(±)-ML 209
Tocris Bioscience, part of Bio-Techne | Catalog # 5987
RORγt inverse agonist; suppresses Th17 cell differentiation
Key Product Details
Description
RORγt inverse agonist; suppresses Th17 cell differentiation
Product Description
(±)-ML 209 is a RORγt inverse agonist (IC50 = 460 nM). Suppresses Th17 cell differentiation and IL17A expression in vitro. Does not suppress transcription of RORα. Minimal activity displayed on ERα, LXRα and thyroid hormone receptors (IC50 values >4.4 μM).Product Specifications
Molecular Weight
441.52
Formula
C25H31NO6
Storage
Store at -20°C
Purity
≥98% (HPLC)
Chemical Name
3-(1,3-Benzodioxol-5-yl)-1-(cis-3,5-dimethyl-1-piperidinyl)-3-(2-hydroxy-4,6-dimethoxyphenyl)-1-propanone
CAS Number
1334526-14-5
PubChem ID
53385590
InChI Key
YEKVAIMYYCZDLI-MCPYQZEQSA-N
SMILES
COC1=CC(OC)=C(C(O)=C1)C(C2=CC=C3OCOC3=C2)CC(N4C[C@@H](C[C@@H](C4)C)C)=O
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 44.15 | 100 |
Preparing Stock Solutions
for (±)-ML 209
The following data is based on the product molecular weight 441.52
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.26 mL | 11.32 mL | 22.65 mL |
| 5 mM | 0.45 mL | 2.26 mL | 4.53 mL |
| 10 mM | 0.23 mL | 1.13 mL | 2.26 mL |
| 50 mM | 0.05 mL | 0.23 mL | 0.45 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Wang Discovery of novel N-(5-(arylcarbonyl)thiazol-2-yl)amides and N-(5-(arylcarbonyl)thiophen-2-yl)amides as potent RORγt inhibitors. Bioorg.Med.Chem. 2014 PMID: 24388993
- Huang DDX5 and its associated lncRNA Rmrp modulate TH17 cell effector functions. Nature 2015 PMID: 26675721
- Kojetin REV-ERB and ROR nuclear receptors as drug targets. Nat.Rev.Drug Discov. 2014 PMID: 24577401
- Huang Identification of Potent and Selective RORγ Antagonists. Probe Reports from the NIH Molecular Libraries Program 2010 PMID: 23658948
Product Specific Notices for (±)-ML 209
For research use only
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