NY2267
CAS No. 886053-73-2
NY2267( Acetic acid, 2-[[6-[2-(cyclohexylamino)-1-[[(4-methoxyphenyl)methyl](2-pyridinylcarbonyl)amino]-2-oxoethyl]-2-naphthalenyl]oxy]-, 1,1-dimethylethyl ester )
Catalog No. M24905 CAS No. 886053-73-2
NY2267 is a disruptor of Myc-Max interaction, with an IC50 of 36.5 μM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 264 | In Stock |
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| 5MG | 187 | In Stock |
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| 10MG | 297 | In Stock |
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| 25MG | 525 | In Stock |
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| 50MG | 732 | In Stock |
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| 100MG | 995 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameNY2267
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NoteResearch use only, not for human use.
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Brief DescriptionNY2267 is a disruptor of Myc-Max interaction, with an IC50 of 36.5 μM.
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DescriptionNY2267 is a disruptor of Myc-Max interaction, with an IC50 of 36.5 μM.
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In Vitro——
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In Vivo——
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SynonymsAcetic acid, 2-[[6-[2-(cyclohexylamino)-1-[[(4-methoxyphenyl)methyl](2-pyridinylcarbonyl)amino]-2-oxoethyl]-2-naphthalenyl]oxy]-, 1,1-dimethylethyl ester
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PathwayCell Cycle/DNA Damage
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Targetc-Myc
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Recptorc-Myc-Max
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Research Area——
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Indication——
Chemical Information
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CAS Number886053-73-2
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Formula Weight637.78
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Molecular FormulaC38H43N3O6
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Purity>98% (HPLC)
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SolubilityDMSO : 250 mg/mL (392.00 mM; Need ultrasonic and warming)
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SMILESO=C(OC(C)(C)C)COC1=CC=C2C=C(C(N(CC3=CC=C(OC)C=C3)C(C4=NC=CC=C4)=O)C(NC5CCCCC5)=O)C=CC2=C1
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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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IRES-C11
A novel, spectfic c-Myc IRES (internal ribosome entry site) function inhibitor that prevents binding of hnRNP A1 to the Myc IRES and specifically inhibits Myc IRES activity in MM cells.
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MYC inhibitor DC-34
MYC inhibitor DC-34 is a potent small molecule that selectively inhibits MYC at the transcriptional level only when a G-quadruplex (G4) is present in the promoter.
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MYCi361
MYCi361 is an inhibitor of MYC (binding to MYC with Kd of 3.2 μM). MYCi361 is a small-molecule MYC inhibitors that inhibits the viability of MYC-dependent cancer cells including prostate cancer (MycCaP, LNCaP, and PC3), leukemia (MV4-11), lymphoma (HL-60 and P493-6), and neuroblastoma (SK-N-B2) with low-micromolar IC50 values.
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