NVP-DKY709
CAS No. 2291360-73-9
NVP-DKY709( —— )
Catalog No. M28913 CAS No. 2291360-73-9
NVP-DKY709 is a potent IKZF2 inhibitor for the treatment of cancers.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 254 | In Stock |
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| 5MG | 231 | In Stock |
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| 10MG | 370 | In Stock |
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| 25MG | 605 | In Stock |
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| 50MG | 732 | In Stock |
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| 100MG | 918 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | 1841 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameNVP-DKY709
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NoteResearch use only, not for human use.
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Brief DescriptionNVP-DKY709 is a potent IKZF2 inhibitor for the treatment of cancers.
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DescriptionNVP-DKY709 is a potent IKZF2 inhibitor for the treatment of cancers.
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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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RecptorApelin receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number2291360-73-9
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Formula Weight417.5
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Molecular FormulaC25H27N3O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 16.67 mg/mL (39.93 mM)
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SMILES——
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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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(Tyr0)-Fibrinopeptid...
(Tyr0)-Fibrinopeptide A
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CALP1
Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site; produces CaM-dependent activation of phosphodiesterase. Also binds to cytoplasmic sites on other Ca2+ channels, including NMDA and HIV-1 gp120-activated channels, inhibiting Ca2+-mediated cytotoxicity and apoptosis (IC50 = 52 μM). Shown to protect pancreatic acinar cells from gossypol induced necrosis. Inhibits VLA-5-mediated adhesion of mast cells to fibronectin in vitro and attenuates inflammatory cell influx in guinea pig lung in vivo.
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CCCP
CCCP inhibits activation of STING and its downstream signalling molecules, TBK1 and IRF3. CCCP inhibits STING-mediated IFN-β production via disrupting mitochondrial membrane potential (MMP).
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