Adenosine A1 receptor activator T62
CAS No. 40312-34-3
Adenosine A1 receptor activator T62( —— )
Catalog No. M26600 CAS No. 40312-34-3
Adenosine A1 receptor activator T62 is an allosteric enhancer of adenosine A1 receptor, and it produces antinociception in animal models of acute pain and also reduces hypersensitivity in models of inflammatory and nerve-injury pain[2][3].
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 197 | In Stock |
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| 5MG | 128 | In Stock |
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| 10MG | 191 | In Stock |
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| 25MG | 307 | In Stock |
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| 50MG | 410 | In Stock |
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| 100MG | 554 | In Stock |
|
| 200MG | 736 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameAdenosine A1 receptor activator T62
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NoteResearch use only, not for human use.
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Brief DescriptionAdenosine A1 receptor activator T62 is an allosteric enhancer of adenosine A1 receptor, and it produces antinociception in animal models of acute pain and also reduces hypersensitivity in models of inflammatory and nerve-injury pain[2][3].
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DescriptionAdenosine A1 receptor activator T62 is an allosteric enhancer of adenosine A1 receptor, and it produces antinociception in animal models of acute pain and also reduces hypersensitivity in models of inflammatory and nerve-injury pain[2][3].(In Vivo):Adenosine A1 receptor activator T62 (0.3-3 μg; intrathecal administration; male SpragueDawley rats) treatment produces a dose-dependent antihypersensitivity effect. However it has no effect on ambulation or activity level.
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In Vitro——
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In VivoAdenosine A1 receptor activator T62 (0.3-3 μg; intrathecal administration; male SpragueDawley rats) treatment produces a dose-dependent antihypersensitivity effect, with no effect on ambulation or activity level. Animal Model:Male SpragueDawley rats (250 g) after paw incision surgery Dosage:0.3 μg, 0.5 μg, 1 μg, and 3 μg Administration:Intrathecal administration Result:Produced a dose-dependent antihypersensitivity effect, with no effect on ambulation or activity level. The ED40 (95% confidence interval) was 0.77 (0.63-0.91) μg.
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Synonyms——
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PathwayApoptosis
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TargetAdenosine Receptor
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RecptorPDE4
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Research Area——
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Indication——
Chemical Information
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CAS Number40312-34-3
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Formula Weight291.79
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Molecular FormulaC15H14ClNOS
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Purity>98% (HPLC)
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Solubility——
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SMILESNc1sc2CCCCc2c1C(=O)c1ccc(Cl)cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Manuel Mata, et al. Piclamilast inhibits the pro-apoptotic and anti-proliferative responses of A549 cells exposed to H(2)O(2) via mechanisms involving AP-1 activation. Free Radic Res. 2012 May;46(5):690-9.
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