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Compile Data Set for Download or QSAR

Found 77 hits with Last Name = 'kitajima' and Initial = 't'   
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))
BDBM50452874
PNG
(CHEMBL4217620)
Show SMILES CO[C@H]1CC[C@]2(Cc3ccc(cc3[C@@]22N=C(C)C(N)=N2)-c2cncc(c2)C#CC)CC1 |r,wU:13.15,5.4,wD:2.1,c:20,t:16,(42.8,-16.77,;41.71,-15.68,;40.22,-16.08,;39.13,-14.99,;37.64,-15.39,;37.25,-16.87,;37.1,-18.41,;35.59,-18.75,;34.81,-20.09,;33.28,-20.09,;32.51,-18.75,;33.27,-17.42,;34.81,-17.41,;35.84,-16.25,;34.46,-15.55,;34.7,-14.03,;33.6,-12.94,;36.22,-13.78,;36.92,-12.4,;36.93,-15.15,;30.97,-18.75,;30.21,-17.42,;28.66,-17.43,;27.9,-18.76,;28.67,-20.08,;30.21,-20.08,;27.9,-21.41,;27.12,-22.74,;26.34,-24.06,;38.34,-17.96,;39.82,-17.56,)|
Show InChI InChI=1S/C26H28N4O/c1-4-5-18-12-21(16-28-15-18)19-6-7-20-14-25(10-8-22(31-3)9-11-25)26(23(20)13-19)29-17(2)24(27)30-26/h6-7,12-13,15-16,22H,8-11,14H2,1-3H3,(H2,27,30)/t22-,25+,26-/m0/s1
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n/an/a 0.600n/an/an/an/an/an/a


TBA

Assay Description
Binding affinity to human recombinant BACE-1 (1 to 460 residue) using CEVNLDAEFK as substrate preincubated for 10 mins followed by substrate addition...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051610
PNG
(CHEMBL3311300)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CC1=CCCCC1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r,t:10|
Show InChI InChI=1S/C51H67N5O9/c1-32(2)27-39(53-48(61)42(56-50(64)65-51(5,6)7)30-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-35-19-13-9-14-20-35/h9-10,13-17,19-26,32-33,39-43H,8,11-12,18,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1
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n/an/a 140n/an/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of fMLP-induced calcium mobilization incubated for 5 mins p...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051690
PNG
(CHEMBL3311137)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r|
Show InChI InChI=1S/C51H63N5O9/c1-32(2)27-39(53-48(61)42(56-50(64)65-51(5,6)7)30-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-35-19-13-9-14-20-35/h8-26,32-33,39-43H,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1
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n/an/a 420n/an/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of fMLP-induced calcium mobilization incubated for 5 mins p...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578243
PNG
(CHEMBL4846642)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(CC(O)=O)cc1 |r|
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n/an/a 430n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578245
PNG
(CHEMBL4857564)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(cc1)C(C)C(O)=O |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578246
PNG
(CHEMBL4859258)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(cc1)C(C)(C)C(O)=O |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578244
PNG
(CHEMBL4850554)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(CCC(O)=O)cc1 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50452874
PNG
(CHEMBL4217620)
Show SMILES CO[C@H]1CC[C@]2(Cc3ccc(cc3[C@@]22N=C(C)C(N)=N2)-c2cncc(c2)C#CC)CC1 |r,wU:13.15,5.4,wD:2.1,c:20,t:16,(42.8,-16.77,;41.71,-15.68,;40.22,-16.08,;39.13,-14.99,;37.64,-15.39,;37.25,-16.87,;37.1,-18.41,;35.59,-18.75,;34.81,-20.09,;33.28,-20.09,;32.51,-18.75,;33.27,-17.42,;34.81,-17.41,;35.84,-16.25,;34.46,-15.55,;34.7,-14.03,;33.6,-12.94,;36.22,-13.78,;36.92,-12.4,;36.93,-15.15,;30.97,-18.75,;30.21,-17.42,;28.66,-17.43,;27.9,-18.76,;28.67,-20.08,;30.21,-20.08,;27.9,-21.41,;27.12,-22.74,;26.34,-24.06,;38.34,-17.96,;39.82,-17.56,)|
Show InChI InChI=1S/C26H28N4O/c1-4-5-18-12-21(16-28-15-18)19-6-7-20-14-25(10-8-22(31-3)9-11-25)26(23(20)13-19)29-17(2)24(27)30-26/h6-7,12-13,15-16,22H,8-11,14H2,1-3H3,(H2,27,30)/t22-,25+,26-/m0/s1
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n/an/a 1.90E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051608
PNG
(CHEMBL3311030)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r|
Show InChI InChI=1S/C44H59N5O8/c1-28(2)23-33(46-41(53)36(26-31-19-13-9-14-20-31)49-43(56)57-44(5,6)7)38(50)47-35(25-30-17-11-8-12-18-30)40(52)45-34(24-29(3)4)39(51)48-37(42(54)55)27-32-21-15-10-16-22-32/h8-22,28-29,33-37H,23-27H2,1-7H3,(H,45,52)(H,46,53)(H,47,50)(H,48,51)(H,49,56)(H,54,55)/t33-,34-,35+,36+,37+/m1/s1
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n/an/a 2.00E+3n/an/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of fMLP-induced calcium mobilization incubated for 5 mins p...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578240
PNG
(CHEMBL4879047)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(cc1)C(C)(C)C |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578249
PNG
(CHEMBL4848236)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1cccc(CC(O)=O)c1 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578236
PNG
(CHEMBL4852055)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(C)cc1 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578255
PNG
(CHEMBL4849016)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNC1CCCCC1 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578251
PNG
(CHEMBL4873667)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(C)c(c1)C(O)=O |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578238
PNG
(CHEMBL4874363)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(CC(C)C)cc1 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578248
PNG
(CHEMBL4865499)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1cccc(c1)C(O)=O |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578239
PNG
(CHEMBL4851168)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(cc1)C1CCCC1 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578253
PNG
(CHEMBL4858655)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1cccc2ccccc12 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578237
PNG
(CHEMBL4876495)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccccc1 |r|
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n/an/a 8.80E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578256
PNG
(CHEMBL4872824)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNC1CCCCCC1 |r|
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n/an/a 9.20E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50110899
PNG
(CHEMBL3604697)
Show SMILES CCC[C@H](NC[C@@H](O)[C@H](Cc1cccs1)NC(=O)[C@H](Cc1cccs1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)CC)C(O)=O |r|
Show InChI InChI=1S/C31H47N5O8S2/c1-4-8-22(31(43)44)33-17-25(37)23(15-19-9-6-13-45-19)34-29(41)24(16-20-10-7-14-46-20)35-30(42)27(18(3)5-2)36-28(40)21(32)11-12-26(38)39/h6-7,9-10,13-14,18,21-25,27,33,37H,4-5,8,11-12,15-17,32H2,1-3H3,(H,34,41)(H,35,42)(H,36,40)(H,38,39)(H,43,44)/t18-,21-,22-,23-,24-,25+,27-/m0/s1
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578257
PNG
(CHEMBL4853052)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNC1CCCCCCC1 |r|
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n/an/a 1.00E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578252
PNG
(CHEMBL4866494)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1cc(C)cc(c1)C(O)=O |r|
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n/an/a 1.30E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578254
PNG
(CHEMBL4864653)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc2CCCCc2c1 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578247
PNG
(CHEMBL4874621)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1cccc(C)c1 |r|
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TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50110911
PNG
(CHEMBL3604595)
Show SMILES CCC[C@H](NC(=O)[C@H](O)[C@H](Cc1cccs1)NC(=O)[C@H](Cc1cccs1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)CC)C(O)=O |r|
Show InChI InChI=1S/C31H45N5O9S2/c1-4-8-21(31(44)45)33-30(43)26(39)22(15-18-9-6-13-46-18)34-28(41)23(16-19-10-7-14-47-19)35-29(42)25(17(3)5-2)36-27(40)20(32)11-12-24(37)38/h6-7,9-10,13-14,17,20-23,25-26,39H,4-5,8,11-12,15-16,32H2,1-3H3,(H,33,43)(H,34,41)(H,35,42)(H,36,40)(H,37,38)(H,44,45)/t17-,20-,21-,22-,23-,25-,26+/m0/s1
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n/an/a 2.60E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578234
PNG
(CHEMBL4857065)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)[C@@H](C)Nc1ccc(C)cc1 |r|
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n/an/a 3.10E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578242
PNG
(CHEMBL4867976)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(cc1)C(O)=O |r|
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n/an/a 3.30E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50110908
PNG
(CHEMBL3604598)
Show SMILES CCC[C@H](NC(=O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1cccs1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)CC)C(O)=O |r|
Show InChI InChI=1S/C33H47N5O9S/c1-4-10-23(33(46)47)35-32(45)28(41)24(17-20-11-7-6-8-12-20)36-30(43)25(18-21-13-9-16-48-21)37-31(44)27(19(3)5-2)38-29(42)22(34)14-15-26(39)40/h6-9,11-13,16,19,22-25,27-28,41H,4-5,10,14-15,17-18,34H2,1-3H3,(H,35,45)(H,36,43)(H,37,44)(H,38,42)(H,39,40)(H,46,47)/t19-,22-,23-,24-,25-,27-,28+/m0/s1
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n/an/a 3.40E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578230
PNG
(CHEMBL4849944)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(C)=O)C(C)C)C(O)C(C)Nc1ccc(C)cc1 |r|
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n/an/a 5.50E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin)


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50110910
PNG
(CHEMBL3604596)
Show SMILES CCC[C@H](NC(=O)[C@H](O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cccs1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)CC)C(O)=O |r|
Show InChI InChI=1S/C30H49N5O9S/c1-6-9-20(30(43)44)32-29(42)25(38)21(14-16(3)4)33-27(40)22(15-18-10-8-13-45-18)34-28(41)24(17(5)7-2)35-26(39)19(31)11-12-23(36)37/h8,10,13,16-17,19-22,24-25,38H,6-7,9,11-12,14-15,31H2,1-5H3,(H,32,42)(H,33,40)(H,34,41)(H,35,39)(H,36,37)(H,43,44)/t17-,19-,20-,21-,22-,24-,25+/m0/s1
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n/an/a 5.60E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50110909
PNG
(CHEMBL3604597)
Show SMILES CCC[C@H](NC(=O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cccs1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)CC)C(O)=O |r|
Show InChI InChI=1S/C33H53N5O9S/c1-4-10-23(33(46)47)35-32(45)28(41)24(17-20-11-7-6-8-12-20)36-30(43)25(18-21-13-9-16-48-21)37-31(44)27(19(3)5-2)38-29(42)22(34)14-15-26(39)40/h9,13,16,19-20,22-25,27-28,41H,4-8,10-12,14-15,17-18,34H2,1-3H3,(H,35,45)(H,36,43)(H,37,44)(H,38,42)(H,39,40)(H,46,47)/t19-,22-,23-,24-,25-,27-,28+/m0/s1
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n/an/a 6.40E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50110898
PNG
(CHEMBL3604698)
Show SMILES CCC[C@H](NC[C@@H](O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cccs1)NC(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)CC)C(O)=O |r|
Show InChI InChI=1S/C30H51N5O8S/c1-6-9-21(30(42)43)32-16-24(36)22(14-17(3)4)33-28(40)23(15-19-10-8-13-44-19)34-29(41)26(18(5)7-2)35-27(39)20(31)11-12-25(37)38/h8,10,13,17-18,20-24,26,32,36H,6-7,9,11-12,14-16,31H2,1-5H3,(H,33,40)(H,34,41)(H,35,39)(H,37,38)(H,42,43)/t18-,20-,21-,22-,23-,24+,26-/m0/s1
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n/an/a 7.20E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578233
PNG
(CHEMBL4855002)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@@H](O)CNc1ccc(C)cc1 |r|
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n/an/a 9.20E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578250
PNG
(CHEMBL4877632)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1cccc(c1)C(=O)OC |r|
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n/an/a 9.30E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578241
PNG
(CHEMBL4848778)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)CNc1ccc(cc1)C(F)(F)F |r|
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n/an/a 1.76E+5n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578231
PNG
(CHEMBL4874674)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@@H](O)[C@@H](C)Nc1ccc(C)cc1 |r|
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n/an/a 8.13E+5n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578235
PNG
(CHEMBL4859851)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@H](O)[C@H](C)Nc1ccc(C)cc1 |r|
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n/an/a>2.00E+6n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM50578232
PNG
(CHEMBL4861075)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCC(O)=O)C(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CC(C)C)[C@@H](O)[C@H](C)Nc1ccc(C)cc1 |r|
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n/an/a>2.00E+6n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant BACE-1 (unknown origin) using H-Ile-Lys-Thr-Glu-Glu-Ile-Ser-Glu-Val-Asn-Leu-Asp-Ala-Glu-Phe-Arg-His-Asp-Ser-Gly-NH2 peptide...


Citation and Details

Article DOI: 10.1016/j.bmc.2021.116459
BindingDB Entry DOI: 10.7270/Q2057KSB
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051609
PNG
(CHEMBL3311301)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CC1=CCCCC1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](CC1CCCCC1)C(O)=O |r,t:10|
Show InChI InChI=1S/C51H73N5O9/c1-32(2)27-39(53-48(61)42(56-50(64)65-51(5,6)7)30-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-35-19-13-9-14-20-35/h10,15-17,21-26,32-33,35,39-43H,8-9,11-14,18-20,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1
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n/an/an/a 6.90n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051610
PNG
(CHEMBL3311300)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](CC1=CCCCC1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r,t:10|
Show InChI InChI=1S/C51H67N5O9/c1-32(2)27-39(53-48(61)42(56-50(64)65-51(5,6)7)30-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-35-19-13-9-14-20-35/h9-10,13-17,19-26,32-33,39-43H,8,11-12,18,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1
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n/an/an/a 2.10n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051611
PNG
(CHEMBL3311299)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccc(cc1)C(=O)c1ccccc1)C(O)=O |r|
Show InChI InChI=1S/C51H63N5O9/c1-32(2)27-39(53-48(61)42(30-35-19-13-9-14-20-35)56-50(64)65-51(5,6)7)45(58)54-41(29-34-17-11-8-12-18-34)47(60)52-40(28-33(3)4)46(59)55-43(49(62)63)31-36-23-25-38(26-24-36)44(57)37-21-15-10-16-22-37/h8-26,32-33,39-43H,27-31H2,1-7H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t39-,40-,41+,42+,43+/m1/s1
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n/an/an/a 150n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051612
PNG
(CHEMBL3311298)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1cn(C(=O)OC(C)(C)C)c2ccccc12)C(O)=O |r|
Show InChI InChI=1S/C51H68N6O10/c1-31(2)25-37(53-46(61)40(28-34-21-15-12-16-22-34)56-48(64)66-50(5,6)7)43(58)54-39(27-33-19-13-11-14-20-33)45(60)52-38(26-32(3)4)44(59)55-41(47(62)63)29-35-30-57(49(65)67-51(8,9)10)42-24-18-17-23-36(35)42/h11-24,30-32,37-41H,25-29H2,1-10H3,(H,52,60)(H,53,61)(H,54,58)(H,55,59)(H,56,64)(H,62,63)/t37-,38-,39+,40+,41+/m1/s1
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n/an/an/a 120n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051613
PNG
(CHEMBL3311297)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O |r|
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n/an/an/a 150n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051614
PNG
(CHEMBL3311296)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccc(OC(C)(C)C)cc1)C(O)=O |r|
Show InChI InChI=1S/C48H67N5O9/c1-30(2)25-36(50-44(57)39(28-33-19-15-12-16-20-33)53-46(60)62-48(8,9)10)41(54)51-38(27-32-17-13-11-14-18-32)43(56)49-37(26-31(3)4)42(55)52-40(45(58)59)29-34-21-23-35(24-22-34)61-47(5,6)7/h11-24,30-31,36-40H,25-29H2,1-10H3,(H,49,56)(H,50,57)(H,51,54)(H,52,55)(H,53,60)(H,58,59)/t36-,37-,38+,39+,40+/m1/s1
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n/an/an/a 68n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051616
PNG
(CHEMBL3311295)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](CC1CCCCC1)C(O)=O |r|
Show InChI InChI=1S/C44H65N5O8/c1-28(2)23-33(46-41(53)36(26-31-19-13-9-14-20-31)49-43(56)57-44(5,6)7)38(50)47-35(25-30-17-11-8-12-18-30)40(52)45-34(24-29(3)4)39(51)48-37(42(54)55)27-32-21-15-10-16-22-32/h8-9,11-14,17-20,28-29,32-37H,10,15-16,21-27H2,1-7H3,(H,45,52)(H,46,53)(H,47,50)(H,48,51)(H,49,56)(H,54,55)/t33-,34-,35+,36+,37+/m1/s1
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n/an/an/a 77n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051622
PNG
(CHEMBL3311294)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)OC(C)(C)C)C(O)=O |r|
Show InChI InChI=1S/C43H65N5O9/c1-26(2)22-31(44-38(51)34(25-30-20-16-13-17-21-30)47-41(55)57-43(9,10)11)36(49)46-33(24-29-18-14-12-15-19-29)37(50)45-32(23-27(3)4)39(52)48-35(40(53)54)28(5)56-42(6,7)8/h12-21,26-28,31-35H,22-25H2,1-11H3,(H,44,51)(H,45,50)(H,46,49)(H,47,55)(H,48,52)(H,53,54)/t28-,31-,32-,33+,34+,35+/m1/s1
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n/an/an/a 130n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051624
PNG
(CHEMBL3311293)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](COC(C)(C)C)C(O)=O |r|
Show InChI InChI=1S/C42H63N5O9/c1-26(2)21-30(44-38(51)33(24-29-19-15-12-16-20-29)47-40(54)56-42(8,9)10)35(48)45-32(23-28-17-13-11-14-18-28)37(50)43-31(22-27(3)4)36(49)46-34(39(52)53)25-55-41(5,6)7/h11-20,26-27,30-34H,21-25H2,1-10H3,(H,43,50)(H,44,51)(H,45,48)(H,46,49)(H,47,54)(H,52,53)/t30-,31-,32+,33+,34+/m1/s1
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n/an/an/a 180n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051631
PNG
(CHEMBL3311292)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(O)=O |r|
Show InChI InChI=1S/C41H61N5O8/c1-25(2)20-30(43-38(50)33(24-29-18-14-11-15-19-29)46-40(53)54-41(7,8)9)35(47)44-32(23-28-16-12-10-13-17-28)37(49)42-31(21-26(3)4)36(48)45-34(39(51)52)22-27(5)6/h10-19,25-27,30-34H,20-24H2,1-9H3,(H,42,49)(H,43,50)(H,44,47)(H,45,48)(H,46,53)(H,51,52)/t30-,31-,32+,33+,34+/m1/s1
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n/an/an/a 130n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM50051639
PNG
(CHEMBL3309281)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(O)=O |r|
Show InChI InChI=1S/C40H59N5O8/c1-24(2)20-29(41-36(48)32(23-28-18-14-11-15-19-28)44-39(52)53-40(7,8)9)34(46)43-31(22-27-16-12-10-13-17-27)35(47)42-30(21-25(3)4)37(49)45-33(26(5)6)38(50)51/h10-19,24-26,29-33H,20-23H2,1-9H3,(H,41,48)(H,42,47)(H,43,46)(H,44,52)(H,45,49)(H,50,51)/t29-,30-,31+,32+,33+/m1/s1
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n/an/an/a 260n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair
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