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Compound Detail

CHEMBL414165

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CC(C)C[C@H]1NC(=O)[C@H](c2cccs2)NC(=O)[C@H]2CCCN2C(=O)[C@H](CC(=O)O)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC1=O

Basic Information

ChEMBL ID CHEMBL414165
Phase Preclinical
Structure Type BOTH
InChI Key KXUDUVUGZWJNHV-PFGYYQCGSA-N
5
Targets
6
Activities
2
Assay Types
0
PK Parameters
4
Publications
0
Known Names

Molecular Properties

650.8
MW (Da)
1.61
ALogP
7
HBA
6
HBD
189.8
PSA (Ų)
0.22
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C32H38N6O7S
MW 650.76
Aromatic Rings 3
Heavy Atoms 46
NP-Likeness 0.31

Activity Summary

IC50 5 meas. best 8.92
Kd 1 meas. best 8.1

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Endothelin-1 receptor
CHEMBL252
IC50 8.92 8.92 1.2 1
Endothelin-1 receptor
CHEMBL4130
IC50 8.52 8.52 3.0 2
Sus scrofa
CHEMBL613488
Kd 8.1 8.1 7.9 1
Endothelin receptor type B
CHEMBL3949
IC50 4.72 4.72 19000.0 1
Endothelin receptor type B
CHEMBL1785
IC50 4.26 4.26 55000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
7473559 10.1021/jm00021a021 Endothelin-1 receptor 3
7473559 10.1021/jm00021a021 Endothelin receptor type B 2
7473559 10.1021/jm00021a021 Sus scrofa 1
7473559 10.1021/jm00021a021 No relevant target 1

Data from ChEMBL 36 via Core Engine