Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Syndrome | D013577 | — | — | 1 | 5 | 1 | — | — | 6 |
Mitochondrial diseases | D028361 | EFO_0000591 | — | 1 | 3 | 2 | — | 1 | 5 |
Ataxia | D001259 | — | R27.0 | — | 4 | 2 | — | — | 5 |
Friedreich ataxia | D005621 | Orphanet_95 | G11.11 | — | 4 | 2 | — | — | 5 |
Cerebellar ataxia | D002524 | HP_0001251 | — | — | 4 | 2 | — | — | 5 |
Leigh disease | D007888 | Orphanet_506 | G31.82 | — | 3 | 1 | — | — | 3 |
Brain diseases | D001927 | HP_0001298 | G93.40 | — | 1 | 1 | — | — | 1 |
Epilepsy | D004827 | EFO_0000474 | G40.9 | — | 1 | 1 | — | — | 1 |
Diffuse cerebral sclerosis of schilder | D002549 | Orphanet_726 | G31.81 | — | 1 | 1 | — | — | 1 |
Drug resistant epilepsy | D000069279 | — | — | — | 1 | 1 | — | — | 1 |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Muscular diseases | D009135 | HP_0003198 | G72.9 | 1 | 2 | — | — | — | 2 |
Inborn genetic diseases | D030342 | EFO_0000508 | — | — | 1 | — | — | — | 1 |
Homocystinuria | D006712 | HP_0002156 | E72.11 | — | 1 | — | — | — | 1 |
Inborn errors lipid metabolism | D008052 | — | — | — | 1 | — | — | — | 1 |
Hearing loss | D034381 | EFO_0004238 | H91.9 | — | 1 | — | — | — | 1 |
Noise-induced hearing loss | D006317 | EFO_1001254 | — | — | 1 | — | — | — | 1 |
Deafness | D003638 | EFO_0001063 | H91.9 | — | 1 | — | — | — | 1 |
Autistic disorder | D001321 | HP_0000717 | F84.0 | — | 1 | — | — | — | 1 |
Autism spectrum disorder | D000067877 | HP_0000729 | F84.0 | — | 1 | — | — | — | 1 |
Pervasive child development disorders | D002659 | EFO_0003756 | F84 | — | 1 | — | — | — | 1 |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Tourette syndrome | D005879 | EFO_0004895 | F95.2 | 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) |