Interactions between Xenobiotics and DME (XEOTIC)
|
Fungicide(s), Herbicide(s) or Insecticide(s) |
Herbicide |
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|
Diuron |
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Induction |
XEOTIC ID |
XEO00973
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Herbicide |
DME Modulation |
Diuron up-regulates the expression of DME AKR1C3 |
[1] |
Pesticide/Insecticide |
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|
Dicrotophos |
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Inhibition |
XEOTIC ID |
XEO01050
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Pesticide/Insecticide |
DME Modulation |
Dicrotophos inhibits the expression of DME AKR1C3 |
[2] |
Health or Environmental Toxicant(s) |
Acute Toxic Substance |
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|
2-butenal |
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Induction |
XEOTIC ID |
XEO01122
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Acute Toxic Substance |
DME Modulation |
2-butenal up-regulates the expression of DME AKR1C3 |
[3] |
Cadmium |
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Induction |
XEOTIC ID |
XEO01503
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Acute Toxic Substance |
DME Modulation |
Cadmium up-regulates the expression of DME AKR1C3 |
[4] |
Formaldehyde |
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Induction |
XEOTIC ID |
XEO01305
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Acute Toxic Substance |
DME Modulation |
Formaldehyde up-regulates the expression of DME AKR1C3 |
[5] |
Ochratoxin A |
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Inhibition |
XEOTIC ID |
XEO01407
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Acute Toxic Substance |
DME Modulation |
Ochratoxin A inhibits the drug-metabolizing activity of DME AKR1C3 |
[6] |
Carcinogen |
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|
Benzo(a)pyrene |
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Induction |
XEOTIC ID |
XEO00898
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Carcinogen |
DME Modulation |
Benzo(a)pyrene up-regulates the expression of DME AKR1C3 |
[7] |
Environmental Pollutant |
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|
Antimony potassium tartrate |
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Induction |
XEOTIC ID |
XEO01201
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Environmental Pollutant |
DME Modulation |
Antimony potassium tartrate induces the drug-metabolizing activity of DME AKR1C3 |
[8] |
Hexyl cinnamic aldehyde |
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Induction |
XEOTIC ID |
XEO00985
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Environmental Pollutant |
DME Modulation |
Hexyl cinnamic aldehyde up-regulates the expression of DME AKR1C3 |
[9] |
Health Hazard/Toxicant |
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|
N-hexane |
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Induction |
XEOTIC ID |
XEO01016
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Health and Environmental Toxicant |
DME Modulation |
N-hexane up-regulates the expression of DME AKR1C3 |
[10] |
Glycidamide |
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Induction |
XEOTIC ID |
XEO01009
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Health Hazard |
DME Modulation |
Glycidamide up-regulates the expression of DME AKR1C3 |
[11] |
Natural Product(s), Extract(s) or Medicine(s) |
Natural Mixture |
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|
Particulate matter |
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Induction |
XEOTIC ID |
XEO00919
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Mixture |
DME Modulation |
Particulate matter induces the drug-metabolizing activity of DME AKR1C3 |
[12] |
Natural Product |
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|
2'-hydroxyflavanone |
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Inhibition |
XEOTIC ID |
XEO01127
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Product |
DME Modulation |
2'-hydroxyflavanone inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 0.1 microM) |
[13] |
7-hydroxycoumarin |
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Induction |
XEOTIC ID |
XEO01174
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Product |
DME Modulation |
7-hydroxycoumarin induces the drug-metabolizing activity of DME AKR1C3 |
[14] |
7-hydroxyflavone |
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Inhibition |
XEOTIC ID |
XEO01176
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Product |
DME Modulation |
7-hydroxyflavone inhibits the drug-metabolizing activity of DME AKR1C3 |
[15] |
Octyl gallate |
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Inhibition |
XEOTIC ID |
XEO01408
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Product |
DME Modulation |
Octyl gallate inhibits the drug-metabolizing activity of DME AKR1C3 |
[16] |
Traditional Medicine |
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|
Jinfukang |
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Induction |
XEOTIC ID |
XEO00760
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Traditional Medicine |
DME Modulation |
Jinfukang up-regulates the expression of DME AKR1C3 |
[17] |
Pharmaceutical Agent(s) |
Approved/Marketed Drug |
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|
Acetaminophen |
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Inhibition |
XEOTIC ID |
XEO00217
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Acetaminophen inhibits the expression of DME AKR1C3 |
[18] |
Arsenic trioxide |
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Induction |
XEOTIC ID |
XEO00339
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Arsenic trioxide up-regulates the expression of DME AKR1C3 |
[19] |
Aspirin |
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Inhibition |
XEOTIC ID |
XEO00213
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Aspirin inhibits the drug-metabolizing activity of DME AKR1C3 |
[20] |
Avobenzone |
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Induction |
XEOTIC ID |
XEO00411
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Avobenzone up-regulates the expression of DME AKR1C3 |
[21] |
Bexarotene |
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Induction |
XEOTIC ID |
XEO00144
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Bexarotene up-regulates the expression of DME AKR1C3 |
[22] |
Bortezomib |
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Induction |
XEOTIC ID |
XEO00159
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Bortezomib up-regulates the expression of DME AKR1C3 |
[23] |
Cisplatin |
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Induction |
XEOTIC ID |
XEO00334
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Cisplatin induces the drug-metabolizing activity of DME AKR1C3 |
[24] |
Copper sulfate |
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Induction |
XEOTIC ID |
XEO00117
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Copper sulfate up-regulates the expression of DME AKR1C3 |
[25] |
Cyclosporine |
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Inhibition |
XEOTIC ID |
XEO00241
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Cyclosporine inhibits the expression of DME AKR1C3 |
[26] |
Dasatinib |
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Induction |
XEOTIC ID |
XEO00181
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Dasatinib up-regulates the expression of DME AKR1C3 |
[27] |
Desogestrel |
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Inhibition |
XEOTIC ID |
XEO00432
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Desogestrel inhibits the drug-metabolizing activity of DME AKR1C3 |
[28] |
Dexamethasone |
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Induction |
XEOTIC ID |
XEO00088
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Dexamethasone up-regulates the expression of DME AKR1C3 |
[29] |
Diazepam |
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Inhibition |
XEOTIC ID |
XEO00024
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Diazepam inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 84 microM) |
[30], [31] |
Disulfiram |
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Induction |
XEOTIC ID |
XEO00028
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Disulfiram up-regulates the expression of DME AKR1C3 |
[9] |
Doxorubicin hydrochloride |
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Inhibition |
XEOTIC ID |
XEO00292
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Doxorubicin hydrochloride inhibits the expression of DME AKR1C3 |
[32] |
Dutasteride |
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Induction |
XEOTIC ID |
XEO00192
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Dutasteride up-regulates the expression of DME AKR1C3 |
[33] |
Dydrogesterone |
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Inhibition |
XEOTIC ID |
XEO00403
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Dydrogesterone inhibits the drug-metabolizing activity of DME AKR1C3 |
[28] |
Estazolam |
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Inhibition |
XEOTIC ID |
XEO00031
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Estazolam inhibits the drug-metabolizing activity of DME AKR1C3 |
[31] |
Estradiol |
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Inhibition |
XEOTIC ID |
XEO00090
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Estradiol inhibits the expression of DME AKR1C3 |
[34], [35] |
Flurbiprofen sodium |
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Inhibition |
XEOTIC ID |
XEO00296
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Flurbiprofen sodium inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 1.56 microM) |
[13] |
Glimepiride |
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Inhibition |
XEOTIC ID |
XEO00043
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Glimepiride inhibits the drug-metabolizing activity of DME AKR1C3 |
[36] |
Glipizide |
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Inhibition |
XEOTIC ID |
XEO00044
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Glipizide inhibits the drug-metabolizing activity of DME AKR1C3 |
[36] |
Glyburide |
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Inhibition |
XEOTIC ID |
XEO00247
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Glyburide inhibits the drug-metabolizing activity of DME AKR1C3 |
[36] |
Hydrogen peroxide |
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Induction |
XEOTIC ID |
XEO00388
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Hydrogen peroxide induces the drug-metabolizing activity of DME AKR1C3 |
[14] |
Ibuprofen |
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Inhibition |
XEOTIC ID |
XEO00248
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Ibuprofen inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 32.7 microM) |
[13] |
Indomethacin |
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Inhibition |
XEOTIC ID |
XEO00047
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Indomethacin inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 0.1 microM) |
[37] |
Levonorgestrel |
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Inhibition |
XEOTIC ID |
XEO00113
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Levonorgestrel inhibits the drug-metabolizing activity of DME AKR1C3 |
[28] |
Meclofenamic acid |
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Inhibition |
XEOTIC ID |
XEO00415
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Meclofenamic acid inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 0.54 microM) |
[13] |
Medroxyprogesterone acetate |
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Inhibition |
XEOTIC ID |
XEO00743
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Medroxyprogesterone acetate inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 0.28 microM) |
[38] |
Naproxen |
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Inhibition |
XEOTIC ID |
XEO00156
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Naproxen inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 0.48 microM) |
[39] |
Progesterone |
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Inhibition |
XEOTIC ID |
XEO00094
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Progesterone inhibits the expression of DME AKR1C3 |
[40] |
Simvastatin |
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Inhibition |
XEOTIC ID |
XEO00125
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Simvastatin inhibits the expression of DME AKR1C3 |
[41] |
Sulindac |
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Inhibition |
XEOTIC ID |
XEO00177
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Sulindac inhibits the drug-metabolizing activity of DME AKR1C3 |
[42] |
Urethane |
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Inhibition |
XEOTIC ID |
XEO00435
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Urethane inhibits the expression of DME AKR1C3 |
[43] |
Vorinostat |
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Inhibition |
XEOTIC ID |
XEO00079
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Vorinostat inhibits the expression of DME AKR1C3 |
[44], [45] |
Benzbromarone |
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Inhibition |
XEOTIC ID |
XEO00492
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Benzbromarone inhibits the drug-metabolizing activity of DME AKR1C3 |
[30] |
Benzoic acid |
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Induction |
XEOTIC ID |
XEO00447
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Benzoic acid up-regulates the expression of DME AKR1C3 |
[9] |
Bromazepam |
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Inhibition |
XEOTIC ID |
XEO00458
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Bromazepam inhibits the drug-metabolizing activity of DME AKR1C3 |
[31] |
Cloxazolam |
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Inhibition |
XEOTIC ID |
XEO01258
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Cloxazolam inhibits the drug-metabolizing activity of DME AKR1C3 (Ki = 1.5 microM) |
[30], [31] |
Flufenamic acid |
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Inhibition |
XEOTIC ID |
XEO00470
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Flufenamic acid inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 0.05 microM) |
[46] |
Flunitrazepam |
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Inhibition |
XEOTIC ID |
XEO00498
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Flunitrazepam inhibits the drug-metabolizing activity of DME AKR1C3 |
[31] |
Gliclazide |
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Inhibition |
XEOTIC ID |
XEO00500
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Gliclazide inhibits the drug-metabolizing activity of DME AKR1C3 |
[36] |
Gliquidone |
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Inhibition |
XEOTIC ID |
XEO00501
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Gliquidone inhibits the drug-metabolizing activity of DME AKR1C3 |
[36] |
Glycyrrhetinic acid |
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Inhibition |
XEOTIC ID |
XEO01319
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Glycyrrhetinic acid inhibits the drug-metabolizing activity of DME AKR1C3 |
[30] |
Hexestrol |
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Inhibition |
XEOTIC ID |
XEO00769
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Hexestrol inhibits the drug-metabolizing activity of DME AKR1C3 |
[30] |
Drug in Phase 3 Clinical Trial |
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|
Dinaciclib |
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Inhibition |
XEOTIC ID |
XEO00678
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 3 |
DME Modulation |
Dinaciclib inhibits the drug-metabolizing activity of DME AKR1C3 |
[47] |
NVP-BKM120 |
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Inhibition |
XEOTIC ID |
XEO00675
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 3 |
DME Modulation |
NVP-BKM120 inhibits the drug-metabolizing activity of DME AKR1C3 |
[31] |
Seocalcitol |
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Induction |
XEOTIC ID |
XEO00652
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 3 |
DME Modulation |
Seocalcitol induces the drug-metabolizing activity of DME AKR1C3 |
[48], [49] |
Triclosan |
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Inhibition |
XEOTIC ID |
XEO00560
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 3 |
DME Modulation |
Triclosan inhibits the expression of DME AKR1C3 |
[50] |
Drug in Phase 2 Clinical Trial |
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|
Butyric acid |
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Induction |
XEOTIC ID |
XEO01230
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 2/3 |
DME Modulation |
Butyric acid up-regulates the expression of DME AKR1C3 |
[7] |
Colforsin |
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Inhibition |
XEOTIC ID |
XEO00606
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 2 |
DME Modulation |
Colforsin inhibits the expression of DME AKR1C3 |
[51] |
Drug in Phase 1 Clinical Trial |
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|
Tolfenamic acid |
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Inhibition |
XEOTIC ID |
XEO00556
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 1/2 |
DME Modulation |
Tolfenamic acid inhibits the drug-metabolizing activity of DME AKR1C3 (Ki = 0.008 microM) |
[52] |
Dinitrochlorobenzene |
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Induction |
XEOTIC ID |
XEO00571
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 1 |
DME Modulation |
Dinitrochlorobenzene up-regulates the expression of DME AKR1C3 |
[9] |
Naringenin |
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Inhibition |
XEOTIC ID |
XEO00573
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 1 |
DME Modulation |
Naringenin inhibits the drug-metabolizing activity of DME AKR1C3 |
[53] |
Phenethyl caffeate |
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Inhibition |
XEOTIC ID |
XEO01233
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 1 |
DME Modulation |
Phenethyl caffeate inhibits the drug-metabolizing activity of DME AKR1C3 (IC50 = 1.7 microM) |
[52] |
Sodium arsenite |
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Induction |
XEOTIC ID |
XEO00632
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 1 |
DME Modulation |
Sodium arsenite induces the drug-metabolizing activity of DME AKR1C3 |
[54], [55] |
Trichostatin A |
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Induction |
XEOTIC ID |
XEO01492
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 1 |
DME Modulation |
Trichostatin A up-regulates the expression of DME AKR1C3 |
[56] |
Preclinical/Patented Drug |
Click to Show/Hide the Full List of Xenobiotics: 3 Xenobiotics
|
Eugenol |
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Induction |
XEOTIC ID |
XEO00885
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Patented Pharmaceutical Agent |
DME Modulation |
Eugenol up-regulates the expression of DME AKR1C3 |
[9] |
GSK-J4 |
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Inhibition |
XEOTIC ID |
XEO01324
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Patented Pharmaceutical Agent |
DME Modulation |
GSK-J4 inhibits the expression of DME AKR1C3 |
[57] |
ICG-001 |
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Inhibition |
XEOTIC ID |
XEO01336
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Patented Pharmaceutical Agent |
DME Modulation |
ICG-001 inhibits the expression of DME AKR1C3 |
[58] |
Investigative Agent |
Click to Show/Hide the Full List of Xenobiotics: 6 Xenobiotics
|
4-hydroxy-2-nonenal |
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Induction |
XEOTIC ID |
XEO00869
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Investigative Agent |
DME Modulation |
4-hydroxy-2-nonenal induces the drug-metabolizing activity of DME AKR1C3 |
[14] |
9,10-phenanthrenequinone |
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Induction |
XEOTIC ID |
XEO00871
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Investigative Agent |
DME Modulation |
9,10-phenanthrenequinone induces the drug-metabolizing activity of DME AKR1C3 |
[59] |
Beta-naphthoflavone |
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Induction |
XEOTIC ID |
XEO01220
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Investigative Agent |
DME Modulation |
Beta-naphthoflavone up-regulates the expression of DME AKR1C3 |
[60] |
Isopropanol |
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Induction |
XEOTIC ID |
XEO01128
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Investigative Agent |
DME Modulation |
Isopropanol up-regulates the expression of DME AKR1C3 |
[9] |
MG-132 |
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Induction |
XEOTIC ID |
XEO01219
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Investigative Agent |
DME Modulation |
MG-132 up-regulates the expression of DME AKR1C3 |
[23], [24] |
Phenylmercuric acetate |
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Induction |
XEOTIC ID |
XEO00818
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Investigative Agent |
DME Modulation |
Phenylmercuric acetate up-regulates the expression of DME AKR1C3 and leads to increasing the drug-metabolizing activity of this enzyme |
[61], [62] |
Other Chemical Compound(s) or Element(s) |
Chemical Compound |
Click to Show/Hide the Full List of Xenobiotics: 2 Xenobiotics
|
1,10-phenanthroline |
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Inhibition |
XEOTIC ID |
XEO00766
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Chemical Compound |
DME Modulation |
1,10-phenanthroline inhibits the drug-metabolizing activity of DME AKR1C3 |
[30] |
Gold |
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Induction |
XEOTIC ID |
XEO01504
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Chemical Compound |
DME Modulation |
Gold up-regulates the expression of DME AKR1C3 |
[63] |
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