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Assay Detail

CHEMBL1011444

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

Binding
Inhibition of thrombin
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Intermediate

Target

Prothrombin (CHEMBL204)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Cyclotheonamides E2 and E3, new potent serine protease inhibitors from the marine sponge of the genus Theonella.
Nakao Y, Oku N, Matsunaga S, Fusetani N.
J Nat Prod (1998) 61 : 667 -670
PubMed 9599274 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 4 8.02 8.54

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL507449 CYCLOTHEONAMIDE E 1 8.54
CHEMBL448342 CYCLOTHEONAMIDE E3 1 8.02
CHEMBL505589 CYCLOTHEONAMIDE E2 1 7.89
CHEMBL342672 CYCLOTHEONAMIDE A 1 7.64

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL507449 CYCLOTHEONAMIDE E IC50 = 2.9 nM 8.54
CHEMBL448342 CYCLOTHEONAMIDE E3 IC50 = 9.5 nM 8.02
CHEMBL505589 CYCLOTHEONAMIDE E2 IC50 = 13.0 nM 7.89
CHEMBL342672 CYCLOTHEONAMIDE A IC50 = 23.0 nM 7.64