Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Non-alcoholic fatty liver disease | D065626 | EFO_0003095 | K75.81 | 1 | 4 | — | — | — | 5 |
Fatty liver | D005234 | EFO_0003934 | — | 1 | 4 | — | — | — | 5 |
Liver diseases | D008107 | HP_0002910 | K70-K77 | 2 | 1 | — | — | — | 3 |
Liver cirrhosis | D008103 | EFO_0001422 | K74.0 | — | 2 | — | — | — | 2 |
Fibrosis | D005355 | — | — | — | 1 | — | — | — | 1 |
Diarrhea | D003967 | HP_0002014 | R19.7 | — | 1 | — | — | — | 1 |
Biliary liver cirrhosis | D008105 | — | K74.3 | — | 1 | — | — | — | 1 |
Cholangitis | D002761 | HP_0030151 | K83.0 | — | 1 | — | — | — | 1 |
Drug common name | TROPIFEXOR |
INN | tropifexor |
Description | Tropifexor is an investigational drug that acts as an agonist of the farnesoid X receptor (FXR). It was discovered by researchers from Novartis and Genomics Institute of the Novartis Research Foundation. Its synthesis and pharmacological properties were published in 2017. It was developed for the treatment of cholestatic liver diseases and nonalcoholic steatohepatitis (NASH). In combination with cenicriviroc, a CCR2 and CCR5 receptor inhibitor, it is undergoing a phase II clinical trial for NASH and liver fibrosis.
|
Classification | Small molecule |
Drug class | atropine derivatives |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | O=C(O)c1cc(F)c2nc(N3[C@H]4CC[C@@H]3C[C@H](OCc3c(-c5ccccc5OC(F)(F)F)noc3C3CC3)C4)sc2c1 |
PDB | — |
CAS-ID | 1383816-29-2 |
RxCUI | — |
ChEMBL ID | CHEMBL4298169 |
ChEBI ID | — |
PubChem CID | 121418176 |
DrugBank | — |
UNII ID | NMZ08KM76Z (ChemIDplus, GSRS) |