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Compound Detail

CHEMBL4476438

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CNC(=N)NCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)NNC(=O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL4476438
Phase Preclinical
Structure Type MOL
InChI Key ZSLCICIBHQVJMP-YDPTYEFTSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

756.9
MW (Da)
0.99
ALogP
7
HBA
10
HBD
248.5
PSA (Ų)
0.04
QED
2
Ro5 Violations
19
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C39H52N10O6
MW 756.91
Aromatic Rings 3
Heavy Atoms 55
NP-Likeness -0.26

Activity Summary

EC50 1 meas. best 9.22

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
KiSS-1 receptor
CHEMBL5413
EC50 9.22 9.22 0.6 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
KiSS-1 receptor EC50 = 0.6 nM 9.22 Agonist activity at human KISS1R expressed in CHO cells assessed as increase in ... 30598349

Literature References

PubMed DOI Target Context # Activities
30598349 10.1016/j.bmcl.2018.12.016 No relevant target 1
30598349 10.1016/j.bmcl.2018.12.016 KiSS-1 receptor 1

Data from ChEMBL 36 via Core Engine