1228097-18-4
1228097-18-4
Chemical Structure
Mifepristone-d6
Synonym(s): RU486-d6; RU 38486-d6
- CAS No.: 1228097-18-4
- Formula:C29H29D6NO2
- Molecular Weight:435.63
InChIKey: VKHAHZOOUSRJNA-SGXGQBIRSA-N
SMILES: C[C@@]12[C@@](C#CC)(O)CC[C@@]1([H])[C@]3([H])CCC4=CC(CCC4=C3[C@@H](C5=CC=C(N(C([2H])([2H])[2H])C([2H])([2H])[2H])C=C5)C2)=O
Biological Activity: Mifepristone-d6 is deuterated labeled Mifepristone (HY-13683). Mifepristone (RU486) is a progesterone receptor (PR) and glucocorticoid receptor (GR) antagonist with IC50s of 0.2 nM and 2.6 nM in in vitro assay[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Mifepristone-d6 | 98.21% | Mifepristone-d6 is deuterated labeled Mifepristone (HY-13683). Mifepristone (RU486) is a progesterone receptor (PR) and glucocorticoid receptor (GR) antagonist with IC50s of 0.2 nM and 2.6 nM in in vitro assay. | ||||||||||||||||||||
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Mifepristone (Standard) | 99.42% | Mifepristone (Standard) is the analytical standard of Mifepristone. This product is intended for research and analytical applications. Mifepristone (RU486) is a progesterone receptor (PR) and glucocorticoid receptor (GR) antagonist with IC50s of 0.2 nM and 2.6 nM in in vitro assay. | ||||||||||||||||||||
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Mifepristone-13C,d3 | Mifepristone-13C,d3 is the 13C- and deuterium labeled Mifepristone. Mifepristone (RU486) is a progesterone receptor (PR) and glucocorticoid receptor (GR) antagonist with IC50s of 0.2 nM and 2.6 nM in in vitro assay. Mifepristone-13C,d3 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | |||||||||||||||||||||
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Mifepristone-d3 | 97.51% | Mifepristone-d3 is the deuterium labeled Mifepristone. Mifepristone (RU486) is a progesterone receptor (PR) and glucocorticoid receptor (GR) antagonist with IC50s of 0.2 nM and 2.6 nM in in vitro assay. | ||||||||||||||||||||
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Mifepristone | 99.88% | Mifepristone (RU486) is a progesterone receptor (PR) and glucocorticoid receptor (GR) antagonist with IC50s of 0.2 nM and 2.6 nM in in vitro assay. | ||||||||||||||||||||
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References
