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Ruxolitinib (S enantiomer)
Cat. No.:
0225LY-1359
Purity:
≥99%
Identity:
Confirmed by NMR.
Size:
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Product Overview
Description:
Ruxolitinib S enantiomer is the specific S-enantiomeric form of ruxolitinib, which is recognized as the inaugural potent and selective inhibitor of JAK1 and JAK2.
Synonym:
S-Ruxolitinib; Ruxolitinib S enantiomer; INCB018424; 941685-37-6; S-Ruxolitinib; S-Ruxolitinib (INCB018424); Ruxolitinib (S enantiomer); (3s)-3-cyclopentyl-3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]propanenitrile; (3S)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrazol-1-yl]propanenitrile; 1H-Pyrazole-1-propanenitrile, beta-cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-, (betaS)-; (3S)-3-Cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile (ent-Ruxolitinib); (S)-Ruxolitinib; (S)-3-(4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-3-cyclopentylpropanenitrile; Ruxolitinib S enantiomer
CAS No.:
941685-37-6
Compound CID:
50878566
Formula:
C17H18N6
Formula Weight:
306.36
Specification
Targets&IC50:
JAK2 (cell-free assay): 2.8 nM; JAK1 (cell-free assay): 3.3 nM; TYK2 (Cell-free assay): 19 nM
Relative Density:
1.40 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Ruxolitinib can be used in stereochemistry studies to evaluate the biological activity of the S-isomer compared to its pharmacological counterpart.
Library Information
Target:
JAK
Receptor:
JAK1; JAK2; Tyk2
Pathways:
JAK/STAT signaling; Chromatin/Epigenetic; Angiogenesis; Stem cell regulation
Plate Number:
AOCL-18
Plate Location:
d9
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
250 mg/mL; 816.03 mM
Water Max Solubility:
5 mg/mL; 16.32 mM
Ethanol Max Solubility:
57 mg/mL; 186.06 mM
ALogP:
2.88
HBA_Count:
3
HBD_Count:
1
Rotatable Bond:
4





