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 quinine atoms shown as spheres conventional color coding pdb4wnv metabolism metabolite side effect detox detoxification interaction drugdrug xenobiotics oxidation substrate metabolic oxygenase grapefruit structure peptide protein 3d rendering amino acid molecule polypeptide polymer science scientific disease health molecular model mixed function oxidase

Cytochrome P450 CYP2D6 Liver Enzyme In Complex With The Drug Quinine. Atoms Are Shown As Spheres With Conventional Color Coding. Royalty-Free Stock Photography


Cytochrome P450 CYP2D6 liver enzyme in complex with the drug quinine. Atoms are shown as spheres with conventional color coding. Stock Photo
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Cytochrome P450 CYP2D6 liver enzyme in complex with the drug quinine. Atoms are shown as spheres with conventional color coding. #188460749
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Cytochrome P450 CYP2D6 liver enzyme in complex with the drug quinine. Atoms are shown as spheres with conventional color coding

Cytochrome P450 CYP2D6 liver enzyme in complex with the drug quinine. Atoms are shown as spheres with conventional color coding.
Cytochrome P450 (CYP2D6) liver enzyme in complex with the drug quinine. Protein: cartoon representation with secondary structure
Cytochrome P450 (CYP3A4) liver enzyme in complex with the antibiotic erythromycin. Cartoon representation with secondary structure
Cytochrome P450 (CYP3A4) liver enzyme in complex with the antibiotic erythromycin. 3D rendering based on protein data bank entry
Cytochrome P450 (CYP3A4) liver enzyme in complex with the antibiotic erythromycin. 3D rendering based on protein data bank entry

Cytochrome P450 (CYP3A4) liver enzyme in complex with the antibiotic erythromycin. 3D rendering based on protein data bank entry
Cytochrome P450 (CYP2D6) liver enzyme, in complex with the alkaloid quinine. 3D rendering based on protein data bank entry 4wnv.

Cytochrome P450 (CYP2D6) liver enzyme, in complex with the alkaloid quinine. 3D rendering based on protein data bank entry 4wnv.
Cobicistat cytochrome P450 inhibiting drug molecule. Increases exposure of various HIV drugs by inhibiting their breakdown by.

Cobicistat cytochrome P450 inhibiting drug molecule. Increases exposure of various HIV drugs by inhibiting their breakdown by.
Cytochrome P450 (CYP2D6) liver enzyme in complex with the drug quinine. Cytochrome P450 (CYP2D6) liver enzyme in complex with the

Cytochrome P450 (CYP3A4) liver enzyme in complex with the antibiotic erythromycin. Cartoon representation with secondary structure
Structure of human cytochrome P450 CYP2C9 with heme and warfarin bound
Cytochrome P450 (CYP2D6) liver enzyme in complex with the drug quinine. 3D render.
Cytochrome P450 molecule. CYP 3A4 is the most promiscuous of the human CYP enzymes. Molecular model. 3D rendering