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Compound Detail

CHEMBL3350562

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CO[C@H]1[C@H](O)[C@@H](O)[C@H](n2c3ccccc3c3c4c(c5c6ccccc6n(C)c5c32)C(=O)OC4=O)O[C@@H]1CO

Basic Information

ChEMBL ID CHEMBL3350562
Phase Preclinical
Structure Type MOL
InChI Key GLOOVDUDWGDMKB-CNFVFWEUSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
6
Publications
0
Known Names

Molecular Properties

516.5
MW (Da)
2.38
ALogP
10
HBA
3
HBD
132.4
PSA (Ų)
0.25
QED
1
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H24N2O8
MW 516.51
Aromatic Rings 5
Heavy Atoms 38
NP-Likeness 1.08

Activity Summary

IC50 1 meas. best 4.51

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
B16
CHEMBL381
IC50 4.51 4.51 31000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
B16 IC50 = 31000.0 nM 4.51 Antiproliferative activity measured against murine B16 melanoma cells 9572888

Literature References

PubMed DOI Target Context # Activities
9572888 10.1021/jm970843+ CEM-SS 2
9572888 10.1021/jm970843+ B16 1
9572888 10.1021/jm970843+ P388 1
9572888 10.1021/jm970843+ Bacillus cereus 1
9572888 10.1021/jm970843+ DNA topoisomerase 1 1
9572888 10.1021/jm970843+ Streptomyces chartreusis 1

Data from ChEMBL 36 via Core Engine