Basic Information

Terpenoid ID TKC020491
Cell line 0
Protein target 7
DiseaseNCIT 0
ORDO 0
ICD 36

Active subnetwork


Terpenoid-cell-disease Activity Association

ID Cell Line Synonyms Value Unit Type NCIt ORDO

Terpenoid-protein target Activity Association

ID Uniport Pref_name Gene name value unit type
TKC020491 P23219 Prostaglandin G/H synthase 1 PTGS1 4000 nM IC50
TKC020491 O42275 Acetylcholinesterase ache 288260 nM IC50
TKC020491 P0DTD1 Replicase polyprotein 1ab rep 21 % Inhibition
TKC020491 P81908 Cholinesterase BCHE 410790 nM IC50
TKC020491 O75762 Transient receptor potential cation channel subfamily A member 1 TRPA1 7000 nM EC50
TKC020491 O75762 Transient receptor potential cation channel subfamily A member 1 TRPA1 17000 nM EC50
TKC020491 O42713 Polyphenol oxidase 2 PPO2 >36 % Inhibition
TKC020491 P0DTE4 UDP-glucuronosyltransferase 2A1 UGT2A1 0 pm/min/mg Activity
TKC020491 P22309 UDP-glucuronosyltransferase 1A1 UGT1A1 0 pm/min/mg Activity
TKC020491 P22310 UDP-glucuronosyltransferase 1A4 UGT1A4 1500000 nM Km
TKC020491 Q75NA5 Gamma-aminobutyric acid receptor subunit beta Rdl 156 % Activity
TKC020491 O60656 UDP-glucuronosyltransferase 1A9 UGT1A9 2700 pm/min/mg Activity
TKC020491 P9WIB9 Secreted chorismate mutase Rv1885c 1060 nM IC50
TKC020491 P19224 UDP-glucuronosyltransferase 1-6 UGT1A6 0 pm/min/mg Activity
TKC020491 P54855 UDP-glucuronosyltransferase 2B15 UGT2B15 3 pm/min/mg Activity
TKC020491 Q13936 Voltage-dependent L-type calcium channel subunit alpha-1C CACNA1C 98000 nM IC50
TKC020491 Q9HAW8 UDP-glucuronosyltransferase 1A10 UGT1A10 0 pm/min/mg Activity
TKC020491 Q9HAW9 UDP-glucuronosyltransferase 1A8 UGT1A8 744 pm/min/mg Activity

Protein target-disease Activity Association

Uniport ID Uniport Name ICD-11
P23219 PGH1_HUMAN Alzheimer disease [ICD-11: 8A20]
P23219 PGH1_HUMAN Endometriosis [ICD-11: GA10]
P23219 PGH1_HUMAN Eye anterior segment structural developmental anomaly [ICD-11: LA11]
P23219 PGH1_HUMAN Female pelvic pain [ICD-11: GA34]
P23219 PGH1_HUMAN Hyper-lipoproteinaemia [ICD-11: 5C80]
P23219 PGH1_HUMAN Indeterminate colitis [ICD-11: DD72]
P23219 PGH1_HUMAN Nutritional deficiency [ICD-11: 5B50-5B71]
P23219 PGH1_HUMAN Osteoarthritis [ICD-11: FA00-FA05]
P23219 PGH1_HUMAN Pain [ICD-11: MG30-MG3Z]
P23219 PGH1_HUMAN Postoperative inflammation [ICD-11: 1A00-CA43]
P23219 PGH1_HUMAN Rheumatoid arthritis [ICD-11: FA20]
P23219 PGH1_HUMAN Seborrhoeic dermatitis [ICD-11: EA81]
P23219 PGH1_HUMAN Tuberculosis [ICD-11: 1B10-1B12]
P23219 PGH1_HUMAN Ulcerative colitis [ICD-11: DD71]
P23219 PGH1_HUMAN Shoulder lesion [ICD-11: FB53]
P23219 PGH1_HUMAN Soft tissue disorder [ICD-11: FB56]
P23219 PGH1_HUMAN Colorectal cancer [ICD-11: 2B91]
P23219 PGH1_HUMAN Solid tumour/cancer [ICD-11: 2A00-2F9Z]
P23219 PGH1_HUMAN Systemic sclerosis [ICD-11: 4A42]
P23219 PGH1_HUMAN Vasculitis [ICD-11: 4A44]
P23219 PGH1_HUMAN Ataxic disorder [ICD-11: 8A03]
P23219 PGH1_HUMAN Muscular dystrophy [ICD-11: 8C70]
P23219 PGH1_HUMAN Neuropathy [ICD-11: 8C0Z]
P23219 PGH1_HUMAN Fever [ICD-11: MG26]
P23219 PGH1_HUMAN Gout [ICD-11: FA25]
P23219 PGH1_HUMAN Sensation disturbance [ICD-11: MB40]
P23219 PGH1_HUMAN Type 2 diabetes mellitus [ICD-11: 5A11]
P23219 PGH1_HUMAN General pain disorder [ICD-11: 8E43]
O75762 TRPA1_HUMAN Upper respiratory tract disorder [ICD-11: CA0Z]
O75762 TRPA1_HUMAN Neuropathy [ICD-11: 8C0Z]
O75762 TRPA1_HUMAN Pain [ICD-11: MG30-MG3Z]
O75762 TRPA1_HUMAN Upper respiratory tract disorder [ICD-11: CA0Z]
O75762 TRPA1_HUMAN Neuropathy [ICD-11: 8C0Z]
O75762 TRPA1_HUMAN Pain [ICD-11: MG30-MG3Z]
P22309 UD11_HUMAN Inborn porphyrin/heme metabolism error [ICD-11: 5C58]
Q13936 CAC1C_HUMAN Alzheimer disease [ICD-11: 8A20]
Q13936 CAC1C_HUMAN Angina pectoris [ICD-11: BA40]
Q13936 CAC1C_HUMAN Genetic cardiac arrhythmia [ICD-11: BC65]
Q13936 CAC1C_HUMAN Unspecific body region injury [ICD-11: ND56]
Q13936 CAC1C_HUMAN Heart failure [ICD-11: BD10-BD1Z]