AKR1C3 inhibitor CRT0093964 Small Molecule (Tool Compound)
Invented by Dr Laurent Rigoreau from Cancer Research Horizons
Invented at Cancer Research Horizons
- Datasheet
- References (2)
- Inventor Info
Info
Catalogue Number | 151880 |
Antigen/Gene or Protein Targets | Type 5 17-β-Hydroxysteroid Dehydrogenase (AKR1C3) |
Type | Inhibitor |
Relevance | CRT0093964 is a highly potent and selective inhibitor of the Type 5 17-β-Hydroxysteroid Dehydrogenase (AKR1C3). |
On Target IC50 | IC50 = 88 nM |
Selectivity | Displays >100-fold selectivity against AKR1C1, AKR1C2 and AKR1C4. Does not display any COX (cyclooxygenase) inhibition at 10 µM in whole blood assay. |
Molecular Formula | C15H20CIN3O2 |
lUPAC | 4-(4-Chloro-phenyl)-piperazin-1-yl]-morpholin-4-yl-methanone |
Molecular Weight (g/mol) | 309.79 |
Research Area | Cell Signaling & Signal Transduction, Metabolism, Neurobiology |
Notes | Referred to as A9 in Khanim et al., 2014. |
References: 2 entries
Khanim et al. 2014. Br J Cancer. 110(6):1506-16. PMID: 24569460.
Selective AKR1C3 inhibitors do not recapitulate the anti-leukaemic activities of the pan-AKR1C inhibitor medroxyprogesterone acetate.
Europe PMC ID: 24569460
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References: 2 entries
Khanim et al. 2014. Br J Cancer. 110(6):1506-16. PMID: 24569460.
Selective AKR1C3 inhibitors do not recapitulate the anti-leukaemic activities of the pan-AKR1C inhibitor medroxyprogesterone acetate.
Add a reference