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Compound Detail

CHEMBL212577

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

Basic Information

ChEMBL ID CHEMBL212577
Phase Preclinical
Structure Type MOL
InChI Key RTRAJNFJVAMWRW-QFIPXVFZSA-N
5
Targets
5
Activities
1
Assay Types
0
PK Parameters
5
Publications
0
Known Names

Molecular Properties

529.7
MW (Da)
0.34
ALogP
7
HBA
6
HBD
197.5
PSA (Ų)
0.18
QED
2
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H35N7O4S
MW 529.67
Aromatic Rings 2
Heavy Atoms 37
NP-Likeness -1.16

Activity Summary

Ki 5 meas. best 7.12

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Suppressor of tumorigenicity 14 protein
CHEMBL3018
Ki 7.12 7.12 75.0 1
Plasminogen
CHEMBL1801
Ki 5.35 5.35 4500.0 1
Prothrombin
CHEMBL204
Ki 5.16 5.16 7000.0 1
Urokinase-type plasminogen activator
CHEMBL3286
Ki 4.96 4.96 11000.0 1
Coagulation factor X
CHEMBL244
Ki 4.46 4.46 35000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
16821772 10.1021/jm051272l Coagulation factor X 1
16821772 10.1021/jm051272l Prothrombin 1
16821772 10.1021/jm051272l Plasminogen 1
16821772 10.1021/jm051272l Urokinase-type plasminogen activator 1
16821772 10.1021/jm051272l Suppressor of tumorigenicity 14 protein 1

Data from ChEMBL 36 via Core Engine