This HTML5 document contains 44 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

PrefixIRI
n2http://linked.opendata.cz/resource/drugbank/drug/
dctermshttp://purl.org/dc/terms/
n4http://linked.opendata.cz/resource/drugbank/drug/DB01762/identifier/pubchem-substance/
n11http://linked.opendata.cz/resource/drugbank/drug/DB01762/identifier/drugbank/
n16http://bio2rdf.org/drugbank:
admshttp://www.w3.org/ns/adms#
n15http://linked.opendata.cz/resource/drugbank/drug/DB01762/identifier/chemspider/
n14http://linked.opendata.cz/resource/drugbank/drug/DB01762/identifier/chebi/
n8http://wifo5-03.informatik.uni-mannheim.de/drugbank/resource/drugs/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
n5http://linked.opendata.cz/ontology/drugbank/
n6http://linked.opendata.cz/resource/drugbank/property/
xsdhhttp://www.w3.org/2001/XMLSchema#
n12http://linked.opendata.cz/resource/drugbank/drug/DB01762/identifier/kegg-compound/
n9http://linked.opendata.cz/resource/drugbank/drug/DB01762/identifier/pdb/
n10http://linked.opendata.cz/resource/drugbank/drug/DB01762/identifier/pubchem-compound/

Statements

Subject Item
n2:DB01762
rdf:type
n5:Drug
n5:generalReferences
# Martin PM, Gopal E, Ananth S, Zhuang L, Itagaki S, Prasad BM, Smith SB, Prasad PD, Ganapathy V: Identity of SMCT1 (SLC5A8) as a neuron-specific Na+-coupled transporter for active uptake of L-lactate and ketone bodies in the brain. J Neurochem. 2006 Jul;98(1):279-88. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/16805814
n5:group
experimental
owl:sameAs
n8:DB01762 n16:DB01762
dcterms:title
Acetoacetic Acid
adms:identifier
n4:46505003 n9:AAE n10:96 n11:DB01762 n12:C00164 n14:15344 n15:94
n5:synthesisReference
Erik Herkenrath, "Process for the production of 1,2-dihydro-2-oxo-4-methyl-7-acetoacetic acid amido-quinoline." U.S. Patent US4064131, issued July, 1956.
n5:IUPAC-Name
n6:271B443A-363D-11E5-9242-09173F13E4C5
n5:InChI
n6:271B4440-363D-11E5-9242-09173F13E4C5
n5:Molecular-Formula
n6:271B443F-363D-11E5-9242-09173F13E4C5
n5:Molecular-Weight
n6:271B443C-363D-11E5-9242-09173F13E4C5
n5:Monoisotopic-Weight
n6:271B443D-363D-11E5-9242-09173F13E4C5
n5:SMILES
n6:271B443E-363D-11E5-9242-09173F13E4C5
n5:Water-Solubility
n6:271B4438-363D-11E5-9242-09173F13E4C5 n6:271B4450-363D-11E5-9242-09173F13E4C5
n5:logP
n6:271B4436-363D-11E5-9242-09173F13E4C5 n6:271B4439-363D-11E5-9242-09173F13E4C5
n5:logS
n6:271B4437-363D-11E5-9242-09173F13E4C5
n5:pKa
n6:271B4452-363D-11E5-9242-09173F13E4C5
n5:H-Bond-Acceptor-Count
n6:271B4446-363D-11E5-9242-09173F13E4C5
n5:H-Bond-Donor-Count
n6:271B4447-363D-11E5-9242-09173F13E4C5
n5:InChIKey
n6:271B4441-363D-11E5-9242-09173F13E4C5
n5:Polar-Surface-Area--PSA-
n6:271B4442-363D-11E5-9242-09173F13E4C5
n5:Polarizability
n6:271B4444-363D-11E5-9242-09173F13E4C5
n5:Refractivity
n6:271B4443-363D-11E5-9242-09173F13E4C5
n5:Rotatable-Bond-Count
n6:271B4445-363D-11E5-9242-09173F13E4C5
n5:casRegistryNumber
541-50-4
n5:Bioavailability
n6:271B444C-363D-11E5-9242-09173F13E4C5
n5:Ghose-Filter
n6:271B444E-363D-11E5-9242-09173F13E4C5
n5:MDDR-Like-Rule
n6:271B444F-363D-11E5-9242-09173F13E4C5
n5:Melting-Point
n6:271B4451-363D-11E5-9242-09173F13E4C5
n5:Number-of-Rings
n6:271B444B-363D-11E5-9242-09173F13E4C5
n5:Physiological-Charge
n6:271B444A-363D-11E5-9242-09173F13E4C5
n5:Rule-of-Five
n6:271B444D-363D-11E5-9242-09173F13E4C5
n5:Traditional-IUPAC-Name
n6:271B443B-363D-11E5-9242-09173F13E4C5
n5:pKa--strongest-acidic-
n6:271B4448-363D-11E5-9242-09173F13E4C5
n5:pKa--strongest-basic-
n6:271B4449-363D-11E5-9242-09173F13E4C5