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Compound Detail

CHEMBL1289277

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Cc1ccc2c(N3CCN(CCc4c(C)ccc5c4ccc(=O)n5C)[C@H](C)C3)cccc2n1

Basic Information

ChEMBL ID CHEMBL1289277
Phase Preclinical
Structure Type MOL
InChI Key UUWQIBYZFVEIMA-OAQYLSRUSA-N
4
Targets
4
Activities
1
Assay Types
5
PK Parameters
8
Publications
0
Known Names

Molecular Properties

440.6
MW (Da)
4.46
ALogP
5
HBA
0
HBD
41.4
PSA (Ų)
0.47
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H32N4O
MW 440.59
Aromatic Rings 4
Heavy Atoms 33
NP-Likeness -0.93

Activity Summary

Ki 4 meas. best 8.9

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 8.9 8.9 1.3 1
5-hydroxytryptamine receptor 1D
CHEMBL1983
Ki 8.6 8.6 2.5 1
Sodium-dependent serotonin transporter
CHEMBL228
Ki 8.4 8.4 4.0 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 5.1 5.1 7943.3 1

Pharmacokinetic Data

Parameter Value Units Species
CL 1.2 mL.min-1.g-1 Homo sapiens
CL 3.8 mL.min-1.g-1 Rattus norvegicus
CL 21.0 mL.min-1.kg-1 Rattus norvegicus
F 31.0 % Rattus norvegicus
T1/2 1.5 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20951584 10.1016/j.bmcl.2010.09.085 Rattus norvegicus 4
20951584 10.1016/j.bmcl.2010.09.085 Liver microsomes 2
20951584 10.1016/j.bmcl.2010.09.085 5-hydroxytryptamine receptor 1A 2
20951584 10.1016/j.bmcl.2010.09.085 5-hydroxytryptamine receptor 1D 2
20951584 10.1016/j.bmcl.2010.09.085 ADMET 1
20951584 10.1016/j.bmcl.2010.09.085 Sodium-dependent serotonin transporter 1
20951584 10.1016/j.bmcl.2010.09.085 Voltage-gated inwardly rectifying potassium channel KCNH2 1
20951584 10.1016/j.bmcl.2010.09.085 5-hydroxytryptamine receptor 1B 1

Data from ChEMBL 36 via Core Engine