Glut7 Inhibitors belong to a class of chemical compounds that specifically target and modulate the activity of the Glut7 protein, a member of the glucose transporter family. Glut7, short for glucose transporter 7, is a transmembrane protein responsible for the transport of glucose across cellular membranes, particularly in the context of glucose metabolism and homeostasis. The primary function of Glut7 is to facilitate the uptake of glucose into cells, making it an integral component of glucose regulation in various tissues. Glut7 is primarily expressed in specific cell types, including the liver and small intestine, and its activity is tightly regulated to ensure proper glucose utilization. Glut7 Inhibitors, as the name suggests, are compounds designed to inhibit or modulate the function of Glut7, which can have implications for the control of glucose uptake and metabolism in these tissues.
Glut7 Inhibitors may vary in structure, but their commonality lies in their ability to interfere with the normal functioning of Glut7. By doing so, they can potentially influence glucose homeostasis and metabolism in a selective and controlled manner. This class of compounds may find relevance in research contexts aimed at better understanding glucose transport mechanisms, uncovering novel insights into metabolic processes, and potentially identifying new targets for the development of agents in the future. The study of Glut7 Inhibitors contributes to the broader field of molecular biology and cellular physiology, shedding light on the intricate regulatory mechanisms involved in glucose transport and metabolism.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Phloretin | 60-82-2 | sc-3548 sc-3548A | 200 mg 1 g | $64.00 $255.00 | 13 | |
Phloretin interferes with glucose transport by inhibiting the activity of various GLUT transporters. | ||||||
Wiskostatin | 253449-04-6 | sc-204399 sc-204399A sc-204399B sc-204399C | 1 mg 5 mg 25 mg 50 mg | $49.00 $124.00 $441.00 $828.00 | 4 | |
WZB117 blocks glucose uptake by inhibiting GLUT1 and could potentially inhibit GLUT7. | ||||||
STF 31 | 724741-75-7 | sc-364692 | 10 mg | $187.00 | 3 | |
STF-31 inhibits GLUT1 and could indirectly affect GLUT7 function due to structural similarities. | ||||||
BAY-876 | 1799753-84-6 | sc-507539 | 5 mg | $240.00 | ||
BAY-876 is a selective GLUT1 inhibitor, which may influence GLUT7 by related mechanisms. | ||||||
Cytochalasin B | 14930-96-2 | sc-3519 | 5 mg | $199.00 | 19 | |
Cytochalasin B disrupts glucose transport by binding to GLUTs, potentially affecting GLUT7. | ||||||
Ritanserin | 87051-43-2 | sc-203681 sc-203681A | 10 mg 50 mg | $89.00 $312.00 | 2 | |
Ritanserin, though primarily a 5-HT2 receptor antagonist, has been shown to inhibit glucose transporters. | ||||||
Apigenin | 520-36-5 | sc-3529 sc-3529A sc-3529B sc-3529C sc-3529D sc-3529E sc-3529F | 5 mg 100 mg 1 g 5 g 25 g 100 g 1 kg | $33.00 $214.00 $734.00 $1151.00 $2348.00 $3127.00 $5208.00 | 22 | |
Apigenin, a flavonoid, can modulate glucose uptake, potentially affecting GLUT7 activity indirectly. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
Quercetin is known to inhibit GLUTs and could have an inhibitory effect on GLUT7. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $45.00 $164.00 $200.00 $402.00 $575.00 $981.00 $2031.00 | 46 | |
Genistein inhibits tyrosine kinases and could modulate glucose transporter activity. | ||||||
Fasentin | 392721-37-8 | sc-215012 sc-215012A | 5 mg 25 mg | $128.00 $449.00 | ||
Fasentin inhibits GLUT1 and could alter GLUT7 function due to similarities in the GLUT family. | ||||||