This HTML5 document contains 51 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/DB04784/identifier/chebi/
n9http://linked.opendata.cz/resource/mesh/concept/
n12http://linked.opendata.cz/resource/drugbank/drug/DB04784/identifier/pdb/
n7http://bio2rdf.org/drugbank:
n13http://linked.opendata.cz/resource/drugbank/drug/DB04784/identifier/pubchem-compound/
admshttp://www.w3.org/ns/adms#
n11http://linked.opendata.cz/resource/drugbank/drug/DB04784/identifier/pubchem-substance/
n6http://wifo5-03.informatik.uni-mannheim.de/drugbank/resource/drugs/
n15http://linked.opendata.cz/resource/drugbank/drug/DB04784/identifier/drugbank/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
n8http://linked.opendata.cz/ontology/mesh/
n3http://linked.opendata.cz/ontology/drugbank/
n4http://linked.opendata.cz/resource/drugbank/property/
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DB04784
rdf:type
n3:Drug
n3:group
experimental
owl:sameAs
n6:DB04784 n7:DB04784
dcterms:title
Methylphenyl carbinol
adms:identifier
n11:46507442 n12:SS2 n13:637516 n14:45616 n15:DB04784
n3:synonym
1-PHENYL-ETHANOL (+)-Methyl phenyl carbinol 1-Phenylethanol (1R)-1-PHENYLETHANOL (R)-1-phenylethanol (R)-alpha-methylbenzenemethanol (R)-alpha-Methylbenzyl alcohol (R)-(+)-1-Phenylethanol
n3:synthesisReference
Leslie Chewter, "Method and apparatus for producing styrene by catalytic dehydration of 1-phenylethanol." U.S. Patent US20040044260, issued March 04, 2004.
n8:hasConcept
n9:M0042474
n3:IUPAC-Name
n4:271B531A-363D-11E5-9242-09173F13E4C5
n3:InChI
n4:271B5320-363D-11E5-9242-09173F13E4C5
n3:Molecular-Formula
n4:271B531F-363D-11E5-9242-09173F13E4C5
n3:Molecular-Weight
n4:271B531C-363D-11E5-9242-09173F13E4C5
n3:Monoisotopic-Weight
n4:271B531D-363D-11E5-9242-09173F13E4C5
n3:SMILES
n4:271B531E-363D-11E5-9242-09173F13E4C5
n3:Water-Solubility
n4:271B5318-363D-11E5-9242-09173F13E4C5 n4:271B5330-363D-11E5-9242-09173F13E4C5
n3:logP
n4:271B5316-363D-11E5-9242-09173F13E4C5 n4:271B5319-363D-11E5-9242-09173F13E4C5 n4:271B5333-363D-11E5-9242-09173F13E4C5
n3:logS
n4:271B5317-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Acceptor-Count
n4:271B5326-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Donor-Count
n4:271B5327-363D-11E5-9242-09173F13E4C5
n3:InChIKey
n4:271B5321-363D-11E5-9242-09173F13E4C5
n3:Polar-Surface-Area--PSA-
n4:271B5322-363D-11E5-9242-09173F13E4C5
n3:Polarizability
n4:271B5324-363D-11E5-9242-09173F13E4C5
n3:Refractivity
n4:271B5323-363D-11E5-9242-09173F13E4C5
n3:Rotatable-Bond-Count
n4:271B5325-363D-11E5-9242-09173F13E4C5
n3:casRegistryNumber
1517-69-7
n3:Bioavailability
n4:271B532C-363D-11E5-9242-09173F13E4C5
n3:Boiling-Point
n4:271B5332-363D-11E5-9242-09173F13E4C5
n3:Ghose-Filter
n4:271B532E-363D-11E5-9242-09173F13E4C5
n3:MDDR-Like-Rule
n4:271B532F-363D-11E5-9242-09173F13E4C5
n3:Melting-Point
n4:271B5331-363D-11E5-9242-09173F13E4C5
n3:Number-of-Rings
n4:271B532B-363D-11E5-9242-09173F13E4C5
n3:Physiological-Charge
n4:271B532A-363D-11E5-9242-09173F13E4C5
n3:Rule-of-Five
n4:271B532D-363D-11E5-9242-09173F13E4C5
n3:Traditional-IUPAC-Name
n4:271B531B-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-acidic-
n4:271B5328-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-basic-
n4:271B5329-363D-11E5-9242-09173F13E4C5