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Elimusertib (BAY-1895344) hydrochloride (Synonyms: BAY-1895344 HCl)

Catalog No.GC25372

Elimusertib (BAY-1895344) hydrochloride is a potent, highly selective and orally available ATR inhibitor with an IC50 of 7 nM.

Products are for research use only. Not for human use. We do not sell to patients.

Elimusertib (BAY-1895344) hydrochloride Chemical Structure

Tamaño Precio Disponibilidad Cantidad
10mM (1mL in DMSO)
166,00 $
Disponible
2mg
67,00 $
Disponible
5mg
109,00 $
Disponible
25mg
327,00 $
Disponible

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Sample solution is provided at 25 µL, 10mM.

Description of Elimusertib (BAY-1895344) hydrochloride

Elimusertib (BAY-1895344) hydrochloride is a potent, highly selective and orally available ATR inhibitor with an IC50 of 7 nM.

In vitro, BAY 1895344 is shown to be a very potent and highly selective ATR inhibitor (IC50 = 7 nM), which potently inhibits proliferation of a broad spectrum of human tumor cell lines (median IC50 = 78 nM). In cellular mechanistic assays BAY 1895344 potently inhibits hydroxyurea-induced H2AX phosphorylation (IC50 = 36 nM)[1].

BAY 1895344 reveals significantly improved aqueous solubility, bioavailability across species and no activity in the hERG patch-clamp assay. It also demonstrates very promising efficacy in monotherapy in DNA damage deficient tumor models as well as combination treatment with DNA damage inducing therapies[1]. BAY 1895344 exhibits strong in vivo anti-tumor efficacy in monotherapy in a variety of xenograft models of different indications that are characterized by DDR deficiencies, inducing stable disease in ovarian and colorectal cancer or even complete tumor remission in mantle cell lymphoma models[2].

[1] Ulrich T. Luecking, et al. AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 983. [2] Antje Margret Wengner, et al. AACR; Cancer Res 2017. 77(13 Suppl):Abstract nr 836.

Chemical Properties of Elimusertib (BAY-1895344) hydrochloride

Cas No. SDF
Sinónimos BAY-1895344 HCl
Formula C20H22ClN7O M.Wt 411.89
Solubility DMSO: 82 mg/mL (199.08 mM);Water: 82 mg/mL (199.08 mM);Ethanol: 82 mg/mL (199.08 mM) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Elimusertib (BAY-1895344) hydrochloride

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.4278 mL 12.1392 mL 24.2783 mL
5 mM 0.4856 mL 2.4278 mL 4.8557 mL
10 mM 0.2428 mL 1.2139 mL 2.4278 mL
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In vivo Formulation Calculator (Clear solution) of Elimusertib (BAY-1895344) hydrochloride

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.

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Average Rating: 5 ★★★★★ (Based on Reviews and 30 reference(s) in Google Scholar.)

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