Ruxolitinib, Free Base

Cat# 288929-50mg

Size : 50mg

Brand : US Biological

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288929 Ruxolitinib, Free Base

Clone Type
Polyclonal
Grade
Highly Purified
Shipping Temp
Blue Ice
Storage Temp
-20°C

Ruxolitinib is a potent and selective Janus kinase (JAK) inhibitor with with IC50's of 2.7 and 4.5nm for JAK1 and JAK2, respectively. Displays clinically significant activity in myelofibrosis. Antineoplastic, anti-inflammatory and immunomodulating agent. Affects DC differentiation and function, leading to impaired T cell activation. Used in the treatment of myeloproliferative neoplasms and psoriasis. Anticancer agent. Shown to induce apoptosis and autophagy.||Synonyms:|(b-R)-b-Cyclopentyl-4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazole-1-propanenitrile; INCB018424, INC18424, NCB018424, NCB18424||CAS No:|941678-49-5||Molecular Formula:|C17H18N6||Molecular Weight:|306.37||Appearance:|White to off-white powder||Purity:|≥98% (HPLC, TLC)||Solubility:|Souble in DMSO at 28mg/ml. Soluble in ethanol at 15mg/ml with warming; very poorly soluble in water; maximum solubility in plain water is estimated to be about 25-50uM; buffers, serum or other additives may increase or decrease the aqueous solubility.||Storage and Stability:|Powder may be stored at -20°C. Stable for 6 months after receipt at -20°C. Reconstitute with DMSO or EtOH. Aliquot to avoid repeated freezing and thawing. Store at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. Light sensitive.

Applications
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. Toxicity and Hazards: All products should be handled by qualified personnel only, trained in laboratory procedures.
Form
White to off-white powder
Purity
≥98% (HPLC, TLC)
References
1. Shilling, A.D. et al., Drug Metab. Disp., 38, 2023 (2010) 2. Mesa, R.A., IDrugs, 13, 394 (2010) 3. Campas-Moya, C., Drugs Fut., 35, 457 (2010)