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PF-07328948

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Catalog No. T88836Cas No. 2936625-34-0
Alias PF07328948

PF-07328948 is a branched-chain keto acid dehydrogenase kinase (BDK) inhibitor, useful in research on cardiovascular disease (CVD) and metabolic disorders.

PF-07328948

PF-07328948

🥰Excellent
Purity: 98.54%
Catalog No. T88836Alias PF07328948Cas No. 2936625-34-0
PF-07328948 is a branched-chain keto acid dehydrogenase kinase (BDK) inhibitor, useful in research on cardiovascular disease (CVD) and metabolic disorders.
Pack SizePriceAvailabilityQuantity
1 mg$359In Stock
5 mg$869In Stock
10 mg$1,190In Stock
25 mg$1,770In Stock
50 mg$2,390In Stock
100 mg$3,230In Stock
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Purity:98.54%
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Product Introduction

Bioactivity
Description
PF-07328948 is a branched-chain keto acid dehydrogenase kinase (BDK) inhibitor, useful in research on cardiovascular disease (CVD) and metabolic disorders.
Targets&IC50
BDK:15 nM
In vitro
PF-07328948 is a selective BDK inhibitor with an IC50 value of 15 nM. [1]
In vivo
After intravenous administration of PF-07328948, the plasma clearance rate (CLp) in rats, dogs and monkeys was 1.36 mL/min/kg, 1.19 mL/min/kg and 9.88 mL/min/kg, respectively.
When fed orally with PF-07328948 (10,50,100 mg/kg for 10 days), plasma biomarkers including BCAA and branched-chain ketoacids (BCKA) were decreased in vivo. [1]
AliasPF07328948
Chemical Properties
Molecular Weight356.29
FormulaC16H8F4O3S
Cas No.2936625-34-0
SmilesO=C(O)C=1SC=2C=C(F)C=CC2C1C=3C=C(F)C(F)=C(OC)C3F
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 80 mg/mL (224.54 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8067 mL14.0335 mL28.0670 mL140.3351 mL
5 mM0.5613 mL2.8067 mL5.6134 mL28.0670 mL
10 mM0.2807 mL1.4034 mL2.8067 mL14.0335 mL
20 mM0.1403 mL0.7017 mL1.4034 mL7.0168 mL
50 mM0.0561 mL0.2807 mL0.5613 mL2.8067 mL
100 mM0.0281 mL0.1403 mL0.2807 mL1.4034 mL

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In Vivo Formulation Calculator (Clear solution)

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.
1 Enter information below:
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2 Enter the in vivo formulation:
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Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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