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CID 16020046

رقم الكتالوجGC35694 Copy One-Click Copy Product Info

CID 16020046 هو مضاد GPR55 قوي وانتقائي ويثبط النشاط التكويني لـ GPR55 مع IC50 من 0.15 ميكرومترCID 16020046 يمنع إشارات Ca2 + بوساطة GPR55 و الفسفرة ERK1 / 2 بوساطة GPR55يقلل CID 16020046 من التئام الجروح في الخلايا البطانية ويشارك في تنظيم وظيفة الصفائح الدموية

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CID 16020046 التركيب الكيميائي

Cas No.: 834903-43-4

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
59٫00
متوفر
1mg
27٫00
متوفر
5mg
63٫00
متوفر
10mg
90٫00
متوفر
25mg
180٫00
متوفر
50mg
261٫00
متوفر
100mg
378٫00
متوفر

Tel:(909) 407-4943 Email: sales@glpbio.com


مراجعات العميل

بناء على آراء العملاء.

Sample solution is provided at 25 µL, 10mM.



Description of CID 16020046

CID 16020046 is a potent and selective GPR55(LPI receptor) antagonist; inhibitsGPR55 constitutive activity with IC50 of 0.15 uM.IC50 value: 0.15 uM [1]Target: GPR55 antagonistIn yeast cells expressing human GPR55, CID16020046 antagonized agonist-induced receptor activation. In human embryonic kidney(HEK293) cells stably expressing human GPR55, the compound behaved as an antagonist on LPI-mediated Ca2+ release and extracellular signal-regulated kinases activation, but not in HEK293 cells expressing cannabinoid receptor 1 or 2.CID16020046 concentration dependently inhibited LPI-induced activation of nuclear factor of activated T-cells (NFAT), nuclear factor k of activated B cells (NF-kB) and serum response element, translocation of NFAT and NF-kB, and GPR55 internalization. It reduced LPI-induced wound healing in primary human lung microvascular endothelial cells and reversed LPI-inhibited platelet aggregation.

[1]. Kargl J, et al. A selective antagonist reveals a potential role of G protein-coupled receptor 55 in platelet and endothelial cell function. J Pharmacol Exp Ther. 2013 Jul;346(1):54-66.

Chemical Properties of CID 16020046

Cas No. 834903-43-4 SDF
Canonical SMILES O=C(N1C(C=C2)=CC=C2C(O)=O)C(NN=C3C4=CC=C(C)C=C4)=C3C1C5=CC(O)=CC=C5
Formula C25H19N3O4 M.Wt 425.44
الذوبان DMSO: 100 mg/mL (235.05 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 CID 16020046

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.3505 mL 11.7525 mL 23.5051 mL
5 mM 470.1 μL 2.3505 mL 4.701 mL
10 mM 235.1 μL 1.1753 mL 2.3505 mL
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In vivo Formulation Calculator (Clear solution) of CID 16020046

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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 saline, 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

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Review for CID 16020046

Average Rating: 5 ★★★★★ (Based on Reviews and 3 reference(s) in Google Scholar.)

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