Synta66

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: Product Name:Synta66
CAS:835904-51-3
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G
Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:Synta66
CAS:835904-51-3
Purity:98.00% Package:10 mg;25 mg;5 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: InvivoChem
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Products Intro: Product Name:Synta66
CAS:835904-51-3
Purity:98% Package:10mg Remarks:V29155
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
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Products Intro: Product Name:Synta66
CAS:835904-51-3
Purity:98% Package:5mg;10mg;25mg
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Products Intro: Product Name:Synta66
CAS:835904-51-3
Purity:>95% Package:1G,5G
Synta66 Basic information
Product Name:Synta66
Synonyms:Synta66;4-Pyridinecarboxamide, N-(2',5'-dimethoxy[1,1'-biphenyl]-4-yl)-3-fluoro-;inhibit,Ca2+ release-activated Ca2+ channels,Calcium release-activated channels,CRAC Channel,Inhibitor,Synta66,Synta 66,Synta-66
CAS:835904-51-3
MF:C20H17FN2O3
MW:352.36
EINECS:
Product Categories:
Mol File:835904-51-3.mol
Synta66 Structure
Synta66 Chemical Properties
storage temp. Store at -20°C
solubility DMSO : 77.5 mg/mL (219.95 mM);Water : < 0.1 mg/mL (insoluble)
form Solid
color White to gray
Safety Information
MSDS Information
Synta66 Usage And Synthesis
Description

Synta66 is an inhibitor of store-operated calcium entry channel Orai, which forms the pore of the CRAC channel, and used for the research of neurological disease.

Synta66 is an inhibitor of Orai, which forms the pore of the CRAC channel. Synta66 (10 μM) attenuates peak SOCE in Müller glia. Synta66 (10 μM) prevents orai channels mediating the residual SOC current in Trpc1-/- Müller cells[1]. Synta66 (10 μM) nearly completely blocks the Ca2+ entry signal evoked by CaCl2 addition, whereas it moderately reduces Ca2+ mobilization from stores with 10% to 30% in platelet. Synta66 (10 μM) suppresses human platelet activation in plasma and whole-blood thrombus formation. Synta66 (10 μM) also inhibits murine platelet responses and thrombus formation[2]. Synta66 (10 μM) inhibits LAD2 human mast cell line. Synta66 (10 μM) significantly inhibits FcεRI stimulated histamine and TNFα secretion, and has differential effects on FcεRI stimulated prostaglandin D2 and cytokine release in human lung mast cells (HLMCs)[3].

References

[1]. Molnár T, et al. Store-Operated Calcium Entry in Müller Glia Is Controlled by Synergistic Activation of TRPC and Orai Channels. J Neurosci. 2016 Mar 16;36(11):3184-98. [2]. van Kruchten R, et al. Antithrombotic potential of blockers of store-operated calcium channels in platelets. Arterioscler Thromb Vasc Biol. 2012 Jul;32(7):1717-23. [3]. Wajdner HE, et al. Orai and TRPC channel characterization in FcεRI-mediated calcium signaling and mediator secretion in human mast cells. Physiol Rep. 2017 Mar;5(5).

Synta66 Preparation Products And Raw materials
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