Local view for "https://dbmi-icode-01.dbmi.pitt.edu/dikb/resource/Evidence/462"
Predicate | Value (sorted: default) |
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rdfs:label | |
rdf:type | |
?:Evidence_assump_list_id |
"87"
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?:Evidence_enzyme_system | |
?:Evidence_type | |
?:claim_assumed_valid_for_evidence_application_evidence_1796 | |
?:content |
"Enzyme system: human liver microsomes
NADPH added: yes
inhibitor used: sulphaphenazole
reaction: haloperidol --> 4-(4-chlorophenyl)-4-hydroxypiperidine
Quote: Ketoconazole was a potent inhibitor of CPHP (4-(4-chlorophenyl)-4-hydroxypiperidine) formation with IC50 values of 0,10, 0,23 and 0,14 micM in microsomes HL-1, HL-6 and HL-9 respectively, wheras sulphaphenazole, furafylline and quinidine showed little inhibition (IC50 > 100micM)"
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dc:creator | |
dc:date | |
rdfs:seeAlso |
All properties reside in the graph file:///home/swish/src/ClioPatria/guidelines/dikb.ttl
The resource appears as object in one triple:
{ cyp2c9_controls_formation_of_4-(4-chlorophenyl)-4-hydroxypiperidine, <http://purl.org/swan/1.2/swan-commons#citesAsRefutingEvidence>, evidence_1796 }