SHP099
CAS No. 1801747-42-1
SHP099( SHP099 free base | SHP099 | SHP-099 | SHP 099 )
Catalog No. M28048 CAS No. 1801747-42-1
SHP099 free base is an effective, selective, orally bioavailable, and efficacious SHP2 inhibitor (IC50 =0.07 μM and p-ERK modulation in cells IC50 = 0.250 μM). SHP099 shows dose-dependent pathway inhibition and antitumor activity in xenograft models.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 40 | Get Quote |
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| 5MG | 65 | Get Quote |
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| 10MG | 91 | Get Quote |
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| 25MG | 159 | Get Quote |
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| 50MG | 213 | Get Quote |
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| 100MG | 388 | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameSHP099
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NoteResearch use only, not for human use.
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Brief DescriptionSHP099 free base is an effective, selective, orally bioavailable, and efficacious SHP2 inhibitor (IC50 =0.07 μM and p-ERK modulation in cells IC50 = 0.250 μM). SHP099 shows dose-dependent pathway inhibition and antitumor activity in xenograft models.
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DescriptionSHP099 free base is an effective, selective, orally bioavailable, and efficacious SHP2 inhibitor (IC50 =0.07 μM and p-ERK modulation in cells IC50 = 0.250 μM). SHP099 shows dose-dependent pathway inhibition and antitumor activity in xenograft models.
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In Vitro——
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In Vivo——
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SynonymsSHP099 free base | SHP099 | SHP-099 | SHP 099
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PathwayMetabolic Enzyme/Protease
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TargetPhosphatase
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RecptorAntifungal
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Research Area——
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Indication——
Chemical Information
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CAS Number1801747-42-1
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Formula Weight352.26
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Molecular FormulaC16H19Cl2N5
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 12 mg/mL (34.07 mM)
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SMILESCC1(N)CCN(CC1)c1cnc(c(N)n1)-c1cccc(Cl)c1Cl
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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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LUPENONE
Lupenone is a natural product isolated from Rhizoma Musae and has good anti-diabetic activityand has anti-inflammatory activity.lupenone were potent PTP1B inhibitors with IC50 values of 15.11±1.23μM.
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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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LFHP-1c
LFHP-1c is a novel PGAM5 inhibitor that shows neuroprotective activity in an ischemic stroke model, preventing BBB destruction after transient middle cerebral artery occlusion (tMCAO) in rats.LFHP-1c can be used to study cerebral ischemic stroke.
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