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/
n14http://linked.opendata.cz/resource/drugbank/drug/DB04528/identifier/pubchem-substance/
n7http://linked.opendata.cz/resource/drugbank/drug/DB04528/identifier/drugbank/
n12http://bio2rdf.org/drugbank:
admshttp://www.w3.org/ns/adms#
n4http://linked.opendata.cz/resource/drugbank/drug/DB04528/identifier/chebi/
n15http://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#
n8http://linked.opendata.cz/ontology/drugbank/
n9http://linked.opendata.cz/resource/drugbank/property/
n5http://linked.opendata.cz/resource/drugbank/drug/DB04528/identifier/pdb/
n10http://linked.opendata.cz/resource/drugbank/drug/DB04528/identifier/kegg-compound/
xsdhhttp://www.w3.org/2001/XMLSchema#
n6http://linked.opendata.cz/resource/drugbank/drug/DB04528/identifier/pubchem-compound/

Statements

Subject Item
n2:DB04528
rdf:type
n8:Drug
n8:description
A toxic dye, chemically related to trinitrophenol (picric acid), used in biochemical studies of oxidative processes where it uncouples oxidative phosphorylation. It is also used as a metabolic stimulant. (Stedman, 26th ed)
n8:group
experimental
owl:sameAs
n12:DB04528 n15:DB04528
dcterms:title
2,4-Dinitrophenol
adms:identifier
n4:918 n5:DNF n6:1493 n7:DB04528 n10:C02496 n14:46507895
n8:synthesisReference
Otto Arndt, Theodor Papenfuhs, "Process for the preparation of 6-chloro-2,4-dinitrophenol." U.S. Patent US4540832, issued September, 1984.
n8:IUPAC-Name
n9:271B6280-363D-11E5-9242-09173F13E4C5
n8:InChI
n9:271B6286-363D-11E5-9242-09173F13E4C5
n8:Molecular-Formula
n9:271B6285-363D-11E5-9242-09173F13E4C5
n8:Molecular-Weight
n9:271B6282-363D-11E5-9242-09173F13E4C5
n8:Monoisotopic-Weight
n9:271B6283-363D-11E5-9242-09173F13E4C5
n8:SMILES
n9:271B6284-363D-11E5-9242-09173F13E4C5
n8:Water-Solubility
n9:271B627E-363D-11E5-9242-09173F13E4C5 n9:271B6296-363D-11E5-9242-09173F13E4C5
n8:logP
n9:271B627F-363D-11E5-9242-09173F13E4C5 n9:271B627C-363D-11E5-9242-09173F13E4C5 n9:271B6298-363D-11E5-9242-09173F13E4C5
n8:logS
n9:271B627D-363D-11E5-9242-09173F13E4C5
n8:pKa
n9:271B6299-363D-11E5-9242-09173F13E4C5
n8:H-Bond-Acceptor-Count
n9:271B628C-363D-11E5-9242-09173F13E4C5
n8:H-Bond-Donor-Count
n9:271B628D-363D-11E5-9242-09173F13E4C5
n8:InChIKey
n9:271B6287-363D-11E5-9242-09173F13E4C5
n8:Polar-Surface-Area--PSA-
n9:271B6288-363D-11E5-9242-09173F13E4C5
n8:Polarizability
n9:271B628A-363D-11E5-9242-09173F13E4C5
n8:Refractivity
n9:271B6289-363D-11E5-9242-09173F13E4C5
n8:Rotatable-Bond-Count
n9:271B628B-363D-11E5-9242-09173F13E4C5
n8:casRegistryNumber
51-28-5
n8:Bioavailability
n9:271B6292-363D-11E5-9242-09173F13E4C5
n8:Ghose-Filter
n9:271B6294-363D-11E5-9242-09173F13E4C5
n8:MDDR-Like-Rule
n9:271B6295-363D-11E5-9242-09173F13E4C5
n8:Melting-Point
n9:271B6297-363D-11E5-9242-09173F13E4C5
n8:Number-of-Rings
n9:271B6291-363D-11E5-9242-09173F13E4C5
n8:Physiological-Charge
n9:271B6290-363D-11E5-9242-09173F13E4C5
n8:Rule-of-Five
n9:271B6293-363D-11E5-9242-09173F13E4C5
n8:Traditional-IUPAC-Name
n9:271B6281-363D-11E5-9242-09173F13E4C5
n8:pKa--strongest-acidic-
n9:271B628E-363D-11E5-9242-09173F13E4C5
n8:pKa--strongest-basic-
n9:271B628F-363D-11E5-9242-09173F13E4C5