Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL817298

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibitory concentration against human tryptase
16
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 4 — Cell-line / Tissue
Curated By Autocuration

Target

Tryptase (CHEMBL2095193)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Synthesis of potent and highly selective inhibitors of human tryptase.
Slusarchyk WA, Bolton SA, Hartl KS, Huang MH, Jacobs G, Meng W, Ogletree ML, Pi Z, Schumacher WA, Seiler SM, Sutton JC, Treuner U, Zahler R, Zhao G, Bisacchi GS.
Bioorg Med Chem Lett (2002) 12 : 3235 -3238
PubMed 12372541 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 7.91 8.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL109504 1 8.72
CHEMBL71037 1 8.40
CHEMBL302058 1 8.40
CHEMBL447534 1 8.34
CHEMBL113591 1 8.22
CHEMBL432835 1 8.05
CHEMBL109733 1 7.92
CHEMBL324621 3 7.20
CHEMBL303437 1 -
CHEMBL326209 1 -
CHEMBL111630 1 -
CHEMBL111173 1 -
CHEMBL70738 1 -
CHEMBL440515 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL109504 IC50 = 1.9 nM 8.72
CHEMBL71037 IC50 = 4.0 nM 8.40
CHEMBL302058 IC50 = 4.0 nM 8.40
CHEMBL447534 IC50 = 4.6 nM 8.34
CHEMBL113591 IC50 = 6.0 nM 8.22
CHEMBL432835 IC50 = 9.0 nM 8.05
CHEMBL109733 IC50 = 12.0 nM 7.92
CHEMBL324621 IC50 = 63.0 nM 7.20
CHEMBL324621 IC50 = 71.0 nM 7.15
CHEMBL324621 IC50 = 204.0 nM 6.69
CHEMBL303437 IC50 < 1.7 nM -
CHEMBL326209 IC50 < 1.7 nM -
CHEMBL111630 IC50 < 1.7 nM -
CHEMBL111173 IC50 < 1.7 nM -
CHEMBL70738 IC50 < 1.7 nM -
CHEMBL440515 IC50 < 1.7 nM -