KY-226
CAS No. 1621673-53-7
KY-226( —— )
Catalog No. M20927 CAS No. 1621673-53-7
KY-226 is a potent inhibitor of protein tyrosine phosphatase 1B (PTP1B)(IC50: 0.25 μM)
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 122 | In Stock |
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| 5MG | 116 | In Stock |
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| 10MG | 170 | In Stock |
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| 25MG | 282 | In Stock |
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| 50MG | 431 | In Stock |
|
| 100MG | 690 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameKY-226
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NoteResearch use only, not for human use.
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Brief DescriptionKY-226 is a potent inhibitor of protein tyrosine phosphatase 1B (PTP1B)(IC50: 0.25 μM)
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DescriptionKY-226 is a potent inhibitor of protein tyrosine phosphatase 1B (PTP1B)(IC50: 0.25 μM).
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In VitroWestern Blot Analysis Cell Line:bEnd.3 cells stimulated with LPS Concentration:1 μM Incubation Time:24 hours Result:Rescued lipopolysaccharide-induced reduction of mRNA and protein levels of ZO-1.
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In VivoAnimal Model:Male db/db mice (8-11 weeks old)Dosage:10 mg/kg and 30 mg/kg Administration:Oral administration; daily; for 4 weeks Result:Significantly reduced plasma glucose and triglyceride levels as well as hemoglobin A1c values without increasing body weight gain.
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Synonyms——
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PathwayMetabolic Enzyme/Protease
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TargetPhosphatase
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RecptorPTP1B
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Research Area——
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Indication——
Chemical Information
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CAS Number1621673-53-7
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Formula Weight481.67
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Molecular FormulaC27H31NO3S2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (519.03 mM)
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SMILESCCCCCCS(=O)(=O)NC(=O)c1ccc(CSCc2ccc(-c3ccccc3)cc2)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
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Rosmanol
Rosmanol has antioxidant activity, it can activate the antioxidant response element. Rosmanol has biphasic modulation of GABAA receptors, demonstrates CNS activity in mouse models of antinociception, antidepressant and anxiolysis.
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JMS-053
JMS-053 is a potent and selective inhibitor of the phosphatase DUSP3, inhibits PTP4A3, PTP4A1, PTP4A2 and CDC25B, inhibits cancer cell migration and sphere growth, and avoids disruption of the microvascular endothelial barrier by vascular endothelial growth factor or lipopolysaccharide.
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Calcineurin Autoinhi...
Selective inhibitor of Ca2+-calmodulin-dependent protein phosphatase (calcineurin) (IC50 ~ 10 μM). Does not inhibit PP1, PP2A or CaM kinase II (IC50 > 100 mM).
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