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Compile Data Set for Download or QSAR

Found 40 hits with Last Name = 'ichikawa' and Initial = 'y'   
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
Tissue alpha-L-fucosidase


(Homo sapiens (Human))
BDBM50104412
PNG
((S)-5-Methyl-piperidine-3,4-diol | CHEMBL86305)
Show SMILES CC1CNC[C@H](O)C1O
Show InChI InChI=1S/C6H13NO2/c1-4-2-7-3-5(8)6(4)9/h4-9H,2-3H2,1H3/t4?,5-,6?/m0/s1
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Article
8.40E+3n/an/an/an/an/an/a6.8n/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-fucosidase from bovine kidney(sigma F 5884) at pH 6.8


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal acid glucosylceramidase


(Homo sapiens (Human))
BDBM50182798
PNG
((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)
Show SMILES O[C@H]1CNC[C@@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4+,5+
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n/an/a 8.80E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-glucosidase from almonds(sigma G 4511).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Tissue alpha-L-fucosidase


(Homo sapiens (Human))
BDBM50104412
PNG
((S)-5-Methyl-piperidine-3,4-diol | CHEMBL86305)
Show SMILES CC1CNC[C@H](O)C1O
Show InChI InChI=1S/C6H13NO2/c1-4-2-7-3-5(8)6(4)9/h4-9H,2-3H2,1H3/t4?,5-,6?/m0/s1
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n/an/a 2.60E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-fucosidase from bovine kidney(sigma F 5884).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Beta-galactosidase


(Homo sapiens (Human))
BDBM50182798
PNG
((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)
Show SMILES O[C@H]1CNC[C@@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4+,5+
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n/an/a 4.00E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-galactosidase from aspergillus oryzae (sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Alpha-galactosidase A


(Homo sapiens (Human))
BDBM50182798
PNG
((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)
Show SMILES O[C@H]1CNC[C@@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4+,5+
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n/an/a 4.00E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-galactosidase from green coffee beans (sigma G 8507).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Beta-galactosidase


(Homo sapiens (Human))
BDBM50288855
PNG
(1-Butyl-piperidine-3,4,5-triol | CHEMBL152232)
Show SMILES CCCCN1CC(O)C(O)C(O)C1
Show InChI InChI=1S/C9H19NO3/c1-2-3-4-10-5-7(11)9(13)8(12)6-10/h7-9,11-13H,2-6H2,1H3
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n/an/a 4.30E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-galactosidase from aspergillus oryzae (sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal acid glucosylceramidase


(Homo sapiens (Human))
BDBM50288853
PNG
(1-Butyl-5-methyl-piperidine-3,4-diol | CHEMBL35602...)
Show SMILES CCCCN1CC(C)C(O)C(O)C1
Show InChI InChI=1S/C10H21NO2/c1-3-4-5-11-6-8(2)10(13)9(12)7-11/h8-10,12-13H,3-7H2,1-2H3
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n/an/a 8.00E+4n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-glucosidase from almonds(sigma G 4511).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Tissue alpha-L-fucosidase


(Homo sapiens (Human))
BDBM50288853
PNG
(1-Butyl-5-methyl-piperidine-3,4-diol | CHEMBL35602...)
Show SMILES CCCCN1CC(C)C(O)C(O)C1
Show InChI InChI=1S/C10H21NO2/c1-3-4-5-11-6-8(2)10(13)9(12)7-11/h8-10,12-13H,3-7H2,1-2H3
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n/an/a 2.70E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-fucosidase from bovine kidney(sigma F 5884).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
alpha-1,2-Mannosidase


(Glycine max)
BDBM50182798
PNG
((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)
Show SMILES O[C@H]1CNC[C@@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4+,5+
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n/an/a 3.60E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of jack bean alpha-mannosidase


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal acid glucosylceramidase


(Homo sapiens (Human))
BDBM50104412
PNG
((S)-5-Methyl-piperidine-3,4-diol | CHEMBL86305)
Show SMILES CC1CNC[C@H](O)C1O
Show InChI InChI=1S/C6H13NO2/c1-4-2-7-3-5(8)6(4)9/h4-9H,2-3H2,1H3/t4?,5-,6?/m0/s1
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n/an/a 5.00E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-glucosidase from almonds(sigma G 4511).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal acid glucosylceramidase


(Homo sapiens (Human))
BDBM50288855
PNG
(1-Butyl-piperidine-3,4,5-triol | CHEMBL152232)
Show SMILES CCCCN1CC(O)C(O)C(O)C1
Show InChI InChI=1S/C9H19NO3/c1-2-3-4-10-5-7(11)9(13)8(12)6-10/h7-9,11-13H,2-6H2,1H3
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n/an/a 5.30E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-glucosidase from almonds(sigma G 4511).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Alpha-galactosidase A


(Homo sapiens (Human))
BDBM50288855
PNG
(1-Butyl-piperidine-3,4,5-triol | CHEMBL152232)
Show SMILES CCCCN1CC(O)C(O)C(O)C1
Show InChI InChI=1S/C9H19NO3/c1-2-3-4-10-5-7(11)9(13)8(12)6-10/h7-9,11-13H,2-6H2,1H3
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n/an/a 7.25E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-galactosidase from green coffee beans (sigma G 8507).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
alpha-1,2-Mannosidase


(Glycine max)
BDBM50288855
PNG
(1-Butyl-piperidine-3,4,5-triol | CHEMBL152232)
Show SMILES CCCCN1CC(O)C(O)C(O)C1
Show InChI InChI=1S/C9H19NO3/c1-2-3-4-10-5-7(11)9(13)8(12)6-10/h7-9,11-13H,2-6H2,1H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of jack bean alpha-mannosidase


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Alpha-galactosidase A


(Homo sapiens (Human))
BDBM50288853
PNG
(1-Butyl-5-methyl-piperidine-3,4-diol | CHEMBL35602...)
Show SMILES CCCCN1CC(C)C(O)C(O)C1
Show InChI InChI=1S/C10H21NO2/c1-3-4-5-11-6-8(2)10(13)9(12)7-11/h8-10,12-13H,3-7H2,1-2H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-galactosidase from green coffee beans (sigma G 8507).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Beta-galactosidase


(Homo sapiens (Human))
BDBM50104412
PNG
((S)-5-Methyl-piperidine-3,4-diol | CHEMBL86305)
Show SMILES CC1CNC[C@H](O)C1O
Show InChI InChI=1S/C6H13NO2/c1-4-2-7-3-5(8)6(4)9/h4-9H,2-3H2,1H3/t4?,5-,6?/m0/s1
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-galactosidase from aspergillus oryzae (sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
alpha-1,2-Mannosidase


(Glycine max)
BDBM50104412
PNG
((S)-5-Methyl-piperidine-3,4-diol | CHEMBL86305)
Show SMILES CC1CNC[C@H](O)C1O
Show InChI InChI=1S/C6H13NO2/c1-4-2-7-3-5(8)6(4)9/h4-9H,2-3H2,1H3/t4?,5-,6?/m0/s1
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of jack bean alpha-mannosidase


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Alpha-galactosidase A


(Homo sapiens (Human))
BDBM50288852
PNG
(5-Methoxy-piperidine-3,4-diol | CHEMBL414447)
Show SMILES COC1CNCC(O)C1O
Show InChI InChI=1S/C6H13NO3/c1-10-5-3-7-2-4(8)6(5)9/h4-9H,2-3H2,1H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-galactosidase from green coffee beans (sigma G 8507).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Alpha-galactosidase A


(Homo sapiens (Human))
BDBM50288854
PNG
(5-Methylene-piperidine-3,4-diol | CHEMBL150938)
Show SMILES OC1CNCC(=C)C1O
Show InChI InChI=1S/C6H11NO2/c1-4-2-7-3-5(8)6(4)9/h5-9H,1-3H2
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-galactosidase from green coffee beans (sigma G 8507).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
alpha-1,2-Mannosidase


(Glycine max)
BDBM50288854
PNG
(5-Methylene-piperidine-3,4-diol | CHEMBL150938)
Show SMILES OC1CNCC(=C)C1O
Show InChI InChI=1S/C6H11NO2/c1-4-2-7-3-5(8)6(4)9/h5-9H,1-3H2
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of jack bean alpha-mannosidase


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Beta-galactosidase


(Homo sapiens (Human))
BDBM50288852
PNG
(5-Methoxy-piperidine-3,4-diol | CHEMBL414447)
Show SMILES COC1CNCC(O)C1O
Show InChI InChI=1S/C6H13NO3/c1-10-5-3-7-2-4(8)6(5)9/h4-9H,2-3H2,1H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-galactosidase from aspergillus oryzae (sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Beta-galactosidase


(Homo sapiens (Human))
BDBM50288854
PNG
(5-Methylene-piperidine-3,4-diol | CHEMBL150938)
Show SMILES OC1CNCC(=C)C1O
Show InChI InChI=1S/C6H11NO2/c1-4-2-7-3-5(8)6(4)9/h5-9H,1-3H2
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-galactosidase from aspergillus oryzae (sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Tissue alpha-L-fucosidase


(Homo sapiens (Human))
BDBM50288852
PNG
(5-Methoxy-piperidine-3,4-diol | CHEMBL414447)
Show SMILES COC1CNCC(O)C1O
Show InChI InChI=1S/C6H13NO3/c1-10-5-3-7-2-4(8)6(5)9/h4-9H,2-3H2,1H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-fucosidase from bovine kidney(sigma F 5884).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal acid glucosylceramidase


(Homo sapiens (Human))
BDBM50288852
PNG
(5-Methoxy-piperidine-3,4-diol | CHEMBL414447)
Show SMILES COC1CNCC(O)C1O
Show InChI InChI=1S/C6H13NO3/c1-10-5-3-7-2-4(8)6(5)9/h4-9H,2-3H2,1H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-glucosidase from almonds(sigma G 4511).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Beta-galactosidase


(Homo sapiens (Human))
BDBM50288853
PNG
(1-Butyl-5-methyl-piperidine-3,4-diol | CHEMBL35602...)
Show SMILES CCCCN1CC(C)C(O)C(O)C1
Show InChI InChI=1S/C10H21NO2/c1-3-4-5-11-6-8(2)10(13)9(12)7-11/h8-10,12-13H,3-7H2,1-2H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-galactosidase from aspergillus oryzae (sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Alpha-galactosidase A


(Homo sapiens (Human))
BDBM50104412
PNG
((S)-5-Methyl-piperidine-3,4-diol | CHEMBL86305)
Show SMILES CC1CNC[C@H](O)C1O
Show InChI InChI=1S/C6H13NO2/c1-4-2-7-3-5(8)6(4)9/h4-9H,2-3H2,1H3/t4?,5-,6?/m0/s1
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-galactosidase from green coffee beans (sigma G 8507).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Tissue alpha-L-fucosidase


(Homo sapiens (Human))
BDBM50288854
PNG
(5-Methylene-piperidine-3,4-diol | CHEMBL150938)
Show SMILES OC1CNCC(=C)C1O
Show InChI InChI=1S/C6H11NO2/c1-4-2-7-3-5(8)6(4)9/h5-9H,1-3H2
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TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-fucosidase from bovine kidney(sigma F 5884).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal acid glucosylceramidase


(Homo sapiens (Human))
BDBM50288854
PNG
(5-Methylene-piperidine-3,4-diol | CHEMBL150938)
Show SMILES OC1CNCC(=C)C1O
Show InChI InChI=1S/C6H11NO2/c1-4-2-7-3-5(8)6(4)9/h5-9H,1-3H2
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TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of beta-glucosidase from almonds(sigma G 4511).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
alpha-1,2-Mannosidase


(Glycine max)
BDBM50288853
PNG
(1-Butyl-5-methyl-piperidine-3,4-diol | CHEMBL35602...)
Show SMILES CCCCN1CC(C)C(O)C(O)C1
Show InChI InChI=1S/C10H21NO2/c1-3-4-5-11-6-8(2)10(13)9(12)7-11/h8-10,12-13H,3-7H2,1-2H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of jack bean alpha-mannosidase


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
alpha-1,2-Mannosidase


(Glycine max)
BDBM50288852
PNG
(5-Methoxy-piperidine-3,4-diol | CHEMBL414447)
Show SMILES COC1CNCC(O)C1O
Show InChI InChI=1S/C6H13NO3/c1-10-5-3-7-2-4(8)6(5)9/h4-9H,2-3H2,1H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of jack bean alpha-mannosidase


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal alpha-glucosidase


(Homo sapiens (Human))
BDBM50288854
PNG
(5-Methylene-piperidine-3,4-diol | CHEMBL150938)
Show SMILES OC1CNCC(=C)C1O
Show InChI InChI=1S/C6H11NO2/c1-4-2-7-3-5(8)6(4)9/h5-9H,1-3H2
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TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-glucosidase from yeast(sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Tissue alpha-L-fucosidase


(Homo sapiens (Human))
BDBM50182798
PNG
((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)
Show SMILES O[C@H]1CNC[C@@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4+,5+
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TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-fucosidase from bovine kidney(sigma F 5884).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal alpha-glucosidase


(Homo sapiens (Human))
BDBM50104412
PNG
((S)-5-Methyl-piperidine-3,4-diol | CHEMBL86305)
Show SMILES CC1CNC[C@H](O)C1O
Show InChI InChI=1S/C6H13NO2/c1-4-2-7-3-5(8)6(4)9/h4-9H,2-3H2,1H3/t4?,5-,6?/m0/s1
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-glucosidase from yeast(sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal alpha-glucosidase


(Homo sapiens (Human))
BDBM50288855
PNG
(1-Butyl-piperidine-3,4,5-triol | CHEMBL152232)
Show SMILES CCCCN1CC(O)C(O)C(O)C1
Show InChI InChI=1S/C9H19NO3/c1-2-3-4-10-5-7(11)9(13)8(12)6-10/h7-9,11-13H,2-6H2,1H3
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TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-glucosidase from yeast(sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal alpha-glucosidase


(Homo sapiens (Human))
BDBM50288852
PNG
(5-Methoxy-piperidine-3,4-diol | CHEMBL414447)
Show SMILES COC1CNCC(O)C1O
Show InChI InChI=1S/C6H13NO3/c1-10-5-3-7-2-4(8)6(5)9/h4-9H,2-3H2,1H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-glucosidase from yeast(sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal alpha-glucosidase


(Homo sapiens (Human))
BDBM50288853
PNG
(1-Butyl-5-methyl-piperidine-3,4-diol | CHEMBL35602...)
Show SMILES CCCCN1CC(C)C(O)C(O)C1
Show InChI InChI=1S/C10H21NO2/c1-3-4-5-11-6-8(2)10(13)9(12)7-11/h8-10,12-13H,3-7H2,1-2H3
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-glucosidase from yeast(sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Lysosomal alpha-glucosidase


(Homo sapiens (Human))
BDBM50182798
PNG
((3R,4r,5S)-piperidine-3,4,5-triol | 1,5-Dideoxy-1,...)
Show SMILES O[C@H]1CNC[C@@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4+,5+
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n/an/a>1.00E+6n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-glucosidase from yeast(sigma G 7256).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Tissue alpha-L-fucosidase


(Homo sapiens (Human))
BDBM50288855
PNG
(1-Butyl-piperidine-3,4,5-triol | CHEMBL152232)
Show SMILES CCCCN1CC(O)C(O)C(O)C1
Show InChI InChI=1S/C9H19NO3/c1-2-3-4-10-5-7(11)9(13)8(12)6-10/h7-9,11-13H,2-6H2,1H3
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TBA

Curated by ChEMBL


Assay Description
Compound was evaluated for inhibition of alpha-fucosidase from bovine kidney(sigma F 5884).


Bioorg Med Chem Lett 6: 553-558 (1996)


Article DOI: 10.1016/0960-894X(96)00068-6
BindingDB Entry DOI: 10.7270/Q2ZS2WHG
More data for this
Ligand-Target Pair
Alpha-(1,3)-fucosyltransferase 10


(Homo sapiens (Human))
BDBM50421338
PNG
(CHEMBL2303754)
Show SMILES OC[C@@H]1NC[C@@H](O)[C@@H](O)[C@@H]1O[C@@H]1O[C@@H](CO)[C@H](O)[C@H](O)[C@@H]1O |r|
Show InChI InChI=1S/C12H23NO9/c14-2-4-11(7(17)5(16)1-13-4)22-12-10(20)9(19)8(18)6(3-15)21-12/h4-20H,1-3H2/t4-,5+,6-,7+,8-,9-,10-,11+,12-/m0/s1
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n/an/a 4.00E+7n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was tested for inhibitory activity against fucosyltransferase


Bioorg Med Chem Lett 1: 425-428 (1991)


Article DOI: 10.1016/S0960-894X(00)80270-X
BindingDB Entry DOI: 10.7270/Q2BK1C7N
More data for this
Ligand-Target Pair
Alpha-(1,3)-fucosyltransferase 10


(Homo sapiens (Human))
BDBM50421339
PNG
(CHEMBL2303753)
Show SMILES OC[C@@H]1O[C@@H](O[C@H]2[C@H](O)C=CO[C@H]2CO)[C@@H](O)[C@@H](O)[C@H]1O |r,c:9|
Show InChI InChI=1S/C12H20O9/c13-3-6-8(16)9(17)10(18)12(20-6)21-11-5(15)1-2-19-7(11)4-14/h1-2,5-18H,3-4H2/t5-,6+,7+,8+,9+,10+,11+,12+/m1/s1
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TBA

Curated by ChEMBL


Assay Description
Compound was tested for inhibitory activity against fucosyltransferase


Bioorg Med Chem Lett 1: 425-428 (1991)


Article DOI: 10.1016/S0960-894X(00)80270-X
BindingDB Entry DOI: 10.7270/Q2BK1C7N
More data for this
Ligand-Target Pair
Alpha-(1,3)-fucosyltransferase 10


(Homo sapiens (Human))
BDBM50421340
PNG
(CHEMBL2303756)
Show SMILES CC(=O)N[C@H]1C[C@H](O[C@@H]2O[C@@H](CO)[C@H](O)[C@H](O)[C@@H]2O)[C@H](CO)O[C@@H]1OCC=C |r|
Show InChI InChI=1S/C17H29NO10/c1-3-4-25-16-9(18-8(2)21)5-10(11(6-19)27-16)26-17-15(24)14(23)13(22)12(7-20)28-17/h3,9-17,19-20,22-24H,1,4-7H2,2H3,(H,18,21)/t9-,10-,11-,12-,13-,14-,15-,16-,17+/m0/s1
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n/an/a>1.25E+8n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was tested for inhibitory activity against fucosyltransferase


Bioorg Med Chem Lett 1: 425-428 (1991)


Article DOI: 10.1016/S0960-894X(00)80270-X
BindingDB Entry DOI: 10.7270/Q2BK1C7N
More data for this
Ligand-Target Pair