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Namespace Prefixes

PrefixIRI
n2http://linked.opendata.cz/resource/drugbank/drug/
dctermshttp://purl.org/dc/terms/
n12http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/chemspider/
n11http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/chebi/
n15http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/wikipedia/
n13http://bio2rdf.org/drugbank:
n17http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/pharmgkb/
admshttp://www.w3.org/ns/adms#
n18http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/pdb/
n8http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/kegg-compound/
n6http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/bindingdb/
n19http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/pubchem-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#
n16http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/pubchem-substance/
n3http://linked.opendata.cz/ontology/drugbank/
n4http://linked.opendata.cz/resource/drugbank/property/
n7http://linked.opendata.cz/resource/drugbank/drug/DB02010/identifier/drugbank/
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DB02010
rdf:type
n3:Drug
n3:description
An indolocarbazole that is a potent protein kinase C inhibitor which enhances cAMP-mediated responses in human neuroblastoma cells. (Biochem Biophys Res Commun 1995;214(3):1114-20)
n3:group
experimental
owl:sameAs
n10:DB02010 n13:DB02010
dcterms:title
Staurosporine
adms:identifier
n6:2579 n7:DB02010 n8:C02079 n11:15738 n12:5089 n15:Staurosporine n16:46504923 n17:PA165109623 n18:STO n19:44120114
n3:synthesisReference
Chikara Murakata, Toshimitsu Takiguchi, Shigeo Katsumata, Akira Mihara, Keiichi Takahashi, Hiromitsu Saito, Shiro Akinaga, Masami Okabe, Yutaka Saito, "Process for producing staurosporine derivatives." U.S. Patent US5344926, issued December, 1990.
n3:IUPAC-Name
n4:271B5C28-363D-11E5-9242-09173F13E4C5
n3:InChI
n4:271B5C2E-363D-11E5-9242-09173F13E4C5
n3:Molecular-Formula
n4:271B5C2D-363D-11E5-9242-09173F13E4C5
n3:Molecular-Weight
n4:271B5C2A-363D-11E5-9242-09173F13E4C5
n3:Monoisotopic-Weight
n4:271B5C2B-363D-11E5-9242-09173F13E4C5
n3:SMILES
n4:271B5C2C-363D-11E5-9242-09173F13E4C5
n3:Water-Solubility
n4:271B5C26-363D-11E5-9242-09173F13E4C5
n3:logP
n4:271B5C27-363D-11E5-9242-09173F13E4C5 n4:271B5C24-363D-11E5-9242-09173F13E4C5
n3:logS
n4:271B5C25-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Acceptor-Count
n4:271B5C34-363D-11E5-9242-09173F13E4C5
n3:H-Bond-Donor-Count
n4:271B5C35-363D-11E5-9242-09173F13E4C5
n3:InChIKey
n4:271B5C2F-363D-11E5-9242-09173F13E4C5
n3:Polar-Surface-Area--PSA-
n4:271B5C30-363D-11E5-9242-09173F13E4C5
n3:Polarizability
n4:271B5C32-363D-11E5-9242-09173F13E4C5
n3:Refractivity
n4:271B5C31-363D-11E5-9242-09173F13E4C5
n3:Rotatable-Bond-Count
n4:271B5C33-363D-11E5-9242-09173F13E4C5
n3:casRegistryNumber
62996-74-1
n3:Bioavailability
n4:271B5C3A-363D-11E5-9242-09173F13E4C5
n3:Ghose-Filter
n4:271B5C3C-363D-11E5-9242-09173F13E4C5
n3:MDDR-Like-Rule
n4:271B5C3D-363D-11E5-9242-09173F13E4C5
n3:Number-of-Rings
n4:271B5C39-363D-11E5-9242-09173F13E4C5
n3:Physiological-Charge
n4:271B5C38-363D-11E5-9242-09173F13E4C5
n3:Rule-of-Five
n4:271B5C3B-363D-11E5-9242-09173F13E4C5
n3:Traditional-IUPAC-Name
n4:271B5C29-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-acidic-
n4:271B5C36-363D-11E5-9242-09173F13E4C5
n3:pKa--strongest-basic-
n4:271B5C37-363D-11E5-9242-09173F13E4C5