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Sandacanol
🥰Excellent
Catalog No. T36898Cas No. 28219-61-6
Alias Sandranol, 2-Ethyl-4-(2,2,3-trimethylcyclopent-3-en-yl)-but-2-en-1-ol
Sandacanol（Sandranol） is a selective olfactory receptor (OR10H1) agonist. Sandacanol can induce cell cycle arrest and partial apoptosis in bladder cancer cells, and can reduce cell migration rate and proliferation rate.
Sandacanol
🥰Excellent
Purity: 99.59%
Catalog No. T36898Alias Sandranol, 2-Ethyl-4-(2,2,3-trimethylcyclopent-3-en-yl)-but-2-en-1-olCas No. 28219-61-6
Sandacanol（Sandranol） is a selective olfactory receptor (OR10H1) agonist. Sandacanol can induce cell cycle arrest and partial apoptosis in bladder cancer cells, and can reduce cell migration rate and proliferation rate.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 25 mg | $38 | In Stock | |
| 50 mg | $52 | In Stock | |
| 100 mg | $72 | In Stock | |
| 500 mg | $170 | In Stock |
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Purity:99.59%
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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 | Sandacanol（Sandranol） is a selective olfactory receptor (OR10H1) agonist. Sandacanol can induce cell cycle arrest and partial apoptosis in bladder cancer cells, and can reduce cell migration rate and proliferation rate. |
| In vitro | Sandranol increases cAMP levels in a concentration-dependent manner, reduces cAMP levels by inhibiting adenylate cyclase, and triggers an increase in intracellular Ca2+ concentration. Treatment with Sandranol (50-700μM; 24 or 48 hours) significantly reduces cell viability, proliferation, and migration, and induces limited apoptosis [1]. |
| Alias | Sandranol, 2-Ethyl-4-(2,2,3-trimethylcyclopent-3-en-yl)-but-2-en-1-ol |
| Molecular Weight | 208.34 |
| Formula | C14H24O |
| Cas No. | 28219-61-6 |
| Smiles | OCC(=CCC1CC=C(C)C1(C)C)CC |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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(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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