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Compound Detail

CHEMBL319667

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COc1cc2cc(C(=O)N3C[C@@H](CCl)c4c3cc(O)c3[nH]c(C)c(C(=O)N5CCN(C)CC5)c43)[nH]c2c(OC)c1OC

Basic Information

ChEMBL ID CHEMBL319667
Phase Preclinical
Structure Type MOL
InChI Key SNALOXUSAFTPNW-QGZVFWFLSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

596.1
MW (Da)
4.06
ALogP
7
HBA
3
HBD
123.4
PSA (Ų)
0.29
QED
1
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C30H34ClN5O6
MW 596.08
Aromatic Rings 4
Heavy Atoms 42
NP-Likeness -0.31

Activity Summary

IC50 2 meas. best 8.39

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HeLa
CHEMBL399
IC50 8.39 7.805 4.1 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
HeLa IC50 = 4.1 nM 8.39 In vitro inhibition HeLa S3 cell growth by 50% after 72 hr. 10425104
HeLa IC50 = 60.0 nM 7.22 In vitro inhibition of HeLa S3 cell growth by 50% after 1 hr. 10425104

Literature References

PubMed DOI Target Context # Activities
10425104 10.1021/jm990094r Mus musculus 3
10425104 10.1021/jm990094r HeLa 2

Data from ChEMBL 36 via Core Engine