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Thioquinapiperifil dihydrochloride

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Catalog No. T9773Cas No. 204077-66-7
Alias KF-31327

Thioquinapiperifil dihydrochloride is a phosphodiesterase (PDE-5) inhibitor (IC50: 0.074 nM) that is potent, selective and non-competitive for investigational maturation.

Thioquinapiperifil dihydrochloride

Thioquinapiperifil dihydrochloride

🥰Excellent
Purity: 98.73%
Catalog No. T9773Alias KF-31327Cas No. 204077-66-7
Thioquinapiperifil dihydrochloride is a phosphodiesterase (PDE-5) inhibitor (IC50: 0.074 nM) that is potent, selective and non-competitive for investigational maturation.
Pack SizePriceAvailabilityQuantity
1 mg$126In Stock
5 mg$313In Stock
10 mg$469In Stock
25 mg$762In Stock
50 mg$987In Stock
100 mg$1,380In Stock
1 mL x 10 mM (in DMSO)$358In Stock
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Purity:98.73%
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Product Introduction

Bioactivity
Description
Thioquinapiperifil dihydrochloride is a phosphodiesterase (PDE-5) inhibitor (IC50: 0.074 nM) that is potent, selective and non-competitive for investigational maturation.
Targets&IC50
PDE1:380 nM, PDE4:800 nM, PDE5:0.074 nM, PDE3:38 nM, PDE2:670 nM
In vitro
Thioquinapiperifil dihydrochloride (KF31327) (0.1-10 μM) inhibits platelet aggregation in a concentration-dependent manner. In the absence of nitroglycerin, higher concentrations of 1 and 10 μM of KF31327 are inhibits platelet aggregation in a concentration-dependent manner.[2]
Thioquinapiperifil dihydrochloride (KF31327) shows a significant increase in cyclic GMP at 10 μM. After 5 min incubation, the mean cyclic GMP levels of KF31327-treated cells is 0.95±0.17 pmol/10 8 cells.[2]
AliasKF-31327
Chemical Properties
Molecular Weight485.05
FormulaC24H29ClN6OS
Cas No.204077-66-7
SmilesCl.Cl.CCn1c2cc3ncnc(NCc4ccccc4N4CCC(CO)CC4)c3cc2[nH]c1=S
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 112.5 mg/mL (215.7 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.0616 mL10.3082 mL20.6164 mL103.0822 mL
5 mM0.4123 mL2.0616 mL4.1233 mL20.6164 mL
10 mM0.2062 mL1.0308 mL2.0616 mL10.3082 mL
20 mM0.1031 mL0.5154 mL1.0308 mL5.1541 mL
50 mM0.0412 mL0.2062 mL0.4123 mL2.0616 mL
100 mM0.0206 mL0.1031 mL0.2062 mL1.0308 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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