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Compile Data Set for Download or QSAR

Found 9 hits Enz. Inhib. hit(s) with all data for entry = 2035   
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))
BDBM16270
PNG
((2R,4S,5S)-N-[(1S)-1-(benzylcarbamoyl)-2-methylpro...)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H]1CC(=O)NC\C=C\CCCOC(=O)N[C@@H](C(C)C)C(=O)N1)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r,t:14|
Show InChI InChI=1S/C38H60N6O8/c1-23(2)19-28(30(45)20-26(7)34(47)43-32(24(3)4)36(49)40-22-27-15-11-10-12-16-27)41-35(48)29-21-31(46)39-17-13-8-9-14-18-52-38(51)44-33(25(5)6)37(50)42-29/h8,10-13,15-16,23-26,28-30,32-33,45H,9,14,17-22H2,1-7H3,(H,39,46)(H,40,49)(H,41,48)(H,42,50)(H,43,47)(H,44,51)/b13-8+/t26-,28+,29+,30+,32+,33+/m1/s1
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PubMed
14.2 -46.6n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM16271
PNG
((2R,4S,5S)-N-[(1S)-1-(benzylcarbamoyl)-2-methylpro...)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H]1CC(=O)NCCCCCCOC(=O)N[C@@H](C(C)C)C(=O)N1)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r|
Show InChI InChI=1S/C38H62N6O8/c1-23(2)19-28(30(45)20-26(7)34(47)43-32(24(3)4)36(49)40-22-27-15-11-10-12-16-27)41-35(48)29-21-31(46)39-17-13-8-9-14-18-52-38(51)44-33(25(5)6)37(50)42-29/h10-12,15-16,23-26,28-30,32-33,45H,8-9,13-14,17-22H2,1-7H3,(H,39,46)(H,40,49)(H,41,48)(H,42,50)(H,43,47)(H,44,51)/t26-,28+,29+,30+,32+,33+/m1/s1
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PubMed
25.1 -45.1n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Beta-secretase 1


(Homo sapiens (Human))
BDBM16263
PNG
(amide-urethane derived inhibitor 12a | prop-2-en-1...)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CC(=O)NCC=C)NC(=O)[C@@H](NC(=O)OCC=C)C(C)C)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r|
Show InChI InChI=1S/C38H60N6O8/c1-10-17-39-31(46)21-29(42-37(50)33(25(7)8)44-38(51)52-18-11-2)35(48)41-28(19-23(3)4)30(45)20-26(9)34(47)43-32(24(5)6)36(49)40-22-27-15-13-12-14-16-27/h10-16,23-26,28-30,32-33,45H,1-2,17-22H2,3-9H3,(H,39,46)(H,40,49)(H,41,48)(H,42,50)(H,43,47)(H,44,51)/t26-,28+,29+,30+,32+,33+/m1/s1
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26.6 -45.0n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM16267
PNG
((2R,4S,5S)-N-[(1S)-1-(benzylcarbamoyl)-2-methylpro...)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H]1CC(=O)NC\C=C\CCOC(=O)N[C@@H](C(C)C)C(=O)N1)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r,t:14|
Show InChI InChI=1S/C37H58N6O8/c1-22(2)18-27(29(44)19-25(7)33(46)42-31(23(3)4)35(48)39-21-26-14-10-8-11-15-26)40-34(47)28-20-30(45)38-16-12-9-13-17-51-37(50)43-32(24(5)6)36(49)41-28/h8-12,14-15,22-25,27-29,31-32,44H,13,16-21H2,1-7H3,(H,38,45)(H,39,48)(H,40,47)(H,41,49)(H,42,46)(H,43,50)/b12-9+/t25-,27+,28+,29+,31+,32+/m1/s1
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28.4 -44.8n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM16266
PNG
(amide-urethane derived inhibitor 12b | but-3-en-1-...)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CC(=O)NCC=C)NC(=O)[C@@H](NC(=O)OCCC=C)C(C)C)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r|
Show InChI InChI=1S/C39H62N6O8/c1-10-12-19-53-39(52)45-34(26(7)8)38(51)43-30(22-32(47)40-18-11-2)36(49)42-29(20-24(3)4)31(46)21-27(9)35(48)44-33(25(5)6)37(50)41-23-28-16-14-13-15-17-28/h10-11,13-17,24-27,29-31,33-34,46H,1-2,12,18-23H2,3-9H3,(H,40,47)(H,41,50)(H,42,49)(H,43,51)(H,44,48)(H,45,52)/t27-,29+,30+,31+,33+,34+/m1/s1
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PubMed
61.4 -42.8n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM16264
PNG
((2R,4S,5S)-N-[(1S)-1-(benzylcarbamoyl)-2-methylpro...)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H]1CC(=O)NC\C=C\COC(=O)N[C@@H](C(C)C)C(=O)N1)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r,t:14|
Show InChI InChI=1S/C36H56N6O8/c1-21(2)17-26(28(43)18-24(7)32(45)41-30(22(3)4)34(47)38-20-25-13-9-8-10-14-25)39-33(46)27-19-29(44)37-15-11-12-16-50-36(49)42-31(23(5)6)35(48)40-27/h8-14,21-24,26-28,30-31,43H,15-20H2,1-7H3,(H,37,44)(H,38,47)(H,39,46)(H,40,48)(H,41,45)(H,42,49)/b12-11+/t24-,26+,27+,28+,30+,31+/m1/s1
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PubMed
87.2 -41.9n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM16268
PNG
((2R,4S,5S)-N-[(1S)-1-(benzylcarbamoyl)-2-methylpro...)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H]1CC(=O)NCCCCCOC(=O)N[C@@H](C(C)C)C(=O)N1)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r|
Show InChI InChI=1S/C37H60N6O8/c1-22(2)18-27(29(44)19-25(7)33(46)42-31(23(3)4)35(48)39-21-26-14-10-8-11-15-26)40-34(47)28-20-30(45)38-16-12-9-13-17-51-37(50)43-32(24(5)6)36(49)41-28/h8,10-11,14-15,22-25,27-29,31-32,44H,9,12-13,16-21H2,1-7H3,(H,38,45)(H,39,48)(H,40,47)(H,41,49)(H,42,46)(H,43,50)/t25-,27+,28+,29+,31+,32+/m1/s1
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PubMed
108 -41.4n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM16269
PNG
(amide-urethane derived inhibitor 12c | pent-4-en-1...)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CC(=O)NCC=C)NC(=O)[C@@H](NC(=O)OCCCC=C)C(C)C)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r|
Show InChI InChI=1S/C40H64N6O8/c1-10-12-16-20-54-40(53)46-35(27(7)8)39(52)44-31(23-33(48)41-19-11-2)37(50)43-30(21-25(3)4)32(47)22-28(9)36(49)45-34(26(5)6)38(51)42-24-29-17-14-13-15-18-29/h10-11,13-15,17-18,25-28,30-32,34-35,47H,1-2,12,16,19-24H2,3-9H3,(H,41,48)(H,42,51)(H,43,50)(H,44,52)(H,45,49)(H,46,53)/t28-,30+,31+,32+,34+,35+/m1/s1
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112 -41.3n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM16265
PNG
((2R,4S,5S)-N-[(1S)-1-(benzylcarbamoyl)-2-methylpro...)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H]1CC(=O)NCCCCOC(=O)N[C@@H](C(C)C)C(=O)N1)[C@@H](O)C[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)NCc1ccccc1 |r|
Show InChI InChI=1S/C36H58N6O8/c1-21(2)17-26(28(43)18-24(7)32(45)41-30(22(3)4)34(47)38-20-25-13-9-8-10-14-25)39-33(46)27-19-29(44)37-15-11-12-16-50-36(49)42-31(23(5)6)35(48)40-27/h8-10,13-14,21-24,26-28,30-31,43H,11-12,15-20H2,1-7H3,(H,37,44)(H,38,47)(H,39,46)(H,40,48)(H,41,45)(H,42,49)/t24-,26+,27+,28+,30+,31+/m1/s1
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PubMed
218 -39.6n/an/an/an/an/a4.537



University of Illinois at Chicago



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


Bioorg Med Chem Lett 15: 15-20 (2005)


Article DOI: 10.1016/j.bmcl.2004.10.084
BindingDB Entry DOI: 10.7270/Q2ZC814B
More data for this
Ligand-Target Pair