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 |
Diabetes mellitus | D003920 | HP_0000819 | E08-E13 | — | 2 | — | — | — | 2 |
Heart failure | D006333 | HP_0001635 | I50 | — | 1 | — | — | — | 1 |
Diabetic nephropathies | D003928 | EFO_0000401 | — | — | 1 | — | — | — | 1 |
Kidney diseases | D007674 | EFO_0003086 | N08 | — | 1 | — | — | — | 1 |
Albuminuria | D000419 | EFO_0004285 | R80.9 | — | 1 | — | — | — | 1 |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Healthy volunteers/patients | — | — | — | 3 | — | — | — | — | 3 |
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 |
PDB | — |
CAS-ID | 1628730-49-3 |
RxCUI | — |
ChEMBL ID | CHEMBL4297214 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | — |
UNII ID | R1S0H458SA (ChemIDplus, GSRS) |