General Information of the Protein
Protein ID
PT02795
Protein Name
Cytochrome P450 2J2
Secondarily
Protein Name
Albendazole monooxygenase (hydroxylating)
Albendazole monooxygenase (sulfoxide-forming)
Arachidonic acid epoxygenase
CYPIIJ2
Hydroperoxy icosatetraenoate isomerase
Gene Name
CYP2J2
Sequence
MLAAMGSLAAALWAVVHPRTLLLGTVAFLLAADFLKRRRPKNYPPGPWRLPFLGNFFLVDFEQSHLEVQLFVKKYGNLFSLELGDISAVLITGLPLIKEALIHMDQNFGNRPVTPMREHIFKKNGLIMSSGQAWKEQRRFTLTALRNFGLGKKSLEERIQEEAQHLTEAIKEENGQPFDPHFKINNAVSNIICSITFGERFEYQDSWFQQLLKLLDEVTYLEASKTCQLYNVFPWIMKFLPGPHQTLFSNWKKLKLFVSHMIDKHRKDWNPAETRDFIDAYLKEMSKHTGNPTSSFHEENLICSTLDLFFAGTETTSTTLRWALLYMALYPEIQEKVQAEIDRVIGQGQQPSTAARESMPYTNAVIHEVQRMGNIIPLNVPREVTVDTTLAGYHLPKGTMILTNLTALHRDPTEWATPDTFNPDHFLENGQFKKREAFMPFSIGKRACLGEQLARTELFIFFTSLMQKFTFRPPNNEKLSLKFRMGITISPVSHRLCAVPQV
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Organism
Homo sapiens, Human
Protein Classification
Enzyme
Function
A cytochrome P450 monooxygenase involved in the metabolism of polyunsaturated fatty acids (PUFA) in the cardiovascular system (PubMed:8631948, PubMed:19965576). Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (NADPH--hemoprotein reductase) (PubMed:8631948, PubMed:19965576). Catalyzes the epoxidation of double bonds of PUFA (PubMed:8631948, PubMed:19965576). Converts arachidonic acid to four regioisomeric epoxyeicosatrienoic acids (EpETrE), likely playing a major role in the epoxidation of endogenous cardiac arachidonic acid pools (PubMed:8631948). In endothelial cells, participates in eicosanoids metabolism by converting hydroperoxide species into hydroxy epoxy metabolites. In combination with 15-lipoxygenase metabolizes arachidonic acid and converts hydroperoxyicosatetraenoates (HpETEs) into hydroxy epoxy eicosatrienoates (HEETs), which are precursors of vasodilatory trihydroxyicosatrienoic acids (THETAs). This hydroperoxide isomerase activity is NADPH- and O2-independent (PubMed:19737933). Catalyzes the monooxygenation of a various xenobiotics, such as danazol, amiodarone, terfenadine, astemizole, thioridazine, tamoxifen, cyclosporin A and nabumetone (PubMed:19923256). Catalyzes hydroxylation of the anthelmintics albendazole and fenbendazole (PubMed:23959307). Catalyzes the sulfoxidation of fenbedazole (PubMed:19923256).
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Uniprot ID
Primary ID:
P51589

Secondarily ID:
B2RD33
Q8TF13
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HGNC ID
HGNC:2634
Subcellular Location
Endoplasmic reticulum membrane
Microsome membrane
Map of Molecular Bioactivity Related to the Protein
Map of Molecular Bioactivity Related to the Protein

Protein
Cell Line
Compound

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Protein
Cell Line ID: CL000013 , Sf9
Compound ID Compound Name Compound Formula
CP0179568
1-(4-allylphenyl)-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butan-1-one
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C31H35NO2
 1
1
IC50 = 400 nM
   TI
   LI
   LO
   TS
CP0205283
4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)-1-(4-propylphenyl)butan-1-one
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C31H37NO2
 2
1
IC50 = 400 nM
   TI
   LI
   LO
   TS
2
Ki = 160 nM
   TI
   LI
   LO
   TS
CP0514374
1-(4-ethylphenyl)-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butan-1-one
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C30H35NO2
 1
1
IC50 = 600 nM
   TI
   LI
   LO
   TS
CP0024490
1-(4-tert-butylphenyl)-4-[4-[hydroxy(diphenyl)methyl]piperidin-1-yl]butan-1-one
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C32H39NO2
 1
1
IC50 = 700 nM
   TI
   LI
   LO
   TS
CP0432828
1-(4-butylphenyl)-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butan-1-one
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C32H39NO2
 1
1
IC50 = 700 nM
   TI
   LI
   LO
   TS
CP0509467
4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)-1-p-tolylbutan-1-one
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C29H33NO2
 1
1
IC50 = 700 nM
   TI
   LI
   LO
   TS
CP0432827
4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)-1-(4-(2-hydroxyethyl)phenyl)butan-1-one
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C30H35NO3
 1
1
IC50 = 1300 nM
   TI
   LI
   LO
   TS
CP0538456
4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)-1-(4-(3-hydroxypropyl)phenyl)butan-1-one
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C31H37NO3
 1
1
IC50 = 1900 nM
   TI
   LI
   LO
   TS
CP0559382
1-(4-(2,2-difluoroethyl)phenyl)-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butan-1-one
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C30H33F2NO2
 1
1
IC50 = 2200 nM
   TI
   LI
   LO
   TS
CP0436965
3-(4-(4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butanoyl)phenyl)propyl acetate
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C33H39NO4
 1
1
IC50 = 2500 nM
   TI
   LI
   LO
   TS
CP0456525
1-(4-bromophenyl)-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butan-1-one
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C28H30BrNO2
 1
1
IC50 = 4200 nM
   TI
   LI
   LO
   TS
CP0522974
1-(benzo[d][1,3]dioxol-5-yl)-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butan-1-one
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C29H31NO4
 1
1
IC50 = 6700 nM
   TI
   LI
   LO
   TS
CP0459774
4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)-1-(4-methoxyphenyl)butan-1-one
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C29H33NO3
 1
1
IC50 = 7600 nM
   TI
   LI
   LO
   TS
CP0033565
(+/-)1-(4-tert-butylphenyl)-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butan-1-ol
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C32H41NO2
 1
1
IC50 = 8100 nM
   TI
   LI
   LO
   TS