Pozanicline
Pozanicline is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
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Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
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ATC Codes
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HCPCS
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Clinical
Clinical Trials
11 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Attention deficit disorder with hyperactivity | D001289 | EFO_0003888 | F90 | — | 7 | — | — | — | 7 |
Alzheimer disease | D000544 | EFO_0000249 | F03 | — | 3 | — | — | — | 3 |
Tobacco use disorder | D014029 | F17 | — | 1 | — | — | — | 1 |
Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | POZANICLINE |
INN | pozanicline |
Description | A-84543 is a drug developed by Abbott, which acts as an agonist at neural nicotinic acetylcholine receptors with high selectivity for the α4β2 subtype. It is widely used in scientific research into the structure and function of this receptor subtype and has been the lead compound for the development of a large family of related derivatives.
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Classification | Small molecule |
Drug class | nicotinic acetylcholine receptor partial agonists/agonists |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | Cc1ncccc1OC[C@@H]1CCCN1 |
Identifiers
PDB | — |
CAS-ID | 161416-43-9 |
RxCUI | — |
ChEMBL ID | CHEMBL127071 |
ChEBI ID | — |
PubChem CID | 9794141 |
DrugBank | — |
UNII ID | CL2002R563 (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
Clinical Variant
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Financial
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 29 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
0 adverse events reported
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