Molecule Information
General Information of the Molecule (ID: Mol01188)
Type(s) of Resistant Mechanism of This Molecule
DISM: Drug Inactivation by Structure Modification
Drug Resistance Data Categorized by Drug
Approved Drug(s)
2 drug(s) in total
Darunavir
Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Human immunodeficiency virus infection | [1] | |||
Sensitive Disease | Human immunodeficiency virus infection [ICD-11: 1C62.0] | |||
Sensitive Drug | Darunavir | |||
Molecule Alteration | Expression | Down-regulation |
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Experimental Note | Identified from the Human Clinical Data | |||
Mechanism Description | Darunavir, a HIV PI that is co-administered with low-dose ritonavir (darunavir/ritonavir), is recommended in combination with other antiretrovirals. The mechanism of ritonavir pharmacokinetic enhancement is through inhibiting cytochrome P450 (CYP) 3A. Ritonavir has intrinsic antiviral activity against HIV-1 when administered at high doses (i.e., 600 mg twice daily) and was the second PI to be licensed. Along with saquinavir and indinavir, it heralded the advent of highly active antiretroviral therapy. |
Oxycodone
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Osteosarcoma | [2] | |||
Resistant Disease | Osteosarcoma [ICD-11: 2B51.0] | |||
Resistant Drug | Oxycodone | |||
Molecule Alteration | Expression | Up-regulation |
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Experimental Note | Identified from the Human Clinical Data | |||
Mechanism Description | Oxycodone is a semisynthetic opioid receptor agonist, and is frequently used for pain control in patients with cancer. Most oxycodone is metabolized by N-demethylation to noroxycodone by CYP3A. Rifampin is a strong inducer of several drug-metabolizing enzymes, including CYP3A. Hence, rifampin-induced CYP3A activity may decrease the effect of oxycodone. |
References
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