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Compound Detail

CHEMBL433636

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CC(C)(C)OC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCCCNC(=O)CCC1CCCCC1)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

Basic Information

ChEMBL ID CHEMBL433636
Phase Preclinical
Structure Type MOL
InChI Key QJQQPZALZJMQMW-ZYADHFCISA-N
3
Targets
3
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

832.0
MW (Da)
3.91
ALogP
8
HBA
8
HBD
250.9
PSA (Ų)
0.07
QED
2
Ro5 Violations
22
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C44H61N7O9
MW 832.01
Aromatic Rings 3
Heavy Atoms 60
NP-Likeness -0.19

Activity Summary

IC50 2 meas. best 6.51
EC50 1 meas. best 4.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cholecystokinin receptor type A
CHEMBL3501
IC50 6.51 6.51 310.0 1
Gastrin/cholecystokinin type B receptor
CHEMBL298
IC50 5.0 5.0 10000.0 1
Cavia porcellus
CHEMBL369
EC50 4.52 4.52 30000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
1375964 10.1021/jm00089a010 Cavia porcellus 2
1375964 10.1021/jm00089a010 Cholecystokinin receptor type A 1
1375964 10.1021/jm00089a010 Gastrin/cholecystokinin type B receptor 1

Data from ChEMBL 36 via Core Engine