Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Mitochondrial diseases | D028361 | EFO_0000591 | — | 1 | 6 | 2 | — | 2 | 9 |
Friedreich ataxia | D005621 | Orphanet_95 | G11.11 | — | 4 | 2 | — | 1 | 6 |
Leigh disease | D007888 | Orphanet_506 | G31.82 | — | 3 | 2 | — | 1 | 5 |
Melas syndrome | D017241 | EFO_0000192 | E88.41 | — | 1 | 2 | — | 1 | 3 |
Diffuse cerebral sclerosis of schilder | D002549 | Orphanet_726 | G31.81 | — | 1 | 2 | — | — | 2 |
Drug resistant epilepsy | D000069279 | — | — | — | 1 | 2 | — | — | 2 |
Merrf syndrome | D017243 | Orphanet_551 | E88.42 | — | 1 | 2 | — | — | 2 |
Seizures | D012640 | — | G40.4 | — | 1 | 1 | — | — | 1 |
Status epilepticus | D013226 | EFO_0008526 | G41 | — | 1 | 1 | — | — | 1 |
Nerve degeneration | D009410 | — | — | — | 1 | 1 | — | — | 1 |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Muscular diseases | D009135 | EFO_0002970 | G72.9 | 1 | 2 | — | — | — | 2 |
Rett syndrome | D015518 | Orphanet_778 | F84.2 | — | 2 | — | — | — | 2 |
Ataxia | D001259 | — | R27.0 | — | 2 | — | — | — | 2 |
Inborn genetic diseases | D030342 | EFO_0000508 | — | — | 1 | — | — | — | 1 |
Retinal diseases | D012164 | — | H35.9 | — | 1 | — | — | — | 1 |
Homocystinuria | D006712 | — | E72.11 | — | 1 | — | — | — | 1 |
Syndrome | D013577 | — | — | — | 1 | — | — | — | 1 |
Inborn errors lipid metabolism | D008052 | — | — | — | 1 | — | — | — | 1 |
Noise-induced hearing loss | D006317 | EFO_1001254 | — | — | 1 | — | — | — | 1 |
Angelman syndrome | D017204 | Orphanet_72 | Q93.51 | — | 1 | — | — | — | 1 |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Tic disorders | D013981 | — | F95 | 1 | — | — | — | — | 1 |
Tourette syndrome | D005879 | EFO_0004895 | F95.2 | 1 | — | — | — | — | 1 |
Tics | D020323 | — | — | 1 | — | — | — | — | 1 |
Alzheimer disease | D000544 | EFO_0000249 | F03 | 1 | — | — | — | — | 1 |
Dementia | D003704 | EFO_0003862 | F03 | 1 | — | — | — | — | 1 |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Optic nerve diseases | D009901 | EFO_1001330 | H47.14 | — | — | — | — | 1 | 1 |
Emergencies | D004630 | — | — | — | — | — | — | 1 | 1 |
Hereditary optic atrophy leber | D029242 | Orphanet_104 | H47.22 | — | — | — | — | 1 | 1 |
Drug common name | Vatiquinone |
INN | vatiquinone |
Description | Vatiquinone is a small molecule pharmaceutical. It is currently being investigated in clinical studies. |
Classification | Small molecule |
Drug class | — |
Image (chem structure or protein) | ![]() |
Structure (InChI/SMILES or Protein Sequence) | CC(C)=CCC/C(C)=C/CC/C(C)=C/CC[C@@](C)(O)CCC1=C(C)C(=O)C(C)=C(C)C1=O |
PDB | — |
CAS-ID | 1213269-98-7 |
RxCUI | — |
ChEMBL ID | CHEMBL1812161 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | — |
UNII ID | 6O85FK9I0X (ChemIDplus, GSRS) |