Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL1716091

SDX-101
🧪 Phase II
Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
🧪 Phase II
CCc1cccc2c3c([nH]c12)[C@@](CC)(CC(=O)O)OCC3

Basic Information

ChEMBL ID CHEMBL1716091
Name SDX-101
Phase Phase II
Structure Type MOL
InChI Key NNYBQONXHNTVIJ-QGZVFWFLSA-N

Known Names

(-)-(r)-etodolac (-)-etodolac Etodolac, (-)- Etodolac, (r)- KS-1056 R-etodolac RAK-593 Sdx-101
1
Targets
3
Activities
1
Assay Types
0
PK Parameters
5
Publications
8
Known Names
2
Indications
1
Mechanisms

Molecular Properties

287.4
MW (Da)
3.38
ALogP
2
HBA
2
HBD
62.3
PSA (Ų)
0.91
QED
0
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Chirality Single Enantiomer

Flags

Natural Product

Extended Properties

Molecular Formula C17H21NO3
MW 287.36
Aromatic Rings 2
Heavy Atoms 21
NP-Likeness 0.44

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Retinoid X receptor alpha modulator MODULATOR Retinoic acid receptor RXR-alpha

Indications

Leukemia, Lymphocytic, Chronic, B-Cell Multiple Myeloma

Activity Summary

IC50 3 meas. best 4.34

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.34 4.34 46000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 46000.0 nM 4.34 Inhibition of Tcf in HEK293 cells by TOPflash luciferase reporter assay 35581674

Literature References

PubMed DOI Target Context # Activities
- 10.6019/CHEMBL4495565 SARS-CoV-2 2
35581674 10.1021/acs.jmedchem.2c00228 Catenin beta-1 2
26182238 10.1021/acs.jmedchem.5b00460 Unchecked 1
- 10.6019/CHEMBL4495564 Replicase polyprotein 1ab 1
35581674 10.1021/acs.jmedchem.2c00228 Unchecked 1

Data from ChEMBL 36 via Core Engine