CSH1 inhibitors represent a specific class of compounds that target **CSH1** (also known as Cystathionine beta-synthase), an enzyme that plays a pivotal role in the transsulfuration pathway, which is essential for cysteine biosynthesis. CSH1 catalyzes the condensation of homocysteine and serine to form cystathionine, which is subsequently converted to cysteine. This process is critical for maintaining cellular redox balance, synthesizing glutathione, and regulating sulfide metabolism. The regulation of CSH1 activity is of particular interest, as it has implications in metabolic pathways related to oxidative stress and amino acid homeostasis.
Inhibitors of CSH1 function by interfering with its enzymatic activity, thereby affecting the overall flux of the transsulfuration pathway. By limiting the production of cystathionine and subsequently cysteine, these compounds can alter the concentrations of key metabolites involved in cellular signaling and stress responses. The exploration of CSH1 inhibitors offers insights into the mechanistic underpinnings of metabolic regulation and how variations in sulfur amino acid metabolism can influence various physiological and biochemical processes. Moreover, CSH1 inhibitors provide researchers with valuable tools to investigate the enzyme's role in different biological contexts, such as cellular adaptation to oxidative stress or metabolic alterations. This understanding can lead to a deeper appreciation of the complexities of amino acid metabolism and its integration with broader metabolic networks.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Mifepristone | 84371-65-3 | sc-203134 | 100 mg | $61.00 | 17 | |
This glucocorticoid receptor antagonist potentially inhibits CSH1 by blocking the hormonal signals required for its expression in placental tissue. | ||||||
Ketoconazole | 65277-42-1 | sc-200496 sc-200496A | 50 mg 500 mg | $63.00 $265.00 | 21 | |
An antifungal agent that inhibits steroid synthesis, which may indirectly reduce CSH1 levels by altering hormonal balances during pregnancy. | ||||||
Trilostane | 13647-35-3 | sc-208469 sc-208469A | 10 mg 100 mg | $228.00 $1217.00 | 2 | |
A steroidogenesis inhibitor that may decrease CSH1 expression by reducing the synthesis of placental hormones. | ||||||
Letrozole | 112809-51-5 | sc-204791 sc-204791A | 25 mg 50 mg | $87.00 $147.00 | 5 | |
An aromatase inhibitor that may indirectly suppress CSH1 by reducing estrogen synthesis, which is crucial for placental development. | ||||||
Finasteride | 98319-26-7 | sc-203954 | 50 mg | $105.00 | 3 | |
By inhibiting 5α-reductase, this compound may lower dihydrotestosterone levels, potentially affecting the hormone regulation of CSH1 expression. | ||||||
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 | |
An androgen receptor antagonist that could potentially decrease CSH1 expression by altering androgenic signaling in the placenta. | ||||||
Spironolactone | 52-01-7 | sc-204294 | 50 mg | $109.00 | 3 | |
This aldosterone antagonist might reduce CSH1 expression by affecting mineralocorticoid pathways in placental tissue. | ||||||
Aminoglutethimide | 125-84-8 | sc-207280 sc-207280A sc-207280B sc-207280C | 1 g 5 g 25 g 100 g | $42.00 $146.00 $541.00 $2060.00 | 2 | |
By inhibiting the synthesis of steroid hormones, this compound could indirectly reduce the expression of CSH1 in the placenta. | ||||||
Copper(II) sulfate | 7758-98-7 | sc-211133 sc-211133A sc-211133B | 100 g 500 g 1 kg | $46.00 $122.00 $189.00 | 3 | |
As a heavy metal, copper sulfate could potentially disrupt placental cellular function, thereby inhibiting CSH1 expression indirectly. | ||||||
Methimazole | 60-56-0 | sc-205747 sc-205747A | 10 g 25 g | $70.00 $112.00 | 4 | |
This thyroid inhibitor might indirectly suppress CSH1 expression by altering the maternal thyroid state during pregnancy. | ||||||