Details of the Drug Inactive Ingredient (DIG)
| General Information of DIG (ID: E0Z0LW) | |||||
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| DIG Name |
Kollicoat IR
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| DIG Function |
Film/Membrane-forming agent
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| Full List of Biological Targets of DIG (DBTs) Regulated by This DIG | ||||||
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| Oxidoreductase (ORase) | ||||||
| DBT Name: Cytochrome P450 2E1 (CYP2E1) | Click to Show/Hide | |||||
| Detailed Information |
DBT Info
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| Experiment for Assessing the Biological Activity of the Studied DIG on This DBT | ||||||
| Biological Activity | IC50 = 598.1 uM (tested by experiment) | [1] | ||||
| Tested Species | Homo sapiens (Human) | |||||
| UniProt ID | CP2E1_HUMAN | |||||
| DBT Name: Cytochrome P450 2C9 (CYP2C9) | Click to Show/Hide | |||||
| Detailed Information |
DBT Info
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| Experiment for Assessing the Biological Activity of the Studied DIG on This DBT | ||||||
| Biological Activity | EC50 = 259.8 uM (tested by experiment) | [1] | ||||
| Tested Species | Homo sapiens (Human) | |||||
| UniProt ID | CP2C9_HUMAN | |||||
| DBT Name: Mephenytoin 4-hydroxylase (CYP2C19) | Click to Show/Hide | |||||
| Detailed Information |
DBT Info
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| Experiment for Assessing the Biological Activity of the Studied DIG on This DBT | ||||||
| Biological Activity | EC50 = 36.1 uM (tested by experiment) | [1] | ||||
| Tested Species | Homo sapiens (Human) | |||||
| UniProt ID | CP2CJ_HUMAN | |||||
| DBT Name: Debrisoquine 4-hydroxylase (CYP2D6) | Click to Show/Hide | |||||
| Detailed Information |
DBT Info
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| Experiment for Assessing the Biological Activity of the Studied DIG on This DBT | ||||||
| Biological Activity | IC50 = 89.9 uM (tested by experiment) | [1] | ||||
| Tested Species | Homo sapiens (Human) | |||||
| UniProt ID | CP2D6_HUMAN | |||||
| Lyase/isomerase/ligase (L/I/G) | ||||||
| DBT Name: Cholesterol 25-hydroxylase (CYP1A2) | Click to Show/Hide | |||||
| Detailed Information |
DBT Info
click to show the detail info of this DBT
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| Experiment for Assessing the Biological Activity of the Studied DIG on This DBT | ||||||
| Biological Activity | IC50 = 10 uM (tested by experiment) | [1] | ||||
| Tested Species | Homo sapiens (Human) | |||||
| UniProt ID | CP1A2_HUMAN | |||||
| References | |||||
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| 1 | Mediation of in vitro cytochrome p450 activity by common pharmaceutical excipients. Mol Pharm. 2013 Jul 1;10(7):2739-48. | ||||
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