Interactions between Xenobiotics and DME (XEOTIC)
|
Fungicide(s), Herbicide(s) or Insecticide(s) |
Herbicide |
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|
Oryzalin |
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Inhibition |
XEOTIC ID |
XEO00977
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Herbicide |
DME Modulation |
Oryzalin inhibits the drug-metabolizing activity of DME CA2 |
[1] |
Health or Environmental Toxicant(s) |
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 CA2 |
[2] |
Environmental Pollutant |
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|
2,6-di-tert-butylphenol |
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Inhibition |
XEOTIC ID |
XEO01115
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Environmental Pollutant |
DME Modulation |
2,6-di-tert-butylphenol inhibits the drug-metabolizing activity of DME CA2 (Ki = 0.51 microM) |
[3] |
Dimethyl amines |
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Inhibition |
XEOTIC ID |
XEO01005
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Environmental Pollutant |
DME Modulation |
Dimethyl amines inhibits the drug-metabolizing activity of DME CA2 |
[4] |
Health Hazard/Toxicant |
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|
1,2,4-triazole |
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Inhibition |
XEOTIC ID |
XEO01087
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Health Hazard |
DME Modulation |
1,2,4-triazole inhibits the drug-metabolizing activity of DME CA2 |
[5] |
Butyraldehyde |
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Induction |
XEOTIC ID |
XEO00999
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Health Hazard |
DME Modulation |
Butyraldehyde up-regulates the expression of DME CA2 |
[6] |
Chloric acid |
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Inhibition |
XEOTIC ID |
XEO01001
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Health Hazard |
DME Modulation |
Chloric acid inhibits the drug-metabolizing activity of DME CA2 (Ki = 850 microM) |
[7] |
Coumarin |
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Inhibition |
XEOTIC ID |
XEO00879
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Health Hazard |
DME Modulation |
Coumarin inhibits the drug-metabolizing activity of DME CA2 (Ki = 9.2 microM) |
[8] |
Lead |
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Inhibition |
XEOTIC ID |
XEO01505
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Health Hazard |
DME Modulation |
Lead inhibits the drug-metabolizing activity of DME CA2 |
[9] |
Natural Product(s), Extract(s) or Medicine(s) |
Natural Mixture |
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|
Flavonoids |
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Inhibition |
XEOTIC ID |
XEO00858
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Mixture |
DME Modulation |
Flavonoids inhibits the drug-metabolizing activity of DME CA2 |
[10] |
Natural Product |
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|
Anthocyanins |
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Inhibition |
XEOTIC ID |
XEO01522
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Product |
DME Modulation |
Anthocyanins inhibits the drug-metabolizing activity of DME CA2 |
[10] |
Malvidin-3-glucoside |
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Inhibition |
XEOTIC ID |
XEO01562
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Product |
DME Modulation |
Malvidin-3-glucoside inhibits the drug-metabolizing activity of DME CA2 |
[11] |
Synephrine |
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Inhibition |
XEOTIC ID |
XEO00908
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Natural Product |
DME Modulation |
Synephrine inhibits the drug-metabolizing activity of DME CA2 |
[12] |
Tunicamycin A |
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Inhibition |
XEOTIC ID |
XEO01494
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Natural Product |
DME Modulation |
Tunicamycin A inhibits the expression of DME CA2 |
[13], [14] |
Pharmaceutical Agent(s) |
Approved/Marketed Drug |
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|
Acetazolamide |
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Inhibition |
XEOTIC ID |
XEO00002
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Acetazolamide inhibits the drug-metabolizing activity of DME CA2 (IC50 < 0.01 microM) |
[15] |
Alitretinoin |
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Induction |
XEOTIC ID |
XEO00167
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Alitretinoin induces the drug-metabolizing activity of DME CA2 |
[16] |
Brinzolamide |
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Inhibition |
XEOTIC ID |
XEO00141
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Brinzolamide inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.0032 microM) |
[17] |
Calcitriol |
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Induction |
XEOTIC ID |
XEO00184
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Calcitriol up-regulates the expression of DME CA2 |
[18], [19] |
Celecoxib |
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Inhibition |
XEOTIC ID |
XEO00013
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Celecoxib inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.021 microM) |
[20] |
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 CA2 |
[21] |
Cyclophosphamide |
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Inhibition |
XEOTIC ID |
XEO00018
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Cyclophosphamide inhibits the expression of DME CA2 |
[22] |
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 CA2 |
[2] |
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 CA2 |
[23] |
Dichlorphenamide |
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Inhibition |
XEOTIC ID |
XEO00025
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Dichlorphenamide inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.038 microM) |
[24], [25] |
Diethylstilbestrol |
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Induction |
XEOTIC ID |
XEO00166
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Diethylstilbestrol up-regulates the expression of DME CA2 |
[26] |
Dorzolamide hydrochloride |
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Inhibition |
XEOTIC ID |
XEO00291
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Dorzolamide hydrochloride inhibits the drug-metabolizing activity of DME CA2 (IC50 < 0.002 microM) |
[27] |
Enalapril |
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Inhibition |
XEOTIC ID |
XEO00356
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Enalapril inhibits the drug-metabolizing activity of DME CA2 |
[28] |
Epinephrine |
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Induction |
XEOTIC ID |
XEO00265
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Epinephrine up-regulates the expression of DME CA2 |
[29] |
Estradiol |
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Induction |
XEOTIC ID |
XEO00090
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Estradiol up-regulates the expression of DME CA2 |
[30], [31] |
Ethinyl estradiol |
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Induction |
XEOTIC ID |
XEO00267
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Ethinyl estradiol up-regulates the expression of DME CA2 |
[32] |
Ethoxzolamide |
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Inhibition |
XEOTIC ID |
XEO00414
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Ethoxzolamide inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.0003 microM) |
[33] |
Furosemide |
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Inhibition |
XEOTIC ID |
XEO00040
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Furosemide inhibits the drug-metabolizing activity of DME CA2 (Ki = 0.065 microM) |
[34] |
Indomethacin |
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Induction |
XEOTIC ID |
XEO00047
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Indomethacin induces the drug-metabolizing activity of DME CA2 |
[35] |
Methazolamide |
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Inhibition |
XEOTIC ID |
XEO00061
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Methazolamide inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.0048 microM) |
[36] |
Progesterone |
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Inhibition |
XEOTIC ID |
XEO00094
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Progesterone inhibits the drug-metabolizing activity of DME CA2 |
[37] |
Propofol |
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Inhibition |
XEOTIC ID |
XEO00075
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Propofol inhibits the drug-metabolizing activity of DME CA2 (Ki = 19.5 microM) |
[3] |
Sulfonamide |
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Inhibition |
XEOTIC ID |
XEO00424
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Sulfonamide inhibits the drug-metabolizing activity of DME CA2 |
[38] |
Titanium dioxide |
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Induction |
XEOTIC ID |
XEO00425
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Titanium dioxide up-regulates the expression of DME CA2 |
[39], [40] |
Topiramate |
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Inhibition |
XEOTIC ID |
XEO00189
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Topiramate inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.005 microM) |
[25] |
Valdecoxib |
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Inhibition |
XEOTIC ID |
XEO00150
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Approved by US FDA |
DME Modulation |
Valdecoxib inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.043 microM) |
[24], [25] |
Valproic acid |
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Induction |
XEOTIC ID |
XEO00029
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Drug Approved by US FDA |
DME Modulation |
Valproic acid up-regulates the expression of DME CA2 |
[41] |
Sulpiride |
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Inhibition |
XEOTIC ID |
XEO00484
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug Marketed but not Approved by US FDA |
DME Modulation |
Sulpiride inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.04 microM) |
[25] |
Drug in Phase 3 Clinical Trial |
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|
Afimoxifene |
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Induction |
XEOTIC ID |
XEO00610
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 3 |
DME Modulation |
Afimoxifene up-regulates the expression of DME CA2 |
[42] |
Guaiacol |
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Inhibition |
XEOTIC ID |
XEO00566
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 3 |
DME Modulation |
Guaiacol inhibits the drug-metabolizing activity of DME CA2 (Ki = 2.94 microM) |
[3] |
Seocalcitol |
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Induction |
XEOTIC ID |
XEO00652
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 3 |
DME Modulation |
Seocalcitol up-regulates the expression of DME CA2 |
[43] |
Drug in Phase 2 Clinical Trial |
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|
Bisphenol A |
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Induction |
XEOTIC ID |
XEO01226
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 2 |
DME Modulation |
Bisphenol A up-regulates the expression of DME CA2 |
[31] |
Chalcone |
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Inhibition |
XEOTIC ID |
XEO01242
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 2 |
DME Modulation |
Chalcone inhibits the drug-metabolizing activity of DME CA2 |
[44] |
Genistein |
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Induction |
XEOTIC ID |
XEO00557
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 2 |
DME Modulation |
Genistein up-regulates the expression of DME CA2 |
[45] |
Indisulam |
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Inhibition |
XEOTIC ID |
XEO01387
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 2 |
DME Modulation |
Indisulam inhibits the drug-metabolizing activity of DME CA2 |
[46] |
Irosustat |
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Inhibition |
XEOTIC ID |
XEO00651
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 2 |
DME Modulation |
Irosustat inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.017 microM) |
[47] |
Drug in Phase 1 Clinical Trial |
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|
Butylated hydroxytoluene |
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Inhibition |
XEOTIC ID |
XEO00601
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 1 |
DME Modulation |
Butylated hydroxytoluene inhibits the drug-metabolizing activity of DME CA2 (Ki = 0.63 microM) |
[3] |
Dinitrochlorobenzene |
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Inhibition |
XEOTIC ID |
XEO00571
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Highest Clinical Status: Phase 1 |
DME Modulation |
Dinitrochlorobenzene inhibits the expression of DME CA2 |
[48] |
Quercetin |
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Induction |
XEOTIC ID |
XEO00538
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Highest Clinical Status: Phase 1 |
DME Modulation |
Quercetin induces the drug-metabolizing activity of DME CA2 |
[49] |
Preclinical/Patented Drug |
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|
STX140 |
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Inhibition |
XEOTIC ID |
XEO00716
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Drug in Preclinical Study |
DME Modulation |
STX140 inhibits the drug-metabolizing activity of DME CA2 (IC50 = 0.379 microM) |
[50], [51] |
Investigative Agent |
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|
Benzolamide |
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Inhibition |
XEOTIC ID |
XEO01216
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Investigative Agent |
DME Modulation |
Benzolamide inhibits the drug-metabolizing activity of DME CA2 (Ki = 0.009 microM) |
[52] |
Thioxolone |
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Inhibition |
XEOTIC ID |
XEO01486
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Investigative Agent |
DME Modulation |
Thioxolone inhibits the drug-metabolizing activity of DME CA2 (IC50 = 1.77 microM) |
[53] |
Other Chemical Compound(s) or Element(s) |
Chemical Compound |
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|
Iodate |
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Inhibition |
XEOTIC ID |
XEO00800
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Chemical Compound |
DME Modulation |
Iodate inhibits the drug-metabolizing activity of DME CA2 |
[7] |
Nitric acid |
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Inhibition |
XEOTIC ID |
XEO01017
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Chemical Compound |
DME Modulation |
Nitric acid inhibits the drug-metabolizing activity of DME CA2 (Ki = 35000 microM) |
[54] |
Sulfamic acid |
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Inhibition |
XEOTIC ID |
XEO00771
XEOTIC Info
|
Gene Form |
Protein |
Classification |
Chemical Compound |
DME Modulation |
Sulfamic acid inhibits the drug-metabolizing activity of DME CA2 (Ki = 0.00039 microM) |
[54] |
Thiophenes |
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Inhibition |
XEOTIC ID |
XEO00781
XEOTIC Info
|
Gene Form |
mRNA |
Classification |
Chemical Compound |
DME Modulation |
Thiophenes inhibits the expression of DME CA2 |
[55] |
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