BDBM50101522 CHEMBL76869::[(S)-2-((S)-2-Cyclohexyl-1-phenethylcarbamoyl-ethylcarbamoyl)-5-p-tolyl-pentyl]-phosphonic acid::[2-(2-Cyclohexyl-1-phenethylcarbamoyl-ethylcarbamoyl)-5-p-tolyl-pentyl]-phosphonic acid

SMILES: Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1

InChI Key: InChIKey=PNOAVGXEWQIVLB-IZLXSDGUSA-N

Data: 9 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50101522   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	2.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of the Gelatinase-A enzyme was determined from purified NSO cells.				Bioorg Med Chem Lett 4: 2747-2752 (1994) Article DOI: 10.1016/S0960-894X(01)80588-6 BindingDB Entry DOI: 10.7270/Q2JH3M3P
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Royal Danish School of Pharmacy Curated by ChEMBL					Assay Description Inhibitory constant against matrix metalloproteinase-2				J Med Chem 44: 2333-43 (2001) BindingDB Entry DOI: 10.7270/Q2JH3KFR
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	277	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of the Stromelysin enzyme was determined from purified NSO cells.				Bioorg Med Chem Lett 4: 2747-2752 (1994) Article DOI: 10.1016/S0960-894X(01)80588-6 BindingDB Entry DOI: 10.7270/Q2JH3M3P
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	277	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Royal Danish School of Pharmacy Curated by ChEMBL					Assay Description Inhibitory constant against matrix metalloproteinase-3				J Med Chem 44: 2333-43 (2001) BindingDB Entry DOI: 10.7270/Q2JH3KFR
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	366	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of the Collagenase enzyme was determined from purified NSO cells.				Bioorg Med Chem Lett 4: 2747-2752 (1994) Article DOI: 10.1016/S0960-894X(01)80588-6 BindingDB Entry DOI: 10.7270/Q2JH3M3P
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Royal Danish School of Pharmacy Curated by ChEMBL					Assay Description Inhibitory constant against matrix metalloproteinase-1				J Med Chem 44: 2333-43 (2001) BindingDB Entry DOI: 10.7270/Q2JH3KFR
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of the Stromelysin enzyme was determined from purified NSO cells.				Bioorg Med Chem Lett 4: 2747-2752 (1994) Article DOI: 10.1016/S0960-894X(01)80588-6 BindingDB Entry DOI: 10.7270/Q2JH3M3P
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	2.12E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of the Gelatinase-A enzyme was determined from purified NSO cells.				Bioorg Med Chem Lett 4: 2747-2752 (1994) Article DOI: 10.1016/S0960-894X(01)80588-6 BindingDB Entry DOI: 10.7270/Q2JH3M3P
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50101522 (CHEMBL76869 | [(S)-2-((S)-2-Cyclohexyl-1-phenethyl...) Show SMILES Cc1ccc(CCC[C@H](CP(O)(O)=O)C(=O)N[C@@H](CC2CCCCC2)C(=O)NCCc2ccccc2)cc1 Show InChI InChI=1S/C30H43N2O5P/c1-23-15-17-25(18-16-23)13-8-14-27(22-38(35,36)37)29(33)32-28(21-26-11-6-3-7-12-26)30(34)31-20-19-24-9-4-2-5-10-24/h2,4-5,9-10,15-18,26-28H,3,6-8,11-14,19-22H2,1H3,(H,31,34)(H,32,33)(H2,35,36,37)/t27-,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of the Collagenase enzyme was determined from purified NSO cells.				Bioorg Med Chem Lett 4: 2747-2752 (1994) Article DOI: 10.1016/S0960-894X(01)80588-6 BindingDB Entry DOI: 10.7270/Q2JH3M3P
					More data for this Ligand-Target Pair