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Compile Data Set for Download or QSAR

Found 244 hits of ic50 for UniProtKB: P40261   
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 N-methyltransferase


(Homo sapiens (Human))
BDBM50566781
PNG
(CHEMBL4867273)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)-c2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

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UniChem
Article
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n/an/a 0.150n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566783
PNG
(CHEMBL4859806)
Show SMILES CN(C)CCCC[C@@H]1NC(=O)[C@H](CC(C)(C)C)NC(=O)[C@@H]2C[C@H](CN2C(=O)[C@H](Cc2ccccc2)N(C)C(=O)CSCCNC(=O)[C@H](Cc2ccc(cc2)-c2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CC(F)(F)CN2C1=O)c1ccccc1 |r|
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
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Article
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n/an/a 0.400n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566776
PNG
(CHEMBL4847740)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2C[C@H](CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O)c1ccccc1 |r|
PDB

UniProtKB/SwissProt

antibodypedia
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UniChem
Article
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n/an/a 0.470n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566782
PNG
(CHEMBL4857394)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)-c2cccc(c2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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n/an/a 0.930n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50598881
PNG
(CHEMBL5194905)
Show SMILES Cc1cc(CN)n(n1)[C@H]1C[C@@H](N(C1)C(=O)c1cnc2[nH]c(C)cc2c1)c1cc2cc(C)ccc2n1Cc1ccc(Cl)cc1 |r|
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n/an/a 1.10n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00919
BindingDB Entry DOI: 10.7270/Q2KS6WJ1
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566772
PNG
(CHEMBL4878738)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)N(C)C(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCCN)NC1=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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PC sid
UniChem
Article
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n/an/a 1.10n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566784
PNG
(CHEMBL4872872)
Show SMILES CN1[C@@H](Cc2ccccc2)C(=O)N2C[C@@H](C[C@H]2C(=O)N[C@@H](CC(C)(C)C)C(=O)N2CCCC[C@H]2C(=O)N2CC(F)(F)C[C@H]2C(=O)N2Cc3ccccc3C[C@H]2C(=O)N[C@@H](Cc2ccc(cc2)-c2ccc(cc2)C(N)=O)C(=O)NCCSCC1=O)c1ccccc1 |r|
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antibodypedia
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n/an/a 1.90n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50588067
PNG
(CHEMBL5189197)
Show SMILES N[C@@H](CCN(C\C=C\c1ccc(cc1)C#N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r|
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n/an/a 3.70n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01094
BindingDB Entry DOI: 10.7270/Q22V2M2Z
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566775
PNG
(CHEMBL4856854)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2C[C@H](CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O)C(F)(F)F |r|
PDB

UniProtKB/SwissProt

antibodypedia
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n/an/a 5.80n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50506000
PNG
(CHEMBL4445337)
Show SMILES N[C@@H](CCN(CC#Cc1cccc(c1)C(N)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r|
Show InChI InChI=1S/C24H28N8O6/c25-15(24(36)37)6-8-31(7-2-4-13-3-1-5-14(9-13)21(27)35)10-16-18(33)19(34)23(38-16)32-12-30-17-20(26)28-11-29-22(17)32/h1,3,5,9,11-12,15-16,18-19,23,33-34H,6-8,10,25H2,(H2,27,35)(H,36,37)(H2,26,28,29)/t15-,16+,18+,19+,23+/m0/s1
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n/an/a 10n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01094
BindingDB Entry DOI: 10.7270/Q22V2M2Z
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50588085
PNG
(CHEMBL5173204)
Show SMILES N[C@@H](CCN(CC=Cc1ccc(cc1)[N+]([O-])=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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UniChem
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n/an/a 10n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01094
BindingDB Entry DOI: 10.7270/Q22V2M2Z
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607544
PNG
(CHEMBL5220889)
Show SMILES C[C@@H]1Cc2c(N1)ncc(C(N)=O)c2C |r|
PDB

UniProtKB/SwissProt

antibodypedia
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UniChem
Article
PubMed
n/an/a 12n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566786
PNG
(CHEMBL4866114)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](CC(C)C)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)CNC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC1=O)C(=O)NCC(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 12n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50588063
PNG
(CHEMBL5172454)
Show SMILES N[C@@H](CCN(C\C=C\c1cccc(c1)C(N)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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UniChem
Article
PubMed
n/an/a 13n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01094
BindingDB Entry DOI: 10.7270/Q22V2M2Z
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566777
PNG
(CHEMBL4848464)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CC(F)(F)CN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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n/an/a 14n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566773
PNG
(CHEMBL4853328)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CC(F)(F)CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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PC sid
UniChem
Article
PubMed
n/an/a 14n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50598880
PNG
(CHEMBL5187248)
Show SMILES Cc1ccc2n(Cc3ccc(Cl)cc3)c(cc2c1)[C@H]1C[C@@H](CN1C(=O)c1cnc2[nH]ccc2c1)n1ccnc1CN |r|
PDB

UniProtKB/SwissProt

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PDB
UniChem
PDB
Article
PubMed
n/an/a 16n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00919
BindingDB Entry DOI: 10.7270/Q2KS6WJ1
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607545
PNG
(CHEMBL5220024)
Show SMILES C[C@H]1Nc2ncc(cc2[C@@H]1C)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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UniChem
Article
PubMed
n/an/a 20n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607541
PNG
(CHEMBL5221106)
Show SMILES Cc1c2CCNc2ncc1C(N)=O
PDB

UniProtKB/SwissProt

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n/an/a 23n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607539
PNG
(CHEMBL5218573)
Show SMILES CNc1cc(C)c(cn1)C(N)=O
PDB

UniProtKB/SwissProt

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PubMed
n/an/a 25n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566759
PNG
(CHEMBL4868588)
Show SMILES NC(=N)NCCC[C@@H]1NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C1=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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n/an/a 28n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566771
PNG
(CHEMBL4859039)
Show SMILES CN1[C@@H](Cc2ccccc2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CC(C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)N2CCC[C@H]2C(=O)N2Cc3ccccc3C[C@H]2C(=O)N[C@@H](Cc2ccc(cc2)C(N)=O)C(=O)N[C@@H](CSCC1=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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n/an/a 36n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607543
PNG
(CHEMBL5220590)
Show SMILES C[C@@H]1Cc2cc(cnc2N1)C(N)=O |r|
PDB

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n/an/a 38n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607543
PNG
(CHEMBL5220590)
Show SMILES C[C@@H]1Cc2cc(cnc2N1)C(N)=O |r|
PDB

UniProtKB/SwissProt

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MCE
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 42n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566765
PNG
(CHEMBL4849636)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)N(C)C(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCNC(N)=N)NC1=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
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n/an/a 42n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607544
PNG
(CHEMBL5220889)
Show SMILES C[C@@H]1Cc2c(N1)ncc(C(N)=O)c2C |r|
PDB

UniProtKB/SwissProt

antibodypedia
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UniChem
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n/an/a 43n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566774
PNG
(CHEMBL4858283)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2C[C@@H](CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O)C(F)(F)F |r|
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Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607562
PNG
(CHEMBL5220955)
Show SMILES C[C@@H]1Cc2c(N1)ncc(C(N)=O)c2Cl |r|
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Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566785
PNG
(CHEMBL4868364)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O |r|
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Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50588087
PNG
(CHEMBL5182376)
Show SMILES N[C@@H](CCN(CCCc1ccc(cc1)C#N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r|
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Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01094
BindingDB Entry DOI: 10.7270/Q22V2M2Z
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50557608
PNG
(CHEMBL4788121)
Show SMILES CC(C)(F)CCCNc1ncc(C(N)=O)c(N[C@@H](CO)C2CC2)n1 |r|
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Assay Description
Inhibition of full length N-terminal His-tagged human NNMT using nicotinamide as substrate incubated for 2 hrs in presence of S-5'adenosyl-L-methioni...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00150
BindingDB Entry DOI: 10.7270/Q23R0XJG
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50588082
PNG
(CHEMBL5196219)
Show SMILES N[C@@H](CCN(C\C=C\c1ccc(Br)cc1)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r|
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Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01094
BindingDB Entry DOI: 10.7270/Q22V2M2Z
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566770
PNG
(CHEMBL4863816)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)N(C)C(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)C(N)=O)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O |r|
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Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50588089
PNG
(CHEMBL5175456)
Show SMILES N[C@@H](CCN(CC#Cc1ccc(cc1)C#N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r|
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Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01094
BindingDB Entry DOI: 10.7270/Q22V2M2Z
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50557606
PNG
(CHEMBL4791213)
Show SMILES CC(C)(F)CCCNc1ncc(C(N)=O)c(NC2(CO)CC2)n1
PDB

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TBA

Assay Description
Inhibition of full length N-terminal His-tagged human NNMT using nicotinamide as substrate incubated for 2 hrs in presence of S-5'adenosyl-L-methioni...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00150
BindingDB Entry DOI: 10.7270/Q23R0XJG
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50557606
PNG
(CHEMBL4791213)
Show SMILES CC(C)(F)CCCNc1ncc(C(N)=O)c(NC2(CO)CC2)n1
PDB

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n/an/a 74n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607542
PNG
(CHEMBL5219823)
Show SMILES NC(=O)c1cnc2NCCc2c1Cl
PDB

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n/an/a 79n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50506011
PNG
(CHEMBL4436698)
Show SMILES N[C@@H](CCN(CCCc1cccc(c1)C(N)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)C(O)=O |r|
Show InChI InChI=1S/C24H32N8O6/c25-15(24(36)37)6-8-31(7-2-4-13-3-1-5-14(9-13)21(27)35)10-16-18(33)19(34)23(38-16)32-12-30-17-20(26)28-11-29-22(17)32/h1,3,5,9,11-12,15-16,18-19,23,33-34H,2,4,6-8,10,25H2,(H2,27,35)(H,36,37)(H2,26,28,29)/t15-,16+,18+,19+,23+/m0/s1
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Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01094
BindingDB Entry DOI: 10.7270/Q22V2M2Z
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607542
PNG
(CHEMBL5219823)
Show SMILES NC(=O)c1cnc2NCCc2c1Cl
PDB

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Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50598882
PNG
(CHEMBL5178360)
Show SMILES [H][C@@]12CCCN1C(=O)[C@H](Cc1c[nH]c3ccccc13)NC(=O)CN(CCCCCC)C(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(cc1)C(N)=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)CSC[C@H](NC2=O)C(N)=O |r|
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Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00919
BindingDB Entry DOI: 10.7270/Q2KS6WJ1
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50598878
PNG
(CHEMBL5174146)
Show SMILES [H][C@@]12CCCN1C(=O)[C@H](Cc1c[nH]c3ccccc13)NC(=O)CN(CCCCCC)C(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(cc1)C(N)=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)CSC[C@H](NC2=O)C(=O)NCC(N)=O |r|
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TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00919
BindingDB Entry DOI: 10.7270/Q2KS6WJ1
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607541
PNG
(CHEMBL5221106)
Show SMILES Cc1c2CCNc2ncc1C(N)=O
PDB

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Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566766
PNG
(CHEMBL4875414)
Show SMILES CN1[C@@H](Cc2ccccc2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N[C@@H](CCCCN)C(=O)N2CCC[C@H]2C(=O)N2Cc3ccccc3C[C@H]2C(=O)N[C@@H](Cc2ccc(cc2)C(N)=O)C(=O)N[C@@H](CSCC1=O)C(N)=O |r|
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n/an/a 108n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607545
PNG
(CHEMBL5220024)
Show SMILES C[C@H]1Nc2ncc(cc2[C@@H]1C)C(N)=O |r|
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Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566760
PNG
(CHEMBL4870987)
Show SMILES CN1[C@@H](Cc2ccccc2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2CCC[C@H]2C(=O)N2Cc3ccccc3C[C@H]2C(=O)N[C@@H](Cc2ccc(cc2)C(N)=O)C(=O)N[C@@H](CSCC1=O)C(N)=O |r|
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n/an/a 125n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566780
PNG
(CHEMBL4860372)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2ccccc2)NC(=O)CSC[C@H](NC(=O)[C@H](Cc2ccc(cc2)-c2ccccc2)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCCN)NC1=O)C(N)=O |r|
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n/an/a 141n/an/an/an/an/an/a


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Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607540
PNG
(CHEMBL5218546)
Show SMILES NC(=O)c1cnc2NCCc2c1
PDB

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n/an/a 142n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50566764
PNG
(CHEMBL4873940)
Show SMILES CN1[C@@H](Cc2ccccc2)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N2CCC[C@H]2C(=O)N2Cc3ccccc3C[C@H]2C(=O)N[C@@H](Cc2ccc(cc2)C(N)=O)C(=O)N[C@@H](CSCC1=O)C(N)=O |r|
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n/an/a 145n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant NNMT using nicotinamide and SAM as substrate assessed as reduction in 1-methyl-nicotinamide formation incubated for 2...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00134
BindingDB Entry DOI: 10.7270/Q21J9FJD
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50598884
PNG
(CHEMBL5191549)
Show SMILES [H][C@@]12CCCN1C(=O)[C@H](Cc1c[nH]c3ccccc13)NC(=O)CN(CCCCCC)C(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@H](Cc1ccccc1)NC(=O)CSC[C@H](NC2=O)C(N)=O |r|
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TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00919
BindingDB Entry DOI: 10.7270/Q2KS6WJ1
More data for this
Ligand-Target Pair
Nicotinamide N-methyltransferase


(Homo sapiens (Human))
BDBM50607540
PNG
(CHEMBL5218546)
Show SMILES NC(=O)c1cnc2NCCc2c1
PDB

UniProtKB/SwissProt

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n/an/a 175n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c01166
BindingDB Entry DOI: 10.7270/Q2H41WHH
More data for this
Ligand-Target Pair
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