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Compound Detail

CHEMBL1083646

(2R)-N-(6-(4-CHLOROPHENYL)-7-(2,4-DICHLOROPHENYL)-2,2-DIMETHYL-3,4-DIHYDRO-2H-PYRANO[2,3-B]PYRIDIN-4-YL)-2-HYDROXYPROPANAMIDE (ENANTIOMERIC MIX)
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C[C@@H](O)C(=O)NC1CC(C)(C)Oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc21

Basic Information

ChEMBL ID CHEMBL1083646
Name (2R)-N-(6-(4-CHLOROPHENYL)-7-(2,4-DICHLOROPHENYL)-2,2-DIMETHYL-3,4-DIHYDRO-2H-PYRANO[2,3-B]PYRIDIN-4-YL)-2-HYDROXYPROPANAMIDE (ENANTIOMERIC MIX)
Phase Preclinical
Structure Type MOL
InChI Key XCFWDLWOCXSJOK-ILRUXTBWSA-N
3
Targets
5
Activities
1
Assay Types
3
PK Parameters
7
Publications
0
Known Names

Molecular Properties

505.8
MW (Da)
6.48
ALogP
4
HBA
2
HBD
71.5
PSA (Ų)
0.43
QED
2
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C25H23Cl3N2O3
MW 505.83
Aromatic Rings 3
Heavy Atoms 33
NP-Likeness -0.24

Activity Summary

IC50 5 meas. best 8.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Cannabinoid receptor 1
CHEMBL218
IC50 8.52 8.16 3.0 2
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 6.92 6.92 120.0 1
Cannabinoid receptor 2
CHEMBL253
IC50 5.46 5.39 3450.0 2

Pharmacokinetic Data

Parameter Value Units Species
CL 4.0 mL.min-1.kg-1 Rattus norvegicus
F 100.0 % Rattus norvegicus
T1/2 7.9 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20483606 10.1016/j.bmcl.2010.04.071 Rattus norvegicus 5
20483606 10.1016/j.bmcl.2010.04.071 Cannabinoid receptor 1 2
20483606 10.1016/j.bmcl.2010.04.071 Cannabinoid receptor 2 2
20483606 10.1016/j.bmcl.2010.04.071 Voltage-gated inwardly rectifying potassium channel KCNH2 1
20483606 10.1016/j.bmcl.2010.04.071 Brain 1
20483606 10.1016/j.bmcl.2010.04.071 Plasma 1
20483606 10.1016/j.bmcl.2010.04.071 ADMET 1

Data from ChEMBL 36 via Core Engine