Terpenoid ID | TKC109625 | |
Cell line | 0 | |
Protein target | 3 | |
DiseaseNCIT | 0 | |
ORDO | 0 | |
ICD | 10 |
ID | Cell Line | Synonyms | Value | Unit | Type | NCIt | ORDO |
---|
ID | Uniport | Pref_name | Gene name | value | unit | type |
---|---|---|---|---|---|---|
TKC109625 | Q9NPD5 | Solute carrier organic anion transporter family member 1B3 | SLCO1B3 | 79 | % | Inhibition |
TKC109625 | Q9Y6L6 | Solute carrier organic anion transporter family member 1B1 | SLCO1B1 | 85 | % | Inhibition |
TKC109625 | O94956 | Solute carrier organic anion transporter family member 2B1 | SLCO2B1 | 54 | % | Inhibition |
TKC109625 | O88397 | Solute carrier organic anion transporter family member 1A5 | Slco1a5 | 4300 | nM | Km |
TKC109625 | Q8TDU6 | G-protein coupled bile acid receptor 1 | GPBAR1 | 1180 | nM | EC50 |
TKC109625 | Q12908 | Ileal sodium/bile acid cotransporter | SLC10A2 | 2000 | nM | Km |
Uniport ID | Uniport Name | ICD-11 |
---|---|---|
Q8TDU6 | GPBAR_HUMAN | Type 2 diabetes mellitus [ICD-11: 5A11] |
Q8TDU6 | GPBAR_HUMAN | Hepatic fibrosis/cirrhosis [ICD-11: DB93] |
Q8TDU6 | GPBAR_HUMAN | Metabolic disorder [ICD-11: 5C50-5D2Z] |
Q12908 | NTCP2_HUMAN | Gallbladder/bile ducts/liver structural developmental anomaly [ICD-11: LB20] |
Q12908 | NTCP2_HUMAN | Inborn lipid metabolism error [ICD-11: 5C52] |
Q12908 | NTCP2_HUMAN | Inborn porphyrin/heme metabolism error [ICD-11: 5C58] |
Q12908 | NTCP2_HUMAN | Autoimmune liver disease [ICD-11: DB96] |
Q12908 | NTCP2_HUMAN | Hyper-lipoproteinaemia [ICD-11: 5C80] |
Q12908 | NTCP2_HUMAN | Pruritus [ICD-11: EC90] |
Q12908 | NTCP2_HUMAN | Type 2 diabetes mellitus [ICD-11: 5A11] |