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BDBM50363494 5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-diol) (4)::CHEMBL374829

SMILES: Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br

InChI Key: InChIKey=AMKNSMNMEAMKDN-UHFFFAOYSA-N

Data: 4 KI  7 IC50

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 11 hits for monomerid = 50363494   
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
Carbonic anhydrase 6 (CA-VI)


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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PubMed
1.78E+4n/an/an/an/an/an/an/an/a



Artvin£oruh University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 6 esterase activity using 4-nitrophenylacetate as substrate


Bioorg Med Chem Lett 22: 1352-7 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.069
BindingDB Entry DOI: 10.7270/Q2WH2QF4
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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2.15E+4n/an/an/an/an/an/an/an/a



Artvin£oruh University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 esterase activity using 4-nitrophenylacetate as substrate


Bioorg Med Chem Lett 22: 1352-7 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.069
BindingDB Entry DOI: 10.7270/Q2WH2QF4
More data for this
Ligand-Target Pair
Carbonic anhydrase 4


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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2.80E+4n/an/an/an/an/an/an/an/a



Artvin£oruh University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 4 esterase activity using 4-nitrophenylacetate as substrate


Bioorg Med Chem Lett 22: 1352-7 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.069
BindingDB Entry DOI: 10.7270/Q2WH2QF4
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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3.51E+4n/an/an/an/an/an/an/an/a



Artvin£oruh University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 esterase activity using 4-nitrophenylacetate as substrate


Bioorg Med Chem Lett 22: 1352-7 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.069
BindingDB Entry DOI: 10.7270/Q2WH2QF4
More data for this
Ligand-Target Pair
Protein-tyrosine phosphatase 1C


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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n/an/a>5.00E+4n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of SHP1 using OMFP as substrate after 3 mins


Bioorg Med Chem Lett 22: 2827-32 (2012)


Article DOI: 10.1016/j.bmcl.2012.02.074
BindingDB Entry DOI: 10.7270/Q28K7B33
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase F (LAR)


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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n/an/a>5.00E+4n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of LAR using OMFP as substrate after 3 mins


Bioorg Med Chem Lett 22: 2827-32 (2012)


Article DOI: 10.1016/j.bmcl.2012.02.074
BindingDB Entry DOI: 10.7270/Q28K7B33
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 11


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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n/an/a>5.00E+4n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of SHP2 using OMFP as substrate after 3 mins


Bioorg Med Chem Lett 22: 2827-32 (2012)


Article DOI: 10.1016/j.bmcl.2012.02.074
BindingDB Entry DOI: 10.7270/Q28K7B33
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 2


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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n/an/a>5.00E+4n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of TCPTP after 3 mins


Bioorg Med Chem Lett 22: 2827-32 (2012)


Article DOI: 10.1016/j.bmcl.2012.02.074
BindingDB Entry DOI: 10.7270/Q28K7B33
More data for this
Ligand-Target Pair
Aldose reductase


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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n/an/a 566n/an/an/an/an/an/a



Jilin Province Academy of Traditional Chinese Medicine and Materia Medica

Curated by ChEMBL


Assay Description
Inhibition of human muscle recombinant aldose reductase by spectrophotometry


J Nat Prod 68: 620-2 (2005)


Article DOI: 10.1021/np040199j
BindingDB Entry DOI: 10.7270/Q2BZ68TQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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n/an/a 3.83E+4n/an/an/an/an/an/a



Atatürk University



Assay Description
Carbonic anhydrase activity was assayed by following the hydration of CO2 according to our previous studies [Soyut et al., Protein Pept. Lett., 15:52...


J Enzyme Inhib Med Chem 27: 43-50 (2012)


Article DOI: 10.3109/14756366.2011.574131
BindingDB Entry DOI: 10.7270/Q2CR5S75
More data for this
Ligand-Target Pair
Protein-tyrosine phosphatase 1B


(Homo sapiens (Human))
BDBM50363494
PNG
(5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-d...)
Show SMILES Oc1c(O)c(Br)c(Cc2c(Br)c(O)c(O)c(Br)c2Br)c(Br)c1Br
Show InChI InChI=1S/C13H6Br6O4/c14-4-2(6(16)10(20)12(22)8(4)18)1-3-5(15)9(19)13(23)11(21)7(3)17/h20-23H,1H2
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n/an/a 680n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of GST-tagged human recombinant PTB1B using pNPP as substrate after 3 mins


Bioorg Med Chem Lett 22: 2827-32 (2012)


Article DOI: 10.1016/j.bmcl.2012.02.074
BindingDB Entry DOI: 10.7270/Q28K7B33
More data for this
Ligand-Target Pair