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BDBM50232505 (2R)-4-[5,5-dimethyl-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::CHEMBL536765

SMILES: CC1(C)CN(Cc2nnc(n12)C(F)(F)F)C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F

InChI Key: InChIKey=TTYGLBGNRGWWAM-SNVBAGLBSA-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 = 50232505   
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 VIII


(Homo sapiens (Human))
BDBM50232505
PNG
((2R)-4-[5,5-dimethyl-3-(trifluoromethyl)-5,6-dihyd...)
Show SMILES CC1(C)CN(Cc2nnc(n12)C(F)(F)F)C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F
Show InChI InChI=1S/C18H19F6N5O/c1-17(2)8-28(7-14-26-27-16(29(14)17)18(22,23)24)15(30)5-10(25)3-9-4-12(20)13(21)6-11(9)19/h4,6,10H,3,5,7-8,25H2,1-2H3/t10-/m1/s1
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PubMed
n/an/a 6.60E+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
Fibroblast activation protein alpha


(Homo sapiens (Human))
BDBM50232505
PNG
((2R)-4-[5,5-dimethyl-3-(trifluoromethyl)-5,6-dihyd...)
Show SMILES CC1(C)CN(Cc2nnc(n12)C(F)(F)F)C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F
Show InChI InChI=1S/C18H19F6N5O/c1-17(2)8-28(7-14-26-27-16(29(14)17)18(22,23)24)15(30)5-10(25)3-9-4-12(20)13(21)6-11(9)19/h4,6,10H,3,5,7-8,25H2,1-2H3/t10-/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 dipeptidase


(Homo sapiens (Human))
BDBM50232505
PNG
((2R)-4-[5,5-dimethyl-3-(trifluoromethyl)-5,6-dihyd...)
Show SMILES CC1(C)CN(Cc2nnc(n12)C(F)(F)F)C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F
Show InChI InChI=1S/C18H19F6N5O/c1-17(2)8-28(7-14-26-27-16(29(14)17)18(22,23)24)15(30)5-10(25)3-9-4-12(20)13(21)6-11(9)19/h4,6,10H,3,5,7-8,25H2,1-2H3/t10-/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
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50232505
PNG
((2R)-4-[5,5-dimethyl-3-(trifluoromethyl)-5,6-dihyd...)
Show SMILES CC1(C)CN(Cc2nnc(n12)C(F)(F)F)C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F
Show InChI InChI=1S/C18H19F6N5O/c1-17(2)8-28(7-14-26-27-16(29(14)17)18(22,23)24)15(30)5-10(25)3-9-4-12(20)13(21)6-11(9)19/h4,6,10H,3,5,7-8,25H2,1-2H3/t10-/m1/s1
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n/an/a 92n/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
Xaa-Pro aminopeptidase 1


(Homo sapiens (Human))
BDBM50232505
PNG
((2R)-4-[5,5-dimethyl-3-(trifluoromethyl)-5,6-dihyd...)
Show SMILES CC1(C)CN(Cc2nnc(n12)C(F)(F)F)C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F
Show InChI InChI=1S/C18H19F6N5O/c1-17(2)8-28(7-14-26-27-16(29(14)17)18(22,23)24)15(30)5-10(25)3-9-4-12(20)13(21)6-11(9)19/h4,6,10H,3,5,7-8,25H2,1-2H3/t10-/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 2 (DPP II)


(Homo sapiens (Human))
BDBM50232505
PNG
((2R)-4-[5,5-dimethyl-3-(trifluoromethyl)-5,6-dihyd...)
Show SMILES CC1(C)CN(Cc2nnc(n12)C(F)(F)F)C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F
Show InChI InChI=1S/C18H19F6N5O/c1-17(2)8-28(7-14-26-27-16(29(14)17)18(22,23)24)15(30)5-10(25)3-9-4-12(20)13(21)6-11(9)19/h4,6,10H,3,5,7-8,25H2,1-2H3/t10-/m1/s1
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n/an/a 7.70E+4n/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
Dipeptidyl peptidase 9


(Homo sapiens (Human))
BDBM50232505
PNG
((2R)-4-[5,5-dimethyl-3-(trifluoromethyl)-5,6-dihyd...)
Show SMILES CC1(C)CN(Cc2nnc(n12)C(F)(F)F)C(=O)C[C@H](N)Cc1cc(F)c(F)cc1F
Show InChI InChI=1S/C18H19F6N5O/c1-17(2)8-28(7-14-26-27-16(29(14)17)18(22,23)24)15(30)5-10(25)3-9-4-12(20)13(21)6-11(9)19/h4,6,10H,3,5,7-8,25H2,1-2H3/t10-/m1/s1
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PubMed
n/an/a 5.40E+4n/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