الصفحة الرئيسية>>Signaling Pathways>> Angiogenesis>> BTK>>JNJ-64264681

JNJ-64264681

رقم الكتالوجGC73427

JNJ-64264681 هو مثبط تساهمي قوي، نشط عن طريق الفم، انتقائي وغير قابل للعكس.

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JNJ-64264681 التركيب الكيميائي

Cas No.: 2101524-34-7

الحجم السعر المخزون الكميّة
5 mg
81٫00
متوفر
10 mg
122٫00
متوفر
25 mg
239٫00
متوفر
50 mg
392٫00
متوفر

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مراجعات العميل

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  • GlpBio Citations

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Sample solution is provided at 25 µL, 10mM.

Description of JNJ-64264681

JNJ-64264681 is a potent, orally active, selective and irreversible covalent BTK inhibitor. JNJ-64264681 exhibits good pharmacokinetic characteristics and can be used for cancer and autoimmune diseases research.

References:
[1]. Mark S Tichenor, et al. Discovery of JNJ-64264681: A Potent and Selective Covalent Inhibitor of Bruton's Tyrosine Kinase. J Med Chem. 2022 Nov 10;65(21):14326-14336.

Chemical Properties of JNJ-64264681

Cas No. 2101524-34-7 SDF
Formula C27H30N6O3S M.Wt 518.63
الذوبان DMSO : 100 mg/mL (192.82 mM; Need ultrasonic) Storage -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 JNJ-64264681

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 1.9282 mL 9.6408 mL 19.2816 mL
5 mM 0.3856 mL 1.9282 mL 3.8563 mL
10 mM 0.1928 mL 0.9641 mL 1.9282 mL
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In vivo Formulation Calculator (Clear solution) of JNJ-64264681

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

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Working concentration: mg/ml;

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.

Product Documents

Quality Control & SDS

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

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