Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Hepatitis c | D006526 | — | B19.2 | — | 4 | — | — | — | 4 |
Chronic hepatitis c | D019698 | EFO_0004220 | B18.2 | — | 4 | — | — | — | 4 |
Hepatitis | D006505 | — | K75.9 | — | 4 | — | — | — | 4 |
Hepatitis a | D006506 | EFO_0007305 | B15 | — | 4 | — | — | — | 4 |
Hiv infections | D015658 | EFO_0000764 | B20 | 1 | 2 | — | — | — | 3 |
Fever | D005334 | — | R50.9 | 2 | 2 | — | — | — | 2 |
Dengue | D003715 | — | A90 | 2 | 2 | — | — | — | 2 |
Chronic hepatitis | D006521 | — | K73.9 | — | 1 | — | — | — | 1 |
Drug common name | CELGOSIVIR |
INN | celgosivir |
Description | Celgosivir, in development by Migenix for the treatment of hepatitis C virus (HCV) infection, is an oral prodrug of the natural product castanospermine that inhibits alpha-glucosidase I, an enzyme that plays a critical role in viral maturation by initiating the processing of the N-linked oligosaccharides of viral envelope glycoproteins. Celgosivir is well absorbed in vitro and in vivo, and is rapidly converted to castanospermine. Celgosivir has a novel mechanism of action (preventing the glycosylation of viral proteins by the host), and demonstrates broad antiviral activity in vitro.
|
Classification | Small molecule |
Drug class | antivirals: glucosidase inhibitors |
Image (chem structure or protein) | ![]() |
Structure (InChI/SMILES or Protein Sequence) | CCCC(=O)O[C@H]1CN2CC[C@H](O)[C@@H]2[C@@H](O)[C@@H]1O |
PDB | — |
CAS-ID | 121104-96-9 |
RxCUI | — |
ChEMBL ID | CHEMBL2110737 |
ChEBI ID | — |
PubChem CID | 60734 |
DrugBank | — |
UNII ID | 895VG117HN (ChemIDplus, GSRS) |