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Compile Data Set for Download or QSAR

Found 16 hits Enz. Inhib. hit(s) with all data for entry = 10653   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557292
PNG
(US11358933, Compound 026)
Show SMILES CC(C)(C)c1cccc(c1)-c1cc2cc(\C=C\C(O)=O)ccc2[nH]1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 200n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557299
PNG
(US11358933, Compound 034)
Show SMILES Cc1ccc(cc1-c1cc2cc(\C=C\C(O)=O)ccc2[nH]1)C(C)(C)C
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 500n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557298
PNG
(US11358933, Compound 032)
Show SMILES CC(C)(C)c1cccc(c1)-c1cc2cc(CC(O)=O)ccc2o1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 2.30E+3n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26A1


(Homo sapiens (Human))
BDBM557292
PNG
(US11358933, Compound 026)
Show SMILES CC(C)(C)c1cccc(c1)-c1cc2cc(\C=C\C(O)=O)ccc2[nH]1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 7.00E+3n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26A1


(Homo sapiens (Human))
BDBM557293
PNG
(US11358933, Compound 027)
Show SMILES CC1(C)CC(C)(C)c2cc(cc(CC=C)c2O1)C(=O)Cc1ccc(CC(O)=O)cc1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 8.60E+3n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26A1


(Homo sapiens (Human))
BDBM557298
PNG
(US11358933, Compound 032)
Show SMILES CC(C)(C)c1cccc(c1)-c1cc2cc(CC(O)=O)ccc2o1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 8.60E+3n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557293
PNG
(US11358933, Compound 027)
Show SMILES CC1(C)CC(C)(C)c2cc(cc(CC=C)c2O1)C(=O)Cc1ccc(CC(O)=O)cc1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 8.80E+3n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26A1


(Homo sapiens (Human))
BDBM557299
PNG
(US11358933, Compound 034)
Show SMILES Cc1ccc(cc1-c1cc2cc(\C=C\C(O)=O)ccc2[nH]1)C(C)(C)C
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 9.60E+3n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557291
PNG
(US11358933, Compound 025)
Show SMILES CC(C)(C)c1cccc(c1)C(=O)Cc1ccc(\C=C\C(O)=O)cc1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1.79E+4n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557297
PNG
(US11358933, Compound 031)
Show SMILES CC(C)(C)c1cccc(c1)-c1cc2cc(\C=C\C(O)=O)ccc2o1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1.83E+4n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26A1


(Homo sapiens (Human))
BDBM557296
PNG
(US11358933, Compound 030)
Show SMILES CC1(C)CC(C)(C)c2cc(cc(C3CC3)c2O1)B1Oc2ccc(CC(O)=O)cc2O1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 3.15E+4n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26A1


(Homo sapiens (Human))
BDBM557291
PNG
(US11358933, Compound 025)
Show SMILES CC(C)(C)c1cccc(c1)C(=O)Cc1ccc(\C=C\C(O)=O)cc1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 4.56E+4n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557295
PNG
(US11358933, Compound 029)
Show SMILES CC(C)(C)c1cccc(c1)B(O)Oc1ccc(\C=C\C(O)=O)cc1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 5.49E+4n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557296
PNG
(US11358933, Compound 030)
Show SMILES CC1(C)CC(C)(C)c2cc(cc(C3CC3)c2O1)B1Oc2ccc(CC(O)=O)cc2O1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 8.81E+4n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26B1


(Homo sapiens (Human))
BDBM557294
PNG
(US11358933, Compound 028)
Show SMILES CC1(C)CC(C)(C)c2cc(cc(C3CC3)c2O1)C(=O)Cc1ccc(CC(O)=O)cc1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a>1.00E+6n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair
Cytochrome P450 26A1


(Homo sapiens (Human))
BDBM557294
PNG
(US11358933, Compound 028)
Show SMILES CC1(C)CC(C)(C)c2cc(cc(C3CC3)c2O1)C(=O)Cc1ccc(CC(O)=O)cc1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a>1.00E+6n/an/an/an/an/an/a


TBA

Assay Description
CYP26 inhibitory activities of various compounds.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2CC13XJ
More data for this
Ligand-Target Pair