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Compound Detail

CHEMBL433393

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COc1cc2cc(C(=O)N3C[C@H]4C[C@@]45C3=CC(=O)c3[nH]c(C)c(C(=O)Sc4ccc6ccccc6c4)c35)[nH]c2c(OC)c1OC

Basic Information

ChEMBL ID CHEMBL433393
Phase Preclinical
Structure Type MOL
InChI Key NDPXUDNFRIAOFX-QGFSVNGOSA-N
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

619.7
MW (Da)
6.41
ALogP
7
HBA
2
HBD
113.7
PSA (Ų)
0.21
QED
2
Ro5 Violations
6
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C35H29N3O6S
MW 619.70
Aromatic Rings 5
Heavy Atoms 45
NP-Likeness -0.12

Activity Summary

IC50 2 meas. best 7.75

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HeLa
CHEMBL399
IC50 7.75 7.32 18.0 2

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
HeLa IC50 = 18.0 nM 7.75 In vitro inhibition HeLa S3 cell growth by 50% after 72 hr. 10425104
HeLa IC50 = 130.0 nM 6.89 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