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Compound Detail

CHEMBL4865613

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COc1ccc(NC(=O)C2=C(c3ccc(C)cc3)C[C@](c3ccc(OCCCC(F)(F)F)cc3)(C(F)(F)F)NC2=O)nn1

Basic Information

ChEMBL ID CHEMBL4865613
Phase Preclinical
Structure Type MOL
InChI Key XGFCNJXKMJWZAX-MHZLTWQESA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

608.5
MW (Da)
5.88
ALogP
6
HBA
2
HBD
102.4
PSA (Ų)
0.18
QED
2
Ro5 Violations
9
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C29H26F6N4O4
MW 608.54
Aromatic Rings 3
Heavy Atoms 43
NP-Likeness -0.87

Activity Summary

IC50 2 meas. best 8.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
CHEMBL2321630
IC50 8.15 8.15 7.1 1
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
CHEMBL2375203
IC50 7.5 7.5 32.0 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