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Compound Detail

CHEMBL433349

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CC[C@H](C)[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(C)=O)C(c1ccccc1)c1ccccc1)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)O)[C@@H](C)CC

Basic Information

ChEMBL ID CHEMBL433349
Phase Preclinical
Structure Type BOTH
InChI Key WXIDXBSXUCQMKX-KUIIPSLPSA-N
3
Targets
4
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

938.1
MW (Da)
4.56
ALogP
8
HBA
9
HBD
265.0
PSA (Ų)
0.04
QED
2
Ro5 Violations
26
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C51H67N7O10
MW 938.14
Aromatic Rings 4
Heavy Atoms 68
NP-Likeness 0.09

Activity Summary

IC50 4 meas. best 7.68

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Endothelin-1 receptor
CHEMBL252
IC50 7.68 7.025 21.0 2
Endothelin receptor type B
CHEMBL4631
IC50 7.22 7.22 60.0 1
Endothelin receptor type B
CHEMBL1785
IC50 5.75 5.75 1800.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
7636842 10.1021/jm00015a003 Endothelin-1 receptor 2
7636842 10.1021/jm00015a003 Endothelin receptor type B 2
7636842 10.1021/jm00015a003 Unchecked 1

Data from ChEMBL 36 via Core Engine