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PSI-697

PSI-697
PSI-697 is an inhibitor of oral P-selectin (IC50: 125 μM).
Catalog No. T16676Cas No. 851546-61-7

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PSI-697

Catalog No. T16676Alias P-Selectin InhibitorCas No. 851546-61-7

PSI-697 is an inhibitor of oral P-selectin (IC50: 125 μM).
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
25 mg$1,8206-8 weeks
50 mg$2,3806-8 weeks
100 mg$3,1006-8 weeks
1 mL x 10 mM (in DMSO)$2786-8 weeks
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Product Introduction

Bioactivity
Description
PSI-697 is an inhibitor of oral P-selectin (IC50: 125 μM).
Targets&IC50
P-selectin:125 μM
In vitro
PSI-697 inhibits the binding of a soluble human P-selectin to PSGL-1. In vitro, as a reproducible concentration-dependent manner inhibiting 50% of binding at a concentration of 125 μM [1].
In vivo
PSI-697 (30 mg/kg; p.o.; daily; 6 days) promotes thrombus resolution and reduces inflammation in a baboon model of venous thrombosis. PSI-697 ((30 mg/kg; i.g.; daily) decreases vein wall injury in a rat stenosis model of venous thrombosis. PSI-697 (100 mg/kg; p.o.) reduces thrombus weight by 18% relative to the vehicle, without prolonging bleeding time in a rat venous thrombosis model. PSI-697 (0-50 mg/kg; p.o.) obviously decreases the number of rolling leukocytes by 39% versus vehicle control[1][2].
AliasP-Selectin Inhibitor
Chemical Properties
Molecular Weight367.83
FormulaC21H18ClNO3
Cas No.851546-61-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 45.8 mg/mL (124.51 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.7186 mL13.5932 mL27.1865 mL135.9324 mL
5 mM0.5437 mL2.7186 mL5.4373 mL27.1865 mL
10 mM0.2719 mL1.3593 mL2.7186 mL13.5932 mL
20 mM0.1359 mL0.6797 mL1.3593 mL6.7966 mL
50 mM0.0544 mL0.2719 mL0.5437 mL2.7186 mL
100 mM0.0272 mL0.1359 mL0.2719 mL1.3593 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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