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Ticlopidine hydrochloride

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Catalog No. T0362Cas No. 53885-35-1
Alias Ticlopidine HCl, Ticlodone, Ticlodix

Ticlopidine hydrochloride (Ticlodix) is an effective inhibitor of platelet aggregation commonly used in the placement of STENTS in CORONARY ARTERIES.

Ticlopidine hydrochloride

Ticlopidine hydrochloride

🥰Excellent
Purity: 99.98%
Catalog No. T0362Alias Ticlopidine HCl, Ticlodone, TiclodixCas No. 53885-35-1
Ticlopidine hydrochloride (Ticlodix) is an effective inhibitor of platelet aggregation commonly used in the placement of STENTS in CORONARY ARTERIES.
Pack SizePriceAvailabilityQuantity
200 mg$29In Stock
1 mL x 10 mM (in DMSO)$30In Stock
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Purity:99.98%
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Product Introduction

Bioactivity
Description
Ticlopidine hydrochloride (Ticlodix) is an effective inhibitor of platelet aggregation commonly used in the placement of STENTS in CORONARY ARTERIES.
Targets&IC50
P2 receptor:2 μM
In vitro
Oral administration of Ticlopidine HCl in rats enhances the affinity of cyclase on platelet membranes for prostaglandin E1, subsequently activating both the basal and prostaglandin E1-stimulated without affecting the enzyme activity induced by adenosine or sodium fluoride. Ticlopidine HCl exhibits an inhibitory effect on platelet aggregation with an IC50 of 2 μM in males.
In vivo
Ticlopidine HCl inhibits platelet aggregation by activating basal PGE1-induced cyclase activity, blocking the enhancement of cyclase activity induced by PGE2, thereby increasing platelet c-AMP levels, and suppressing prostaglandin synthesis from endogenous substrates. Additionally, it alters platelet membrane function and inhibits aggregation through the blockade of ADP receptors.
AliasTiclopidine HCl, Ticlodone, Ticlodix
Chemical Properties
Molecular Weight300.25
FormulaC14H15Cl2NS
Cas No.53885-35-1
SmilesCl.Clc1ccccc1CN1CCc2c(C1)ccs2
Relative Density.1.37 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 30 mg/mL (100 mM)
DMSO: 65 mg/mL (216.49 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM3.3306 mL16.6528 mL33.3056 mL166.5279 mL
5 mM0.6661 mL3.3306 mL6.6611 mL33.3056 mL
10 mM0.3331 mL1.6653 mL3.3306 mL16.6528 mL
20 mM0.1665 mL0.8326 mL1.6653 mL8.3264 mL
50 mM0.0666 mL0.3331 mL0.6661 mL3.3306 mL
100 mM0.0333 mL0.1665 mL0.3331 mL1.6653 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
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