Find where to buy products from UK suppliers, including: distributors, industrial manufacturers, wholesalers, raw ingredients, bulk supplies and finished goods for sale.
Search for products or services, then visit the suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the USA.
| Product | Description | |
|---|---|---|
| 17-Methyltestosterone | 5g Pack Size. Group: Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C20H30O2. CAS No. 58-18-4. Prepack ID : 49273437-5g. Molecular Weight : 302.45. |  |
| Abarelix | Abarelix is a synthetic decapeptide and antagonist of naturally occurring gonadotropin-releasing hormone (GnRH). Abarelix directly and competitively binds to and blocks the gonadotropin releasing hormone receptor in the anterior pituitary gland, thereby inhibiting the secretion and release of luteinizing hormone (LH) and follicle stimulating hormone (FSH). In males, the inhibition of LH secretion prevents the release of testosterone. As a result, this may relieve symptoms associated with prostate hypertrophy or prostate cancer, since testosterone is required to sustain prostate growth. Check for active clinical trials or closed clinical trials using this agent. Group: Pharmaceutical. CAS No. 183552-38-7. Pack Sizes: 10 mg. Product ID: BAT-006166. Molecular formula: Custom synthesis is available. Send your inquiries for more information. |  London |
| 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 |
| Degarelix | Degarelix acetate is a reversible gonadotropin-releasing hormone receptor (GnRHR) antagonist. Degarelix reduces the secretion of luteinizing hormone (LH) and testosterone via blocking GnRHR. Degarelix can be used for the treatment of prostate cancer. Group: Pharmaceutical. CAS No. 214766-78-6. Pack Sizes: 10 mg. Product ID: BAT-010776. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Degarelix acetate hydrate | Degarelix acetate is a synthetic peptide that acts as a gonadotrophin-releasing hormone (GnRH) antagonist. Degarelix targets GnRH receptors in the pituitary gland, resulting in reduction of luteinizing hormone (LH), follicle-stimulating hormone (FSH) and suppression of testosterone. Group: Pharmaceutical. CAS No. 934246-14-7. Pack Sizes: 100 mg. Product ID: BAT-010777. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Finasteride | Finasteride (INN, USAN, BAN) (brand names Proscar, and Propecia by Merck, among other generic names; former developmental code name MK-906) is a drug used for the treatment of benign prostatic hyperplasia (BPH) and male pattern baldness (MPB). It is a type II and type III 5α-reductase inhibitor; 5α-reductase, an enzyme, converts testosterone to dihydrotestosterone (DHT). Uses: Api. Group: Pharmaceutical. CAS No. 98319-26-7. Pack Sizes: 50 g. Product ID: NP3378. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Finasteride EP Impurity B | An intermediate in the synthesis of Finasteride. Finasteride is a 4-azasteroid analog of testosterone that competitively blocks type II 5α-reductase activity with 100-fold greater affinity than for the type I enzyme. Group: Pharmaceutical. CAS No. 103335-41-7. Pack Sizes: 100 mg. Product ID: B2694-255935. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| FOXO4-DRI | FOXO4-DRI is a peptide acting as a specific FOXO4 blocker. It has been demonstrated to alleviate age-related testosterone secretion insufficiency by targeting senescent Leydig cells in aged mice. Group: Pharmaceutical. Pack Sizes: 1 mg. Product ID: BAT-006150. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Nilutamide | Nilutamide is a non-steroidal and silent antiandrogen that binds to androgen receptors and also inhibits androgen biosynthesis in vitro. In rats in vivo it inhibits androgen-induced prostate weight increase and inhibits negative androgen-dependent gonadotropin feedback leading to an increase in luteinising hormone and testosterone. Uses: Antineoplastic agents. Group: Pharmaceutical. CAS No. 63612-50-0. Pack Sizes: 10 g. Product ID: B2693-465325. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| ODM-201 | ODM-201 is a new-generation, potent and selective androgen receptor (AR) inhibitor which is potential useful for treatment of castration-resistant prostate cancer (CRPC). ODM-201 is a full and high-affinity AR antagonist that, similar to second-generation antiandrogens enzalutamide and ARN-509, inhibits testosterone-induced nuclear translocation of AR. Group: Pharmaceutical. CAS No. 1297538-32-9. Pack Sizes: 100 mg. Product ID: B0084-470833. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Paeoniflorin | Paeoniflorin is a herbal constituent extracted from the root of Paeonia albiflora Pall. Paeoniflorin has antiandrogenic properties. Paeoniflorin inhibits the production of testosterone and promotes the activity of aromatase-the enzyme that converts testosterone into estrogen. Uses: Antiandrogenic properties. Group: Pharmaceutical. CAS No. 23180-57-6. Pack Sizes: 500 mg. Product ID: NP4515. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Secalciferol | Secalciferol is a metabolite of Vitamin D, a possibly anti-inflammatory steroid which is involved in bone ossification. lt mediates calcium and phosphorus homeostasis and inhibits calcium channels in osteosarcoma cells via suppressing the effects of 1α, 25-dihydroxyvitamin D3 and testosterone. lt also can decrease the abundance of p53 and Pi-induced cytochrome c translocation. Uses: Bone density conservation agents. Group: Pharmaceutical. CAS No. 55721-11-4. Pack Sizes: 1 mg. Product ID: B0084-375020. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
Our database is helping our users find suppliers everyday.
