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Compound Detail

CHEMBL2372932

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C[C@@H]1NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@@H]2CCCN2C(=O)[C@@H](Cc2ccccc2)N(C)C(=O)[C@@H]2CCCCN2C(=O)[C@H]2CCCCN2C1=O

Basic Information

ChEMBL ID CHEMBL2372932
Phase Preclinical
Structure Type BOTH
InChI Key JERDGULXMFCRDK-MCBGOINZSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

698.9
MW (Da)
2.06
ALogP
6
HBA
2
HBD
139.4
PSA (Ų)
0.50
QED
1
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C39H50N6O6
MW 698.87
Aromatic Rings 2
Heavy Atoms 51
NP-Likeness 0.69

Activity Summary

Ki 1 meas. best 4.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Oxytocin receptor
CHEMBL3996
Ki 4.92 4.92 12000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Oxytocin receptor Ki = 12000.0 nM 4.92 Inhibition of [3H]- oxytocin binding to rat uterine Oxytocin receptor 2163451

Literature References

PubMed DOI Target Context # Activities
2163451 10.1021/jm00169a001 Oxytocin receptor 1
2163451 10.1021/jm00169a001 Vasopressin V1 receptor 1
2163451 10.1021/jm00169a001 Vasopressin V2 receptor 1

Data from ChEMBL 36 via Core Engine