RN486 is a reversible inhibitor of Btk with IC50 value of 4.0 nM [1].
Bruton's tyrosine kinase (Btk) is a type of kinase protein which is expressed by immune system-related cells (B-lymphocyte, monocytes, macrophages, neutrophils and mast cells) and plays a pivotal role in cell differentiation and proliferation at the transition from pre-B to later B cell stages as well as in the process of both BCR and FcR signaling [2]. It has been reported that aberrant BCR signaling is associated with autoimmune diseases, for example, rheumatoid arthritis (RA) [3].
RN486 is a selective Btk inhibitor. When tested with human Ramos B cells or whole blood, RN486 treatment reduced the expression of CD69/B cells proliferation and IgG production by blocking BCR and FcR Signaling [1].
In NZB × NZW mouse model with systemic lupus erythematosus (SLE), compared with control group, RN486 treatment completely stopped disease progression by inhibiting BTK signaling and targeting other autoantibody-producing and effector cells [4]. In a PCA (type I hypersensitivity) mouse model or rPCA (type III hypersensitivity) mouse model, RN486 treatment significantly inhibited inflammatory response. In mouse model of RA, administration of RN486 orally could reduce both paw swelling and inflammatory markers in the blood by inhibiting both joint and systemic inflammation alone or in combination with methotrexate [1].
RN486 may also play a pivotal role in reducing immune complex-mediated activation of human monocytes and down-regulating the expression of macrophage-related and interferon-inducible genes [4].
References:
[1]. Xu, D., et al., RN486, a selective Bruton's tyrosine kinase inhibitor, abrogates immune hypersensitivity responses and arthritis in rodents. J Pharmacol Exp Ther, 2012. 341(1): p. 90-103.
[2]. Kil, L.P., et al., Btk levels set the threshold for B-cell activation and negative selection of autoreactive B cells in mice. Blood, 2012. 119(16): p. 3744-56.
[3]. Hartkamp, L.M., et al., Btk inhibition suppresses agonist-induced human macrophage activation and inflammatory gene expression in RA synovial tissue explants. Ann Rheum Dis, 2014.
[4]. Mina-Osorio, P., et al., Suppression of glomerulonephritis in lupus-prone NZB x NZW mice by RN486, a selective inhibitor of Bruton's tyrosine kinase. Arthritis Rheum, 2013. 65(9): p. 2380-91.
引用文献 (Citations)
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製品資料 (Product Documents)
Purity:>99.50%Appearance:A solid
化学的性質 (Chemical Properties)
CAS番号
1242156-23-5
化学名
6-cyclopropyl-8-fluoro-2-[2-(hydroxymethyl)-3-[1-methyl-5-[[5-(4-methylpiperazin-1-yl)pyridin-2-yl]amino]-6-oxopyridin-3-yl]phenyl]isoquinolin-1-one
SMILES
CN1CCN(CC1)C2=CN=C(C=C2)NC3=CC(=CN(C3=O)C)C4=C(C(=CC=C4)N5C=CC6=CC(=CC(=C6C5=O)F)C7CC7)CO
分子式
C35H35FN6O3
分子量
606.69
溶解性
≥ 30.35mg/mL in DMSO with gentle warming
保存条件
Store at -20°C
一般的な注意事項
製品の溶解性データに基づいて適切な溶媒を選択してください。調製後は、凍結融解の繰り返しを避けるため、ストック溶液を小分けしてください。
ストック溶液は、-80°Cで保存する場合は6か月以内、-20°Cで保存する場合は1か月以内に使用してください。
溶解性を高めるには、チューブを37°Cに温め、適切な時間超音波処理してください。
ストック溶液は、-80°Cで保存する場合は6か月以内、-20°Cで保存する場合は1か月以内に使用してください。
溶解性を高めるには、チューブを37°Cに温め、適切な時間超音波処理してください。
配送条件
評価用サンプルは保冷剤とともに発送します。その他の容量は室温で発送し、ご要望に応じて保冷剤を同梱します。
計算ツール (Calculators)モル濃度 / 希釈 / 分子量 / 単位変換 / in vivo製剤 / 溶解度
g/mol
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