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Literature summary for 3.4.14.2 extracted from

  • Danilova, O.; Li, B.; Szardenings, A.K.; Huber, B.T.; Rosenblum, J.S.
    Synthesis and activity of a potent, specific azabicyclo[3.3.0]-octane-based DPP II inhibitor (2007), Bioorg. Med. Chem. Lett., 17, 507-510.
    View publication on PubMedView publication on EuropePMC

Inhibitors

Inhibitors Comment Organism Structure
(3S)-4-[(3aR,6aR)-hexahydrocyclopenta[b]pyrrol-1(2H)-yl]-4-oxobutane-1,3-diamine AX8819, potent and selective inhibitor of DPP II Homo sapiens
[(1R)-1-[[(2S)-2,4-diaminobutanoyl]amino]pentyl]boronic acid
-
Homo sapiens

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
58000
-
SDS-PAGE Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Posttranslational Modification

Posttranslational Modification Comment Organism
glycoprotein
-
Homo sapiens

Source Tissue

Source Tissue Comment Organism Textmining
HEK-293T cell
-
Homo sapiens
-

Synonyms

Synonyms Comment Organism
DPP II
-
Homo sapiens
DPP2
-
Homo sapiens
DPP7
-
Homo sapiens
QPP
-
Homo sapiens
quiescent cell proline dipeptidase
-
Homo sapiens

pH Range

pH Minimum pH Maximum Comment Organism
5.5 7
-
Homo sapiens

IC50 Value

IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
0.00000048
-
-
Homo sapiens [(1R)-1-[[(2S)-2,4-diaminobutanoyl]amino]pentyl]boronic acid
0.00000088
-
-
Homo sapiens (3S)-4-[(3aR,6aR)-hexahydrocyclopenta[b]pyrrol-1(2H)-yl]-4-oxobutane-1,3-diamine