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Assay Detail

CHEMBL1008372

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Binding
Inhibition of human MMP2
19
Total Activities
19
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

72 kDa type IV collagenase (CHEMBL333)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Compelling P1 substituent affect on metalloprotease binding profile enables the design of a novel cyclohexyl core scaffold with excellent MMP selectivity and HER-2 sheddase inhibition.
Burns DM, Li YL, Shi E, He C, Xu M, Zhuo J, Zhang C, Qian DQ, Li Y, Wynn R, Covington MB, Katiyar K, Marando CA, Fridman JS, Scherle P, Friedman S, Metcalf B, Yao W.
Bioorg Med Chem Lett (2009) 19 : 3525 -3530
PubMed 19457660 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 6.69 8.10

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL495596 1 8.10
CHEMBL497222 1 7.17
CHEMBL496211 1 7.09
CHEMBL496018 1 7.04
CHEMBL496628 1 7.00
CHEMBL521719 1 6.97
CHEMBL387202 1 6.82
CHEMBL497032 1 6.81
CHEMBL496212 1 6.75
CHEMBL221857 1 6.70
CHEMBL496825 1 6.63
CHEMBL523076 1 6.57
CHEMBL497026 1 6.49
CHEMBL252246 1 6.00
CHEMBL496629 1 5.96
CHEMBL445717 1 5.89
CHEMBL495797 1 5.78
CHEMBL496829 1 -
CHEMBL497645 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL495596 IC50 = 8.0 nM 8.10
CHEMBL497222 IC50 = 68.0 nM 7.17
CHEMBL496211 IC50 = 81.0 nM 7.09
CHEMBL496018 IC50 = 92.0 nM 7.04
CHEMBL496628 IC50 = 100.0 nM 7.00
CHEMBL521719 IC50 = 106.0 nM 6.97
CHEMBL387202 IC50 = 150.0 nM 6.82
CHEMBL497032 IC50 = 156.0 nM 6.81
CHEMBL496212 IC50 = 180.0 nM 6.75
CHEMBL221857 IC50 = 200.0 nM 6.70
CHEMBL496825 IC50 = 236.0 nM 6.63
CHEMBL523076 IC50 = 271.0 nM 6.57
CHEMBL497026 IC50 = 321.0 nM 6.49
CHEMBL252246 IC50 = 998.0 nM 6.00
CHEMBL496629 IC50 = 1090.0 nM 5.96
CHEMBL445717 IC50 = 1277.0 nM 5.89
CHEMBL495797 IC50 = 1662.0 nM 5.78
CHEMBL496829 IC50 > 5000.0 nM -
CHEMBL497645 IC50 > 5000.0 nM -