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ANI-7

Catalog No.GC39284 Copy One-Click Copy Product Info

ANI-7 es un activador de la vÍa del receptor de hidrocarburos de arilo (AhR). ANI-7 inhibe el crecimiento de mÚltiples células cancerosas e inhibe potente y selectivamente el crecimiento de células de cÁncer de mama MCF-7 con un GI50 de 0,56 μM. ANI-7 induce monooxigenasas que metabolizan CYP1 mediante la activaciÓn de la vÍa AhR, y también induce daÑo en el ADN, activaciÓn del punto de control de la quinasa 2 (Chk2), detenciÓn del ciclo celular en fase S y muerte celular en lÍneas celulares de cÁncer de mama sensibles.

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

ANI-7 Chemical Structure

Cas No.: 931417-26-4

Tamaño Precio Disponibilidad Cantidad
10mM (in 1mL DMSO)
69,00 $
Disponible
5mg
63,00 $
Disponible
10mg
108,00 $
Disponible
50mg
342,00 $
Disponible
100mg
522,00 $
Disponible

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Sample solution is provided at 25 µL, 10mM.



Description of ANI-7

ANI-7 is an activator of aryl hydrocarbon receptor (AhR) pathway. ANI-7 inhibits the growth of multiple cancer cells, and potently and selectively inhibits the growth of MCF-7 breast cancer cells with a GI50 of 0.56 μM. ANI-7 induces CYP1-metabolizing mono-oxygenases by activating AhR pathway, and also induces DNA damage, checkpoint Kinase 2 (Chk2) activation, S-phase cell cycle arrest, and cell death in sensitive breast cancer cell lines[1][2][3].

[1]. ilbert J, et al. (Z)-2-(3,4-Dichlorophenyl)-3-(1H-Pyrrol-2-yl)Acrylonitrile Exhibits Selective Antitumor Activity in Breast Cancer Cell Lines via the Aryl Hydrocarbon Receptor Pathway. Mol Pharmacol. 2018 Feb;93(2):168-177. [2]. Baker JR, et al. Dichlorophenylacrylonitriles as AhR Ligands That Display Selective Breast Cancer Cytotoxicity in vitro. ChemMedChem. 2018 Jul 18;13(14):1447-1458. [3]. Mark Tarleton, et al. Library synthesis and cytotoxicity of a family of 2-phenylacrylonitriles and discovery of an estrogen dependent breast cancer lead compound.  Medicinal Chemistry Communication. January 20112. (1):31-37.

Chemical Properties of ANI-7

Cas No. 931417-26-4 SDF
Canonical SMILES ClC1=CC(/C(C#N)=C/C2=CC=CN2)=CC=C1Cl
Formula C13H8Cl2N2 M.Wt 263.12
Solubility DMSO: 20.83 mg/mL (79.17 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 ANI-7

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 3.8005 mL 19.0027 mL 38.0055 mL
5 mM 760.1 μL 3.8005 mL 7.6011 mL
10 mM 380.1 μL 1.9003 mL 3.8005 mL
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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 ANI-7

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

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