Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL137537

Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
CCSc1nsnc1C1CN2CCC[C@H]1C2

Basic Information

ChEMBL ID CHEMBL137537
Phase Preclinical
Structure Type MOL
InChI Key MHCPBZXRJZKIQK-IENPIDJESA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

255.4
MW (Da)
2.46
ALogP
5
HBA
0
HBD
29.0
PSA (Ų)
0.78
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C11H17N3S2
MW 255.41
Aromatic Rings 1
Heavy Atoms 16
NP-Likeness -0.44

Activity Summary

IC50 1 meas. best 8.89

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 8.89 8.89 1.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 1.3 nM 8.89 In vitro inhibition of [3H]Oxo-Mas binding to M1 and M4 receptors in rat brain h... 9784113

Literature References

PubMed DOI Target Context # Activities
9784113 10.1021/jm981048e Rattus norvegicus 2
9784113 10.1021/jm981048e Unchecked 1
9784113 10.1021/jm981048e Mus musculus 1

Data from ChEMBL 36 via Core Engine