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Compound Detail

CHEMBL4518378

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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)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)CCc1ccncc1)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL4518378
Phase Preclinical
Structure Type MOL
InChI Key PZMQLGZEKMHLAI-DUGSHLAESA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

987.1
MW (Da)
-2.45
ALogP
12
HBA
14
HBD
382.9
PSA (Ų)
0.02
QED
3
Ro5 Violations
28
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C47H66N14O10
MW 987.13
Aromatic Rings 3
Heavy Atoms 71
NP-Likeness -0.11

Activity Summary

EC50 1 meas. best 8.82

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
KiSS-1 receptor
CHEMBL5413
EC50 8.82 8.82 1.5 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
KiSS-1 receptor EC50 = 1.5 nM 8.82 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