylic acid","logp":"0.476801055","pka":"6.287584372617771","alogps_solubility":"2.89e+01 g/l","alogps_logp":"0.81","alogps_logs":"-0.65","acceptor_count":"3","donor_count":"2","rotatable_bond_count":"1","polar_surface_area":"70.67","refractivity":"26.9393","polarizability":"10.85476857727577","formal_charge":"0","physiological_charge":"-2","pka_strongest_basic":"-5.2088140406705135","pka_strongest_acidic":"3.1341256897095877","bioavailability":"1","number_of_rings":"1","rule_of_five":"1","ghose_filter":"0","veber_rule":"0","mddr_like_rule":"0","synonyms":["5-hydroxy monocarboxylic acid"],"pathways":[],"growth_conditions":[],"references":[{"pubmed_id":17439666,"citation":"Castrillo, J. I., Zeef, L. A., Hoyle, D. C., Zhang, N., Hayes, A., Gardner, D. C., Cornell, M. J., Petty, J., Hakes, L., Wardleworth, L., Rash, B., Brown, M., Dunn, W. B., Broadhurst, D., O'Donoghue, K., Hester, S. S., Dunkley, T. P., Hart, S. R., Swainston, N., Li, P., Gaskell, S. J., Paton, N. W., Lilley, K. S., Kell, D. B., Oliver, S. G. (2007). \"Growth control of the eukaryote cell: a systems biology study in yeast.\" J Biol 6:4."}],"proteins":[]}