Found 9 hits for monomerid = 50513937 Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
N-acetyl-beta-D-glucosaminidase (O-GlcNAcase)
(Homo sapiens (Human)) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| >3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Inhibition of recombinant human OGA |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |
Beta-hexosaminidase subunit beta (Hex B)
(Homo sapiens (Human)) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Inhibition of human beta hexosaminidase assessed as inhibitory constant using 4-methylumbelliferyl N-acetyl-beta-D-glucosaminide dihydrate as substra... |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |
Sodium channel protein type 5 subunit alpha
(Homo sapiens (Human)) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Inhibition of Nav1.5 (unknown origin) |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |
1,3-beta-glucan synthase component GLS2
(Saccharomyces cerevisiae) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | KEGG
UniProtKB/SwissProt
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Displacement of MK-0499 from human ERG |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |
L-type calcium channel alpha-1c/beta-2/alpha2delta-1
(Homo sapiens (Human)) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Inhibition of Cav1.2 (unknown origin) |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Inhibition of CYP3A4 (unknown origin) |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C9
(Homo sapiens (Human)) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Inhibition of CYP2C9 (unknown origin) |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |
Cytochrome P450 2D6
(Homo sapiens (Human)) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Inhibition of CYP2D6 (unknown origin) |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |
Pregnane X receptor
(Homo sapiens (Human)) | BDBM50513937
![PNG](/data/jpeg/tenK5051/BindingDB_50513937.png) (CHEMBL4520749)Show SMILES [H][C@]12O[C@H](CO)C[C@H](O)[C@@]1([H])N=C(NCC)S2 |r,t:12| Show InChI InChI=1S/C9H16N2O3S/c1-2-10-9-11-7-6(13)3-5(4-12)14-8(7)15-9/h5-8,12-13H,2-4H2,1H3,(H,10,11)/t5-,6-,7+,8+/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | n/a | n/a | >3.00E+4 | n/a | n/a | n/a | n/a |
Merck & Co.
Curated by ChEMBL
| Assay Description Activation of PXR (unknown origin) assessed as CYP3A4 induction |
J Med Chem 62: 10062-10097 (2019)
Article DOI: 10.1021/acs.jmedchem.9b01090 |
More data for this Ligand-Target Pair | |