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SIRT2-IN-9
🥰Excellent
Catalog No. T62515Cas No. 522650-91-5
SIRT2-IN-9 is a selective SRIT2 inhibitor with an IC50 value of 1.3 μM.SIRT2-IN-9 inhibits the proliferation of MCF-7 breast cancer cells.SIRT2-IN-9 can be used for cancer research.
SIRT2-IN-9
🥰Excellent
Purity: 99.5%
Catalog No. T62515Cas No. 522650-91-5
SIRT2-IN-9 is a selective SRIT2 inhibitor with an IC50 value of 1.3 μM.SIRT2-IN-9 inhibits the proliferation of MCF-7 breast cancer cells.SIRT2-IN-9 can be used for cancer research.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $68 | In Stock | |
| 10 mg | $118 | In Stock | |
| 25 mg | $247 | In Stock | |
| 50 mg | $392 | In Stock | |
| 100 mg | $588 | In Stock |
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Purity:99.5%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| Description | SIRT2-IN-9 is a selective SRIT2 inhibitor with an IC50 value of 1.3 μM.SIRT2-IN-9 inhibits the proliferation of MCF-7 breast cancer cells.SIRT2-IN-9 can be used for cancer research. |
| Targets&IC50 | SIRT2:1.3 μM |
| In vitro | SIRT2-IN-9 (1-100 μM; 15 min) dose-dependently inhibits SIRT2 (IC50=1.3 μM) while also inhibiting SIRT1 and SIRT3 (IC50s >300 μM).[1] Additionally, SIRT2-IN-9 (0-50 μM; 72 h) affects the cell viability and dose-dependently inhibits the proliferation of MCF-7 breast cancer cells.[1] SIRT2-IN-9 (0-50 μM; 6 h) also impacts the acetylation of α-tubulin protein.[1] |
| Molecular Weight | 438.57 |
| Formula | C21H22N6OS2 |
| Cas No. | 522650-91-5 |
| Smiles | CCCn1c2ccccc2c2nnc(SCC(=O)Nc3nc4CCCCc4s3)nc12 |
Storage & Solubility Information
| Storage | Shipping with blue ice. | |||||||||||||||
| Solubility Information | DMSO: 4.0 mg/mL (9.2 mM), Sonication and heating to 70℃ are recommended. | |||||||||||||||
Solution Preparation Table | ||||||||||||||||
DMSO
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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:
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DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (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.
(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 DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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