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Apoptosis inducer 43

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Catalog No. T212266

Apoptosis inducer43 is an agent that promotes apoptosis. It has the capability to induce apoptosis in HCT116 cells, cause cell cycle arrest at the SubG0-G1 phase, trigger secondary necrosis, and increase the expression of caspase-3, p53, and Bax/Bcl-2. This compound also inhibits tumor growth in solid Ehrlich carcinoma (SEC) mouse models. Apoptosis inducer43 is applicable for research in colon cancer, leukemia, non-small cell lung cancer, and other cancers.

Apoptosis inducer 43

Apoptosis inducer 43

😃Good
Catalog No. T212266
Apoptosis inducer43 is an agent that promotes apoptosis. It has the capability to induce apoptosis in HCT116 cells, cause cell cycle arrest at the SubG0-G1 phase, trigger secondary necrosis, and increase the expression of caspase-3, p53, and Bax/Bcl-2. This compound also inhibits tumor growth in solid Ehrlich carcinoma (SEC) mouse models. Apoptosis inducer43 is applicable for research in colon cancer, leukemia, non-small cell lung cancer, and other cancers.
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Product Introduction

Bioactivity
Description
Apoptosis inducer43 is an agent that promotes apoptosis. It has the capability to induce apoptosis in HCT116 cells, cause cell cycle arrest at the SubG0-G1 phase, trigger secondary necrosis, and increase the expression of caspase-3, p53, and Bax/Bcl-2. This compound also inhibits tumor growth in solid Ehrlich carcinoma (SEC) mouse models. Apoptosis inducer43 is applicable for research in colon cancer, leukemia, non-small cell lung cancer, and other cancers.
In vitro
Apoptosis inducer 43 (Compound 5f) at a concentration of 10 μM demonstrates anticancer activity, achieving an average inhibition rate of over 80% in NCI 60 cell lines, which include leukemia, non-small cell lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, renal cancer, prostate cancer, and breast cancer, with an average GI50 below 5 μM. Additionally, when used at 1.79-10 μM for 24 hours, it induces cell cycle arrest in the HCT-116 cells, primarily at the SubG0/G1 phase, and triggers apoptosis.
In vivo
Compound 5f, known as Apoptosis inducer 43, administered intraperitoneally at 10 mg/kg three times a week for 14 days, demonstrated antitumor activity in a solid Ehrlich carcinoma (SEC) mouse model.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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