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2 similar compounds to monomer 50128307

Wt: 367.4
BDBM50128298
Wt: 337.4
BDBM50128310

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50128298,50128310   
Target
(Institution)
LigandTarget
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
pHTemp
°C
Ecdysone receptor


(Choristoneura fumiferana)
BDBM50128298
PNG
(CHEMBL299671 | N-[1-(3,5-Dimethyl-benzoyl)-1-ethyl...)
Show SMILES CCC(CC)(NC(=O)c1cccc(OC)c1C)C(=O)c1cc(C)cc(C)c1
Show InChI InChI=1S/C23H29NO3/c1-7-23(8-2,21(25)18-13-15(3)12-16(4)14-18)24-22(26)19-10-9-11-20(27-6)17(19)5/h9-14H,7-8H2,1-6H3,(H,24,26)
PDB
MMDB

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

AffyNet 
PubMed
n/an/an/an/a 6.23E+3n/an/an/an/a



RHeoGene

Curated by ChEMBL


Assay Description
Dose affording 50% of maximum transactivation for ecdysone receptor from Choristoneura fumiferana (CfEcR) and a luciferase reporter gene in CHO cells


Bioorg Med Chem Lett 13: 1883-6 (2003)

More data for this
Ligand-Target Pair
Ecdysone receptor


(Choristoneura fumiferana)
BDBM50128310
PNG
(CHEMBL55953 | N-[1-(3,5-Dimethyl-benzoyl)-cyclopro...)
Show SMILES COc1cccc(C(=O)NC2(CC2)C(=O)c2cc(C)cc(C)c2)c1C
Show InChI InChI=1S/C21H23NO3/c1-13-10-14(2)12-16(11-13)19(23)21(8-9-21)22-20(24)17-6-5-7-18(25-4)15(17)3/h5-7,10-12H,8-9H2,1-4H3,(H,22,24)
PDB
MMDB

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

AffyNet 
PubMed
n/an/an/an/a 3.33E+4n/an/an/an/a



RHeoGene

Curated by ChEMBL


Assay Description
Dose affording 50% of maximum transactivation for ecdysone receptor from Choristoneura fumiferana (CfEcR) and a luciferase reporter gene in CHO cells


Bioorg Med Chem Lett 13: 1883-6 (2003)

More data for this
Ligand-Target Pair
Ecdysone receptor


(Bombyx mori)
BDBM50128310
PNG
(CHEMBL55953 | N-[1-(3,5-Dimethyl-benzoyl)-cyclopro...)
Show SMILES COc1cccc(C(=O)NC2(CC2)C(=O)c2cc(C)cc(C)c2)c1C
Show InChI InChI=1S/C21H23NO3/c1-13-10-14(2)12-16(11-13)19(23)21(8-9-21)22-20(24)17-6-5-7-18(25-4)15(17)3/h5-7,10-12H,8-9H2,1-4H3,(H,22,24)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

AffyNet 
PubMed
n/an/an/an/a 2.04E+4n/an/an/an/a



RHeoGene

Curated by ChEMBL


Assay Description
Dose affording 50% of maximum transactivation for ecdysone receptor from Bombyx mori (BmEcR) and a beta-galactosidase reporter gene in HEK-293 cell-l...


Bioorg Med Chem Lett 13: 1883-6 (2003)

More data for this
Ligand-Target Pair
Ecdysone receptor


(Bombyx mori)
BDBM50128298
PNG
(CHEMBL299671 | N-[1-(3,5-Dimethyl-benzoyl)-1-ethyl...)
Show SMILES CCC(CC)(NC(=O)c1cccc(OC)c1C)C(=O)c1cc(C)cc(C)c1
Show InChI InChI=1S/C23H29NO3/c1-7-23(8-2,21(25)18-13-15(3)12-16(4)14-18)24-22(26)19-10-9-11-20(27-6)17(19)5/h9-14H,7-8H2,1-6H3,(H,24,26)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

AffyNet 
PubMed
n/an/an/an/a 4.53E+3n/an/an/an/a



RHeoGene

Curated by ChEMBL


Assay Description
Dose affording 50% of maximum transactivation for ecdysone receptor from Bombyx mori (BmEcR) and a beta-galactosidase reporter gene in HEK-293 cell-l...


Bioorg Med Chem Lett 13: 1883-6 (2003)

More data for this
Ligand-Target Pair