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Compound Detail

CHEMBL334949

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C/C(=C\Cc1c(O)c(C=O)c(C)c(Cl)c1OC(=O)CCCC(=O)O)CC/C=C(\C)[C@@H]1CC(=O)C(C)(C)O1

Basic Information

ChEMBL ID CHEMBL334949
Phase Preclinical
Structure Type MOL
InChI Key YOYLIRUMGOYFDU-LBSMODEVSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
7
Publications
0
Known Names

Molecular Properties

535.0
MW (Da)
5.68
ALogP
7
HBA
2
HBD
127.2
PSA (Ų)
0.15
QED
2
Ro5 Violations
12
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C28H35ClO8
MW 535.03
Aromatic Rings 1
Heavy Atoms 37
NP-Likeness 1.60

Activity Summary

IC50 1 meas. best 5.5

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
C3H 10T1/2
CHEMBL614531
IC50 5.5 5.5 3200.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
C3H 10T1/2 IC50 = 3200.0 nM 5.5 Concentration required for inhibition of C3H10T1/2 progenitor cell growth 12954063

Literature References

PubMed DOI Target Context # Activities
12954063 10.1021/jm0205649 C3H 10T1/2 1
12954063 10.1021/jm0205649 Peroxisome proliferator-activated receptor gamma 1
12954063 10.1021/jm0205649 Peroxisome proliferator-activated receptor alpha 1
12954063 10.1021/jm0205649 Nuclear receptor subfamily 1 group I member 2 1
12954063 10.1021/jm0205649 Estrogen receptor 1
12954063 10.1021/jm0205649 Estrogen receptor beta 1
12954063 10.1021/jm0205649 Androgen receptor 1

Data from ChEMBL 36 via Core Engine