Values CatLog read from this paper

Identification of rat and human cytochrome p450 isoforms and a rat serum esterase that metabolize the pyrethroid insecticides deltamethrin and esfenvalerate

PMID 17576809doi:10.1124/dmd.107.015388Open in Browse

The paper itself is not on this site: read it at the publisher. This page lists only the values CatLog read from it.

CatLog read 12 records (25 values) from this paper: CYP2C11, CYP2C19, CYP2C6 and 4 more from Rattus norvegicus, Homo sapiens.

Read from the paper by an AI model and checked against the paper by a second, separate AI run; code converted the units. Values are in CatLog's units; each record opens in Browse with the line the paper prints and the checks. CatLog calculated the 11 kcat/Km values marked “calc.” from kcat and Km; no printed kcat/Km was read for those records.

EC 1.14.14.1, EC 1.14.14.51, EC 1.14.14.52, EC 1.14.14.53, EC 1.14.14.75, EC 3.1.1.1

Records read from this paper
EnzymeOrganismSubstratekcat (s⁻¹)Km (mM)kcat/Km (mM⁻¹ s⁻¹)ConditionsOpen record
CYP2C11Rattus norvegicus(alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate3.430.0319108 calc.pH 7.4, 37 °COpen record: CYP2C11, (alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate
CYP2C11Rattus norvegicus(alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate3.6570.0335109 calc.pH 7.4, 37 °COpen record: CYP2C11, (alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate
CYP2C19Homo sapiens(alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate1.0270.009110 calc.pH 7.4, 37 °COpen record: CYP2C19, (alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate
CYP2C19Homo sapiens(alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate1.0730.0041260 calc.pH 7.4, 37 °COpen record: CYP2C19, (alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate
CYP2C6Rattus norvegicus(alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate2.50.0216120 calc.pH 7.4, 37 °COpen record: CYP2C6, (alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate
CYP2C6Rattus norvegicus(alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate2.6370.038269.0 calc.pH 7.4, 37 °COpen record: CYP2C6, (alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate
CYP2C8Homo sapiens(alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate0.7120.010269.8 calc.pH 7.4, 37 °COpen record: CYP2C8, (alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate
CYP2C8Homo sapiens(alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate0.9870.019151.7 calc.pH 7.4, 37 °COpen record: CYP2C8, (alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate
CYP2C9*1Homo sapiens(alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate1.330.024354.7 calc.pH 7.4, 37 °COpen record: CYP2C9*1, (alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate
CYP3A2Rattus norvegicus(alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate0.4320.006467 calc.pH 7.4, 37 °COpen record: CYP3A2, (alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate
CYP3A2Rattus norvegicus(alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate0.6580.0043150 calc.pH 7.4, 37 °COpen record: CYP3A2, (alphaS)-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate
serum carboxylesterase (CE)Rattus norvegicus(alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate0.0080.01260.63pH 7.4, 37 °COpen record: serum carboxylesterase (CE), (alphaS)-cyano-3-phenoxybenzyl (1R, 3R)-cis-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropane carboxylate