null

SMILES: N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1

InChI Key: InChIKey=FFOSLNTUQPRRRB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 8876   

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
Cytochrome P450 11B1, mitochondrial (Homo sapiens (Human))	BDBM8876 ((1E)-1-(1H-Imidazol-5-ylmethylene)indane-5-carboni...) Show SMILES N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H11N3/c15-7-10-1-4-14-11(5-10)2-3-12(14)6-13-8-16-9-17-13/h1,4-6,8-9H,2-3H2,(H,16,17)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	7.4	37
Saarland University					Assay Description The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...				J Med Chem 48: 1796-805 (2005) Article DOI: 10.1021/jm049600p BindingDB Entry DOI: 10.7270/Q2RN362H
					More data for this Ligand-Target Pair
Cytochrome P450 11B1, mitochondrial (Homo sapiens (Human))	BDBM8876 ((1E)-1-(1H-Imidazol-5-ylmethylene)indane-5-carboni...) Show SMILES N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H11N3/c15-7-10-1-4-14-11(5-10)2-3-12(14)6-13-8-16-9-17-13/h1,4-6,8-9H,2-3H2,(H,16,17)	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	12.3	n/a	n/a	n/a	n/a	7.4	37
Saarland University					Assay Description The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...				J Med Chem 48: 1796-805 (2005) Article DOI: 10.1021/jm049600p BindingDB Entry DOI: 10.7270/Q2RN362H
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM8876 ((1E)-1-(1H-Imidazol-5-ylmethylene)indane-5-carboni...) Show SMILES N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H11N3/c15-7-10-1-4-14-11(5-10)2-3-12(14)6-13-8-16-9-17-13/h1,4-6,8-9H,2-3H2,(H,16,17)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	35.9	n/a	n/a	n/a	n/a	n/a	n/a
Saarland University					Assay Description The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...				J Med Chem 48: 1796-805 (2005) Article DOI: 10.1021/jm049600p BindingDB Entry DOI: 10.7270/Q2RN362H
					More data for this Ligand-Target Pair
Steroid 17-alpha-hydroxylase/17,20 lyase (Homo sapiens (Human))	BDBM8876 ((1E)-1-(1H-Imidazol-5-ylmethylene)indane-5-carboni...) Show SMILES N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H11N3/c15-7-10-1-4-14-11(5-10)2-3-12(14)6-13-8-16-9-17-13/h1,4-6,8-9H,2-3H2,(H,16,17)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Saarland University					Assay Description The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...				J Med Chem 48: 1796-805 (2005) Article DOI: 10.1021/jm049600p BindingDB Entry DOI: 10.7270/Q2RN362H
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM8876 ((1E)-1-(1H-Imidazol-5-ylmethylene)indane-5-carboni...) Show SMILES N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H11N3/c15-7-10-1-4-14-11(5-10)2-3-12(14)6-13-8-16-9-17-13/h1,4-6,8-9H,2-3H2,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	119	n/a	n/a	n/a	n/a	n/a	n/a
Saarland University					Assay Description The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...				J Med Chem 48: 1796-805 (2005) Article DOI: 10.1021/jm049600p BindingDB Entry DOI: 10.7270/Q2RN362H
					More data for this Ligand-Target Pair
Aromatase (Homo sapiens (Human))	BDBM8876 ((1E)-1-(1H-Imidazol-5-ylmethylene)indane-5-carboni...) Show SMILES N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H11N3/c15-7-10-1-4-14-11(5-10)2-3-12(14)6-13-8-16-9-17-13/h1,4-6,8-9H,2-3H2,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
Saarland University					Assay Description The enzyme activity was assayed by measuring the 3H-labeled H2O formed from [1beta,2beta-3H]testosterone during aromatization. After incubation, the ...				J Med Chem 48: 1796-805 (2005) Article DOI: 10.1021/jm049600p BindingDB Entry DOI: 10.7270/Q2RN362H
					More data for this Ligand-Target Pair
Steroid 17-alpha-hydroxylase/17,20 lyase (Homo sapiens (Human))	BDBM8876 ((1E)-1-(1H-Imidazol-5-ylmethylene)indane-5-carboni...) Show SMILES N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H11N3/c15-7-10-1-4-14-11(5-10)2-3-12(14)6-13-8-16-9-17-13/h1,4-6,8-9H,2-3H2,(H,16,17)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Saarland University					Assay Description The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...				J Med Chem 48: 1796-805 (2005) Article DOI: 10.1021/jm049600p BindingDB Entry DOI: 10.7270/Q2RN362H
					More data for this Ligand-Target Pair
Cytochrome P450 11B2, mitochondrial (Homo sapiens (Human))	BDBM8876 ((1E)-1-(1H-Imidazol-5-ylmethylene)indane-5-carboni...) Show SMILES N#Cc1ccc2C(CCc2c1)=Cc1cnc[nH]1 |w:11.13| Show InChI InChI=1S/C14H11N3/c15-7-10-1-4-14-11(5-10)2-3-12(14)6-13-8-16-9-17-13/h1,4-6,8-9H,2-3H2,(H,16,17)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	35.7	n/a	n/a	n/a	n/a	n/a	n/a
Saarland University					Assay Description The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...				J Med Chem 48: 1796-805 (2005) Article DOI: 10.1021/jm049600p BindingDB Entry DOI: 10.7270/Q2RN362H
					More data for this Ligand-Target Pair