Bifeprunox
Bifeprunox is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
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Clinical
Clinical Trials
20 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Schizophrenia | D012559 | EFO_0000692 | F20 | — | 3 | 12 | — | — | 15 |
| Psychotic disorders | D011618 | — | F20.81 | — | 3 | 2 | — | — | 5 |
| Bipolar disorder | D001714 | EFO_0000289 | F30.9 | — | 2 | 2 | — | — | 4 |
| Depression | D003863 | — | F33.9 | — | — | 2 | — | — | 2 |
| Schizophrenia spectrum and other psychotic disorders | D019967 | — | — | — | — | 1 | — | — | 1 |
| Alzheimer disease | D000544 | EFO_0000249 | F03 | — | — | 1 | — | — | 1 |
| Dementia | D003704 | EFO_0003862 | F03 | — | — | 1 | — | — | 1 |
| Mental disorders | D001523 | EFO_0000677 | F91.9 | — | — | 1 | — | — | 1 |
| Problem behavior | D000066553 | — | — | — | — | 1 | — | — | 1 |
| Body weight changes | D001836 | — | — | — | — | 1 | — | — | 1 |
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Indications Phases 2
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Healthy volunteers/patients | — | — | — | 1 | — | — | — | — | 1 |
Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Bifeprunox |
| INN | bifeprunox |
| Description | Bifeprunox is a member of biphenyls. |
| Classification | Small molecule |
| Drug class | — |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | O=c1[nH]c2cccc(N3CCN(Cc4cccc(-c5ccccc5)c4)CC3)c2o1 |
Identifiers
| PDB | — |
| CAS-ID | 350992-10-8 |
| RxCUI | — |
| ChEMBL ID | CHEMBL218166 |
| ChEBI ID | — |
| PubChem CID | 208951 |
| DrugBank | DB04888 |
| UNII ID | AP69E83Z79 (ChemIDplus, GSRS) |
Target
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Variants
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Financial
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Trends
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Additional graphs summarizing 161 documents
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Safety
Black-box Warning
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Adverse Events
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22 adverse events reported
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