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Compound Detail

CHEMBL5092327

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CC(=O)N[C@H]1CC(=O)NCCCC[C@@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)c2nc3ccc(N[C@H](C(N)=O)C(C)C)cc3s2)NC(=O)[C@H](CC(C)C)NC1=O

Basic Information

ChEMBL ID CHEMBL5092327
Phase Preclinical
Structure Type MOL
InChI Key BVIZJIXKCBABFU-YIHYGEMESA-N
5
Targets
5
Activities
1
Assay Types
3
PK Parameters
6
Publications
0
Known Names

Molecular Properties

786.0
MW (Da)
0.36
ALogP
11
HBA
10
HBD
292.5
PSA (Ų)
0.05
QED
3
Ro5 Violations
15
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H55N11O7S
MW 785.97
Aromatic Rings 2
Heavy Atoms 55
NP-Likeness -0.12

Activity Summary

IC50 5 meas. best 8.27

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Serine protease hepsin
CHEMBL2079849
IC50 8.27 8.27 5.4 1
Suppressor of tumorigenicity 14 protein
CHEMBL3018
IC50 7.96 7.96 11.0 1
Prothrombin
CHEMBL204
IC50 7.47 7.47 34.0 1
Coagulation factor X
CHEMBL244
IC50 6.93 6.93 118.0 1
Hepatocyte growth factor activator
CHEMBL3351190
IC50 5.27 5.27 5378.0 1

Pharmacokinetic Data

Parameter Value Units Species
Fu - - Mus musculus
T1/2 4.818 hr Mus musculus
T1/2 4.818 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34902246 10.1021/acs.jmedchem.1c01671 ADMET 3
34902246 10.1021/acs.jmedchem.1c01671 Prothrombin 1
34902246 10.1021/acs.jmedchem.1c01671 Hepatocyte growth factor activator 1
34902246 10.1021/acs.jmedchem.1c01671 Suppressor of tumorigenicity 14 protein 1
34902246 10.1021/acs.jmedchem.1c01671 Serine protease hepsin 1
34902246 10.1021/acs.jmedchem.1c01671 Coagulation factor X 1

Data from ChEMBL 36 via Core Engine