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Compound Detail

CHEMBL2402893

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CC(C)(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1

Basic Information

ChEMBL ID CHEMBL2402893
Phase Preclinical
Structure Type MOL
InChI Key RCBBDNFCXSBDIT-UHFFFAOYSA-N
2
Targets
3
Activities
2
Assay Types
1
PK Parameters
4
Publications
0
Known Names

Molecular Properties

534.7
MW (Da)
1.24
ALogP
7
HBA
3
HBD
121.9
PSA (Ų)
0.47
QED
1
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C26H42N6O4S
MW 534.73
Aromatic Rings 2
Heavy Atoms 37
NP-Likeness -1.36

Activity Summary

Ki 2 meas. best 7.9
EC50 1 meas. best 8.5

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5-hydroxytryptamine receptor 4
CHEMBL1875
EC50 8.5 8.5 3.2 1
5-hydroxytryptamine receptor 4
CHEMBL1875
Ki 7.9 7.9 12.6 1
5-hydroxytryptamine receptor 3A
CHEMBL1899
Ki 4.4 4.4 39810.7 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 1.5 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
23756062 10.1016/j.bmcl.2013.05.018 5-hydroxytryptamine receptor 4 3
23756062 10.1016/j.bmcl.2013.05.018 Liver microsomes 1
23756062 10.1016/j.bmcl.2013.05.018 Caco-2 1
23756062 10.1016/j.bmcl.2013.05.018 5-hydroxytryptamine receptor 3A 1

Data from ChEMBL 36 via Core Engine