| Drug Name: | Interferon gamma-1b (82115-62-6) |
|---|---|
| PubChem ID: | 124081005 |
| SMILES: | CCN1C[C@]2(CC[C@H]([C@@]34[C@@H]2[C@@H]([C@@]([C@@H]31)([C@@]5(C[C@@H]([C@H]6C[C@@H]4[C@@H]5[C@H]6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)C[C@H](C8=O)C.C(C(=O)O)C(CC(=O)O)(C(=O)O)O |
| InchiKey: | INBLZNJHDLEWPS-OXVGBIBJSA-N |
| Therapeutic Category: |
| Molecular Weight (dalton) | : | 874.934 |
| LogP | : | 0.7866 |
| Ring Count | : | 1 |
| Hydrogen Bond Acceptor Count | : | 15 |
| Hydrogen Bond Donor Count | : | 6 |
| Total Polar Surface Area | : | 276.43 |
This panel provides information on interacting drugs and their ADRs along with references
| Interacting drug | Toxicity | Interaction Type | Mechanism | Reference |
|---|
This panel provides drug-protein interaction and their ADRs along with references
| Toxicity | Interacting Protein | Mechanism | Reference |
|---|---|---|---|
| Analgesia | Adenosine A1 receptor (P30542) | Formalin-induced pain and mu-opioid receptor density in brain and spinal cord are modulated by A1 and A2a adenosine aGOnists in mice@which lead to dose-dependent analgesia [ ADR Type 1 ] | Formalin-induced pain and mu-opioid receptor density in brain and spinal cord are modulated by A1 and A2a adenosine agonists in mice |
| Analgesia | Mu-Type opioid receptor (P35372) | Formalin-induced pain and mu-opioid receptor density in brain and spinal cord are modulated by A1 and A2a adenosine agonists in mice@which lead to dose-dependent analgesia. [ ADR Type 1 ] | Formalin-induced pain and mu-opioid receptor density in brain and spinal cord are modulated by A1 and A2a adenosine agonists in mice |
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 |
|---|
This panel provides information on drug category