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FKK

Catalog No. T19322Cas No. 78299-79-3

FKK [N-(heptyloxycarbonylaminosulfonyl)-2-aminobenzamide] is an indazole derivative and a novel bronchodilator.

FKK

FKK

Catalog No. T19322Cas No. 78299-79-3
FKK [N-(heptyloxycarbonylaminosulfonyl)-2-aminobenzamide] is an indazole derivative and a novel bronchodilator.
Pack SizePriceAvailabilityQuantity
25 mg$1,5206-8 weeks
50 mg$1,9806-8 weeks
100 mg$2,5006-8 weeks
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Product Introduction

Bioactivity
Description
FKK [N-(heptyloxycarbonylaminosulfonyl)-2-aminobenzamide] is an indazole derivative and a novel bronchodilator.
In vivo
FKK, an indazole derivative and novel bronchodilator, induces direct vasodilation in the coronary, mesenteric, and femoral vessels without affecting the renal vasculature. Notably, at a dosage of 30 mg/kg, intradermally (i.d.), FKK effectively causes bronchodilation without significantly impacting the cardiovascular system, unlike aminophylline at the same dosage and administration route. Additionally, FKK administered intravenously (i.v.) at dosages ranging from 0.1 to 3.0 mg/kg modestly elevates respiratory frequency, maximizes the rate of left ventricular (LV) pressure rise (dp/dt max), and enhances myocardial contractile strength. This administration also leads to a transient increase followed by a decrease in both systemic blood pressure and LV systolic pressure.
Chemical Properties
Molecular Weight329.23
FormulaC17H17BrN2
Cas No.78299-79-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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