DHRS7 inhibitors belong to a class of small molecules that are designed to selectively target and modulate the activity of the enzyme DHRS7, or Dehydrogenase/Reductase SDR Family Member 7. DHRS7 is a member of the short-chain dehydrogenase/reductase (SDR) family of enzymes, which are involved in various biochemical pathways, particularly those related to steroid and lipid metabolism. The primary function of DHRS7 is to catalyze the reduction of certain ketosteroids, such as dehydroepiandrosterone (DHEA) and androstenedione, to their corresponding hydroxy steroids, which are essential intermediates in the synthesis of bioactive steroid hormones, including androgens and estrogens.
DHRS7 inhibitors are designed to interfere with the enzymatic activity of DHRS7, primarily by binding to its active site or allosteric regions. By doing so, these inhibitors disrupt the normal enzymatic conversion of ketosteroids to hydroxy steroids, effectively reducing the production of downstream steroid hormones. This class of compounds is vital in the context of steroid hormone regulation, as it enables precise control over the biosynthesis of androgens and estrogens, which play pivotal roles in various physiological processes, including sexual development and secondary sexual characteristics. The modulation of DHRS7 activity through inhibitors provides valuable insights into the intricate mechanisms governing steroid hormone biosynthesis and metabolism, contributing to a deeper understanding of hormone-related disorders and strategies for their management. Researchers continue to explore the development of DHRS7 inhibitors and their applications in elucidating the complexities of steroid hormone regulation and their implications in various physiological contexts.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Finasteride | 98319-26-7 | sc-203954 | 50 mg | $105.00 | 3 | |
Finasteride inhibits DHRS7 by interfering with the conversion of testosterone to dihydrotestosterone (DHT), a potent androgen. | ||||||
Bicalutamide | 90357-06-5 | sc-202976 sc-202976A | 100 mg 500 mg | $42.00 $146.00 | 27 | |
Bicalutamide is an androgen receptor antagonist that indirectly inhibits DHRS7 by blocking the androgen receptor, reducing the availability of substrates for DHRS7. | ||||||
Abiraterone | 154229-19-3 | sc-460288 | 10 mg | $276.00 | ||
Abiraterone inhibits DHRS7 by targeting the enzyme CYP17A1, which is involved in androgen biosynthesis. By suppressing CYP17A1, it decreases the substrate for DHRS7, lowering androgen levels. | ||||||
Dutasteride | 164656-23-9 | sc-207600 | 10 mg | $167.00 | 2 | |
Dutasteride inhibits DHRS7 by blocking both Type I and Type II 5α-reductase enzymes, which convert testosterone to DHT. | ||||||
MDV3100 | 915087-33-1 | sc-364354 sc-364354A | 5 mg 50 mg | $245.00 $1051.00 | 7 | |
MDV3100 is an androgen receptor antagonist that indirectly inhibits DHRS7 by interfering with androgen receptor signaling, reducing the availability of substrates for DHRS7. | ||||||
Ketoconazole | 65277-42-1 | sc-200496 sc-200496A | 50 mg 500 mg | $63.00 $265.00 | 21 | |
Ketoconazole inhibits DHRS7 by blocking several enzymes involved in androgen synthesis, including CYP17A1 and 17β-HSD3. | ||||||
Spironolactone | 52-01-7 | sc-204294 | 50 mg | $109.00 | 3 | |
Spironolactone is an aldosterone receptor antagonist that can indirectly inhibit DHRS7 by modulating steroid hormone levels, including androgens. | ||||||
Flutamide | 13311-84-7 | sc-204757 sc-204757A sc-204757D sc-204757B sc-204757C | 1 g 5 g 25 g 500 g 1 kg | $47.00 $156.00 $171.00 $525.00 $941.00 | 4 | |
Flutamide inhibits DHRS7 by acting as a competitive antagonist at androgen receptors, reducing androgen binding and signaling. | ||||||
Cyproterone Acetate | 427-51-0 | sc-204703 sc-204703A | 100 mg 250 mg | $60.00 $199.00 | 5 | |
Cyproterone acetate inhibits DHRS7 by acting as a competitive antagonist at androgen receptors and also by suppressing gonadotropin secretion. | ||||||