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Compound Detail

CHEMBL471047

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Cc1ccc2c(N3CCN(CCc4cccc5c4OCC(=O)N5C)[C@@H](C)C3)cccc2n1

Basic Information

ChEMBL ID CHEMBL471047
Phase Preclinical
Structure Type MOL
InChI Key WNZKLSJSPOZSAM-IBGZPJMESA-N
5
Targets
5
Activities
1
Assay Types
5
PK Parameters
8
Publications
0
Known Names

Molecular Properties

430.6
MW (Da)
3.65
ALogP
5
HBA
0
HBD
48.9
PSA (Ų)
0.63
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 C26H30N4O2
MW 430.55
Aromatic Rings 3
Heavy Atoms 32
NP-Likeness -1.01

Activity Summary

Ki 5 meas. best 9.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 1A
CHEMBL214
Ki 9.4 9.4 0.4 1
5-hydroxytryptamine receptor 1D
CHEMBL1983
Ki 8.8 8.8 1.6 1
Sodium-dependent serotonin transporter
CHEMBL228
Ki 7.9 7.9 12.6 1
5-hydroxytryptamine receptor 1B
CHEMBL1898
Ki 7.8 7.8 15.8 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
Ki 4.9 4.9 12589.2 1

Pharmacokinetic Data

Parameter Value Units Species
CL 1.1 mL.min-1.g-1 Rattus norvegicus
CL 3.5 mL.min-1.g-1 Homo sapiens
CL 44.0 mL.min-1.kg-1 Rattus norvegicus
F 31.0 % Rattus norvegicus
T1/2 0.8 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19286377 10.1016/j.bmcl.2009.02.056 Rattus norvegicus 4
19286377 10.1016/j.bmcl.2009.02.056 5-hydroxytryptamine receptor 1A 2
19286377 10.1016/j.bmcl.2009.02.056 5-hydroxytryptamine receptor 1B 2
19286377 10.1016/j.bmcl.2009.02.056 5-hydroxytryptamine receptor 1D 2
19286377 10.1016/j.bmcl.2009.02.056 Liver microsomes 2
19286377 10.1016/j.bmcl.2009.02.056 Sodium-dependent serotonin transporter 1
19286377 10.1016/j.bmcl.2009.02.056 Voltage-gated inwardly rectifying potassium channel KCNH2 1
19286377 10.1016/j.bmcl.2009.02.056 ADMET 1

Data from ChEMBL 36 via Core Engine