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Namespace Prefixes

PrefixIRI
n2http://linked.opendata.cz/resource/drugbank/drug/
dctermshttp://purl.org/dc/terms/
n9http://linked.opendata.cz/resource/drugbank/drug/DB04628/identifier/pubchem-substance/
n13http://linked.opendata.cz/resource/mesh/concept/
n4http://linked.opendata.cz/resource/drugbank/drug/DB04628/identifier/drugbank/
n17http://bio2rdf.org/drugbank:
n6http://linked.opendata.cz/resource/drugbank/drug/DB04628/identifier/chemspider/
admshttp://www.w3.org/ns/adms#
n15http://wifo5-03.informatik.uni-mannheim.de/drugbank/resource/drugs/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n12http://linked.opendata.cz/ontology/mesh/
owlhttp://www.w3.org/2002/07/owl#
n7http://linked.opendata.cz/ontology/drugbank/
n8http://linked.opendata.cz/resource/drugbank/property/
n5http://linked.opendata.cz/resource/drugbank/drug/DB04628/identifier/kegg-compound/
n10http://linked.opendata.cz/resource/drugbank/drug/DB04628/identifier/pdb/
xsdhhttp://www.w3.org/2001/XMLSchema#
n11http://linked.opendata.cz/resource/drugbank/drug/DB04628/identifier/pubchem-compound/

Statements

Subject Item
n2:DB04628
rdf:type
n7:Drug
n7:description
Allosamidin exhibits extremely potent inhibitory activity against chitinases from a number of sources, particularly from <i>Candida albicans</i>, and can be utilized as potent antifungal agent.
n7:group
experimental
owl:sameAs
n15:DB04628 n17:DB04628
dcterms:title
Allosamidin
adms:identifier
n4:DB04628 n5:C05346 n6:10670675 n9:46506500 n10:AO3 n11:119339
n7:synonym
NAA-(1-4)NAA-(1-4)AMI Allosamidine
n12:hasConcept
n13:M0154700
n7:IUPAC-Name
n8:271B4499-363D-11E5-9242-09173F13E4C5
n7:InChI
n8:271B449F-363D-11E5-9242-09173F13E4C5
n7:Molecular-Formula
n8:271B449E-363D-11E5-9242-09173F13E4C5
n7:Molecular-Weight
n8:271B449B-363D-11E5-9242-09173F13E4C5
n7:Monoisotopic-Weight
n8:271B449C-363D-11E5-9242-09173F13E4C5
n7:SMILES
n8:271B449D-363D-11E5-9242-09173F13E4C5
n7:Water-Solubility
n8:271B4497-363D-11E5-9242-09173F13E4C5
n7:logP
n8:271B4495-363D-11E5-9242-09173F13E4C5 n8:271B4498-363D-11E5-9242-09173F13E4C5
n7:logS
n8:271B4496-363D-11E5-9242-09173F13E4C5
n7:H-Bond-Acceptor-Count
n8:271B44A5-363D-11E5-9242-09173F13E4C5
n7:H-Bond-Donor-Count
n8:271B44A6-363D-11E5-9242-09173F13E4C5
n7:InChIKey
n8:271B44A0-363D-11E5-9242-09173F13E4C5
n7:Polar-Surface-Area--PSA-
n8:271B44A1-363D-11E5-9242-09173F13E4C5
n7:Polarizability
n8:271B44A3-363D-11E5-9242-09173F13E4C5
n7:Refractivity
n8:271B44A2-363D-11E5-9242-09173F13E4C5
n7:Rotatable-Bond-Count
n8:271B44A4-363D-11E5-9242-09173F13E4C5
n7:casRegistryNumber
103782-08-7
n7:category
n7:Bioavailability
n8:271B44AB-363D-11E5-9242-09173F13E4C5
n7:Ghose-Filter
n8:271B44AD-363D-11E5-9242-09173F13E4C5
n7:MDDR-Like-Rule
n8:271B44AE-363D-11E5-9242-09173F13E4C5
n7:Number-of-Rings
n8:271B44AA-363D-11E5-9242-09173F13E4C5
n7:Physiological-Charge
n8:271B44A9-363D-11E5-9242-09173F13E4C5
n7:Rule-of-Five
n8:271B44AC-363D-11E5-9242-09173F13E4C5
n7:Traditional-IUPAC-Name
n8:271B449A-363D-11E5-9242-09173F13E4C5
n7:pKa--strongest-acidic-
n8:271B44A7-363D-11E5-9242-09173F13E4C5
n7:pKa--strongest-basic-
n8:271B44A8-363D-11E5-9242-09173F13E4C5