BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 852 hits of ec50 for UniProtKB: P43490   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50438936
PNG
(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/an/an/an/a 1.10n/an/an/an/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
3D Structure (crystal)
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50011266
PNG
(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/an/an/an/a 1.20n/an/an/an/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


(Homo sapiens (Human))
BDBM50609428
PNG
(CHEMBL5266272)
Show SMILES CC(NC(=O)C1CC(O)CN1C(=O)C(NC(=O)COCCOCCOCCOCCNC(=O)c1ccc(CN2CCN(CC2)S(=O)(=O)c2ccc(NC(=S)NCc3ccccc3)cc2)cc1)C(C)(C)C)c1ccc(cc1)-c1scnc1C
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 7.10n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM656348
PNG
(N-[2-(3-Methoxyphenyl)-2H-indazol-6-yl]-N′-[...)
Show SMILES COc1cccc(c1)-n1cc2ccc(NC(=O)NCc3ccncc3)cc2n1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 10n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM656325
PNG
(N-(5-Fluoro-2-phenyl-1,3-benzoxazol-6-yl)-N′...)
Show SMILES Fc1cc2nc(oc2cc1NC(=O)NCc1ccncc1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 10n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50570832
PNG
(CHEMBL4848594)
Show SMILES O=C(NCc1ccncc1)Nc1ccc2cc(nn2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 12n/an/an/an/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))
BDBM656330
PNG
(N-[2-(2-Butylphenyl)[1,2,4]triazolo[1,5-a]pyridin-...)
Show SMILES CCCCc1ccccc1-c1nc2ccc(NC(=O)NCc3ccncc3)cn2n1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 20n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50570834
PNG
(CHEMBL4877644 | US11918568, Example 9)
Show SMILES O=C(NCc1cn[nH]c1)Nc1ccc2nc(nn2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 20n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50570834
PNG
(CHEMBL4877644 | US11918568, Example 9)
Show SMILES O=C(NCc1cn[nH]c1)Nc1ccc2nc(nn2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 22n/an/an/an/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))
BDBM572570
PNG
(1-[4-(4-Chloro-benzenesulfonyl)-phenyl]-3-(1H-pyra...)
Show SMILES Clc1ccc(cc1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 23n/an/an/an/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))
BDBM50569533
PNG
(CHEMBL4858231 | US11452717, Compound TableB-2.166)
Show SMILES CN(Cc1ccccc1)S(=O)(=O)c1ccc(NC(=O)NCc2ccncc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 23n/an/an/an/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
PNG
(CHEMBL4859010 | US11452717, Compound TableB-1.48)
Show SMILES O=C(NCc1cn[nH]c1)Nc1ccc(cc1)S(=O)(=O)c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 28n/an/an/an/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))
BDBM656373
PNG
(N-Benzyl-N-ethyl-6-({[(pyridin-4-yl)methyl]carbamo...)
Show SMILES CCN(Cc1ccccc1)C(=O)c1noc2cc(NC(=O)NCc3ccncc3)ccc12
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 30n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50570831
PNG
(CHEMBL4846468 | US11918568, Example 26)
Show SMILES O=C(NCc1ccncc1)Nc1ccc2cn(nc2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 40n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50570831
PNG
(CHEMBL4846468 | US11918568, Example 26)
Show SMILES O=C(NCc1ccncc1)Nc1ccc2cn(nc2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 40n/an/an/an/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))
BDBM656342
PNG
(N-(3-Cyano-2-phenylpyrazolo[1,5-a]pyridin-6-yl)-N&...)
Show SMILES O=C(NCc1ccncc1)Nc1ccc2c(C#N)c(nn2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 50n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM656336
PNG
(N,N-Diethyl-2-phenyl-6-({[(pyridin-4-yl)methyl]car...)
Show SMILES CCN(CC)C(=O)c1n(nc2cc(NC(=O)NCc3ccncc3)ccc12)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 50n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM656321
PNG
(N-(2-Phenyl-1,3-benzoxazol-6-yl)-N′-[(pyridi...)
Show SMILES O=C(NCc1ccncc1)Nc1ccc2nc(oc2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 50n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM656347
PNG
(N-{2-[2-(2-Methoxyethoxy)phenyl]-2H-indazol-6-yl}-...)
Show SMILES COCCOc1ccccc1-n1cc2ccc(NC(=O)NCc3ccncc3)cc2n1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 60n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50569529
PNG
(CHEMBL4867743 | US11452717, Compound TableB-2.173)
Show SMILES CCN(C1CCCC1)S(=O)(=O)c1ccc(NC(=O)NCc2ccncc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 60n/an/an/an/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))
BDBM656363
PNG
(N-[2-(3-Methoxyphenyl)pyrazolo[1,5-a]pyridin-6-yl]...)
Show SMILES COc1cccc(c1)-c1cc2ccc(NC(=O)NCc3ccncc3)cn2n1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 60n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50569536
PNG
(CHEMBL4852773 | US11452717, Compound TableB-2.219)
Show SMILES Clc1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2ccncc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 69n/an/an/an/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
PNG
(CHEMBL4860172)
Show SMILES FC(F)(F)Oc1ccccc1-c1nc2ccc(NC(=O)NCc3ccncc3)cn2n1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 70n/an/an/an/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))
BDBM656343
PNG
(N-(3-Methyl-2-phenylpyrazolo[1,5-a]pyridin-6-yl)-N...)
Show SMILES Cc1c(nn2cc(NC(=O)NCc3ccncc3)ccc12)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 70n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50569541
PNG
(CHEMBL4859855 | US11452717, Compound TableB-5.29)
Show SMILES FC(F)(F)Oc1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2cnco2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 70n/an/an/an/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
PNG
(CHEMBL4868976 | US11452717, Compound TableB-1.47)
Show SMILES O=C(NCc1cnco1)Nc1ccc(cc1)S(=O)(=O)c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 77n/an/an/an/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
PNG
(CHEMBL4856434 | US11452717, Compound TableB-2.221)
Show SMILES Clc1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2ccncc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 79n/an/an/an/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))
BDBM656340
PNG
(N-[3-(1-Methyl-1H-pyrazol-5-yl)-2-phenylpyrazolo[1...)
Show SMILES Cn1nccc1-c1c(nn2cc(NC(=O)NCc3ccncc3)ccc12)-c1ccccc1 |(2,3.28,;3.54,3.28,;4.45,4.53,;5.91,4.05,;5.91,2.51,;4.45,2.03,;3.97,.57,;4.88,-.68,;3.97,-1.92,;2.51,-1.45,;1.17,-2.22,;-.16,-1.45,;-1.49,-2.22,;-2.83,-1.45,;-2.83,.09,;-4.16,-2.22,;-5.5,-1.45,;-6.83,-2.22,;-6.83,-3.76,;-8.16,-4.53,;-9.5,-3.76,;-9.5,-2.22,;-8.16,-1.45,;-.16,.09,;1.17,.86,;2.51,.09,;6.42,-.68,;7.19,.66,;8.73,.66,;9.5,-.68,;8.73,-2.01,;7.19,-2.01,)|
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 80n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50570833
PNG
(CHEMBL4861097 | US11918568, Example 8)
Show SMILES O=C(NCc1ccncc1)Nc1ccc2nc(nn2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 80n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM656370
PNG
(N-[(2S*,3S*)-2-(3-Methoxyphenyl)-3-methyl-2,3-dihy...)
Show SMILES COc1cccc(c1)[C@H]1Oc2cc(NC(=O)NCc3ccncc3)ccc2[C@@H]1C |r|
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 80n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM656369
PNG
(N-[2-(3-Methoxyphenyl)-2,3-dihydro-1-benzofuran-6-...)
Show SMILES COc1cccc(c1)C1Cc2ccc(NC(=O)NCc3ccncc3)cc2O1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 80n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM50570833
PNG
(CHEMBL4861097 | US11918568, Example 8)
Show SMILES O=C(NCc1ccncc1)Nc1ccc2nc(nn2c1)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 83n/an/an/an/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))
BDBM50570844
PNG
(CHEMBL4877360)
Show SMILES COCCn1nccc1-c1nc2ccc(NC(=O)NCc3ccncc3)cn2n1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 83n/an/an/an/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
PNG
(CHEMBL4868692 | US11452717, Compound TableB-2.224)
Show SMILES O=C(NCc1ccncc1)Nc1ccc(cc1)S(=O)(=O)c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 85n/an/an/an/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))
BDBM656360
PNG
(N-(1-Methyl-2-phenyl-1H-indol-5-yl)-N′-[(pyr...)
Show SMILES Cn1c(cc2cc(NC(=O)NCc3ccncc3)ccc12)-c1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/an/an/a 100n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Nicotinamide phosphoribosyltransferase


(Homo sapiens (Human))
BDBM572812
PNG
(3-Chloro-N-[4-(3-pyridin-4-ylmethyl-ureido)-phenyl...)
Show SMILES Clc1cccc(c1)S(=O)(=O)Nc1ccc(NC(=O)NCc2ccncc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(4-Chloro-N-[4-(3-pyridin-4-ylmethyl-ureido)-phenyl...)
Show SMILES Clc1ccc(cc1)S(=O)(=O)Nc1ccc(NC(=O)NCc2ccncc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(N-[4-(3-Benzyl-ureido)-phenyl]-C-phenyl-methanesul...)
Show SMILES O=C(NCc1ccccc1)Nc1ccc(NS(=O)(=O)Cc2ccccc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(1-(2-chlorophenyl)-N-(4-(3-(pyridin-4-ylmethyl)ure...)
Show SMILES Clc1ccccc1CS(=O)(=O)Nc1ccc(NC(=O)NCc2ccncc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(1-(3-chlorophenyl)-N-(4-(3-(pyridin-4-ylmethyl)ure...)
Show SMILES Clc1cccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3ccncc3)cc2)c1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(1-(4-chlorophenyl)-N-(4-(3-(pyridin-4-ylmethyl)ure...)
Show SMILES Clc1ccc(CS(=O)(=O)Nc2ccc(NC(=O)NCc3ccncc3)cc2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(N-Methyl-C-phenyl-N-[4-(3-pyridin-4-ylmethyl-ureid...)
Show SMILES CN(c1ccc(NC(=O)NCc2ccncc2)cc1)S(=O)(=O)Cc1ccccc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(1-((1H-Pyrazol-4-yl)methyl)-3-(4-((2-fluorophenyl)...)
Show SMILES Fc1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(1-((1H-Pyrazol-4-yl)methyl)-3-(4-((3-fluorophenyl)...)
Show SMILES Fc1cccc(c1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(1-((1H-Pyrazol-4-yl)methyl)-3-(4-((4-fluorophenyl)...)
Show SMILES Fc1ccc(cc1)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(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
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(1-(1H-Pyrazol-4-ylmethyl)-3-[4-(toluene-2-sulfonyl...)
Show SMILES Cc1ccccc1S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(1-[4-(3,4-Dichloro-benzenesulfonyl)-phenyl]-3-(1H-...)
Show SMILES Clc1ccc(cc1Cl)S(=O)(=O)c1ccc(NC(=O)NCc2cn[nH]c2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(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
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
PNG
(C-(2-Chloro-phenyl)-N-{4-[3-(1H-pyrazol-4-ylmethyl...)
Show SMILES Clc1ccccc1CS(=O)(=O)Nc1ccc(NC(=O)NCc2cn[nH]c2)cc1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a<100n/an/an/an/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
Displayed 1 to 50 (of 852 total )  |  Next  |  Last  >>
Jump to: