Drug Name: | Minocycline (10118-90-8) |
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PubChem ID: | 54675783 |
SMILES: | CN(C)[C@H]1[C@@H]2C[C@@H]3CC4=C(C=CC(=C4C(=C3C(=O)[C@@]2(C(=C(C1=O)C(=O)N)O)O)O)O)N(C)C |
InchiKey: | FFTVPQUHLQBXQZ-KVUCHLLUSA-N |
Therapeutic Category: | Anti-Bacterial Agents, Anti-Infective Agents |
Molecular Weight (dalton) | : | 457.483 |
LogP | : | 0.03 |
Ring Count | : | 1 |
Hydrogen Bond Acceptor Count | : | 9 |
Hydrogen Bond Donor Count | : | 5 |
Total Polar Surface Area | : | 164.63 |
This panel provides information on interacting drugs and their ADRs along with references
Interacting drug | Toxicity | Interaction Type | Mechanism | Reference |
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Ethinyl Estradiol (57-63-6) | Melasma | Additive | Not understood. It seems possible that the facial pigmentation (melasma, chloasma) that can occur with oral contraceptives may have been additive with the effects of the minocycline | Minocycline-induced pigmentation occurring in two sisters |
Perphenazine (58-39-9) | Galactorrhoea | Additive | Unknown | Black galactorrhea as a consequence of minocycline and phenothiazine therapy |
This panel provides drug-protein interaction and their ADRs along with references
Toxicity | Interacting Protein | Mechanism | Reference |
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Dangerous Side Effects | Cytochrome P450 2E1 (P05181) | Theophylline inhibits CYP2E1 activity@ thus leads to reduction of minocylcine clearance and causes dangerous side effects. [ ADR Type 4 ] | Possible theophylline-minocycline interaction |
This panel provides drug-food interactions and their ADRs along with references
Food | Toxicity | Reference |
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This panel provides information on metabolites and their ADRs along with references
Metabolite | Toxicity | Place of Metabolism | Mechanism | Reference |
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This panel provides information on drug category