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MY-5445

Catalog No. T16164Cas No. 78351-75-4
Alias N-(3-chlorophenyl)-4-phenylphthalazin-1-amine

MY-5445 (N-(3-chlorophenyl)-4-phenylphthalazin-1-amine) is a specific inhibitor of phosphodiesterase type 5 (PDE5). MY-5445 selectively inhibits cGMP PDE (Ki:1.3 μM).

MY-5445

MY-5445

Purity: 99.77%
Catalog No. T16164Alias N-(3-chlorophenyl)-4-phenylphthalazin-1-amineCas No. 78351-75-4
MY-5445 (N-(3-chlorophenyl)-4-phenylphthalazin-1-amine) is a specific inhibitor of phosphodiesterase type 5 (PDE5). MY-5445 selectively inhibits cGMP PDE (Ki:1.3 μM).
Pack SizePriceAvailabilityQuantity
5 mg$38In Stock
10 mg$58In Stock
25 mg$97In Stock
50 mg$143In Stock
1 mL x 10 mM (in DMSO)$42In Stock
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Purity:99.77%
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Product Introduction

Bioactivity
Description
MY-5445 (N-(3-chlorophenyl)-4-phenylphthalazin-1-amine) is a specific inhibitor of phosphodiesterase type 5 (PDE5). MY-5445 selectively inhibits cGMP PDE (Ki:1.3 μM).
Targets&IC50
PDE5:1.3 μM (Ki), PDE5:6.7 μM , PDE4:37 μM
In vitro
in ABCG2-overexpressing cells, MY-5445 selectively reverses ABCG2-mediated multidrug resistance. MY-5445 reverses ABCG2-mediated multidrug resistance (MDR) by potentiating the cytotoxicity of an ABCG2 substrate drug in ABCG2-overexpressing multidrug-resistant cancer cells, possibly by modulating the function and/or the protein expression of ABCG2[2]. In the S1-M1-80 cell, MY-5445 (3 μM; 48 hours) substantially increases the topotecan-induced apoptosis[2].
In vivo
I.p administration of 0.5-3 mg/kg twice a day for 15 days) produces significant relief of mechanical hypersensitivity[3].
AliasN-(3-chlorophenyl)-4-phenylphthalazin-1-amine
Chemical Properties
Molecular Weight331.8
FormulaC20H14ClN3
Cas No.78351-75-4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 40 mg/mL (120.55 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0139 mL15.0693 mL30.1386 mL150.6932 mL
5 mM0.6028 mL3.0139 mL6.0277 mL30.1386 mL
10 mM0.3014 mL1.5069 mL3.0139 mL15.0693 mL
20 mM0.1507 mL0.7535 mL1.5069 mL7.5347 mL
50 mM0.0603 mL0.3014 mL0.6028 mL3.0139 mL
100 mM0.0301 mL0.1507 mL0.3014 mL1.5069 mL

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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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