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| Product | Description | |
|---|---|---|
| Androstenedione Impurities | Androstenedione Impurities are often utilized in the pharmaceutical industry to study and refine the synthesis of steroids, including corticosteroids and anabolic steroids. These impurities help in developing accurate quality control measures and understanding metabolic pathways associated with endocrine disorders and hormonal therapies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. |  London |
| 19-Norandrostene-3,17-dione | 1g Pack Size. Group: Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C18H24O2. CAS No. 734-32-7. Prepack ID : 59378954-1g. Molecular Weight : 272.4. |  |
| 3β-Aecetoxy-4-androsten-17-one | 3β-Aecetoxy-4-androsten-17-on (CAS# 2398-62-1 ) is a useful research chemical. Group: Pharmaceutical. CAS No. 2398-62-1. Pack Sizes: 500 mg. Product ID: B2699-008635. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| 4-Androstene-3,17-dione | 5g Pack Size. Group: Bioactive Small Molecules, Building Blocks, Research Organics & Inorganics. Formula: C19H26O2. CAS No. 63-05-8. Prepack ID : 15237310-5g. Molecular Weight : 286.41. | |
| ASP-9521 | ASP9521 is a novel, selective, orally bioavailable inhibitor of 17β-hydroxysteroid dehydrogenase type 5 (17βHSD5; AKR1C3). ASP9521 has demonstrated anti-tumour activity in in vitro and in vivo preclinical models. ASP9521 inhibited conversion of androstenedione (AD) into testosterone (T) by recombinant human or cynomolgus monkey AKR1C3 in a concentration-dependent manner. Group: Pharmaceutical. CAS No. 1126084-37-4. Pack Sizes: 100 mg. Product ID: B0084-462669. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Estrone | Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol. Group: Pharmaceutical. CAS No. 53-16-7. Pack Sizes: 50 g. Product ID: NP6101. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
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