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BDBM50232521 (2R)-4-[(6R)-6-methyl-3-(trifluoromethyl)-5,6-dihydro[[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl]-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-amine hydrochloride::CHEMBL553787

SMILES: C[C@@H]1Cn2c(CN1C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F)nnc2C(F)(F)F

InChI Key: InChIKey=VXEJFPVVOIXCFP-PSASIEDQSA-N

Data: 7 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50232521   
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
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM50232521
PNG
((2R)-4-[(6R)-6-methyl-3-(trifluoromethyl)-5,6-dihy...)
Show SMILES C[C@@H]1Cn2c(CN1C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F)nnc2C(F)(F)F
Show InChI InChI=1S/C17H17F6N5O/c1-8-6-28-14(25-26-16(28)17(21,22)23)7-27(8)15(29)4-10(24)2-9-3-12(19)13(20)5-11(9)18/h3,5,8,10H,2,4,6-7,24H2,1H3/t8-,10-/m1/s1
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n/an/a>1.00E+5n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of QPP


J Med Chem 51: 589-602 (2008)


Article DOI: 10.1021/jm070330v
BindingDB Entry DOI: 10.7270/Q2B27W4M
More data for this
Ligand-Target Pair
Fibroblast activation protein alpha


(Homo sapiens (Human))
BDBM50232521
PNG
((2R)-4-[(6R)-6-methyl-3-(trifluoromethyl)-5,6-dihy...)
Show SMILES C[C@@H]1Cn2c(CN1C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F)nnc2C(F)(F)F
Show InChI InChI=1S/C17H17F6N5O/c1-8-6-28-14(25-26-16(28)17(21,22)23)7-27(8)15(29)4-10(24)2-9-3-12(19)13(20)5-11(9)18/h3,5,8,10H,2,4,6-7,24H2,1H3/t8-,10-/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of FAP


J Med Chem 51: 589-602 (2008)


Article DOI: 10.1021/jm070330v
BindingDB Entry DOI: 10.7270/Q2B27W4M
More data for this
Ligand-Target Pair
Xaa-Pro aminopeptidase 1


(Homo sapiens (Human))
BDBM50232521
PNG
((2R)-4-[(6R)-6-methyl-3-(trifluoromethyl)-5,6-dihy...)
Show SMILES C[C@@H]1Cn2c(CN1C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F)nnc2C(F)(F)F
Show InChI InChI=1S/C17H17F6N5O/c1-8-6-28-14(25-26-16(28)17(21,22)23)7-27(8)15(29)4-10(24)2-9-3-12(19)13(20)5-11(9)18/h3,5,8,10H,2,4,6-7,24H2,1H3/t8-,10-/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of amino peptidase P


J Med Chem 51: 589-602 (2008)


Article DOI: 10.1021/jm070330v
BindingDB Entry DOI: 10.7270/Q2B27W4M
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50232521
PNG
((2R)-4-[(6R)-6-methyl-3-(trifluoromethyl)-5,6-dihy...)
Show SMILES C[C@@H]1Cn2c(CN1C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F)nnc2C(F)(F)F
Show InChI InChI=1S/C17H17F6N5O/c1-8-6-28-14(25-26-16(28)17(21,22)23)7-27(8)15(29)4-10(24)2-9-3-12(19)13(20)5-11(9)18/h3,5,8,10H,2,4,6-7,24H2,1H3/t8-,10-/m1/s1
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n/an/a 42n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of DPP4


J Med Chem 51: 589-602 (2008)


Article DOI: 10.1021/jm070330v
BindingDB Entry DOI: 10.7270/Q2B27W4M
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM50232521
PNG
((2R)-4-[(6R)-6-methyl-3-(trifluoromethyl)-5,6-dihy...)
Show SMILES C[C@@H]1Cn2c(CN1C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F)nnc2C(F)(F)F
Show InChI InChI=1S/C17H17F6N5O/c1-8-6-28-14(25-26-16(28)17(21,22)23)7-27(8)15(29)4-10(24)2-9-3-12(19)13(20)5-11(9)18/h3,5,8,10H,2,4,6-7,24H2,1H3/t8-,10-/m1/s1
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n/an/a 7.50E+4n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of DPP8


J Med Chem 51: 589-602 (2008)


Article DOI: 10.1021/jm070330v
BindingDB Entry DOI: 10.7270/Q2B27W4M
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 9


(Homo sapiens (Human))
BDBM50232521
PNG
((2R)-4-[(6R)-6-methyl-3-(trifluoromethyl)-5,6-dihy...)
Show SMILES C[C@@H]1Cn2c(CN1C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F)nnc2C(F)(F)F
Show InChI InChI=1S/C17H17F6N5O/c1-8-6-28-14(25-26-16(28)17(21,22)23)7-27(8)15(29)4-10(24)2-9-3-12(19)13(20)5-11(9)18/h3,5,8,10H,2,4,6-7,24H2,1H3/t8-,10-/m1/s1
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n/an/a>1.00E+5n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of DPP9


J Med Chem 51: 589-602 (2008)


Article DOI: 10.1021/jm070330v
BindingDB Entry DOI: 10.7270/Q2B27W4M
More data for this
Ligand-Target Pair
Xaa-Pro dipeptidase


(Homo sapiens (Human))
BDBM50232521
PNG
((2R)-4-[(6R)-6-methyl-3-(trifluoromethyl)-5,6-dihy...)
Show SMILES C[C@@H]1Cn2c(CN1C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F)nnc2C(F)(F)F
Show InChI InChI=1S/C17H17F6N5O/c1-8-6-28-14(25-26-16(28)17(21,22)23)7-27(8)15(29)4-10(24)2-9-3-12(19)13(20)5-11(9)18/h3,5,8,10H,2,4,6-7,24H2,1H3/t8-,10-/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of prolidase


J Med Chem 51: 589-602 (2008)


Article DOI: 10.1021/jm070330v
BindingDB Entry DOI: 10.7270/Q2B27W4M
More data for this
Ligand-Target Pair