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BDBM50203970 CHEMBL232004::N-(4-(2-(4-isobutoxy-2-methylphenoxy)thiazol-5-yl)but-3-yn-2-yl)acetamide

SMILES: CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c(C)c1

InChI Key: InChIKey=FHNWBOFIOKDQPP-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50203970   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Acetyl-CoA carboxylase 1 (ACC1)


(Homo sapiens (Human))
BDBM50203970
PNG
(CHEMBL232004 | N-(4-(2-(4-isobutoxy-2-methylphenox...)
Show SMILES CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c(C)c1 |w:17.18|
Show InChI InChI=1S/C20H24N2O3S/c1-13(2)12-24-17-7-9-19(14(3)10-17)25-20-21-11-18(26-20)8-6-15(4)22-16(5)23/h7,9-11,13,15H,12H2,1-5H3,(H,22,23)
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human recombinant ACC1


Bioorg Med Chem Lett 17: 1961-5 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.022
BindingDB Entry DOI: 10.7270/Q2W095KS
More data for this
Ligand-Target Pair
Acetyl-CoA carboxylase 2 (ACC2)


(Homo sapiens (Human))
BDBM50203970
PNG
(CHEMBL232004 | N-(4-(2-(4-isobutoxy-2-methylphenox...)
Show SMILES CC(C)COc1ccc(Oc2ncc(s2)C#CC(C)NC(C)=O)c(C)c1 |w:17.18|
Show InChI InChI=1S/C20H24N2O3S/c1-13(2)12-24-17-7-9-19(14(3)10-17)25-20-21-11-18(26-20)8-6-15(4)22-16(5)23/h7,9-11,13,15H,12H2,1-5H3,(H,22,23)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 9n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human recombinant ACC2


Bioorg Med Chem Lett 17: 1961-5 (2007)


Article DOI: 10.1016/j.bmcl.2007.01.022
BindingDB Entry DOI: 10.7270/Q2W095KS
More data for this
Ligand-Target Pair