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BDBM50045698 1-Cyclopropyl-7-(2,6-dimethyl-pyridin-4-yl)-6,8-difluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid::CHEMBL8179::WIN-57294

SMILES: Cc1cc(cc(C)n1)-c1c(F)cc2c(c1F)n(cc(C(O)=O)c2=O)C1CC1

InChI Key: InChIKey=WHXJSJBKDGZVDA-UHFFFAOYSA-N

Data: 6 EC50

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 6 hits for monomerid = 50045698   
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
DNA topoisomerase II


(Homo sapiens (Human))
BDBM50045698
PNG
(1-Cyclopropyl-7-(2,6-dimethyl-pyridin-4-yl)-6,8-di...)
Show SMILES Cc1cc(cc(C)n1)-c1c(F)cc2c(c1F)n(cc(C(O)=O)c2=O)C1CC1
Show InChI InChI=1S/C20H16F2N2O3/c1-9-5-11(6-10(2)23-9)16-15(21)7-13-18(17(16)22)24(12-3-4-12)8-14(19(13)25)20(26)27/h5-8,12H,3-4H2,1-2H3,(H,26,27)
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Article
n/an/an/an/a>5.40E+4n/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of calf thymus DNA/ethidium bromide complex formation.


Bioorg Med Chem Lett 5: 405-410 (1995)


Article DOI: 10.1016/0960-894X(95)00044-T
BindingDB Entry DOI: 10.7270/Q2CZ37N7
More data for this
Ligand-Target Pair
DNA topoisomerase II


(Homo sapiens (Human))
BDBM50045698
PNG
(1-Cyclopropyl-7-(2,6-dimethyl-pyridin-4-yl)-6,8-di...)
Show SMILES Cc1cc(cc(C)n1)-c1c(F)cc2c(c1F)n(cc(C(O)=O)c2=O)C1CC1
Show InChI InChI=1S/C20H16F2N2O3/c1-9-5-11(6-10(2)23-9)16-15(21)7-13-18(17(16)22)24(12-3-4-12)8-14(19(13)25)20(26)27/h5-8,12H,3-4H2,1-2H3,(H,26,27)
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n/an/an/an/a 7.60E+3n/an/an/an/a


TBA

Assay Description
Inhibitory activity against HeLa cell Topoisomerase II


Citation and Details

BindingDB Entry DOI: 10.7270/Q2TX3HJW
More data for this
Ligand-Target Pair
DNA topoisomerase II


(Homo sapiens (Human))
BDBM50045698
PNG
(1-Cyclopropyl-7-(2,6-dimethyl-pyridin-4-yl)-6,8-di...)
Show SMILES Cc1cc(cc(C)n1)-c1c(F)cc2c(c1F)n(cc(C(O)=O)c2=O)C1CC1
Show InChI InChI=1S/C20H16F2N2O3/c1-9-5-11(6-10(2)23-9)16-15(21)7-13-18(17(16)22)24(12-3-4-12)8-14(19(13)25)20(26)27/h5-8,12H,3-4H2,1-2H3,(H,26,27)
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PubMed
n/an/an/an/a 7.60E+3n/an/an/an/a



Dainippon Pharmaceutical Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibitory activity in a DNA cleavage assay using HeLa DNA topoisomerase II yielding its effective concentration


J Med Chem 45: 5564-75 (2002)


Article DOI: 10.1021/jm010057b
BindingDB Entry DOI: 10.7270/Q2XS5Z46
More data for this
Ligand-Target Pair
DNA topoisomerase II


(Homo sapiens (Human))
BDBM50045698
PNG
(1-Cyclopropyl-7-(2,6-dimethyl-pyridin-4-yl)-6,8-di...)
Show SMILES Cc1cc(cc(C)n1)-c1c(F)cc2c(c1F)n(cc(C(O)=O)c2=O)C1CC1
Show InChI InChI=1S/C20H16F2N2O3/c1-9-5-11(6-10(2)23-9)16-15(21)7-13-18(17(16)22)24(12-3-4-12)8-14(19(13)25)20(26)27/h5-8,12H,3-4H2,1-2H3,(H,26,27)
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Article
n/an/an/an/a 7.60E+3n/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was tested for topoisomerase II inhibition in purified HeLa cells by SDS/K+ precipitation method


Bioorg Med Chem Lett 5: 405-410 (1995)


Article DOI: 10.1016/0960-894X(95)00044-T
BindingDB Entry DOI: 10.7270/Q2CZ37N7
More data for this
Ligand-Target Pair
DNA topoisomerase II


(Homo sapiens (Human))
BDBM50045698
PNG
(1-Cyclopropyl-7-(2,6-dimethyl-pyridin-4-yl)-6,8-di...)
Show SMILES Cc1cc(cc(C)n1)-c1c(F)cc2c(c1F)n(cc(C(O)=O)c2=O)C1CC1
Show InChI InChI=1S/C20H16F2N2O3/c1-9-5-11(6-10(2)23-9)16-15(21)7-13-18(17(16)22)24(12-3-4-12)8-14(19(13)25)20(26)27/h5-8,12H,3-4H2,1-2H3,(H,26,27)
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Article
PubMed
n/an/an/an/a 7.60E+3n/an/an/an/a



Sterling Winthrop Pharmaceuticals Research Division

Curated by ChEMBL


Assay Description
Tested for inhibition of topoisomerase II isolated from HeLa cells by DNA-cleavage assay


J Med Chem 36: 2801-9 (1993)


Article DOI: 10.1021/jm00071a010
BindingDB Entry DOI: 10.7270/Q2NK3H89
More data for this
Ligand-Target Pair
DNA topoisomerase II


(Homo sapiens (Human))
BDBM50045698
PNG
(1-Cyclopropyl-7-(2,6-dimethyl-pyridin-4-yl)-6,8-di...)
Show SMILES Cc1cc(cc(C)n1)-c1c(F)cc2c(c1F)n(cc(C(O)=O)c2=O)C1CC1
Show InChI InChI=1S/C20H16F2N2O3/c1-9-5-11(6-10(2)23-9)16-15(21)7-13-18(17(16)22)24(12-3-4-12)8-14(19(13)25)20(26)27/h5-8,12H,3-4H2,1-2H3,(H,26,27)
PDB

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antibodypedia
antibodypedia
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PC cid
PC sid
UniChem

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n/an/an/an/a 7.60E+3n/an/an/an/a


TBA

Assay Description
Inhibitory activity in a cell-free assay of DNA cleavage mediated by purified HeLa cell topoisomerase II.


Citation and Details

BindingDB Entry DOI: 10.7270/Q2R49SXV
More data for this
Ligand-Target Pair