BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 22 hits Enz. Inhib. hit(s) with Target = 'Beta-1,4-galactosyltransferase 1'   
Target
(Institution)
LigandTarget
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
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50427121
PNG
(CHEMBL2323429 | CHEMBL2323430)
Show SMILES C[n+]1ccn(CCCCCCCCCCCCCCCCCCCCn2cc[n+](C)c2)c1
Show InChI InChI=1S/C28H52N4/c1-29-23-25-31(27-29)21-19-17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-20-22-32-26-24-30(2)28-32/h23-28H,3-22H2,1-2H3/q+2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
PubMed
n/an/a 7.30E+5n/an/an/an/an/an/a



Queen's University

Curated by ChEMBL


Assay Description
Inhibition of bovine milk beta4-GalT1 using GlcNAcbeta-Bn as substrate after 1 hr relative to control


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50427121
PNG
(CHEMBL2323429 | CHEMBL2323430)
Show SMILES C[n+]1ccn(CCCCCCCCCCCCCCCCCCCCn2cc[n+](C)c2)c1
Show InChI InChI=1S/C28H52N4/c1-29-23-25-31(27-29)21-19-17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-20-22-32-26-24-30(2)28-32/h23-28H,3-22H2,1-2H3/q+2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
PubMed
n/an/a 1.96E+6n/an/an/an/an/an/a



Queen's University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant soluble His-tagged beta4-GalT1 expressed in Escherichia coli BL21 using GlcNAcbeta-Bn as substrate after 1 hr relativ...


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50324492
PNG
(CHEMBL1214871 | NA)
Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@H](COCCOCCOCCOCc3ccc4ccccc4c3)[C@H](O)[C@H](O)[C@H]2O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O
Show InChI InChI=1S/C32H44N2O20P2/c35-24-7-8-34(32(41)33-24)30-28(39)26(37)23(51-30)18-50-55(42,43)54-56(44,45)53-31-29(40)27(38)25(36)22(52-31)17-49-14-12-47-10-9-46-11-13-48-16-19-5-6-20-3-1-2-4-21(20)15-19/h1-8,15,22-23,25-31,36-40H,9-14,16-18H2,(H,42,43)(H,44,45)(H,33,35,41)/t22-,23-,25+,26-,27+,28-,29-,30-,31-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
PubMed
1.86E+3n/an/an/an/an/an/an/an/a



Hokkaido University

Curated by ChEMBL


Assay Description
Inhibition of human Beta-1,4-galactosyltransferase 1


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50370676
PNG
(CHEMBL607907)
Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@@H](COCCOCCOCCOCc3ccc4ccccc4c3)[C@H](O)[C@H](O)[C@@H]2O)OC([C@@H]1O)n1ccc(=O)[nH]c1=O
Show InChI InChI=1S/C32H44N2O20P2/c35-24-7-8-34(32(41)33-24)30-28(39)26(37)23(51-30)18-50-55(42,43)54-56(44,45)53-31-29(40)27(38)25(36)22(52-31)17-49-14-12-47-10-9-46-11-13-48-16-19-5-6-20-3-1-2-4-21(20)15-19/h1-8,15,22-23,25-31,36-40H,9-14,16-18H2,(H,42,43)(H,44,45)(H,33,35,41)/t22-,23+,25-,26+,27-,28+,29-,30?,31+/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
PubMed
1.86E+3n/an/an/an/an/an/an/an/a



Hokkaido University

Curated by ChEMBL


Assay Description
Inhibitory constant against human galactosyltransferase using UDP-Gal


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50072694
PNG
(CHEMBL320104 | N-[4,5-Dihydroxy-6-hydroxymethyl-2-...)
Show SMILES COc1ccc2cc(OC3OC(CO)C(O)C(O)C3NC(C)=O)ccc2c1
Show InChI InChI=1S/C19H23NO7/c1-10(22)20-16-18(24)17(23)15(9-21)27-19(16)26-14-6-4-11-7-13(25-2)5-3-12(11)8-14/h3-8,15-19,21,23-24H,9H2,1-2H3,(H,20,22)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
PubMed
3.50E+3n/an/an/an/an/an/an/an/a



Scripps Research Institute

Curated by ChEMBL


Assay Description
Compound was tested for the inhibition recombinant bovine beta -1,4 -galactosyl transferase (beta-1,4-GalT)


Bioorg Med Chem Lett 8: 3359-64 (1999)

More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50370674
PNG
(UDP-GALACTOSE)
Show SMILES OC[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)c2cc(=O)[nH]c(=O)[nH]2)[C@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C15H24N2O17P2/c18-2-5-8(20)10(22)12(24)14(32-5)33-36(28,29)34-35(26,27)30-3-6-9(21)11(23)13(31-6)4-1-7(19)17-15(25)16-4/h1,5-6,8-14,18,20-24H,2-3H2,(H,26,27)(H,28,29)(H2,16,17,19,25)/t5-,6-,8+,9-,10+,11-,12-,13+,14-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
AffyNet 
Article
PubMed
4.91E+3n/an/an/an/an/an/an/an/a



Hokkaido University

Curated by ChEMBL


Assay Description
Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase I


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50072688
PNG
(CHEMBL111972 | N-[2-(6-Bromo-naphthalen-2-yloxy)-4...)
Show SMILES CC(=O)NC1C(O)C(O)C(CO)OC1Oc1ccc2cc(Br)ccc2c1
Show InChI InChI=1S/C18H20BrNO6/c1-9(22)20-15-17(24)16(23)14(8-21)26-18(15)25-13-5-3-10-6-12(19)4-2-11(10)7-13/h2-7,14-18,21,23-24H,8H2,1H3,(H,20,22)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

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



Scripps Research Institute

Curated by ChEMBL


Assay Description
Compound was tested for the inhibition recombinant bovine beta -1,4 -galactosyl transferase (beta-1,4-GalT)


Bioorg Med Chem Lett 8: 3359-64 (1999)

More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50072689
PNG
(CHEMBL112241 | N-[4,5-Dihydroxy-6-hydroxymethyl-2-...)
Show SMILES CC(=O)NC1C(O)C(O)C(CO)OC1Oc1ccc2ccccc2c1
Show InChI InChI=1S/C18H21NO6/c1-10(21)19-15-17(23)16(22)14(9-20)25-18(15)24-13-7-6-11-4-2-3-5-12(11)8-13/h2-8,14-18,20,22-23H,9H2,1H3,(H,19,21)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

AffyNet 
PubMed
9.50E+3n/an/an/an/an/an/an/an/a



Scripps Research Institute

Curated by ChEMBL


Assay Description
Compound was tested for the inhibition recombinant bovine beta -1,4 -galactosyl transferase (beta-1,4-GalT)


Bioorg Med Chem Lett 8: 3359-64 (1999)

More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50370675
PNG
(CHEMBL607908)
Show SMILES OC[C@@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2OC([C@H](O)[C@@H]2O)n2ccc(=O)[nH]c2=O)[C@@H](OCCOCCOCCOCc2ccc3ccccc3c2)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C32H44N2O20P2/c35-16-22-25(37)27(39)29(49-14-13-47-10-9-46-11-12-48-17-19-5-6-20-3-1-2-4-21(20)15-19)31(52-22)53-56(44,45)54-55(42,43)50-18-23-26(38)28(40)30(51-23)34-8-7-24(36)33-32(34)41/h1-8,15,22-23,25-31,35,37-40H,9-14,16-18H2,(H,42,43)(H,44,45)(H,33,36,41)/t22-,23+,25-,26+,27-,28+,29-,30?,31+/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
PubMed
1.17E+4n/an/an/an/an/an/an/an/a



Hokkaido University

Curated by ChEMBL


Assay Description
Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase I


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50370678
PNG
(CHEMBL611116)
Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]2O[C@@H](CNNC(=O)COCCOCCOCc3ccc4ccccc4c3)[C@H](O)[C@H](O)[C@@H]2O)OC([C@@H]1O)n1ccc(=O)[nH]c1=O
Show InChI InChI=1S/C32H44N4O20P2/c37-23-7-8-36(32(44)34-23)30-28(42)26(40)22(53-30)16-52-57(45,46)56-58(47,48)55-31-29(43)27(41)25(39)21(54-31)14-33-35-24(38)17-51-12-10-49-9-11-50-15-18-5-6-19-3-1-2-4-20(19)13-18/h1-8,13,21-22,25-31,33,39-43H,9-12,14-17H2,(H,35,38)(H,45,46)(H,47,48)(H,34,37,44)/t21-,22+,25-,26+,27-,28+,29-,30?,31+/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
PubMed
2.06E+4n/an/an/an/an/an/an/an/a



Hokkaido University

Curated by ChEMBL


Assay Description
Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase I


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50072693
PNG
(CHEMBL114323 | N-[4,5-Dihydroxy-6-hydroxymethyl-2-...)
Show SMILES CC(=O)NC1C(O)C(O)C(CO)OC1Oc1cccc2ccccc12
Show InChI InChI=1S/C18H21NO6/c1-10(21)19-15-17(23)16(22)14(9-20)25-18(15)24-13-8-4-6-11-5-2-3-7-12(11)13/h2-8,14-18,20,22-23H,9H2,1H3,(H,19,21)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

AffyNet 
PubMed
2.20E+4n/an/an/an/an/an/an/an/a



Scripps Research Institute

Curated by ChEMBL


Assay Description
Compound was tested for the inhibition recombinant bovine beta -1,4 -galactosyl transferase (beta-1,4-GalT)


Bioorg Med Chem Lett 8: 3359-64 (1999)

More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50370677
PNG
(CHEMBL609634)
Show SMILES Cc1ccc2ccc(COC(=O)COCCOCC(=O)NC[C@@H]3O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]4OC([C@H](O)[C@@H]4O)n4ccc(=O)[nH]c4=O)[C@@H](O)[C@@H](O)[C@H]3O)cc2c1
Show InChI InChI=1S/C33H43N3O21P2/c1-17-2-4-19-5-3-18(11-20(19)10-17)13-52-25(39)16-51-9-8-50-15-24(38)34-12-21-26(40)28(42)30(44)32(55-21)56-59(48,49)57-58(46,47)53-14-22-27(41)29(43)31(54-22)36-7-6-23(37)35-33(36)45/h2-7,10-11,21-22,26-32,40-44H,8-9,12-16H2,1H3,(H,34,38)(H,46,47)(H,48,49)(H,35,37,45)/t21-,22+,26-,27+,28-,29+,30-,31?,32+/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
PubMed
2.23E+4n/an/an/an/an/an/an/an/a



Hokkaido University

Curated by ChEMBL


Assay Description
Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase I


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50366328
PNG
(CHEMBL606075)
Show SMILES OCC1OC(CP(O)(=O)OP(O)(=O)OC[C@H]2OC([C@H](O)[C@@H]2O)n2ccc(=O)[nH]c2=O)=CC(O)C1O
Show InChI InChI=1S/C16H24N2O15P2/c19-4-9-12(22)8(20)3-7(31-9)6-34(26,27)33-35(28,29)30-5-10-13(23)14(24)15(32-10)18-2-1-11(21)17-16(18)25/h1-3,8-10,12-15,19-20,22-24H,4-6H2,(H,26,27)(H,28,29)(H,17,21,25)/t8?,9?,10-,12?,13-,14-,15?/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
6.20E+4n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition constant of compound was tested against Beta-galactosyltransferase from bovine milk


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50173721
PNG
(CHEMBL196432 | Uridine-5'-diphosphogalactose deriv...)
Show SMILES CN(C)c1cccc2c(cccc12)S(=O)(=O)NCCCOC1OC(CO)C(O)C(O)C1NC(C)=O
Show InChI InChI=1S/C23H33N3O8S/c1-14(28)25-20-22(30)21(29)18(13-27)34-23(20)33-12-6-11-24-35(31,32)19-10-5-7-15-16(19)8-4-9-17(15)26(2)3/h4-5,7-10,18,20-24,27,29-30H,6,11-13H2,1-3H3,(H,25,28)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
AffyNet 
Article
PubMed
7.67E+4n/an/an/an/an/an/an/an/a



Hokkaido University

Curated by ChEMBL


Assay Description
Inhibitory constant against human Beta-1,4-galactosyltransferase I using UDP-Gal (0-160 uM)


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50366330
PNG
(CHEMBL605663)
Show SMILES O[C@@H]1[C@@H](COP(O)(=O)CP(O)(=O)OC2OC(O)C(O)C(O)C2O)OC([C@@H]1O)n1ccc(=O)[nH]c1=O
Show InChI InChI=1S/C15H24N2O16P2/c18-6-1-2-17(15(25)16-6)12-9(21)7(19)5(31-12)3-30-34(26,27)4-35(28,29)33-14-11(23)8(20)10(22)13(24)32-14/h1-2,5,7-14,19-24H,3-4H2,(H,26,27)(H,28,29)(H,16,18,25)/t5-,7-,8?,9-,10?,11?,12?,13?,14?/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
9.69E+4n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition constant of compound was tested against Beta-galactosyltransferase from bovine milk


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50118213
PNG
(5'-UTP | CHEMBL336296 | H4utp | UTP | uridine 5'-(...)
Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]([C@@H]1O)n1ccc(=O)[nH]c1=O
Show InChI InChI=1S/C9H15N2O15P3/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(24-8)3-23-28(19,20)26-29(21,22)25-27(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
Purchase

CHEMBL
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents


Similars

AffyNet 
Article
1.28E+5n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition constant of compound was tested against Beta-galactosyltransferase from bovine milk


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Homo sapiens)
BDBM50370679
PNG
(CHEMBL611112)
Show SMILES COCCOCCOCCOC[C@@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2OC([C@H](O)[C@@H]2O)n2ccc(=O)[nH]c2=O)[C@@H](O)[C@@H](O)[C@H]1O
Show InChI InChI=1S/C22H38N2O20P2/c1-36-4-5-37-6-7-38-8-9-39-10-12-15(26)17(28)19(30)21(42-12)43-46(34,35)44-45(32,33)40-11-13-16(27)18(29)20(41-13)24-3-2-14(25)23-22(24)31/h2-3,12-13,15-21,26-30H,4-11H2,1H3,(H,32,33)(H,34,35)(H,23,25,31)/t12-,13+,15-,16+,17-,18+,19-,20?,21+/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
PubMed
1.49E+5n/an/an/an/an/an/an/an/a



Hokkaido University

Curated by ChEMBL


Assay Description
Inhibitory constant against human recombinant Beta-1,4-galactosyltransferase I


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50366329
PNG
(CHEMBL605030)
Show SMILES O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)C2OC(O)C(O)C(O)C2O)OC([C@@H]1O)n1ccc(=O)[nH]c1=O
Show InChI InChI=1S/C14H22N2O16P2/c17-5-1-2-16(14(24)15-5)11-8(20)6(18)4(30-11)3-29-34(27,28)32-33(25,26)13-10(22)7(19)9(21)12(23)31-13/h1-2,4,6-13,18-23H,3H2,(H,25,26)(H,27,28)(H,15,17,24)/t4-,6-,7?,8-,9?,10?,11?,12?,13?/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
1.65E+5n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition constant of compound was tested against Beta-galactosyltransferase from bovine milk


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50072695
PNG
(CHEMBL115776 | N-(5-Amino-2-benzyloxy-4-hydroxy-6-...)
Show SMILES CC(=O)NC1C(O)C(N)C(CO)OC1OCc1ccccc1
Show InChI InChI=1S/C15H22N2O5/c1-9(19)17-13-14(20)12(16)11(7-18)22-15(13)21-8-10-5-3-2-4-6-10/h2-6,11-15,18,20H,7-8,16H2,1H3,(H,17,19)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

AffyNet 
PubMed
8.50E+5n/an/an/an/an/an/an/an/a



Scripps Research Institute

Curated by ChEMBL


Assay Description
Compound was tested for the inhibition recombinant bovine beta -1,4 -galactosyl transferase (beta-1,4-GalT)


Bioorg Med Chem Lett 8: 3359-64 (1999)

More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50283877
PNG
(CHEMBL125848 | N-((2R,3R,4S,5S,6S)-5-Amino-2-benzy...)
Show SMILES CC(=O)N[C@@H]1[C@@H](O)[C@H](N)[C@@H](CO)O[C@H]1OCc1ccccc1
Show InChI InChI=1S/C15H22N2O5/c1-9(19)17-13-14(20)12(16)11(7-18)22-15(13)21-8-10-5-3-2-4-6-10/h2-6,11-15,18,20H,7-8,16H2,1H3,(H,17,19)/t11-,12-,13-,14+,15-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
Article
8.50E+5n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibitory activity against bovine Beta-1,4-galactosyltransferase at 100 microM concentration


Citation and Details
More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50072691
PNG
(CHEMBL2303731 | N-[2-(3,5-Dihydroxy-2-hydroxymethy...)
Show SMILES CO[C@@H]1O[C@@H](CO)[C@H](O)[C@H](O[C@@H]2O[C@@H](CS)[C@@H](O)[C@H](O)[C@@H]2NC(C)=O)[C@@H]1O
Show InChI InChI=1S/C15H27NO10S/c1-5(18)16-8-11(21)9(19)7(4-27)25-14(8)26-13-10(20)6(3-17)24-15(23-2)12(13)22/h6-15,17,19-22,27H,3-4H2,1-2H3,(H,16,18)/t6-,7-,8-,9+,10-,11+,12-,13-,14-,15+/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

AffyNet 
PubMed
1.00E+6n/an/an/an/an/an/an/an/a



Scripps Research Institute

Curated by ChEMBL


Assay Description
Compound was tested for the inhibition recombinant bovine beta -1,4 -galactosyl transferase (beta-1,4-GalT)


Bioorg Med Chem Lett 8: 3359-64 (1999)

More data for this
Ligand-Target Pair
Beta-1,4-galactosyltransferase 1


(Bos taurus)
BDBM50282179
PNG
((4,5-Dihydroxy-6-hydroxymethyl-5,6-dihydro-4H-pyra...)
Show SMILES OCC1OC(CP(O)(O)=O)=CC(O)C1O
Show InChI InChI=1S/C7H13O7P/c8-2-6-7(10)5(9)1-4(14-6)3-15(11,12)13/h1,5-10H,2-3H2,(H2,11,12,13)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
AffyNet 
Article
1.43E+6n/an/an/an/an/an/an/an/a


TBA

Assay Description
Inhibition constant of compound was tested against Beta-galactosyltransferase from bovine milk


Citation and Details
More data for this
Ligand-Target Pair