Compile Data Set for Download or QSAR

Found 44 hits with Last Name = 'wustman' and Initial = 'ba'   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Beta-galactosidase (Homo sapiens (Human))	BDBM50358321 (CHEMBL1922579 | CHEMBL1922581) Show SMILES CCCCCCCCN[C@@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O |r,t:10| Show InChI InChI=1S/C15H29NO4/c1-2-3-4-5-6-7-8-16-12-9-11(10-17)13(18)15(20)14(12)19/h9,12-20H,2-8,10H2,1H3/t12-,13+,14+,15+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Amicus Therapeutics Curated by ChEMBL					Assay Description Inhibition of human beta galactosidase				J Med Chem 56: 2705-25 (2013) Article DOI: 10.1021/jm301557k BindingDB Entry DOI: 10.7270/Q26111N4
					More data for this Ligand-Target Pair				3D Structure (crystal)
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175515 (US9119845, 16) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1CC1CCNCC1 |r| Show InChI InChI=1S/C12H24N2O3/c15-8-10-12(17)11(16)3-6-14(10)7-9-1-4-13-5-2-9/h9-13,15-17H,1-8H2/t10-,11-,12-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	440	n/a	1.07E+3	n/a	6.90E+3	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238210 (US9402837, 16) Show SMILES OC[C@H]1CN(CC2CCNCC2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C12H24N2O3/c15-8-10-6-14(7-11(16)12(10)17)5-9-1-3-13-4-2-9/h9-13,15-17H,1-8H2/t10-,11-,12-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	440	n/a	1.07E+3	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175523 (US9119845, 24) Show SMILES CC(C)CCCN1CC[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C12H25NO3/c1-9(2)4-3-6-13-7-5-11(15)12(16)10(13)8-14/h9-12,14-16H,3-8H2,1-2H3/t10-,11-,12-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	880	n/a	2.13E+3	n/a	3.05E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238214 (US9402837, 24) Show SMILES CC(C)CCCN1C[C@@H](O)[C@H](O)[C@@H](CO)C1 Show InChI InChI=1S/C12H25NO3/c1-9(2)4-3-5-13-6-10(8-14)12(16)11(15)7-13/h9-12,14-16H,3-8H2,1-2H3/t10-,11-,12-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	880	n/a	2.13E+3	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175503 (US9119845, 4) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#7]-1-[#6]-[#6]-[#6@@H](-[#8])-[#6@H](-[#8])-[#6@H]-1-[#6]-[#8] |r| Show InChI InChI=1S/C11H21NO3/c1-8(2)3-5-12-6-4-10(14)11(15)9(12)7-13/h3,9-11,13-15H,4-7H2,1-2H3/t9-,10-,11-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.66E+3	n/a	4.00E+3	n/a	6.30E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238200 (US9402837, 4) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-[#7]-1-[#6]-[#6@@H](-[#8])-[#6@H](-[#8])-[#6@@H](-[#6]-[#8])-[#6]-1 Show InChI InChI=1S/C11H21NO3/c1-8(2)3-4-12-5-9(7-13)11(15)10(14)6-12/h3,9-11,13-15H,4-7H2,1-2H3/t9-,10-,11-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.66E+3	n/a	4.00E+3	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175504 (US9119845, 5) Show SMILES COCCN1CC[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C9H19NO4/c1-14-5-4-10-3-2-8(12)9(13)7(10)6-11/h7-9,11-13H,2-6H2,1H3/t7-,8-,9-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	2.48E+3	n/a	5.99E+3	n/a	6.07E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238201 (US9402837, 5) Show SMILES COCCN1C[C@@H](O)[C@H](O)[C@@H](CO)C1 Show InChI InChI=1S/C9H19NO4/c1-14-3-2-10-4-7(6-11)9(13)8(12)5-10/h7-9,11-13H,2-6H2,1H3/t7-,8-,9-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.48E+3	n/a	5.99E+3	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175512 (US9119845, 13) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1CCc1ccccc1 |r| Show InChI InChI=1S/C14H21NO3/c16-10-12-14(18)13(17)7-9-15(12)8-6-11-4-2-1-3-5-11/h1-5,12-14,16-18H,6-10H2/t12-,13-,14-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3.11E+3	n/a	7.50E+3	n/a	2.20E+3	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238208 (US9402837, 13) Show SMILES OC[C@H]1CN(CCc2ccccc2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C14H21NO3/c16-10-12-8-15(9-13(17)14(12)18)7-6-11-4-2-1-3-5-11/h1-5,12-14,16-18H,6-10H2/t12-,13-,14-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3.11E+3	n/a	7.50E+3	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175511 (US9119845, 12) Show SMILES Nc1ccc(CN2CC[C@@H](O)[C@H](O)[C@H]2CO)cc1 |r| Show InChI InChI=1S/C13H20N2O3/c14-10-3-1-9(2-4-10)7-15-6-5-12(17)13(18)11(15)8-16/h1-4,11-13,16-18H,5-8,14H2/t11-,12-,13-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	3.88E+3	n/a	9.36E+3	n/a	7.70E+3	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238207 (US9402837, 12) Show SMILES Nc1ccc(CN2C[C@@H](O)[C@H](O)[C@@H](CO)C2)cc1 Show InChI InChI=1S/C13H20N2O3/c14-11-3-1-9(2-4-11)5-15-6-10(8-16)13(18)12(17)7-15/h1-4,10,12-13,16-18H,5-8,14H2/t10-,12-,13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	3.88E+3	n/a	9.36E+3	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175507 (US9119845, 8) Show SMILES Cc1cccc(CN2CC[C@@H](O)[C@H](O)[C@H]2CO)c1 |r| Show InChI InChI=1S/C14H21NO3/c1-10-3-2-4-11(7-10)8-15-6-5-13(17)14(18)12(15)9-16/h2-4,7,12-14,16-18H,5-6,8-9H2,1H3/t12-,13-,14-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	5.26E+3	n/a	1.27E+4	n/a	1.16E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238204 (US9402837, 8) Show SMILES Cc1cccc(CN2C[C@@H](O)[C@H](O)[C@@H](CO)C2)c1 Show InChI InChI=1S/C14H21NO3/c1-10-3-2-4-11(5-10)6-15-7-12(9-16)14(18)13(17)8-15/h2-5,12-14,16-18H,6-9H2,1H3/t12-,13-,14-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	5.26E+3	n/a	1.27E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238213 (US9402837, 23) Show SMILES OC[C@H]1CN(CC2CCCC2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C12H23NO3/c14-8-10-6-13(7-11(15)12(10)16)5-9-3-1-2-4-9/h9-12,14-16H,1-8H2/t10-,11-,12-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	6.48E+3	n/a	1.56E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175522 (US9119845, 23) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1CC1CCCC1 |r| Show InChI InChI=1S/C12H23NO3/c14-8-10-12(16)11(15)5-6-13(10)7-9-3-1-2-4-9/h9-12,14-16H,1-8H2/t10-,11-,12-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	6.48E+3	n/a	1.56E+4	n/a	1.88E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238212 (US9402837, 19) Show SMILES OC[C@H]1CN(Cc2ccncc2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C12H18N2O3/c15-8-10-6-14(7-11(16)12(10)17)5-9-1-3-13-4-2-9/h1-4,10-12,15-17H,5-8H2/t10-,11-,12-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	8.02E+3	n/a	1.94E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175518 (US9119845, 19) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1Cc1ccncc1 |r| Show InChI InChI=1S/C12H18N2O3/c15-8-10-12(17)11(16)3-6-14(10)7-9-1-4-13-5-2-9/h1-2,4-5,10-12,15-17H,3,6-8H2/t10-,11-,12-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	8.02E+3	n/a	1.94E+4	n/a	3.50E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238216 (US9402837, 18) Show SMILES OC[C@H]1CN(Cc2cccs2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C11H17NO3S/c13-7-8-4-12(6-10(14)11(8)15)5-9-2-1-3-16-9/h1-3,8,10-11,13-15H,4-7H2/t8-,10-,11-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.14E+4	n/a	2.76E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175517 (US9119845, 18) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1Cc1cccs1 |r| Show InChI InChI=1S/C11H17NO3S/c13-7-9-11(15)10(14)3-4-12(9)6-8-2-1-5-16-8/h1-2,5,9-11,13-15H,3-4,6-7H2/t9-,10-,11-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.14E+4	n/a	2.76E+4	n/a	1.39E+5	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238197 (US9402837, 1) Show SMILES CCCN1C[C@@H](O)[C@H](O)[C@@H](CO)C1 Show InChI InChI=1S/C9H19NO3/c1-2-3-10-4-7(6-11)9(13)8(12)5-10/h7-9,11-13H,2-6H2,1H3/t7-,8-,9-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.48E+4	n/a	3.58E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175500 (US9119845, 1) Show SMILES CCCN1CC[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C9H19NO3/c1-2-4-10-5-3-8(12)9(13)7(10)6-11/h7-9,11-13H,2-6H2,1H3/t7-,8-,9-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	1.48E+4	n/a	3.58E+4	n/a	6.59E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175502 (US9119845, 3) Show SMILES CCCCCCCN1CC[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C13H27NO3/c1-2-3-4-5-6-8-14-9-7-12(16)13(17)11(14)10-15/h11-13,15-17H,2-10H2,1H3/t11-,12-,13-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	1.73E+4	n/a	4.17E+4	n/a	9.99E+3	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238199 (US9402837, 3) Show SMILES CCCCCCCN1C[C@@H](O)[C@H](O)[C@@H](CO)C1 Show InChI InChI=1S/C13H27NO3/c1-2-3-4-5-6-7-14-8-11(10-15)13(17)12(16)9-14/h11-13,15-17H,2-10H2,1H3/t11-,12-,13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.73E+4	n/a	4.17E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238215 (US9402837, 25) Show SMILES OC[C@H]1CN(Cc2ccc(cc2)[N+]([O-])=O)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C13H18N2O5/c16-8-10-6-14(7-12(17)13(10)18)5-9-1-3-11(4-2-9)15(19)20/h1-4,10,12-13,16-18H,5-8H2/t10-,12-,13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.86E+4	n/a	4.50E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175524 (US9119845, 25) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1Cc1ccc(cc1)[N+]([O-])=O |r| Show InChI InChI=1S/C13H18N2O5/c16-8-11-13(18)12(17)5-6-14(11)7-9-1-3-10(4-2-9)15(19)20/h1-4,11-13,16-18H,5-8H2/t11-,12-,13-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	1.86E+4	n/a	4.50E+4	n/a	1.64E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238209 (US9402837, 15) Show SMILES OC[C@H]1CN(CC2CCOCC2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C12H23NO4/c14-8-10-6-13(7-11(15)12(10)16)5-9-1-3-17-4-2-9/h9-12,14-16H,1-8H2/t10-,11-,12-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.04E+4	n/a	4.92E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175514 (US9119845, 15) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1CC1CCOCC1 |r| Show InChI InChI=1S/C12H23NO4/c14-8-10-12(16)11(15)1-4-13(10)7-9-2-5-17-6-3-9/h9-12,14-16H,1-8H2/t10-,11-,12-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	2.04E+4	n/a	4.92E+4	n/a	6.83E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175506 (US9119845, 7) Show SMILES Cc1ccccc1CN1CC[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C14H21NO3/c1-10-4-2-3-5-11(10)8-15-7-6-13(17)14(18)12(15)9-16/h2-5,12-14,16-18H,6-9H2,1H3/t12-,13-,14-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	2.88E+4	n/a	6.95E+4	n/a	4.64E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238203 (US9402837, 7) Show SMILES Cc1ccccc1CN1C[C@@H](O)[C@H](O)[C@@H](CO)C1 Show InChI InChI=1S/C14H21NO3/c1-10-4-2-3-5-11(10)6-15-7-12(9-16)14(18)13(17)8-15/h2-5,12-14,16-18H,6-9H2,1H3/t12-,13-,14-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	2.88E+4	n/a	6.95E+4	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238205 (US9402837, 9) Show SMILES Cc1ccc(CN2C[C@@H](O)[C@H](O)[C@@H](CO)C2)cc1 Show InChI InChI=1S/C14H21NO3/c1-10-2-4-11(5-3-10)6-15-7-12(9-16)14(18)13(17)8-15/h2-5,12-14,16-18H,6-9H2,1H3/t12-,13-,14-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	5.37E+4	n/a	1.30E+5	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175508 (US9119845, 9) Show SMILES Cc1ccc(CN2CC[C@@H](O)[C@H](O)[C@H]2CO)cc1 |r| Show InChI InChI=1S/C14H21NO3/c1-10-2-4-11(5-3-10)8-15-7-6-13(17)14(18)12(15)9-16/h2-5,12-14,16-18H,6-9H2,1H3/t12-,13-,14-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	5.37E+4	n/a	1.30E+5	n/a	1.45E+5	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238202 (US9402837, 6) Show SMILES OC[C@H]1CN(Cc2ccccc2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C13H19NO3/c15-9-11-7-14(8-12(16)13(11)17)6-10-4-2-1-3-5-10/h1-5,11-13,15-17H,6-9H2/t11-,12-,13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	8.30E+4	n/a	2.00E+5	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175505 (US9119845, 6) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1Cc1ccccc1 |r| Show InChI InChI=1S/C13H19NO3/c15-9-11-13(17)12(16)6-7-14(11)8-10-4-2-1-3-5-10/h1-5,11-13,15-17H,6-9H2/t11-,12-,13-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	8.30E+4	n/a	2.00E+5	n/a	1.15E+5	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238206 (US9402837, 10) Show SMILES OC[C@H]1CN(Cc2ccc(F)cc2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C13H18FNO3/c14-11-3-1-9(2-4-11)5-15-6-10(8-16)13(18)12(17)7-15/h1-4,10,12-13,16-18H,5-8H2/t10-,12-,13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.12E+5	n/a	2.70E+5	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175509 (US9119845, 10) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1Cc1ccc(F)cc1 |r| Show InChI InChI=1S/C13H18FNO3/c14-10-3-1-9(2-4-10)7-15-6-5-12(17)13(18)11(15)8-16/h1-4,11-13,16-18H,5-8H2/t11-,12-,13-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	1.12E+5	n/a	2.70E+5	n/a	7.06E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238211 (US9402837, 17) Show SMILES OC[C@H]1CN(Cc2ccco2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C11H17NO4/c13-7-8-4-12(6-10(14)11(8)15)5-9-2-1-3-16-9/h1-3,8,10-11,13-15H,4-7H2/t8-,10-,11-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.16E+5	n/a	2.80E+5	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175516 (US9119845, 17) Show SMILES OC[C@@H]1[C@@H](O)[C@H](O)CCN1Cc1ccco1 |r| Show InChI InChI=1S/C11H17NO4/c13-7-9-11(15)10(14)3-4-12(9)6-8-2-1-5-16-8/h1-2,5,9-11,13-15H,3-4,6-7H2/t9-,10-,11-/m1/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.16E+5	n/a	2.80E+5	n/a	6.56E+4	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM238198 (US9402837, 2) Show SMILES CCCCCN1C[C@@H](O)[C@H](O)[C@@H](CO)C1 Show InChI InChI=1S/C11H23NO3/c1-2-3-4-5-12-6-9(8-13)11(15)10(14)7-12/h9-11,13-15H,2-8H2,1H3/t9-,10-,11-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	4.06E+5	n/a	9.80E+5	n/a	n/a	n/a	n/a	4.5	n/a
Amicus Therapeutics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 μ...				US Patent US9402837 (2016) BindingDB Entry DOI: 10.7270/Q2MS3RPB
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Mus musculus (Mouse))	BDBM175501 (US9119845, 2) Show SMILES CCCCCC1CC[C@@H](O)[C@H](O)[C@H]1CO |r| Show InChI InChI=1S/C12H24O3/c1-2-3-4-5-9-6-7-11(14)12(15)10(9)8-13/h9-15H,2-8H2,1H3/t9?,10-,11+,12+/m0/s1	PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	4.06E+5	n/a	9.80E+5	n/a	2.66E+5	n/a	n/a	4.5	n/a
Amicus Therapeautics, Inc. US Patent					Assay Description To 2.5 μl of supernatant (in 96-well plates) was added 17.5 μl reaction buffer (citrate phosphate buffer, pH 4.5, no Triton X-100), and 50 ...				US Patent US9119845 (2015) BindingDB Entry DOI: 10.7270/Q2V40T0P
					More data for this Ligand-Target Pair
Lysosomal acid glucosylceramidase (Homo sapiens (Human))	BDBM50182801 ((3R,4R,5R)-5-(Hydroxymethyl)piperidine-3,4-diol, 8...) Show SMILES OC[C@H]1CNC[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C6H13NO3/c8-3-4-1-7-2-5(9)6(4)10/h4-10H,1-3H2/t4-,5-,6-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	59	n/a	n/a	n/a	n/a	n/a	n/a
Harvard Medical School Curated by ChEMBL					Assay Description Inhibition of GCase assessed as 4-methylumbelliferone release assay after 30 mins by fluorimetry				Nat Chem Biol 3: 101-7 (2007) Article DOI: 10.1038/nchembio850 BindingDB Entry DOI: 10.7270/Q2639PX9
					More data for this Ligand-Target Pair				3D Structure (crystal)
Palmitoyl-protein thioesterase 1 (Homo sapiens (Human))	BDBM50429511 (CHEMBL2332876) Show SMILES CCCCCCCCCCCCCCCC(=O)NC[C@H](NC(=O)CNC(=O)CCNc1ccc([N+]([O-])=O)c2nonc12)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(O)=O |r| Show InChI InChI=1S/C59H103N15O13/c1-6-8-9-10-11-12-13-14-15-16-17-18-19-29-47(75)64-37-45(66-49(77)38-65-48(76)32-36-63-41-30-31-46(74(85)86)53-52(41)72-87-73-53)56(80)70-50(39(3)4)57(81)67-43(27-21-24-34-61)55(79)71-51(40(5)7-2)58(82)68-42(26-20-23-33-60)54(78)69-44(59(83)84)28-22-25-35-62/h30-31,39-40,42-45,50-51,63H,6-29,32-38,60-62H2,1-5H3,(H,64,75)(H,65,76)(H,66,77)(H,67,81)(H,68,82)(H,69,78)(H,70,80)(H,71,79)(H,83,84)/t40-,42-,43-,44-,45-,50-,51-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Amicus Therapeutics Curated by ChEMBL					Assay Description Inhibition of PPT1 in human fibroblast/lymphoblast cell lysate using fluorescent-based MUGSP as substrate after 1 to 3 hrs				J Med Chem 56: 2705-25 (2013) Article DOI: 10.1021/jm301557k BindingDB Entry DOI: 10.7270/Q26111N4
					More data for this Ligand-Target Pair
Palmitoyl-protein thioesterase 1 (Homo sapiens (Human))	BDBM50429510 (CHEMBL2332875) Show SMILES CCCCCCCCCCCCCCCC(=O)NC[C@H](NC(=O)CNC(C)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(O)=O |r| Show InChI InChI=1S/C52H99N11O10/c1-7-9-10-11-12-13-14-15-16-17-18-19-20-30-43(65)57-34-42(58-44(66)35-56-38(6)64)49(69)62-45(36(3)4)50(70)59-40(28-22-25-32-54)48(68)63-46(37(5)8-2)51(71)60-39(27-21-24-31-53)47(67)61-41(52(72)73)29-23-26-33-55/h36-37,39-42,45-46H,7-35,53-55H2,1-6H3,(H,56,64)(H,57,65)(H,58,66)(H,59,70)(H,60,71)(H,61,67)(H,62,69)(H,63,68)(H,72,73)/t37-,39-,40-,41-,42-,45-,46-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Amicus Therapeutics Curated by ChEMBL					Assay Description Inhibition of PPT1 (unknown origin) in cell lysates using fluorescent-based MUGSP as substrate after 1 to 3 hrs				J Med Chem 56: 2705-25 (2013) Article DOI: 10.1021/jm301557k BindingDB Entry DOI: 10.7270/Q26111N4
					More data for this Ligand-Target Pair