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Compound Detail

CHEMBL4081023

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CO[C@H]1[C@@H](OC(=O)c2ccccc2)[C@@H](C)O[C@@H](O[C@H]2CC[C@]3(C=O)[C@H]4CC[C@]5(C)[C@@H](C6=CC(=O)OC6)CC[C@]5(O)[C@@H]4CC[C@]3(O)C2)[C@@H]1OC

Basic Information

ChEMBL ID CHEMBL4081023
Phase Preclinical
Structure Type MOL
InChI Key BTGUOWWXHVNMMP-KXYSHMIISA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

682.8
MW (Da)
3.92
ALogP
11
HBA
2
HBD
147.1
PSA (Ų)
0.23
QED
2
Ro5 Violations
8
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H50O11
MW 682.81
Aromatic Rings 1
Heavy Atoms 49
NP-Likeness 2.47

Activity Summary

IC50 1 meas. best 5.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HT-29
CHEMBL384
IC50 5.92 5.92 1200.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
HT-29 IC50 = 1200.0 nM 5.92 Cytotoxicity against human HT-29 cells incubated for 72 hrs by SRB assay 27983842

Literature References

PubMed DOI Target Context # Activities
27983842 10.1021/acs.jnatprod.6b00924 HT-29 1

Data from ChEMBL 36 via Core Engine