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2 similar compounds to monomer 50427446

Compile data set for download or QSAR
Wt: 464.3
BDBM50427444		Wt: 302.2
BDBM50427445

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50427444,50427445   
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
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427444
PNG
(CHEMBL2326313)
Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1
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 1.17E+5n/an/an/an/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by STD NMR analysis in presence of magnesium ions

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427444
PNG
(CHEMBL2326313)
Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1
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 5.65E+5n/an/an/an/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Competitive inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by Michaelis-Menten equation analysis in presence of m...

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427445
PNG
(CHEMBL1235497)
Show SMILES OC[C@@H](O)[C@@H](O)[C@H](O)Cn1c2[nH]c(=O)[nH]c(=O)c2[nH]c1=O
Show InChI InChI=1S/C10H14N4O7/c15-2-4(17)6(18)3(16)1-14-7-5(11-10(14)21)8(19)13-9(20)12-7/h3-4,6,15-18H,1-2H2,(H,11,21)(H2,12,13,19,20)/t3-,4-,6+/m1/s1
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 5.71E+5n/an/an/an/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by STD NMR analysis in presence of magnesium ions

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427444
PNG
(CHEMBL2326313)
Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1
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 1.50E+6n/an/an/an/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Inhibition of human blood group B Galactosyltransferase using radiolabeled UDP-Gal as substrate in presence of manganese ions

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427445
PNG
(CHEMBL1235497)
Show SMILES OC[C@@H](O)[C@@H](O)[C@H](O)Cn1c2[nH]c(=O)[nH]c(=O)c2[nH]c1=O
Show InChI InChI=1S/C10H14N4O7/c15-2-4(17)6(18)3(16)1-14-7-5(11-10(14)21)8(19)13-9(20)12-7/h3-4,6,15-18H,1-2H2,(H,11,21)(H2,12,13,19,20)/t3-,4-,6+/m1/s1
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 2.20E+6n/an/an/an/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Inhibition of human blood group B Galactosyltransferase using radiolabeled UDP-Gal as substrate in presence of manganese ions

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427444
PNG
(CHEMBL2326313)
Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1
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n/an/a 3.89E+5n/an/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Inhibition of human blood group B Galactosyltransferase using UDP-Gal as substrate by STD NMR analysis in presence of magnesium ions

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427444
PNG
(CHEMBL2326313)
Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1
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n/an/an/a 2.54E+5n/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Binding affinity to human blood group B Galactosyltransferase after 300 secs by SPR analysis

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427445
PNG
(CHEMBL1235497)
Show SMILES OC[C@@H](O)[C@@H](O)[C@H](O)Cn1c2[nH]c(=O)[nH]c(=O)c2[nH]c1=O
Show InChI InChI=1S/C10H14N4O7/c15-2-4(17)6(18)3(16)1-14-7-5(11-10(14)21)8(19)13-9(20)12-7/h3-4,6,15-18H,1-2H2,(H,11,21)(H2,12,13,19,20)/t3-,4-,6+/m1/s1
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n/an/an/a 2.30E+6n/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Binding affinity to human blood group B Galactosyltransferase after 300 secs by SPR analysis

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427444
PNG
(CHEMBL2326313)
Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1
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n/an/an/a 1.82E+5n/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Binding affinity to human blood group B Galactosyltransferase by STD NMR analysis in presence of magnesium ions

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair
Histo-blood group ABO system transferase


(Homo sapiens (Human))		BDBM50427444
PNG
(CHEMBL2326313)
Show SMILES OC[C@H]1O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O)Cn2c3[nH]c(=O)[nH]c(=O)c3[nH]c2=O)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C16H24N4O12/c21-2-6-9(25)10(26)11(27)14(32-6)31-3-5(23)8(24)4(22)1-20-12-7(17-16(20)30)13(28)19-15(29)18-12/h4-6,8-11,14,21-27H,1-3H2,(H,17,30)(H2,18,19,28,29)/t4-,5-,6-,8+,9+,10+,11-,14+/m1/s1
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n/an/a 1.60E+6n/an/an/an/an/an/a



University of Hamburg

Curated by ChEMBL


Assay Description
Inhibition of human blood group B Galactosyltransferase using radiolabeled UDP-Gal as substrate in presence of manganese ions

J Med Chem 56: 2150-4 (2013)


Article DOI: 10.1021/jm300642a
BindingDB Entry DOI: 10.7270/Q26T0P01
More data for this
Ligand-Target Pair