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PSI-697

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Catalog No. T16676Cas No. 851546-61-7
Alias P-Selectin Inhibitor

PSI-697 is an inhibitor of oral P-selectin (IC50: 125 μM).

PSI-697

PSI-697

😃Good
Catalog No. T16676Alias P-Selectin InhibitorCas No. 851546-61-7
PSI-697 is an inhibitor of oral P-selectin (IC50: 125 μM).
Pack SizePriceAvailabilityQuantity
25 mg1.729 €1-2 weeks
50 mg2.261 €1-2 weeks
100 mg2.945 €1-2 weeks
1 mL x 10 mM (in DMSO)264 €1-2 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
Relative Density.1.383 g/cm3 (Predicted)
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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