Terpenoid ID | TKC162951 |
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Cell line | 0 | |
Protein target | 9 | |
DiseaseNCIT | 0 | |
ORDO | 0 | |
ICD | 16 |
ID | Cell Line | Synonyms | Value | Unit | Type | NCIt | ORDO |
---|---|---|---|---|---|---|---|
TKC162951 | HepG2 | 35481.0 | nM | Potency | C3728 | Orphanet_449 |
ID | Uniport | Pref_name | Gene name | value | unit | type |
---|---|---|---|---|---|---|
TKC162951 | Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | TDP1 | 20596 | nM | Potency |
TKC162951 | P84022 | Mothers against decapentaplegic homolog 3 | SMAD3 | 25119 | nM | Potency |
TKC162951 | Q16236 | Nuclear factor erythroid 2-related factor 2 | NFE2L2 | 3162 | nM | Potency |
TKC162951 | Q99700 | Ataxin-2 | ATXN2 | 10000 | nM | Potency |
TKC162951 | O75496 | Geminin | GMNN | 18356 | nM | Potency |
TKC162951 | P01215 | Glycoprotein hormones alpha chain | CGA | 7943 | nM | Potency |
TKC162951 | P83916 | Chromobox protein homolog 1 | CBX1 | 89125 | nM | Potency |
TKC162951 | Q96QE3 | ATPase family AAA domain-containing protein 5 | ATAD5 | 29081 | nM | Potency |
TKC162951 | O00255 | Menin | MEN1 | 39811 | nM | Potency |
Uniport ID | Uniport Name | ICD-11 |
---|---|---|
P84022 | SMAD3_HUMAN | Herpes simplex infection [ICD-11: 1F00] |
P84022 | SMAD3_HUMAN | Kidney fibrosis [ICD-11: GC01] |
Q16236 | NF2L2_HUMAN | Ataxic disorder [ICD-11: 8A03] |
Q16236 | NF2L2_HUMAN | Breast cancer [ICD-11: 2C60-2C6Y] |
Q16236 | NF2L2_HUMAN | Glaucoma [ICD-11: 9C61] |
Q16236 | NF2L2_HUMAN | Lung cancer [ICD-11: 2C25] |
Q16236 | NF2L2_HUMAN | Macular degeneration [ICD-11: 9B75] |
Q16236 | NF2L2_HUMAN | Melanoma [ICD-11: 2C30] |
Q16236 | NF2L2_HUMAN | Mental/behavioural/neurodevelopmental disorder [ICD-11: 6E20-6E8Z] |
Q16236 | NF2L2_HUMAN | Pulmonary hypertension [ICD-11: BB01] |
Q16236 | NF2L2_HUMAN | Subarachnoid haemorrhage [ICD-11: 8B01] |
Q16236 | NF2L2_HUMAN | Urinary system clinical sympton [ICD-11: MF8Y] |
Q16236 | NF2L2_HUMAN | Non-alcoholic fatty liver disease [ICD-11: DB92] |
Q16236 | NF2L2_HUMAN | Alpha-1-antitrypsin deficiency [ICD-11: 5C5A] |
Q16236 | NF2L2_HUMAN | Motor neuron disease [ICD-11: 8B60] |
Q16236 | NF2L2_HUMAN | Multiple sclerosis [ICD-11: 8A40] |