Praliciguat
Praliciguat is a small molecule pharmaceutical. It is currently being investigated in clinical studies. It is known to target guanylate cyclase soluble subunit beta-1.
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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
7 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 |
---|---|---|---|---|---|---|---|---|---|
Type 2 diabetes mellitus | D003924 | EFO_0001360 | E11 | — | 3 | — | — | — | 3 |
Hypertension | D006973 | EFO_0000537 | I10 | — | 2 | — | — | — | 2 |
Heart failure | D006333 | EFO_0003144 | I50 | — | 1 | — | — | — | 1 |
Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Healthy volunteers/patients | — | 3 | — | — | — | — | 3 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | PRALICIGUAT |
INN | praliciguat |
Description | Praliciguat is a member of the class of pyrazoles that is 5-fluoro-2-(1H-pyrazol-3-yl)pyrimidine which is substituted by a 2-fluorobenzyl group at position 1, 1,2-oxazol-3-yl group at position 5, and by a [3,3,3-trifluoro-2-hydroxy-2-(trifluoromethyl)propyl]nitrilo group at position 4. It is a soluble guanylate cyclase stimulator under clinical development for the treatment of heart failure with preserved ejection fraction. It has a role as a soluble guanylate cyclase activator, an anti-inflammatory agent, a vasodilator agent and an antihypertensive agent. It is a member of isoxazoles, a member of pyrazoles, an organofluorine compound, an aminopyrimidine, a tertiary alcohol, a secondary amino compound and a member of monofluorobenzenes. |
Classification | Small molecule |
Drug class | guanaline cyclase activators |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | OC(CNc1nc(-c2cc(-c3ccon3)n(Cc3ccccc3F)n2)ncc1F)(C(F)(F)F)C(F)(F)F |
Identifiers
PDB | — |
CAS-ID | 1628730-49-3 |
RxCUI | — |
ChEMBL ID | CHEMBL4297214 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | — |
UNII ID | R1S0H458SA (ChemIDplus, GSRS) |
Target
Agency Approved
No data
Alternate
GUCY1B1
GUCY1B1
Organism
Homo sapiens
Gene name
GUCY1B1
Gene synonyms
GUC1B3, GUCSB3, GUCY1B3
NCBI Gene ID
Protein name
guanylate cyclase soluble subunit beta-1
Protein synonyms
GCS-beta-1, GCS-beta-3, guanylate cyclase 1, soluble, beta 3, Guanylate cyclase soluble subunit beta-3, Soluble guanylate cyclase small subunit
Uniprot ID
Mouse ortholog
Gucy1b1 (54195)
guanylate cyclase soluble subunit beta-1 (O54865)
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 92 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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