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INCA-6

CAS No.: 3519-82-2

INCA-6 (Triptycene-1,4-quinone) is a cell-permeable NFAT inhibitor. INCA-6 inhibits of CN-NFAT signaling by targeting of
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Description INCA-6 (Triptycene-1,4-quinone) is a cell-permeable NFAT inhibitor. INCA-6 inhibits of CN-NFAT signaling by targeting of NFAT(P) substrate to the calcineurin (CN) phosphatase site.
In vitro 在人类视网膜微血管内皮细胞中,INCA-6(1.0, 2.5μM)显著降低VEGF及血清诱导的增殖,但不影响基线增殖[1]。在3-Hz细胞中,INCA-6(5μM)防止瞬时外向K+流的下调[2]。INCA-6(10μM)显著抑制大鼠初代微胶质细胞和BV-2细胞ATP诱导的CXCL2表达[3]。INCA-6(5μM)减少蛋白表达并降低与thapsigargin有无相关的SERCA2转录水平[4]。
In vivo INCA-6(2.5、5.0和25.0 μM;眼内注射)显著减少了氧气诱导的视网膜病变中的病理性新生血管,并以剂量依赖的方式降低了OIR的严重性[1]。
Synonyms Triptycene-1,4-quinone
molecular weight 284.31
Molecular formula C20H12O2
CAS 3519-82-2
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility DMSO: 2.84 mg/mL (10 mM), Sonication is recommended.
References 1. Colin A Bretz, et al. The role of the NFAT signaling pathway in retinal neovascularization. Invest Ophthalmol Vis Sci. 2013 Oct 25;54(10):7020-7. 2. Ling Xiao, et al. Mechanisms underlying rate-dependent remodeling of transient outward potassium current in canine ventricular myocytes. Circ Res. 2008 Sep 26;103(7):733-42. 3. Miho Shiratori,et al. P2X7 receptor activation induces CXCL2 production in microglia through NFAT and PKC/MAPK pathways. J Neurochem. 2010 Aug;114(3):810-9. 4. Anand Mohan Prasad, et al. Silencing calcineurin A subunit reduces SERCA2 expression in cardiac myocytes. Am J Physiol Heart Circ Physiol. 2011 Jan;300(1):H173-80.