ERK5-IN-2
CAS No. 1888305-96-1
ERK5-IN-2( —— )
Catalog No. M20408 CAS No. 1888305-96-1
ERK5-IN-2 is an orally active sub-micromolar selective ERK5 inhibitor with IC50s of 0.82 μM 3 μM for ERK5 and ERK5 MEF2D respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 53 | In Stock |
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| 5MG | 87 | In Stock |
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| 10MG | 155 | In Stock |
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| 25MG | 302 | In Stock |
|
| 50MG | 507 | In Stock |
|
| 100MG | 712 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameERK5-IN-2
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NoteResearch use only, not for human use.
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Brief DescriptionERK5-IN-2 is an orally active sub-micromolar selective ERK5 inhibitor with IC50s of 0.82 μM 3 μM for ERK5 and ERK5 MEF2D respectively.
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DescriptionERK5-IN-2 is an orally active sub-micromolar selective ERK5 inhibitor with IC50s of 0.82 μM 3 μM for ERK5 and ERK5 MEF2D respectively.
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In Vitro——
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In VivoAnimal Model:Female CD1 mice (8-10 weeks old) with Matrigel inoculation and female CD1 nude (nu/nu) mice (8-10 weeks old) bearing A2780 human ovarian carcinoma xenografts Dosage:100?mg/kg Administration:P.o.; twice-daily; CD1 mice for 7 days and CD1 nude (nu/nu) mice for 10 days Result:Tumor volumes were significantly reduced. Animal Model:Female CD1 mice at 8-10 weeks of age Dosage:10 mg/kg Administration:I.v. or p.o.; 0.083-24?hours Result:The terminal plasma half-life was 38?min, with a plasma clearance of 27?mL/min/kg, and oral bioavailability of 68%.
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Synonyms——
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PathwayMAPK/ERK Signaling
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TargetERK
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RecptorERK5
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Research Area——
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Indication——
Chemical Information
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CAS Number1888305-96-1
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Formula Weight388.19
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Molecular FormulaC17H11BrFN3O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (644.01 mM)
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SMILESFc1cccc(Br)c1C(=O)c1c[nH]c(c1)C(=O)Nc1cccnc1
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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.Myers SM Miller DC Molyneux L et al .Identification of a novel orally bioavailable ERK5 inhibitor with selectivity over p38α and BRD4[J].Eur J Med Chem. 2019 Sep 15;178:530-543.
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