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Assay Detail

CHEMBL3083372

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of Escherichia coli GR19N NDH1 assessed as deaminoNADH-DB reductase activity
54
Total Activities
54
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Escherichia coli
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Comparison of the inhibitory action of synthetic capsaicin analogues with various NADH-ubiquinone oxidoreductases.
Satoh T, Miyoshi H, Sakamoto K, Iwamura H.
Biochim Biophys Acta (1996) 1273 : 21 -30
PubMed 8573592 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 54 5.24 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2273119 1 7.00
CHEMBL2273118 1 7.00
CHEMBL2268817 1 6.82
CHEMBL2268816 1 6.74
CHEMBL2273116 1 6.72
CHEMBL272733 PIERICIDIN A 1 6.63
CHEMBL2273117 1 6.60
CHEMBL2273115 1 6.35
CHEMBL2268818 1 6.30
CHEMBL1443698 1 6.15
CHEMBL2273110 1 5.82
CHEMBL2273113 1 5.72
CHEMBL2268815 1 5.71
CHEMBL2268799 1 5.70
CHEMBL2268801 1 5.58
CHEMBL2273102 N-(2,4-DIMETHOXYBENZYL)DODECANAMIDE 1 5.40
CHEMBL2273114 1 5.30
CHEMBL2268820 1 5.30
CHEMBL2268488 1 5.30
CHEMBL2273104 N-(3,5-DIMETHOXYBENZYL)DODECANAMIDE 1 5.30
CHEMBL2268804 1 5.26
CHEMBL2273098 HEPTYLHYDROXYQUINOLINE N-OXIDE 1 5.15
CHEMBL2268813 1 5.10
CHEMBL365100 FENPYROXYMATE 1 5.00
CHEMBL2268802 1 4.96
CHEMBL429023 ROTENONE 1 4.90
CHEMBL294199 CAPSAICIN 4.0 1 4.77
CHEMBL2268812 1 4.77
CHEMBL2268800 1 4.70
CHEMBL2268819 1 4.70

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2273119 IC50 = 100.0 nM 7.00
CHEMBL2273118 IC50 = 100.0 nM 7.00
CHEMBL2268817 IC50 = 151.36 nM 6.82
CHEMBL2268816 IC50 = 181.97 nM 6.74
CHEMBL2273116 IC50 = 190.55 nM 6.72
CHEMBL272733 PIERICIDIN A IC50 = 234.42 nM 6.63
CHEMBL2273117 IC50 = 251.19 nM 6.60
CHEMBL2273115 IC50 = 446.68 nM 6.35
CHEMBL2268818 IC50 = 501.19 nM 6.30
CHEMBL1443698 IC50 = 707.95 nM 6.15
CHEMBL2273110 IC50 = 1513.56 nM 5.82
CHEMBL2273113 IC50 = 1905.46 nM 5.72
CHEMBL2268815 IC50 = 1949.84 nM 5.71
CHEMBL2268799 IC50 = 1995.26 nM 5.70
CHEMBL2268801 IC50 = 2630.27 nM 5.58
CHEMBL2273102 N-(2,4-DIMETHOXYBENZYL)DODECANAMIDE IC50 = 3981.07 nM 5.40
CHEMBL2273114 IC50 = 5011.87 nM 5.30
CHEMBL2268820 IC50 = 5011.87 nM 5.30
CHEMBL2268488 IC50 = 5011.87 nM 5.30
CHEMBL2273104 N-(3,5-DIMETHOXYBENZYL)DODECANAMIDE IC50 = 5011.87 nM 5.30
CHEMBL2268804 IC50 = 5495.41 nM 5.26
CHEMBL2273098 HEPTYLHYDROXYQUINOLINE N-OXIDE IC50 = 7079.46 nM 5.15
CHEMBL2268813 IC50 = 7943.28 nM 5.10
CHEMBL365100 FENPYROXYMATE IC50 = 10000.0 nM 5.00
CHEMBL2268802 IC50 = 10964.78 nM 4.96
CHEMBL429023 ROTENONE IC50 = 12589.25 nM 4.90
CHEMBL2268812 IC50 = 16982.44 nM 4.77
CHEMBL294199 CAPSAICIN IC50 = 16982.44 nM 4.77
CHEMBL2268800 IC50 = 19952.62 nM 4.70
CHEMBL2268819 IC50 = 19952.62 nM 4.70
CHEMBL2273107 N-(4-METHOXYBENZYL)DODECANAMIDE IC50 = 25703.96 nM 4.59
CHEMBL2268811 IC50 = 30199.52 nM 4.52
CHEMBL2273120 IC50 = 34673.69 nM 4.46
CHEMBL2268798 IC50 = 50118.72 nM 4.30
CHEMBL2273100 N-(3,4-DIMETHOXYBENZYL)DODECANAMIDE IC50 = 50118.72 nM 4.30
CHEMBL2268805 IC50 = 63095.73 nM 4.20
CHEMBL2268806 IC50 = 70794.58 nM 4.15
CHEMBL2273105 N-(2-METHOXYBENZYL)DODECANAMIDE IC50 = 79432.82 nM 4.10
CHEMBL2273106 N-(3-METHOXYBENZYL)DODECANAMIDE IC50 = 83176.38 nM 4.08
CHEMBL2268803 IC50 = 93325.43 nM 4.03
CHEMBL2273121 IC50 = 100000.0 nM 4.00
CHEMBL2273109 N-(3,4-DIMETHYLBENZYL)DODECANAMIDE IC50 = 100000.0 nM 4.00
CHEMBL2273108 N-(2,5-DIMETHYLBENZYL)DODECANAMIDE IC50 = 100000.0 nM 4.00
CHEMBL2273103 N-(2,5-DIMETHOXYBENZYL)DODECANAMIDE IC50 > 100000.0 nM -
CHEMBL86638 IC50 > 100000.0 nM -
CHEMBL2268807 IC50 > 100000.0 nM -
CHEMBL2268808 IC50 > 100000.0 nM -
CHEMBL2268809 IC50 > 100000.0 nM -
CHEMBL2268814 IC50 > 100000.0 nM -
CHEMBL2273111 IC50 > 100000.0 nM -