UK-5099 [56396-35-1]

Référence T4441-10mg

Conditionnement : 10mg

Marque : TargetMol

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UK-5099

(Synonyms: UK5099, UK 5099, PF-1005023) Copy Product Info
UK-5099 (PF-1005023) is a specific and potent inhibitor of MPC carrier activity, effectively inhibiting pyruvate-dependent oxygen consumption in rat heart mitochondria with an IC50 of 50 nM [1].
UK-5099
Cas No. 56396-35-1
For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:98.43%
Color:White to Yellow

Product Introduction

Bioactivity
Description
UK-5099 (PF-1005023) is a specific and potent inhibitor of MPC carrier activity, effectively inhibiting pyruvate-dependent oxygen consumption in rat heart mitochondria with an IC50 of 50 nM [1].
Targets & IC50
MPC:50 nM
In vitro
The trypanosomal pyruvate carrier is found to be rather insensitive to inhibition by alpha-cyano-4-hydroxycinnamate (Ki: 17 mM) but can be completely blocked by UK-5099 (Ki: 49 μM)[2]. UK-5099 also inhibits the monocarboxylate transporter (MCT) [3]. UK5099 dose-dependently significantly inhibits the glucose-stimulated rise in oxygen consumption and at 150 μM reduced oxygen consumption below basal levels. UK5099 reduces ATP levels and increases ADP and AMP levels in 832/13 cells[4]. The UK5099 treated cells show a significantly higher proportion of side population fraction and express higher levels of stemness markers Oct3/4 and Nanog. The UK5099 application may be an ideal model for Warburg effect studies[5].
In vivo
UK5099 increases the glucose excursion seen during an intraperitoneal glucose tolerance test in C57BLK mice[4].
SynonymsUK5099, UK 5099, PF-1005023
Cell Research
The 832/13 cell line derived from INS-1 rat insulinoma cells is used for experiments. Cell viability is measured using CellTiter Blue. The assay is based on the cellular reduction of resazurin to resorufin. The appearance of resorufin is monitored by fluorescence emission at 585 nm using a Spectramax M5 microplate reader with excitation at 555 nm. For UK5099-treated cells, cells are allowed to recover for 1 h before measuring cell viability. Data are expressed as -fold relative to no treatment or siCtrl[4].
Animal Research
C57BLK mice are fasted for 16 h prior to glucose challenge. UK5099 (32 μmol/kg of body weight) or DMSO in PBS is injected into the intraperitoneal cavity 30 min before injecting glucose (1.5 mg of glucose/g of body weight). Blood glucose levels are measured at 0, 10, 20, 30, 60, and 120 min after glucose injection[4].
Chemical Properties
Molecular Weight288.3
FormulaC18H12N2O2
Cas No.56396-35-1
SmilesOC(=O)C(=Cc1cn(-c2ccccc2)c2ccccc12)C#N
Relative Density.1.20 g/cm3
Storage & Solubility Information
StorageStore at low temperature,Keep away from direct sunlight Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 16.67 mg/mL (57.82 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1.67 mg/mL (5.79 mM), Solution.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.4686 mL17.3430 mL34.6861 mL173.4305 mL
5 mM0.6937 mL3.4686 mL6.9372 mL34.6861 mL
10 mM0.3469 mL1.7343 mL3.4686 mL17.3430 mL
20 mM0.1734 mL0.8672 mL1.7343 mL8.6715 mL
50 mM0.0694 mL0.3469 mL0.6937 mL3.4686 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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