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CB30865

🥰Excellent
Catalog No. T14882Cas No. 206275-15-2
Alias ZM-242421, ZM242421, ZM 242421

CB30865 (ZM 242421) is a selective and highly effective nicotinamide phosphoribosyltransferase (Nampt) inhibitor with potential antitumor activity.

CB30865

CB30865

🥰Excellent
Purity: 99.04%
Catalog No. T14882Alias ZM-242421, ZM242421, ZM 242421Cas No. 206275-15-2
CB30865 (ZM 242421) is a selective and highly effective nicotinamide phosphoribosyltransferase (Nampt) inhibitor with potential antitumor activity.
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2 mg$166In Stock
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Purity:99.04%
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Product Introduction

Bioactivity
Description
CB30865 (ZM 242421) is a selective and highly effective nicotinamide phosphoribosyltransferase (Nampt) inhibitor with potential antitumor activity.
In vitro
CB30865 showed dramatically increased W1L2 cytotoxicity (EC50=2.8 nM) that was not rescued by precursors or end-products of folate metabolism.
CB30865 represents a class of compounds with unique biochemical characteristics such as a delayed, non-phase specific, cell-cycle arrest. [1]
CB30865 represents a class of compounds with unique biochemical characteristics such as a delayed, non-phase specific, cell-cycle arrest. [3]
AliasZM-242421, ZM242421, ZM 242421
Chemical Properties
Molecular Weight516.39
FormulaC26H22BrN5O2
Cas No.206275-15-2
SmilesO=C1N=C(NC2=CC(Br)=C(C=C12)CN(C3=CC=C(C=C3)C(=O)NCC=4C=NC=CC4)CC#C)C
Relative Density.1.38 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: < 0.1 mg/mL (insoluble)
DMSO: 30 mg/mL (58.10 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9365 mL9.6826 mL19.3652 mL96.8260 mL
5 mM0.3873 mL1.9365 mL3.8730 mL19.3652 mL
10 mM0.1937 mL0.9683 mL1.9365 mL9.6826 mL
20 mM0.0968 mL0.4841 mL0.9683 mL4.8413 mL
50 mM0.0387 mL0.1937 mL0.3873 mL1.9365 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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