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Compound Detail

CHEMBL4872367

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Cc1ccc(C2=C(c3nnn[nH]3)C(=O)N[C@@](c3ccc(OCCCC(F)(F)F)c(F)c3)(C(F)(F)F)C2)cc1

Basic Information

ChEMBL ID CHEMBL4872367
Phase Preclinical
Structure Type MOL
InChI Key SYUPLDIFIXZWGE-QFIPXVFZSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

543.4
MW (Da)
5.26
ALogP
5
HBA
2
HBD
92.8
PSA (Ų)
0.31
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H20F7N5O2
MW 543.44
Aromatic Rings 3
Heavy Atoms 38
NP-Likeness -0.94

Activity Summary

IC50 2 meas. best 8.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
CHEMBL2321630
IC50 8.0 8.0 10.0 1
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
CHEMBL2375203
IC50 7.66 7.66 22.0 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