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Compound Detail

CHEMBL513339

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N=C(N)c1cccc(C[C@H](NS(=O)(=O)c2cccc(NC(=O)CCO)c2)C(=O)N2CCC(CCN)CC2)c1

Basic Information

ChEMBL ID CHEMBL513339
Phase Preclinical
Structure Type MOL
InChI Key NFFDOZRPFRQRCW-QHCPKHFHSA-N
5
Targets
6
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

544.7
MW (Da)
0.77
ALogP
7
HBA
6
HBD
191.7
PSA (Ų)
0.17
QED
2
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H36N6O5S
MW 544.68
Aromatic Rings 2
Heavy Atoms 38
NP-Likeness -0.99

Activity Summary

Ki 6 meas. best 6.93

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Suppressor of tumorigenicity 14 protein
CHEMBL3018
Ki 6.93 6.925 117.0 2
Plasminogen
CHEMBL1801
Ki 5.58 5.58 2600.0 1
Urokinase-type plasminogen activator
CHEMBL3286
Ki 5.52 5.52 3000.0 1
Prothrombin
CHEMBL204
Ki 5.26 5.26 5500.0 1
Coagulation factor X
CHEMBL244
Ki 4.21 4.21 61000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19036586 10.1016/j.bmcl.2008.11.019 Suppressor of tumorigenicity 14 protein 1
19036586 10.1016/j.bmcl.2008.11.019 Plasminogen 1
19036586 10.1016/j.bmcl.2008.11.019 Urokinase-type plasminogen activator 1
19036586 10.1016/j.bmcl.2008.11.019 Prothrombin 1
19036586 10.1016/j.bmcl.2008.11.019 Coagulation factor X 1

Data from ChEMBL 36 via Core Engine