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Epiandrosterone
🥰Excellent
Catalog No. T2195Cas No. 481-29-8
Alias trans-Androsterone, iso-Androsterone, EpiA, 3β-Androsterone
Epiandrosterone (EpiA) is a dehydroepiandrosterone metabolite and a precursor of testosterone and estradiol with hypolipidemic and anabolic property.
Epiandrosterone
🥰Excellent
Purity: 99.88%
Catalog No. T2195Alias trans-Androsterone, iso-Androsterone, EpiA, 3β-AndrosteroneCas No. 481-29-8
Epiandrosterone (EpiA) is a dehydroepiandrosterone metabolite and a precursor of testosterone and estradiol with hypolipidemic and anabolic property.
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CitedSelect Batch
Purity:99.88%
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With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.Product Introduction
Bioactivity
Chemical Properties
| Description | Epiandrosterone (EpiA) is a dehydroepiandrosterone metabolite and a precursor of testosterone and estradiol with hypolipidemic and anabolic property. |
| In vivo | Epiandrosterone is only a weak androgen, but is widely recognized to inhibit the pentose phosphate pathway and reduce intracellular levels of reduced coenzyme II.Epiandrosterone is formed in peripheral tissues, released into the circulation, and ultimately excreted in the urine.Epiandrosterone reduces NO-induced relaxation of the pulmonary arteries, and, while Epiandrosterone acts on isolated lungs to inhibit angiotensin II- and hypoxia-induced vasoconstriction and to relax isolated pulmonary arteries preconstricted by KCl. |
| Alias | trans-Androsterone, iso-Androsterone, EpiA, 3β-Androsterone |
| Molecular Weight | 290.44 |
| Formula | C19H30O2 |
| Cas No. | 481-29-8 |
| Smiles | C[C@]12CC[C@@H](C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2([C@H]1CCC2=O)C)O |
| Relative Density. | 1.085 g/cm3 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||||||||||||
| Solubility Information | H2O: <1 mg/mL Ethanol: 54 mg/mL (185.92 mM), Sonication is recommended. DMSO: 28 mg/mL (96.41 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||||||||||||
DMSO/Ethanol
Ethanol
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For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
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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