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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 536.5
BDBM501319

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 4 hits in this display   
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))
BDBM501319
PNG
(US11021493, Example 238)
Show SMILES CN1C(N)=N[C@@](C)(CS1(=O)=O)c1cc(\C=C(/F)c2cnc(OCc3nc(C)oc3C)cn2)cc(F)c1F |r,c:3|
Show InChI InChI=1S/C23H23F3N6O4S/c1-12-19(30-13(2)36-12)10-35-20-9-28-18(8-29-20)16(24)6-14-5-15(21(26)17(25)7-14)23(3)11-37(33,34)32(4)22(27)31-23/h5-9H,10-11H2,1-4H3,(H2,27,31)/b16-6-/t23-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 6n/an/an/an/an/an/a



Amgen Inc.

US Patent


Assay Description
The cDNAs for both human recombinant BACE1 and 2 with C-terminal 6-His Tags were cloned into transient protein expression vectors, which were subsequ...


US Patent US11021493 (2021)


BindingDB Entry DOI: 10.7270/Q2CZ3B90
More data for this
Ligand-Target Pair
Beta-secretase 1


(Homo sapiens (Human))
BDBM501319
PNG
(US11021493, Example 238)
Show SMILES CN1C(N)=N[C@@](C)(CS1(=O)=O)c1cc(\C=C(/F)c2cnc(OCc3nc(C)oc3C)cn2)cc(F)c1F |r,c:3|
Show InChI InChI=1S/C23H23F3N6O4S/c1-12-19(30-13(2)36-12)10-35-20-9-28-18(8-29-20)16(24)6-14-5-15(21(26)17(25)7-14)23(3)11-37(33,34)32(4)22(27)31-23/h5-9H,10-11H2,1-4H3,(H2,27,31)/b16-6-/t23-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 42n/an/an/an/an/an/a



Amgen Inc.

US Patent


Assay Description
The cell-based assay measures inhibition or reduction of Aβ40 in conditioned medium of test compound treated cells expressing amyloid precursor ...


US Patent US11021493 (2021)


BindingDB Entry DOI: 10.7270/Q2CZ3B90
More data for this
Ligand-Target Pair
Beta-secretase 2


(Homo sapiens (Human))
BDBM501319
PNG
(US11021493, Example 238)
Show SMILES CN1C(N)=N[C@@](C)(CS1(=O)=O)c1cc(\C=C(/F)c2cnc(OCc3nc(C)oc3C)cn2)cc(F)c1F |r,c:3|
Show InChI InChI=1S/C23H23F3N6O4S/c1-12-19(30-13(2)36-12)10-35-20-9-28-18(8-29-20)16(24)6-14-5-15(21(26)17(25)7-14)23(3)11-37(33,34)32(4)22(27)31-23/h5-9H,10-11H2,1-4H3,(H2,27,31)/b16-6-/t23-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 94n/an/an/an/an/an/a



Amgen Inc.

US Patent


Assay Description
The cDNAs for both human recombinant BACE1 and 2 with C-terminal 6-His Tags were cloned into transient protein expression vectors, which were subsequ...


US Patent US11021493 (2021)


BindingDB Entry DOI: 10.7270/Q2CZ3B90
More data for this
Ligand-Target Pair
Cathepsin D


(Homo sapiens (Human))
BDBM501319
PNG
(US11021493, Example 238)
Show SMILES CN1C(N)=N[C@@](C)(CS1(=O)=O)c1cc(\C=C(/F)c2cnc(OCc3nc(C)oc3C)cn2)cc(F)c1F |r,c:3|
Show InChI InChI=1S/C23H23F3N6O4S/c1-12-19(30-13(2)36-12)10-35-20-9-28-18(8-29-20)16(24)6-14-5-15(21(26)17(25)7-14)23(3)11-37(33,34)32(4)22(27)31-23/h5-9H,10-11H2,1-4H3,(H2,27,31)/b16-6-/t23-/m0/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 4.68E+4n/an/an/an/an/an/a



Amgen Inc.

US Patent


Assay Description
Recombinant CatD was expressed in CHO cells. The assay buffer for CatD was 0.05 M citrate pH 3.5, 10% DMSO final, 5 mM CHAPS. The CatD enzyme (9 nM) ...


US Patent US11021493 (2021)


BindingDB Entry DOI: 10.7270/Q2CZ3B90
More data for this
Ligand-Target Pair