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Compound Detail

CHEMBL4764335

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CC1=C(O)C(=O)C=C2C1=CC=C1[C@@]2(C)CC[C@@]2(C)[C@@H]3C[C@](C)(C(=O)OCc4cccc(Br)c4)CC[C@]3(C)CC[C@]12C

Basic Information

ChEMBL ID CHEMBL4764335
Phase Preclinical
Structure Type MOL
InChI Key BNIQXTMLISRWIR-WFVGHVPHSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

619.6
MW (Da)
9.12
ALogP
4
HBA
1
HBD
63.6
PSA (Ų)
0.34
QED
2
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C36H43BrO4
MW 619.64
Aromatic Rings 1
Heavy Atoms 41
NP-Likeness 2.36

Activity Summary

IC50 1 meas. best 5.97

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 5.97 5.97 1070.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 1070.0 nM 5.97 Antiproliferative activity against Con A-induced BALB/c mouse T cell after 48 hr... 32822186

Literature References

PubMed DOI Target Context # Activities
32822186 10.1021/acs.jnatprod.0c00067 Unchecked 3

Data from ChEMBL 36 via Core Engine