BindingDB logo
myBDB logout

PubMed code 26003339

Compile data set for download or QSAR
Found 12 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Beta-secretase 1


(Homo sapiens (Human))
BDBM16034
PNG
(1-N-[(2S,3R)-4-(cyclopropylamino)-3-hydroxy-1-phen...)
Show SMILES C[C@@H](NC(=O)c1cc(cc(c1)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)CNC1CC1)N(C)S(C)(=O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C31H38N4O5S/c1-21(23-12-8-5-9-13-23)33-30(37)24-17-25(19-27(18-24)35(2)41(3,39)40)31(38)34-28(16-22-10-6-4-7-11-22)29(36)20-32-26-14-15-26/h4-13,17-19,21,26,28-29,32,36H,14-16,20H2,1-3H3,(H,33,37)(H,34,38)/t21-,28+,29-/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
MMDB
PC cid
PC sid
PDB
UniChem

Similars

MMDB
PDB
Article
PubMed
n/an/a 20n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant BACE1 using M-2420 as substrate preincubated with enzyme for 1 hr by FRET assay


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50308280
PNG
(2-{4-[(Benzylmethylamino)methyl]benzylidene}-6-(5-...)
Show SMILES CN(Cc1ccccc1)Cc1ccc(\C=C2/CCc3cc(OCCCCCN4CCCCC4)ccc3C2=O)cc1
Show InChI InChI=1S/C36H44N2O2/c1-37(27-30-11-5-2-6-12-30)28-31-15-13-29(14-16-31)25-33-18-17-32-26-34(19-20-35(32)36(33)39)40-24-10-4-9-23-38-21-7-3-8-22-38/h2,5-6,11-16,19-20,25-26H,3-4,7-10,17-18,21-24,27-28H2,1H3/b33-25+
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 52n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated with enzyme for 20 mins prior to substrate addition by ...


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50308265
PNG
(2-{4-[(Benzylmethylamino)methyl]benzylidene}-6-(5-...)
Show SMILES CN(Cc1ccccc1)Cc1ccc(\C=C2/Cc3ccc(OCCCCCN4CCCCC4)cc3C2=O)cc1
Show InChI InChI=1S/C35H42N2O2/c1-36(26-29-11-5-2-6-12-29)27-30-15-13-28(14-16-30)23-32-24-31-17-18-33(25-34(31)35(32)38)39-22-10-4-9-21-37-19-7-3-8-20-37/h2,5-6,11-18,23,25H,3-4,7-10,19-22,24,26-27H2,1H3/b32-23+
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 200n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated with enzyme for 20 mins prior to substrate addition by ...


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM8961
PNG
(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)
Show SMILES Nc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents


Similars

PDB
Article
PubMed
n/an/a 300n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated with enzyme for 20 mins prior to substrate addition by ...


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Beta-secretase 1


(Homo sapiens (Human))
BDBM50105795
PNG
(CHEMBL3597554)
Show SMILES CN(Cc1ccccc1)Cc1ccc(\C=C2/Cc3ccc(OCCCCCN4CCN(CC4)C(c4ccc(F)cc4)c4ccc(F)cc4)cc3C2=O)cc1
Show InChI InChI=1S/C47H49F2N3O2/c1-50(33-36-8-4-2-5-9-36)34-37-12-10-35(11-13-37)30-41-31-40-18-23-44(32-45(40)47(41)53)54-29-7-3-6-24-51-25-27-52(28-26-51)46(38-14-19-42(48)20-15-38)39-16-21-43(49)22-17-39/h2,4-5,8-23,30,32,46H,3,6-7,24-29,31,33-34H2,1H3/b41-30+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
MMDB
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 2.49E+3n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant BACE1 using M-2420 as substrate preincubated with enzyme for 1 hr by FRET assay


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50105796
PNG
(CHEMBL3597552)
Show SMILES CN(Cc1ccccc1)Cc1ccc(\C=C2/Cc3ccc(OCCCCCN4CCN(CC4)OC(=O)C(C)(C)C)cc3C2=O)cc1
Show InChI InChI=1S/C39H49N3O4/c1-39(2,3)38(44)46-42-22-20-41(21-23-42)19-9-6-10-24-45-35-18-17-33-26-34(37(43)36(33)27-35)25-30-13-15-32(16-14-30)29-40(4)28-31-11-7-5-8-12-31/h5,7-8,11-18,25,27H,6,9-10,19-24,26,28-29H2,1-4H3/b34-25+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 3.21E+3n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant BACE1 using M-2420 as substrate preincubated with enzyme for 1 hr by FRET assay


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50105794
PNG
(CHEMBL3597555)
Show SMILES [#6]-[#7](-[#6]-c1ccccc1)-[#6]-c1ccc(\[#6]=[#6]-2/[#6]-c3ccc(-[#8]-[#6]-[#6]-[#6]-[#6]-[#6]-[#7]-4-[#6]-[#6]\[#6](-[#6]-[#6]-4)=[#6](\c4ccc(F)cc4)-c4ccc(F)cc4)cc3-[#6]-2=O)cc1
Show InChI InChI=1S/C48H48F2N2O2/c1-51(33-36-8-4-2-5-9-36)34-37-12-10-35(11-13-37)30-42-31-41-18-23-45(32-46(41)48(42)53)54-29-7-3-6-26-52-27-24-40(25-28-52)47(38-14-19-43(49)20-15-38)39-16-21-44(50)22-17-39/h2,4-5,8-23,30,32H,3,6-7,24-29,31,33-34H2,1H3/b42-30+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 5.95E+3n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant BACE1 using M-2420 as substrate preincubated with enzyme for 1 hr by FRET assay


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50105800
PNG
(CHEMBL3597556)
Show SMILES CN(Cc1ccccc1)Cc1ccc(\C=C2/CCc3cc(OCCCCCN4CCN(Cc5ccc(F)cc5)CC4)ccc3C2=O)cc1
Show InChI InChI=1S/C42H48FN3O2/c1-44(30-34-8-4-2-5-9-34)31-35-12-10-33(11-13-35)28-38-17-16-37-29-40(20-21-41(37)42(38)47)48-27-7-3-6-22-45-23-25-46(26-24-45)32-36-14-18-39(43)19-15-36/h2,4-5,8-15,18-21,28-29H,3,6-7,16-17,22-27,30-32H2,1H3/b38-28+
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 7.83E+3n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated with enzyme for 20 mins prior to substrate addition by ...


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50105797
PNG
(CHEMBL3597550)
Show SMILES CCOC(=O)C1(CCN(CCCCCOc2ccc3C\C(=C/c4ccc(CN(C)Cc5ccccc5)cc4)C(=O)c3c2)CC1)c1ccccc1
Show InChI InChI=1S/C44H50N2O4/c1-3-49-43(48)44(39-15-9-5-10-16-39)23-26-46(27-24-44)25-11-6-12-28-50-40-22-21-37-30-38(42(47)41(37)31-40)29-34-17-19-36(20-18-34)33-45(2)32-35-13-7-4-8-14-35/h4-5,7-10,13-22,29,31H,3,6,11-12,23-28,30,32-33H2,1-2H3/b38-29+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 8.23E+3n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant BACE1 using M-2420 as substrate preincubated with enzyme for 1 hr by FRET assay


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50105798
PNG
(CHEMBL3597549)
Show SMILES CN(Cc1ccccc1)Cc1ccc(\C=C2/Cc3ccc(OCCCCCN4CCN(CC4)c4ccccc4)cc3C2=O)cc1
Show InChI InChI=1S/C40H45N3O2/c1-41(30-33-11-5-2-6-12-33)31-34-17-15-32(16-18-34)27-36-28-35-19-20-38(29-39(35)40(36)44)45-26-10-4-9-21-42-22-24-43(25-23-42)37-13-7-3-8-14-37/h2-3,5-8,11-20,27,29H,4,9-10,21-26,28,30-31H2,1H3/b36-27+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.17E+4n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant BACE1 using M-2420 as substrate preincubated with enzyme for 1 hr by FRET assay


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50105799
PNG
(CHEMBL3597548)
Show SMILES CN(Cc1ccccc1)Cc1ccc(\C=C2/Cc3ccc(OCCCCCN4CCC(CC4)c4ccccc4)cc3C2=O)cc1
Show InChI InChI=1S/C41H46N2O2/c1-42(30-33-11-5-2-6-12-33)31-34-17-15-32(16-18-34)27-38-28-37-19-20-39(29-40(37)41(38)44)45-26-10-4-9-23-43-24-21-36(22-25-43)35-13-7-3-8-14-35/h2-3,5-8,11-20,27,29,36H,4,9-10,21-26,28,30-31H2,1H3/b38-27+
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.34E+4n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant BACE1 using M-2420 as substrate preincubated with enzyme for 1 hr by FRET assay


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50105799
PNG
(CHEMBL3597548)
Show SMILES CN(Cc1ccccc1)Cc1ccc(\C=C2/Cc3ccc(OCCCCCN4CCC(CC4)c4ccccc4)cc3C2=O)cc1
Show InChI InChI=1S/C41H46N2O2/c1-42(30-33-11-5-2-6-12-33)31-34-17-15-32(16-18-34)27-38-28-37-19-20-39(29-40(37)41(38)44)45-26-10-4-9-23-43-24-21-36(22-25-43)35-13-7-3-8-14-35/h2-3,5-8,11-20,27,29,36H,4,9-10,21-26,28,30-31H2,1H3/b38-27+
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 6.20E+4n/an/an/an/an/an/a



University of Bologna

Curated by ChEMBL


Assay Description
Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated with enzyme for 20 mins prior to substrate addition by ...


Bioorg Med Chem Lett 25: 2804-8 (2015)


Article DOI: 10.1016/j.bmcl.2015.05.002
BindingDB Entry DOI: 10.7270/Q2TB18P5
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%