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Compound Detail

CHEMBL320010

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

Basic Information

ChEMBL ID CHEMBL320010
Phase Preclinical
Structure Type MOL
InChI Key MVNAZJPBWZGBLB-OAHLLOKOSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

527.0
MW (Da)
4.73
ALogP
6
HBA
3
HBD
103.0
PSA (Ų)
0.30
QED
1
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H31ClN4O5
MW 527.02
Aromatic Rings 4
Heavy Atoms 37
NP-Likeness -0.15

Activity Summary

IC50 2 meas. best 9.8

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HeLa
CHEMBL399
IC50 9.8 9.675 0.2 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
HeLa IC50 = 0.16 nM 9.8 In vitro inhibition HeLa S3 cell growth by 50% after 72 hr. 10425104
HeLa IC50 = 0.28 nM 9.55 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