Ubiquitination-IN-1
CAS No. 1819330-15-8
Ubiquitination-IN-1( —— )
Catalog No. M26494 CAS No. 1819330-15-8
Ubiquitination-IN-1 is an inhibitor of ubiquitination and Cksl-Skp2 protein-protein interaction (IC50: 0.17 μM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 58 | Get Quote |
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| 10MG | 87 | Get Quote |
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| 25MG | 159 | Get Quote |
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| 50MG | 264 | Get Quote |
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| 100MG | 395 | Get Quote |
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| 500MG | 888 | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameUbiquitination-IN-1
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NoteResearch use only, not for human use.
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Brief DescriptionUbiquitination-IN-1 is an inhibitor of ubiquitination and Cksl-Skp2 protein-protein interaction (IC50: 0.17 μM).
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DescriptionUbiquitination-IN-1 is an inhibitor of ubiquitination and Cksl-Skp2 protein-protein interaction (IC50: 0.17 μM).(In Vitro):Ubiquitination-IN-1 inhibits A549 and HT1080 cells (IC50s: 0.91 and 0.4 μM).
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorPim2
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Research Area——
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Indication——
Chemical Information
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CAS Number1819330-15-8
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Formula Weight429.42
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Molecular FormulaC21H14F3N3O2S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 83.33 mg/mL (194.06 mM)
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SMILESFC(F)(F)c1cccc(c1)S(=O)(=O)Nc1ccc(-c2cccnc2)c2cccnc12
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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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Oxytroflavoside D
The branches of Magnolia utilis.
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Syk Inhibitor II hyd...
The impact of spleen tyrosine kinase (Syk) signaling might be prominent in lupus because (i) Syk is a shared downstream signaling molecule among circulating immune complex, LPS, and (1→3)-β-D-glucan (BG), and (ii) all of these factors are detectable in the serum of Fc gamma receptor IIb-deficient (FcgRIIb-/-) mice with sepsis. Syk inhibition downregulated several inflammatory pathways in FcgRIIb-/- macrophages activated with BG + LPS suggesting the potential anti-inflammatory impact of Syk inhibitors in lupus.
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Naringenin triacetat...
Naringenin triacetate exhibits a better binding affinity with multiple crystal structures of first bromodomain BRD4 (BRD4 BD1) when compared with the known inhibitors.
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