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Assay Detail

CHEMBL3083296

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Binding
Inhibition of Solanum tuberosum (potato) submitochondrial particle NDH1 assessed as deaminoNADH-DB reductase activity
54
Total Activities
54
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Solanum tuberosum
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 44 4.96 7.82
pI50 10 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL272733 PIERICIDIN A 1 7.82
CHEMBL365100 FENPYROXYMATE 1 6.26
CHEMBL2273119 1 5.62
CHEMBL2273120 1 5.56
CHEMBL2273116 1 5.50
CHEMBL1443698 1 5.40
CHEMBL2273117 1 5.40
CHEMBL2268817 1 5.30
CHEMBL429023 ROTENONE 1 5.30
CHEMBL2268820 1 5.28
CHEMBL2268799 1 5.27
CHEMBL2273118 1 5.15
CHEMBL2273102 N-(2,4-DIMETHOXYBENZYL)DODECANAMIDE 1 5.05
CHEMBL2268801 1 5.01
CHEMBL2268810 1 5.00
CHEMBL2273103 N-(2,5-DIMETHOXYBENZYL)DODECANAMIDE 1 5.00
CHEMBL2268800 1 5.00
CHEMBL2273104 N-(3,5-DIMETHOXYBENZYL)DODECANAMIDE 1 4.92
CHEMBL2273099 N-BENZYLDODECANAMIDE 1 4.92
CHEMBL2268807 1 4.90
CHEMBL2268805 1 4.90
CHEMBL2268819 1 4.89
CHEMBL2268818 1 4.86
CHEMBL2268811 1 4.80
CHEMBL2273107 N-(4-METHOXYBENZYL)DODECANAMIDE 1 4.80
CHEMBL2268803 1 4.74
CHEMBL2268806 1 4.74
CHEMBL2273109 N-(3,4-DIMETHYLBENZYL)DODECANAMIDE 1 4.66
CHEMBL2268804 1 4.60
CHEMBL2273121 1 4.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL272733 PIERICIDIN A IC50 = 15.14 nM 7.82
CHEMBL365100 FENPYROXYMATE IC50 = 549.54 nM 6.26
CHEMBL2273119 IC50 = 2398.83 nM 5.62
CHEMBL2273120 IC50 = 2754.23 nM 5.56
CHEMBL2273116 IC50 = 3162.28 nM 5.50
CHEMBL1443698 IC50 = 3981.07 nM 5.40
CHEMBL2273117 IC50 = 3981.07 nM 5.40
CHEMBL2268817 IC50 = 5011.87 nM 5.30
CHEMBL429023 ROTENONE IC50 = 5011.87 nM 5.30
CHEMBL2268820 IC50 = 5248.07 nM 5.28
CHEMBL2268799 IC50 = 5370.32 nM 5.27
CHEMBL2273118 IC50 = 7079.46 nM 5.15
CHEMBL2273102 N-(2,4-DIMETHOXYBENZYL)DODECANAMIDE IC50 = 8912.51 nM 5.05
CHEMBL2268801 IC50 = 9772.37 nM 5.01
CHEMBL2268800 IC50 = 10000.0 nM 5.00
CHEMBL2273103 N-(2,5-DIMETHOXYBENZYL)DODECANAMIDE IC50 = 10000.0 nM 5.00
CHEMBL2268810 IC50 = 10000.0 nM 5.00
CHEMBL2273104 N-(3,5-DIMETHOXYBENZYL)DODECANAMIDE IC50 = 12022.64 nM 4.92
CHEMBL2273099 N-BENZYLDODECANAMIDE IC50 = 12022.64 nM 4.92
CHEMBL2268807 IC50 = 12589.25 nM 4.90
CHEMBL2268805 IC50 = 12589.25 nM 4.90
CHEMBL2268819 IC50 = 12882.5 nM 4.89
CHEMBL2268818 IC50 = 13803.84 nM 4.86
CHEMBL2268811 IC50 = 15848.93 nM 4.80
CHEMBL2273107 N-(4-METHOXYBENZYL)DODECANAMIDE IC50 = 15848.93 nM 4.80
CHEMBL2268803 IC50 = 18197.01 nM 4.74
CHEMBL2268806 IC50 = 18197.01 nM 4.74
CHEMBL2273109 N-(3,4-DIMETHYLBENZYL)DODECANAMIDE IC50 = 21877.62 nM 4.66
CHEMBL2268804 IC50 = 25118.86 nM 4.60
CHEMBL2273121 IC50 = 30199.52 nM 4.52
CHEMBL2268812 IC50 = 30199.52 nM 4.52
CHEMBL2273108 N-(2,5-DIMETHYLBENZYL)DODECANAMIDE IC50 = 30199.52 nM 4.52
CHEMBL2273105 N-(2-METHOXYBENZYL)DODECANAMIDE IC50 = 30199.52 nM 4.52
CHEMBL2268808 IC50 = 34673.69 nM 4.46
CHEMBL2273113 IC50 = 37153.52 nM 4.43
CHEMBL2273100 N-(3,4-DIMETHOXYBENZYL)DODECANAMIDE IC50 = 37153.52 nM 4.43
CHEMBL2273112 IC50 = 70794.58 nM 4.15
CHEMBL2273106 N-(3-METHOXYBENZYL)DODECANAMIDE IC50 = 100000.0 nM 4.00
CHEMBL2273101 N-(2,3-DIMETHOXYBENZYL)DODECANAMIDE IC50 = 100000.0 nM 4.00
CHEMBL2268802 IC50 = 100000.0 nM 4.00
CHEMBL2268798 IC50 = 120226.44 nM -
CHEMBL294199 CAPSAICIN IC50 = 134896.29 nM -
CHEMBL2273098 HEPTYLHYDROXYQUINOLINE N-OXIDE IC50 > 100000.0 nM -
CHEMBL2268488 IC50 = 301995.17 nM -
CHEMBL86638 pI50 - -
CHEMBL2268809 pI50 - -
CHEMBL2268813 pI50 - -
CHEMBL2268814 pI50 - -
CHEMBL2268815 pI50 - -
CHEMBL2268816 pI50 - -