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Seratrodast

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Catalog No. T0212Cas No. 112665-43-7
Alias ABT-001, AA 2414

Seratrodast (ABT-001) (INN), a thromboxane A2 (TXA2) receptor (TP receptor) antagonist, is mainly used in the therapy of asthma. It was the first TP receptor antagonist developed as an anti-asthmatic drug and attained marketing qualification in Japan in 1997.

Seratrodast

Seratrodast

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Purity: 99.69%
Catalog No. T0212Alias ABT-001, AA 2414Cas No. 112665-43-7
Seratrodast (ABT-001) (INN), a thromboxane A2 (TXA2) receptor (TP receptor) antagonist, is mainly used in the therapy of asthma. It was the first TP receptor antagonist developed as an anti-asthmatic drug and attained marketing qualification in Japan in 1997.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$34In StockIn Stock
25 mg$61In StockIn Stock
50 mg$85In StockIn Stock
100 mg$123In StockIn Stock
500 mg$297-In Stock
1 mL x 10 mM (in DMSO)$37In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.69%
Appearance:Solid
Color:White
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Product Introduction

Seratrodast AI Summary
Seratrodast exhibits a broad range of bioactivities across multiple assays and targets. It shows potent inhibition of U-46619-induced contraction of guinea pig lung membranes (Kd = 5.129 nM) and U-44069-induced aggregation of guinea pig platelets (IC50 = 350.0 nM). Demonstrating significant efficacy in various biological systems, it effectively inhibits U-44,069-induced contraction of rabbit aorta and platelet aggregation, and possesses anti-bronchoconstriction properties validated by in vivo studies. Despite this, its inhibition effects on the vitamin D receptor, malarial parasite plastid, USP1/UAF1, and others, display significantly lower potency, most notably with USP1/UAF1 (89,125.1 nM) and vitamin D receptor (44,668.4 nM). Seratrodast shows moderate metabolic stability with high lipophilicity (LogD7.4 = 2.48), an intrinsic clearance of 85.0 uL.min-1.(10^6 cells)-1 in rat hepatocytes, and 3.0 mL.min-1.g-1 in human liver microsomes. It exhibits a high plasma protein binding of 98.0%. It also acts as an inhibitor of human BSEP (IC50 < 14,310.0 nM) and shows mixed results on cell viability across various cell types, such as HEK293T and U2OS cells. While exhibiting some antiviral activities against SARS-CoV-2 and Ebola Virus with low and mixed inhibitory effects, Seratrodast also demonstrates HDAC6 inhibition (36.44% inhibition in enzyme assay). Additionally, it affects the thermal stability of various protein domains and has significant, though variable, impacts on GPCR beta-arrestin recruitment assays across multiple targets. Overall, Seratrodast has significant potential in anti-inflammatory and anti-contraction applications with a diverse range of biological activities, though with relatively lower potency against several enzymes and receptors..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Seratrodast (ABT-001) (INN), a thromboxane A2 (TXA2) receptor (TP receptor) antagonist, is mainly used in the therapy of asthma. It was the first TP receptor antagonist developed as an anti-asthmatic drug and attained marketing qualification in Japan in 1997.
SynonymsABT-001, AA 2414
Chemical Properties
Molecular Weight354.44
FormulaC22H26O4
Cas No.112665-43-7
SmilesC(CCCCCC(O)=O)(C1=C(C)C(=O)C(C)=C(C)C1=O)C2=CC=CC=C2
Relative Density.1.14 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 50 mg/mL (141.07 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Saline: 2.5 mg/mL (7.05 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8214 mL14.1068 mL28.2135 mL141.0676 mL
5 mM0.5643 mL2.8214 mL5.6427 mL28.2135 mL
10 mM0.2821 mL1.4107 mL2.8214 mL14.1068 mL
20 mM0.1411 mL0.7053 mL1.4107 mL7.0534 mL
50 mM0.0564 mL0.2821 mL0.5643 mL2.8214 mL
100 mM0.0282 mL0.1411 mL0.2821 mL1.4107 mL

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In Vivo Formulation Calculator (Clear solution)

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:
% DMSO
%
% Tween 80
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