KJ-Pyr-9
CAS No. 581073-80-5
KJ-Pyr-9( KJ Pyr9 )
Catalog No. M15131 CAS No. 581073-80-5
KJ-Pyr-9 is a novel small-molecule inhibitor of c-Myc (Kd=6.5 ± 1.0 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 54 | In Stock |
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| 2MG | 31 | In Stock |
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| 5MG | 49 | In Stock |
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| 10MG | 70 | In Stock |
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| 25MG | 141 | In Stock |
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| 50MG | 272 | In Stock |
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| 100MG | 498 | In Stock |
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| 200MG | 669 | In Stock |
|
| 500MG | 1042 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameKJ-Pyr-9
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NoteResearch use only, not for human use.
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Brief DescriptionKJ-Pyr-9 is a novel small-molecule inhibitor of c-Myc (Kd=6.5 ± 1.0 nM).
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DescriptionKJ-Pyr-9 is a novel small-molecule inhibitor of c-Myc (Kd=6.5 ± 1.0 nM); interferes with MYC-MAX complex formation and inhibits MYC-induced oncogenic transformation in cells; active in xenograft mice.
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In Vitro——
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In Vivo——
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SynonymsKJ Pyr9
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PathwayCell Cycle/DNA Damage
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Targetc-Myc
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Recptorc-Myc
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number581073-80-5
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Formula Weight385.3722
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Molecular FormulaC22H15N3O4
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO=C(N)C1=CC=C(C2=CC(C3=CC=CO3)=NC(C4=CC=C([N+]([O-])=O)C=C4)=C2)C=C1
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Chemical NameBenzamide, 4-[2-(2-furanyl)-6-(4-nitrophenyl)-4-pyridinyl]-
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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MYCMI-6
MYCMI-6 (NSC354961) is a selective, high affinity inhibitor of MYC-MAX interaction.
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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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MYCi975
MYCi975 is an orally active inhibitor of MYC.MYCi975 inhibits P493-6, MV411,SK-N-B2 cells viability in an MYC-dependent manner(IC50s of 3.7, 3.9, 6.4 μM, respectively).The initial lead, MYC inhibitor 361 (MYCi361), suppressed in vivo tumor growth in mice, increased tumor immune cell infiltration, upregulated PD-L1 on tumors, and sensitized tumors to anti-PD1 immunotherapy. However, 361 demonstrated a narrow therapeutic index.
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