Compile Data Set for Download or QSAR

Found 653 hits of ec50 data for polymerid = 4910,50006593,50006594   

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
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50438936 (CHEMBL2420629 | GNE-617) Show SMILES Fc1cc(F)cc(c1)S(=O)(=O)c1ccc(CNC(=O)c2ccc3nccn3c2)cc1 Show InChI InChI=1S/C21H15F2N3O3S/c22-16-9-17(23)11-19(10-16)30(28,29)18-4-1-14(2-5-18)12-25-21(27)15-3-6-20-24-7-8-26(20)13-15/h1-11,13H,12H2,(H,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Similars	PDB Article PubMed	n/a	n/a	n/a	n/a	1.10	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of NAMPT in human PC3 cells assessed as reduction in NAD level after 48 hrs by mass spectrometry				Bioorg Med Chem Lett 23: 5488-97 (2013) Article DOI: 10.1016/j.bmcl.2013.08.074 BindingDB Entry DOI: 10.7270/Q2DF6SQ1
					More data for this Ligand-Target Pair				3D Structure (crystal)
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50011266 (CHEMBL3260358) Show SMILES FC(F)(F)c1cccc(c1)S(=O)(=O)c1ccc(CNC(=O)c2cnc3[nH]ncc3c2)cc1 Show InChI InChI=1S/C21H15F3N4O3S/c22-21(23,24)16-2-1-3-18(9-16)32(30,31)17-6-4-13(5-7-17)10-26-20(29)15-8-14-12-27-28-19(14)25-11-15/h1-9,11-12H,10H2,(H,26,29)(H,25,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.20	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of NAMPT in human PC3 cells assessed as reduction in NAD level after 48 hrs by mass spectrometry				Bioorg Med Chem Lett 23: 5488-97 (2013) Article DOI: 10.1016/j.bmcl.2013.08.074 BindingDB Entry DOI: 10.7270/Q2DF6SQ1
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Mus musculus)	BDBM50438936 (CHEMBL2420629 | GNE-617) Show SMILES Fc1cc(F)cc(c1)S(=O)(=O)c1ccc(CNC(=O)c2ccc3nccn3c2)cc1 Show InChI InChI=1S/C21H15F2N3O3S/c22-16-9-17(23)11-19(10-16)30(28,29)18-4-1-14(2-5-18)12-25-21(27)15-3-6-20-24-7-8-26(20)13-15/h1-11,13H,12H2,(H,25,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Similars	PDB Article PubMed	n/a	n/a	n/a	n/a	1.30	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of NAMPT in mouse cells assessed as reduction in NAD level after 48 hrs by mass spectrometry				Bioorg Med Chem Lett 23: 5488-97 (2013) Article DOI: 10.1016/j.bmcl.2013.08.074 BindingDB Entry DOI: 10.7270/Q2DF6SQ1
					More data for this Ligand-Target Pair				3D Structure (crystal)
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50570832 (CHEMBL4848594) Show SMILES O=C(NCc1ccncc1)Nc1ccc2cc(nn2c1)-c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	12	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT assessed as increase in NMN production by fluorescence based analysis				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128048 BindingDB Entry DOI: 10.7270/Q27W6H07
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50570834 (CHEMBL4877644) Show SMILES O=C(NCc1cn[nH]c1)Nc1ccc2nc(nn2c1)-c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	22	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT assessed as increase in NMN production by fluorescence based analysis				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128048 BindingDB Entry DOI: 10.7270/Q27W6H07
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50569533 (CHEMBL4858231 | US11452717, Compound TableB-2.166) Show SMILES CN(Cc1ccccc1)S(=O)(=O)c1ccc(NC(=O)NCc2ccncc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	23	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572570 (1-[4-(4-Chloro-benzenesulfonyl)-phenyl]-3-(1H-pyra...) Show SMILES Clc1ccc(cc1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	23	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50569538 (CHEMBL4859010 | US11452717, Compound TableB-1.48) Show SMILES O=C(NCc1cn[nH]c1)Nc1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	28	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50570831 (CHEMBL4846468) Show SMILES O=C(NCc1ccncc1)Nc1ccc2cn(nc2c1)-c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	40	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT assessed as increase in NMN production by fluorescence based analysis				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128048 BindingDB Entry DOI: 10.7270/Q27W6H07
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50569529 (CHEMBL4867743 | US11452717, Compound TableB-2.173) Show SMILES CCN(C1CCCC1)S(=O)(=O)c1ccc(NC(=O)NCc2ccncc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	60	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50569536 (CHEMBL4852773 | US11452717, Compound TableB-2.219) Show SMILES Clc1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2ccncc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	69	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50570836 (CHEMBL4860172) Show SMILES FC(F)(F)Oc1ccccc1-c1nc2ccc(NC(=O)NCc3ccncc3)cn2n1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	70	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT assessed as increase in NMN production by fluorescence based analysis				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128048 BindingDB Entry DOI: 10.7270/Q27W6H07
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Mus musculus)	BDBM50011266 (CHEMBL3260358) Show SMILES FC(F)(F)c1cccc(c1)S(=O)(=O)c1ccc(CNC(=O)c2cnc3[nH]ncc3c2)cc1 Show InChI InChI=1S/C21H15F3N4O3S/c22-21(23,24)16-2-1-3-18(9-16)32(30,31)17-6-4-13(5-7-17)10-26-20(29)15-8-14-12-27-28-19(14)25-11-15/h1-9,11-12H,10H2,(H,26,29)(H,25,27,28)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	70	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of NAMPT in mouse cells assessed as reduction in NAD level after 48 hrs by mass spectrometry				Bioorg Med Chem Lett 23: 5488-97 (2013) Article DOI: 10.1016/j.bmcl.2013.08.074 BindingDB Entry DOI: 10.7270/Q2DF6SQ1
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50569541 (CHEMBL4859855 | US11452717, Compound TableB-5.29) Show SMILES FC(F)(F)Oc1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2cnco2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	70	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50569540 (CHEMBL4868976 | US11452717, Compound TableB-1.47) Show SMILES O=C(NCc1cnco1)Nc1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	77	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50569535 (CHEMBL4856434 | US11452717, Compound TableB-2.221) Show SMILES Clc1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2ccncc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	79	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50570844 (CHEMBL4877360) Show SMILES COCCn1nccc1-c1nc2ccc(NC(=O)NCc3ccncc3)cn2n1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	83	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT assessed as increase in NMN production by fluorescence based analysis				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128048 BindingDB Entry DOI: 10.7270/Q27W6H07
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50570833 (CHEMBL4861097) Show SMILES O=C(NCc1ccncc1)Nc1ccc2nc(nn2c1)-c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	83	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT assessed as increase in NMN production by fluorescence based analysis				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128048 BindingDB Entry DOI: 10.7270/Q27W6H07
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM50569534 (CHEMBL4868692 | US11452717, Compound TableB-2.224) Show SMILES O=C(NCc1ccncc1)Nc1ccc(cc1)S(=O)(=O)c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	85	n/a	n/a	n/a	n/a
TBA					Assay Description Activation of human NAMPT				Citation and Details Article DOI: 10.1016/j.bmcl.2021.128007 BindingDB Entry DOI: 10.7270/Q2MK6HPH
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572812 (3-Chloro-N-[4-(3-pyridin-4-ylmethyl-ureido)-phenyl...) Show SMILES Clc1cccc(c1)S(=O)(=O)Nc1ccc(NC(=O)NCc2ccncc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572813 (4-Chloro-N-[4-(3-pyridin-4-ylmethyl-ureido)-phenyl...) Show SMILES Clc1ccc(cc1)S(=O)(=O)Nc1ccc(NC(=O)NCc2ccncc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572814 (N-[4-(3-Benzyl-ureido)-phenyl]-C-phenyl-methanesul...) Show SMILES O=C(NCc1ccccc1)Nc1ccc(NS(=O)(=O)Cc2ccccc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572815 (1-(2-chlorophenyl)-N-(4-(3-(pyridin-4-ylmethyl)ure...) Show SMILES Clc1ccccc1CS(=O)(=O)Nc1ccc(NC(=O)NCc2ccncc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572816 (1-(3-chlorophenyl)-N-(4-(3-(pyridin-4-ylmethyl)ure...) Show SMILES Clc1cccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3ccncc3)cc2)c1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572817 (1-(4-chlorophenyl)-N-(4-(3-(pyridin-4-ylmethyl)ure...) Show SMILES Clc1ccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3ccncc3)cc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572818 (N-Methyl-C-phenyl-N-[4-(3-pyridin-4-ylmethyl-ureid...) Show SMILES CN(c1ccc(NC(=O)NCc2ccncc2)cc1)S(=O)(=O)Cc1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572861 (1-((1H-Pyrazol-4-yl)methyl)-3-(4-((2-fluorophenyl)...) Show SMILES Fc1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572862 (1-((1H-Pyrazol-4-yl)methyl)-3-(4-((3-fluorophenyl)...) Show SMILES Fc1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572863 (1-((1H-Pyrazol-4-yl)methyl)-3-(4-((4-fluorophenyl)...) Show SMILES Fc1ccc(cc1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572864 (1-((1H-Pyrazol-4-yl)methyl)-3-(4-((3-(trifluoromet...) Show SMILES FC(F)(F)c1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572869 (1-(1H-Pyrazol-4-ylmethyl)-3-[4-(toluene-2-sulfonyl...) Show SMILES Cc1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572871 (1-[4-(3,4-Dichloro-benzenesulfonyl)-phenyl]-3-(1H-...) Show SMILES Clc1ccc(cc1Cl)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572872 (C-(3-Chloro-phenyl)-N-{4-[3-(1H-pyrazol-4-ylmethyl...) Show SMILES Clc1cccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3cn[nH]c3)cc2)c1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572873 (C-(2-Chloro-phenyl)-N-{4-[3-(1H-pyrazol-4-ylmethyl...) Show SMILES Clc1ccccc1CS(=O)(=O)Nc1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572874 (C-(4-Chloro-phenyl)-N-{4-[3-(1H-pyrazol-4-ylmethyl...) Show SMILES Clc1ccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3cn[nH]c3)cc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572877 (C-(3,4-Dichloro-phenyl)-N-{4-[3-(1H-pyrazol-4-ylme...) Show SMILES Clc1ccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3cn[nH]c3)cc2)cc1Cl Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572882 (1-(1H-Pyrazol-4-ylmethyl)-3-[4-(2-trifluoromethoxy...) Show SMILES FC(F)(F)Oc1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572883 (1-(1H-Pyrazol-4-ylmethyl)-3-[4-(3-trifluoromethoxy...) Show SMILES FC(F)(F)Oc1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572891 (1-[4-(3,5-Difluoro-benzenesulfonyl)-phenyl]-3-(1H-...) Show SMILES Fc1cc(F)cc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572892 (1-[4-(1-Isopropyl-1H-pyrazole-4-sulfonyl)-phenyl]-...) Show SMILES CC(C)n1cc(cn1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572897 (1-[4-(2,4-Difluoro-benzenesulfonyl)-phenyl]-3-(1H-...) Show SMILES Fc1ccc(c(F)c1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572929 (1-((1H-Pyrazol-4-yl)methyl)-3-(4-([1,1'-biphenyl]-...) Show SMILES O=C(NCc1cn[nH]c1)Nc1ccc(cc1)S(=O)(=O)c1ccccc1-c1ccccc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572939 (1-[4-(3-Iodo-benzenesulfonyl)-phenyl]-3-(1H-pyrazo...) Show SMILES Ic1ccc(cc1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572940 (1-[4-(2'-Fluoro-biphenyl-2-sulfonyl)-phenyl]-3-(1H...) Show SMILES Fc1ccccc1-c1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572941 (1-[4-(3'-Fluoro-biphenyl-2-sulfonyl)-phenyl]-3-(1H...) Show SMILES Fc1cccc(c1)-c1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572957 (1-(3-Chlorophenyl)-N-(4-(3-(oxazol-5-ylmethyl)urei...) Show SMILES Clc1cccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3cnco3)cc2)c1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572958 (1-(4-Chlorophenyl)-N-(4-(3-(oxazol-5-ylmethyl)urei...) Show SMILES Clc1ccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3cnco3)cc2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572959 (1-(3,4-Dichlorophenyl)-N-(4-(3-(oxazol-5-ylmethyl)...) Show SMILES Clc1ccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3cnco3)cc2)cc1Cl Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572960 (1-(2-Chlorophenyl)-N-(4-(3-(oxazol-5-ylmethyl)urei...) Show SMILES Clc1ccccc1CS(=O)(=O)Nc1ccc(NC(=O)NCc2cnco2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair
Nicotinamide phosphoribosyltransferase (Homo sapiens (Human))	BDBM572964 (1-(4-((3-Chlorophenyl)sulfonyl)phenyl)-3-(oxazol-5...) Show SMILES Clc1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2cnco2)cc1 Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	<100	n/a	n/a	n/a	n/a
TBA					Assay Description NAMPT reaction was performed in 50 mM HEPES, pH 7.5, containing 5 mM MgCl2, 0.1% Prionex, 0.005% Tween 20, and 1 mM TCEP at room temperature in Grein...				Citation and Details BindingDB Entry DOI: 10.7270/Q2M048P0
					More data for this Ligand-Target Pair

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