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Compound Detail

CHEMBL4851952

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CCCCSc1ccc([C@]2(C(F)(F)F)CC(c3ccc(C)cc3)=C(c3nnn[nH]3)C(=O)N2)cc1

Basic Information

ChEMBL ID CHEMBL4851952
Phase Preclinical
Structure Type MOL
InChI Key HWZWJXDOSMQTGI-QHCPKHFHSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

487.6
MW (Da)
5.29
ALogP
5
HBA
2
HBD
83.6
PSA (Ų)
0.35
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H24F3N5OS
MW 487.55
Aromatic Rings 3
Heavy Atoms 34
NP-Likeness -0.93

Activity Summary

IC50 2 meas. best 8.26

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
CHEMBL2321630
IC50 8.26 8.26 5.5 1
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
CHEMBL2375203
IC50 7.02 7.02 96.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
34613725 10.1021/acs.jmedchem.1c01356 Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase 2
34613725 10.1021/acs.jmedchem.1c01356 ADMET 2

Data from ChEMBL 36 via Core Engine