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

CHEMBL819273

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

Binding
Binding affinity towards human trypsin
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Trypsin (CHEMBL2095204)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Synthesis and SAR of benzamidine factor Xa inhibitors containing a vicinally-substituted heterocyclic core.
Fevig JM, Pinto DJ, Han Q, Quan ML, Pruitt JR, Jacobson IC, Galemmo RA, Wang S, Orwat MJ, Bostrom LL, Knabb RM, Wong PC, Lam PYS, Wexler RR.
Bioorg Med Chem Lett (2001) 11 : 641 -645
PubMed 11266160 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 17 7.15 8.47

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL157417 1 8.47
CHEMBL160489 1 8.19
CHEMBL356016 1 7.82
CHEMBL152854 1 7.80
CHEMBL153611 1 7.68
CHEMBL349323 1 7.58
CHEMBL346825 1 7.57
CHEMBL152274 1 7.25
CHEMBL156924 1 7.22
CHEMBL160575 1 7.01
CHEMBL160958 1 6.72
CHEMBL347606 1 6.66
CHEMBL351755 1 6.58
CHEMBL157299 1 6.58
CHEMBL156505 1 6.41
CHEMBL160515 1 6.11
CHEMBL159204 1 5.96

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL157417 Ki = 3.4 nM 8.47
CHEMBL160489 Ki = 6.4 nM 8.19
CHEMBL356016 Ki = 15.0 nM 7.82
CHEMBL152854 Ki = 16.0 nM 7.80
CHEMBL153611 Ki = 21.0 nM 7.68
CHEMBL349323 Ki = 26.0 nM 7.58
CHEMBL346825 Ki = 27.0 nM 7.57
CHEMBL152274 Ki = 56.0 nM 7.25
CHEMBL156924 Ki = 60.0 nM 7.22
CHEMBL160575 Ki = 97.0 nM 7.01
CHEMBL160958 Ki = 190.0 nM 6.72
CHEMBL347606 Ki = 220.0 nM 6.66
CHEMBL351755 Ki = 260.0 nM 6.58
CHEMBL157299 Ki = 261.0 nM 6.58
CHEMBL156505 Ki = 390.0 nM 6.41
CHEMBL160515 Ki = 780.0 nM 6.11
CHEMBL159204 Ki = 1100.0 nM 5.96