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Amiprilose

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TargetMol
Catalog No. T25080Cas No. 56824-20-5
Alias SM-1213, SM1213, SM 1213

Amiprilose (SM 1213) has anti-inflammatory activity and inhibits the proliferation of a variety of hyperproliferative cell types.Amiprilose induces lymphokine-induced macrophage activation and may be used in studies of rheumatoid arthritis and psoriasis.

Amiprilose

Amiprilose

😃Good
TargetMol
Purity: 99.82%
Catalog No. T25080Alias SM-1213, SM1213, SM 1213Cas No. 56824-20-5
Amiprilose (SM 1213) has anti-inflammatory activity and inhibits the proliferation of a variety of hyperproliferative cell types.Amiprilose induces lymphokine-induced macrophage activation and may be used in studies of rheumatoid arthritis and psoriasis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$293-In Stock
5 mg$722-In Stock
10 mg$987-In Stock
25 mg$1,520-In Stock
50 mg$1,980-In Stock
100 mg$2,500-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.82%
ee:100%
Appearance:Oil
Color:White
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Product Introduction

Bioactivity
Description
Amiprilose (SM 1213) has anti-inflammatory activity and inhibits the proliferation of a variety of hyperproliferative cell types.Amiprilose induces lymphokine-induced macrophage activation and may be used in studies of rheumatoid arthritis and psoriasis.
In vitro
Low concentrations of Amiprilose hydrochloride (1-100 μg/ml) stimulated proliferation of mouse thymocytes and enhanced IL-1-stimulated proliferative responses in human synovial fibroblasts.[1];In all three models, Amiprilose hydrochloride at concentrations of 0.1% (w/v) or less was not toxic to fibroblasts and keratinocytes and did not interfere with the differentiation of skin equivalents and developing skin equivalents. When tested in skin equivalents, Amiprilose hydrochloride concentrations between 0.1% and 0.5% resulted in altered fibroblast morphology with large intracellular vacuoles, and concentrations above 5% were toxic. In mature skin equivalents, Amiprilose hydrochloride at concentrations of 1% to 10% affected the epidermis in addition to changes in fibroblast morphology. During differentiation, epidermal keratinocytes are also affected when 0.5% Amiprilose hydrochloride is present in developing skin equivalents.[2]
In vivo
In 8 consecutive experiments, 90 Louvain (LOU) rats and 91 Sprague-Dawley (SD) rats were immunized with chick type II collagen and administered amiprilose HCl aqueous (1 mg/mL). In LOU rats, the incidence of arthritis was 7/46 (15%) in the amiprilose HCl group compared with 16/44 (36%) in the aqueous group (P less than 0.01). In SD rats, the incidence of arthritis was 28/46 (60%) in the experimental group and 33/45 (73%) in the control group (p greater than NS), but the incidence of arthritis was significantly lower in the experimental group on days 16 and 21 (p less than 0.03). In the LOU assay, amiprilose HCl did not affect antibody titers or delayed hypersensitivity to collagen, nor did it affect the distribution of T cell subsets. At a nontoxic concentration of 1 mg/mL, amiprilose HCl reduced 3H thymidine incorporation in cultured rabbit synovial fibroblasts by 78% and resulted in the presence of numerous intracytoplasmic granules/vacuoles. amiprilose HCl system also reduced prostaglandin E2 levels in rabbit synovial cell supernatant in a dose-related manner by as much as 73% without affecting collagenase activity. collagenase activity.[5]
SynonymsSM-1213, SM1213, SM 1213
Chemical Properties
Molecular Weight305.37
FormulaC14H27NO6
Cas No.56824-20-5
SmilesO(CCCN(C)C)[C@@H]1[C@@]2([C@](O[C@@]1([C@@H](CO)O)[H])(OC(C)(C)O2)[H])[H]
Relative Density.1.21g/cm3
Storage & Solubility Information
StoragePure form: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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