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Compound Detail

CHEMBL183521

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CSSCCC(=O)O[C@@H](C(=O)O[C@H]1C[C@@]2(O)[C@@H](OC(=O)c3ccccc3)[C@@H]3[C@]4(OC(C)=O)CO[C@@H]4C[C@H](O)[C@@]3(C)C(=O)[C@H](OC(C)=O)C(=C1C)C2(C)C)[C@H](C=C(C)C)NC(=O)OC(C)(C)C

Basic Information

ChEMBL ID CHEMBL183521
Phase Preclinical
Structure Type MOL
InChI Key IOIIBVLZAYPAHK-CQSHRALKSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

962.1
MW (Da)
5.38
ALogP
18
HBA
3
HBD
236.6
PSA (Ų)
0.07
QED
3
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C47H63NO16S2
MW 962.15
Aromatic Rings 1
Heavy Atoms 66
NP-Likeness 1.94

Activity Summary

IC50 1 meas. best 9.05

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
A549
CHEMBL392
IC50 9.05 9.05 0.9 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
A549 IC50 = 0.9 nM 9.05 Compound was tested for its cytotoxicity by inhibiting the growth of A-549 cell ... 15225730

Literature References

PubMed DOI Target Context # Activities
15225730 10.1016/j.bmcl.2004.05.027 A-431 1
15225730 10.1016/j.bmcl.2004.05.027 A549 1

Data from ChEMBL 36 via Core Engine