This HTML5 document contains 40 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
n2http://linked.opendata.cz/resource/drugbank/drug/
dctermshttp://purl.org/dc/terms/
n6http://linked.opendata.cz/resource/drugbank/drug/DB02556/identifier/chebi/
n11http://bio2rdf.org/drugbank:
admshttp://www.w3.org/ns/adms#
n12http://linked.opendata.cz/resource/drugbank/drug/DB02556/identifier/pdb/
n13http://linked.opendata.cz/resource/drugbank/drug/DB02556/identifier/kegg-compound/
n10http://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#
n3http://linked.opendata.cz/ontology/drugbank/
n4http://linked.opendata.cz/resource/drugbank/property/
xsdhhttp://www.w3.org/2001/XMLSchema#
n7http://linked.opendata.cz/resource/drugbank/drug/DB02556/identifier/drugbank/

Statements

Subject Item
n2:DB02556
rdf:type
n3:Drug
n3:description
An essential aromatic amino acid that is a precursor of melanin; dopamine; noradrenalin (norepinephrine), and thyroxine. [PubChem]
n3:generalReferences
# Yanagida O, Kanai Y, Chairoungdua A, Kim DK, Segawa H, Nii T, Cha SH, Matsuo H, Fukushima J, Fukasawa Y, Tani Y, Taketani Y, Uchino H, Kim JY, Inatomi J, Okayasu I, Miyamoto K, Takeda E, Goya T, Endou H: Human L-type amino acid transporter 1 (LAT1): characterization of function and expression in tumor cell lines. Biochim Biophys Acta. 2001 Oct 1;1514(2):291-302. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/11557028
n3:group
experimental
owl:sameAs
n10:DB02556 n11:DB02556
dcterms:title
D-Phenylalanine
adms:identifier
n6:16998 n7:DB02556 n12:DPN n13:C02265
n3:synthesisReference
Dennis P. Bauer, "Process for producing N-acyl-D-phenylalanine ester." U.S. Patent US4262092, issued November, 1977.
n3:IUPAC-Name
n4:271B425D-363D-11E5-9242-09173F13E4C5
n3:InChI
n4:271B4263-363D-11E5-9242-09173F13E4C5
n3:Molecular-Formula
n4:271B4262-363D-11E5-9242-09173F13E4C5
n3:Molecular-Weight
n4:271B425F-363D-11E5-9242-09173F13E4C5
n3:Monoisotopic-Weight
n4:271B4260-363D-11E5-9242-09173F13E4C5
n3:SMILES
n4:271B4261-363D-11E5-9242-09173F13E4C5
n3:Water-Solubility
n4:271B425B-363D-11E5-9242-09173F13E4C5 n4:271B4273-363D-11E5-9242-09173F13E4C5
n3:logP
n4:271B4259-363D-11E5-9242-09173F13E4C5 n4:271B425C-363D-11E5-9242-09173F13E4C5
n3:logS
n4:271B425A-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Acceptor-Count
n4:271B4269-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Donor-Count
n4:271B426A-363D-11E5-9242-09173F13E4C5
n3:InChIKey
n4:271B4264-363D-11E5-9242-09173F13E4C5
n3:Polar-Surface-Area--PSA-
n4:271B4265-363D-11E5-9242-09173F13E4C5
n3:Polarizability
n4:271B4267-363D-11E5-9242-09173F13E4C5
n3:Refractivity
n4:271B4266-363D-11E5-9242-09173F13E4C5
n3:Rotatable-Bond-Count
n4:271B4268-363D-11E5-9242-09173F13E4C5
n3:casRegistryNumber
673-06-3
n3:Bioavailability
n4:271B426F-363D-11E5-9242-09173F13E4C5
n3:Ghose-Filter
n4:271B4271-363D-11E5-9242-09173F13E4C5
n3:MDDR-Like-Rule
n4:271B4272-363D-11E5-9242-09173F13E4C5
n3:Number-of-Rings
n4:271B426E-363D-11E5-9242-09173F13E4C5
n3:Physiological-Charge
n4:271B426D-363D-11E5-9242-09173F13E4C5
n3:Rule-of-Five
n4:271B4270-363D-11E5-9242-09173F13E4C5
n3:Traditional-IUPAC-Name
n4:271B425E-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-acidic-
n4:271B426B-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-basic-
n4:271B426C-363D-11E5-9242-09173F13E4C5