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Compile Data Set for Download or QSAR

Found 11 hits of ic50 for UniProtKB: P56817   
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
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM186049
PNG
(US9163011, 3)
Show SMILES CC1(C)OC(N)=N[C@](C)(c2nc(NC(=O)c3ncc(cc3Cl)C#N)ccc2F)C1(F)F |r,c:5|
Show InChI InChI=1S/C19H16ClF3N6O2/c1-17(2)19(22,23)18(3,29-16(25)31-17)14-11(21)4-5-12(27-14)28-15(30)13-10(20)6-9(7-24)8-26-13/h4-6,8H,1-3H3,(H2,25,29)(H,27,28,30)/t18-/m1/s1
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n/an/a 7n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of BACE1/BACE2 (unknown origin) transfected in CHO cells assessed as release of amyloid beta (1 to 40) after 24 hrs by immunoassay


ACS Med Chem Lett 4: 433-4 (2013)


Article DOI: 10.1021/ml400104f
BindingDB Entry DOI: 10.7270/Q24M97F6
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM186080
PNG
(US9163011, 35)
Show SMILES C[C@@]1(N=C(N)OCC1(F)F)c1nc(NC(=O)c2ccc(cn2)C#N)ccc1F |r,t:2|
Show InChI InChI=1S/C17H13F3N6O2/c1-16(17(19,20)8-28-15(22)26-16)13-10(18)3-5-12(24-13)25-14(27)11-4-2-9(6-21)7-23-11/h2-5,7H,8H2,1H3,(H2,22,26)(H,24,25,27)/t16-/m1/s1
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n/an/a 7n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of BACE1/BACE2 (unknown origin) transfected in CHO cells assessed as release of amyloid beta (1 to 40) after 24 hrs by immunoassay


ACS Med Chem Lett 4: 433-4 (2013)


Article DOI: 10.1021/ml400104f
BindingDB Entry DOI: 10.7270/Q24M97F6
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM186048
PNG
(US9163011, 2)
Show SMILES C[C@@]1(N=C(N)OCC1(F)F)c1nc(NC(=O)c2ncc(cc2Cl)C#N)ccc1F |r,t:2|
Show InChI InChI=1S/C17H12ClF3N6O2/c1-16(17(20,21)7-29-15(23)27-16)13-10(19)2-3-11(25-13)26-14(28)12-9(18)4-8(5-22)6-24-12/h2-4,6H,7H2,1H3,(H2,23,27)(H,25,26,28)/t16-/m1/s1
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n/an/a 8n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of BACE1/BACE2 (unknown origin) transfected in CHO cells assessed as release of amyloid beta (1 to 40) after 24 hrs by immunoassay


ACS Med Chem Lett 4: 433-4 (2013)


Article DOI: 10.1021/ml400104f
BindingDB Entry DOI: 10.7270/Q24M97F6
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM186055
PNG
(US9163011, 9)
Show SMILES C[C@@]1(N=C(N)OCC1(F)F)c1nc(NC(=O)c2ncc(Cl)cc2Cl)ccc1F |r,t:2|
Show InChI InChI=1S/C16H12Cl2F3N5O2/c1-15(16(20,21)6-28-14(22)26-15)12-9(19)2-3-10(24-12)25-13(27)11-8(18)4-7(17)5-23-11/h2-5H,6H2,1H3,(H2,22,26)(H,24,25,27)/t15-/m1/s1
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n/an/a 12n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of BACE1/BACE2 (unknown origin) transfected in CHO cells assessed as release of amyloid beta (1 to 40) after 24 hrs by immunoassay


ACS Med Chem Lett 4: 433-4 (2013)


Article DOI: 10.1021/ml400104f
BindingDB Entry DOI: 10.7270/Q24M97F6
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM186075
PNG
(US9163011, 30)
Show SMILES C[C@@]1(N=C(N)OCC1(F)F)c1nc(NC(=O)c2nn(cc2Cl)C(F)F)ccc1F |r,t:2|
Show InChI InChI=1S/C15H12ClF5N6O2/c1-14(15(20,21)5-29-13(22)25-14)10-7(17)2-3-8(23-10)24-11(28)9-6(16)4-27(26-9)12(18)19/h2-4,12H,5H2,1H3,(H2,22,25)(H,23,24,28)/t14-/m1/s1
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n/an/a 13n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of BACE1/BACE2 (unknown origin) transfected in CHO cells assessed as release of amyloid beta (1 to 40) after 24 hrs by immunoassay


ACS Med Chem Lett 4: 433-4 (2013)


Article DOI: 10.1021/ml400104f
BindingDB Entry DOI: 10.7270/Q24M97F6
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM186053
PNG
(US9163011, 7)
Show SMILES C[C@@]1(N=C(N)OCC1(F)F)c1nc(NC(=O)c2ncc(cc2Cl)C(F)(F)F)ccc1F |r,t:2|
Show InChI InChI=1S/C17H12ClF6N5O2/c1-15(16(20,21)6-31-14(25)29-15)12-9(19)2-3-10(27-12)28-13(30)11-8(18)4-7(5-26-11)17(22,23)24/h2-5H,6H2,1H3,(H2,25,29)(H,27,28,30)/t15-/m1/s1
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n/an/a 27n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of BACE1/BACE2 (unknown origin) transfected in CHO cells assessed as release of amyloid beta (1 to 40) after 24 hrs by immunoassay


ACS Med Chem Lett 4: 433-4 (2013)


Article DOI: 10.1021/ml400104f
BindingDB Entry DOI: 10.7270/Q24M97F6
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM50100436
PNG
(CHEMBL412768 | NH2-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val...)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CCCCN)[C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)[C@@H](O)CC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1ccccc1)C(O)=O
Show InChI InChI=1S/C73H118N16O27/c1-11-37(8)59(88-66(108)45(23-27-56(101)102)79-63(105)43(21-25-54(97)98)81-72(114)60(39(10)91)89-62(104)41(75)19-15-16-28-74)71(113)85-49(33-90)68(110)80-44(22-26-55(99)100)65(107)87-58(36(6)7)70(112)83-47(31-51(76)93)67(109)82-46(29-34(2)3)50(92)32-52(94)86-57(35(4)5)69(111)77-38(9)61(103)78-42(20-24-53(95)96)64(106)84-48(73(115)116)30-40-17-13-12-14-18-40/h12-14,17-18,34-39,41-50,57-60,90-92H,11,15-16,19-33,74-75H2,1-10H3,(H2,76,93)(H,77,111)(H,78,103)(H,79,105)(H,80,110)(H,81,114)(H,82,109)(H,83,112)(H,84,106)(H,85,113)(H,86,94)(H,87,107)(H,88,108)(H,89,104)(H,95,96)(H,97,98)(H,99,100)(H,101,102)(H,115,116)/t37-,38-,39+,41-,42-,43-,44-,45-,46-,47-,48-,49-,50-,57-,58-,59-,60-/m0/s1
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n/an/a 30n/an/an/an/an/an/a



Harvard Medical School

Curated by ChEMBL


Assay Description
In vitro inhibition of beta-secretase was evaluated


J Med Chem 44: 2039-60 (2001)


BindingDB Entry DOI: 10.7270/Q27S7PGX
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM186050
PNG
(US9163011, 4)
Show SMILES COCC[C@@]1(N=C(N)OCC1(F)F)c1nc(NC(=O)c2ncc(cc2C)C#N)ccc1F |r,t:5|
Show InChI InChI=1S/C20H19F3N6O3/c1-11-7-12(8-24)9-26-15(11)17(30)28-14-4-3-13(21)16(27-14)19(5-6-31-2)20(22,23)10-32-18(25)29-19/h3-4,7,9H,5-6,10H2,1-2H3,(H2,25,29)(H,27,28,30)/t19-/m1/s1
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n/an/a 49n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of BACE1/BACE2 (unknown origin) transfected in CHO cells assessed as release of amyloid beta (1 to 40) after 24 hrs by immunoassay


ACS Med Chem Lett 4: 433-4 (2013)


Article DOI: 10.1021/ml400104f
BindingDB Entry DOI: 10.7270/Q24M97F6
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM50100434
PNG
(CHEMBL302004 | L-68458 | L-685458 | tert-butyl (2S...)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H](C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(N)=O
Show InChI InChI=1S/C39H52N4O6/c1-26(2)21-33(37(47)41-32(35(40)45)24-29-19-13-8-14-20-29)42-36(46)30(22-27-15-9-6-10-16-27)25-34(44)31(23-28-17-11-7-12-18-28)43-38(48)49-39(3,4)5/h6-20,26,30-34,44H,21-25H2,1-5H3,(H2,40,45)(H,41,47)(H,42,46)(H,43,48)/t30-,31+,32+,33+,34-/m1/s1
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n/an/a 300n/an/an/an/an/an/a



Harvard Medical School

Curated by ChEMBL


Assay Description
Inhibition of beta-secretase activity


J Med Chem 44: 2039-60 (2001)


BindingDB Entry DOI: 10.7270/Q27S7PGX
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM186057
PNG
(US9163011, 11)
Show SMILES C[C@@]1(N=C(N)OCC1(F)F)c1nc(NC(=O)c2ncc(OCC(F)F)nc2N)ccc1F |r,t:2|
Show InChI InChI=1S/C17H16F5N7O3/c1-16(17(21,22)6-32-15(24)29-16)12-7(18)2-3-9(26-12)27-14(30)11-13(23)28-10(4-25-11)31-5-8(19)20/h2-4,8H,5-6H2,1H3,(H2,23,28)(H2,24,29)(H,26,27,30)/t16-/m1/s1
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n/an/a 440n/an/an/an/an/an/a



Dart Neuroscience LLC

Curated by ChEMBL


Assay Description
Inhibition of BACE1/BACE2 (unknown origin) transfected in CHO cells assessed as release of amyloid beta (1 to 40) after 24 hrs by immunoassay


ACS Med Chem Lett 4: 433-4 (2013)


Article DOI: 10.1021/ml400104f
BindingDB Entry DOI: 10.7270/Q24M97F6
More data for this
Ligand-Target Pair
Beta-secretase 1/2


(Homo sapiens (Human))
BDBM50470133
PNG
(CHEMBL277046)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(C)=O)C(=O)NC(CC(C)C)C(O)CC(=O)N[C@@H](CC(C)C)C(N)=O
Show InChI InChI=1S/C31H51N5O6/c1-8-20(6)28(36-30(41)25(33-21(7)37)16-22-12-10-9-11-13-22)31(42)35-23(14-18(2)3)26(38)17-27(39)34-24(29(32)40)15-19(4)5/h9-13,18-20,23-26,28,38H,8,14-17H2,1-7H3,(H2,32,40)(H,33,37)(H,34,39)(H,35,42)(H,36,41)/t20-,23?,24-,25-,26?,28-/m0/s1
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n/an/a 1.40E+3n/an/an/an/an/an/a



Affymax Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against aspartyl protease


J Med Chem 37: 1233-51 (1994)


Article DOI: 10.1021/jm00035a001
BindingDB Entry DOI: 10.7270/Q2GT5QWG
More data for this
Ligand-Target Pair