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EIT hydrobromide

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Catalog No. T22761Cas No. 1071-37-0
Alias S-Ethylisothiourea hydrobromide, 2-Ethyl-2-thiopseudourea hydrobromide

EIT hydrobromide (S-Ethylisothiourea hydrobromide) is an iNOS inhibitor.

EIT hydrobromide

EIT hydrobromide

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Purity: 99.81%
Catalog No. T22761Alias S-Ethylisothiourea hydrobromide, 2-Ethyl-2-thiopseudourea hydrobromideCas No. 1071-37-0
EIT hydrobromide (S-Ethylisothiourea hydrobromide) is an iNOS inhibitor.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 g$294-6 weeks4-6 weeks
1 mL x 10 mM (in DMSO)$50-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:99.81%
Appearance:Solid
Color:White
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Product Introduction

EIT hydrobromide AI Summary
EIT hydrobromide exhibits a diverse range of bioactivities. It induces the erasure of genomic imprints with a potency of 6309.6 nM and inhibits several enzymes, including Tyrosyl-DNA Phosphodiesterase (TDP1) with a potency of 3548.1 nM, Bloom's syndrome helicase (BLM) with a potency of 2.8 nM, GCN5L2 with a potency of 31622.8 nM, and Human Apurinic/apyrimidinic Endonuclease 1 (APE1) with a potency of 12589.3 nM. Additionally, it serves as a differential inhibitor of proliferation of Plasmodium falciparum with a potency of 22387.2 nM and acts as a delayed death inhibitor of the malarial parasite plastid with a potency of 3696.4 nM. It also inhibits binding or entry into cells for Marburg Virus with a potency of 23099.9 nM. In terms of antiviral activity, EIT hydrobromide inhibits SARS-CoV-2 induced cytotoxicity in Caco-2 cells by 25.71% at 10 µM after 48 hours and inhibits the SARS-CoV-2 3CL-Pro protease by 11.88% at 20 µM. However, the inhibition rate in VERO-6 cells is lower, showing 0.41% inhibition at 10 µM after 48 hours..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
EIT hydrobromide (S-Ethylisothiourea hydrobromide) is an iNOS inhibitor.
SynonymsS-Ethylisothiourea hydrobromide, 2-Ethyl-2-thiopseudourea hydrobromide
Chemical Properties
Molecular Weight185.09
FormulaC3H9BrN2S
Cas No.1071-37-0
SmilesBr.CCSC(N)=N
Relative Density.1.19 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 60 mg/mL (324.17 mM), Sonication is recommended.
H2O: ≥7.85 mg/mL, Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM5.4028 mL27.0139 mL54.0278 mL270.1389 mL
5 mM1.0806 mL5.4028 mL10.8056 mL54.0278 mL
10 mM0.5403 mL2.7014 mL5.4028 mL27.0139 mL
20 mM0.2701 mL1.3507 mL2.7014 mL13.5069 mL
50 mM0.1081 mL0.5403 mL1.0806 mL5.4028 mL
100 mM0.0540 mL0.2701 mL0.5403 mL2.7014 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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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