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PK095

Catalog No. T67763Cas No. 380314-37-4

PK095 is a proprietary compound in the guanidine - based F1F0-ATPase inhibitor family.

PK095

PK095

Purity: 96.84%
Catalog No. T67763Cas No. 380314-37-4
PK095 is a proprietary compound in the guanidine - based F1F0-ATPase inhibitor family.
Pack SizePriceAvailabilityQuantity
1 mg$88In Stock
5 mg$208In Stock
10 mg$296In Stock
25 mg$473In Stock
50 mg$653In Stock
100 mg$882In Stock
200 mg$1,180In Stock
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Purity:96.84%
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Product Introduction

Bioactivity
Description
PK095 is a proprietary compound in the guanidine - based F1F0-ATPase inhibitor family.
Chemical Properties
Molecular Weight378.45
FormulaC20H18N4O2S
Cas No.380314-37-4
Storage & Solubility Information
StorageShipping with blue ice.
Solubility Information
DMSO: 3.79 mg/mL (10 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6424 mL13.2118 mL26.4236 mL132.1178 mL
5 mM0.5285 mL2.6424 mL5.2847 mL26.4236 mL
10 mM0.2642 mL1.3212 mL2.6424 mL13.2118 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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