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ZL006

Catalog No. T17293Cas No. 1181226-02-7

ZL006 is an effective inhibitor of nNOS/PSD-95 interaction. ZL006 also inhibits NMDA receptor-mediated NO synthesis.

ZL006

ZL006

Purity: 98.29%
Catalog No. T17293Cas No. 1181226-02-7
ZL006 is an effective inhibitor of nNOS/PSD-95 interaction. ZL006 also inhibits NMDA receptor-mediated NO synthesis.
Pack SizePriceAvailabilityQuantity
1 mg$32In Stock
2 mg$45In Stock
5 mg$72In Stock
10 mg$101In Stock
25 mg$198In Stock
50 mg$315In Stock
100 mg$539In Stock
200 mg$778In Stock
500 mg$1,180In Stock
1 mL x 10 mM (in DMSO)$81In Stock
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Purity:98.29%
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Product Introduction

Bioactivity
Description
ZL006 is an effective inhibitor of nNOS/PSD-95 interaction. ZL006 also inhibits NMDA receptor-mediated NO synthesis.
In vitro
ZL006 growth inhibition of BCECs is not found at a low concentration of 0.001, 0.01, 0.1, 1, and 10 μg/mL. The cytotoxicity of T7-P-LPs/ZL006 is obviously enhanced at the concentration of 10 μg/mL. Cellular uptake of ZL006 loads P-LPs and T7-P-LPs after incubation for 0.5 h at the concentrations range from 100 μg/mL to 600 μg/mL in BCECs [1][2].
In vivo
T7-P-LPs/ZL006 displays a significant enhance in drug accumulation in the brain tissue due to its better brain targeting delivery compared with P-LPs/ZL006 and free ZL006. P-LPs/ZL006 and T7-P-LPs/ZL006 show a significant decrease in drug accumulation in the liver and kidney compared with free ZL006 [1].
Chemical Properties
Molecular Weight328.15
FormulaC14H11Cl2NO4
Cas No.1181226-02-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 29 mg/mL (88.37 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0474 mL15.2369 mL30.4739 mL152.3693 mL
5 mM0.6095 mL3.0474 mL6.0948 mL30.4739 mL
10 mM0.3047 mL1.5237 mL3.0474 mL15.2369 mL
20 mM0.1524 mL0.7618 mL1.5237 mL7.6185 mL
50 mM0.0609 mL0.3047 mL0.6095 mL3.0474 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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