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MYCi361

Catalog No. T12132Cas No. 2289690-31-7
Alias NUCC-0196361

MYCi361 (NUCC-0196361) is an inhibitor of MYC (binding to MYC with Kd of 3.2 μM).

MYCi361

MYCi361

Purity: 99.52%
Catalog No. T12132Alias NUCC-0196361Cas No. 2289690-31-7
MYCi361 (NUCC-0196361) is an inhibitor of MYC (binding to MYC with Kd of 3.2 μM).
Pack SizePriceAvailabilityQuantity
1 mg$118In Stock
5 mg$287In Stock
10 mg$457In Stock
25 mg$753In Stock
50 mg$1,060In Stock
100 mg$1,430In Stock
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Purity:99.52%
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Product Introduction

Bioactivity
Description
MYCi361 (NUCC-0196361) is an inhibitor of MYC (binding to MYC with Kd of 3.2 μM).
Targets&IC50
MYC:3.2 μM(Kd)
In vitro
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[1].
In vivo
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.
Animal Research
FVB or NSG male mice of 6-8 weeks of age and 25 g bearing established MycCaP tumors.MYCi361 treatment i.p. initially at 50 mg/kg twice daily for 2 days, then 70 mg/kg/day for 9 days
AliasNUCC-0196361
Chemical Properties
Molecular Weight594.86
FormulaC26H16ClF9N2O2
Cas No.2289690-31-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 100 mg/mL (168.1 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6811 mL8.4053 mL16.8107 mL84.0534 mL
5 mM0.3362 mL1.6811 mL3.3621 mL16.8107 mL
10 mM0.1681 mL0.8405 mL1.6811 mL8.4053 mL
20 mM0.0841 mL0.4203 mL0.8405 mL4.2027 mL
50 mM0.0336 mL0.1681 mL0.3362 mL1.6811 mL
100 mM0.0168 mL0.0841 mL0.1681 mL0.8405 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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