Connexin 46 inhibitors are a class of chemical compounds that specifically target and inhibit the function of connexin 46, a protein encoded by the GJA3 (gap junction protein alpha 3) gene. Connexin 46 is a member of the connexin family of proteins, which are integral components of gap junctions. These gap junctions are specialized intercellular channels that allow for direct communication between adjacent cells by facilitating the passage of ions, metabolites, and other small molecules. Connexin 46, in particular, is predominantly expressed in the lens of the eye, where it plays a crucial role in maintaining lens transparency and homeostasis. By forming gap junction channels, connexin 46 enables the diffusion of essential nutrients and the removal of metabolic waste products, ensuring proper cellular function within the lens.
Structurally, connexin 46 inhibitors are diverse and can include small molecules or peptides specifically designed to interfere with the assembly, opening, or functioning of connexin 46 channels. These inhibitors can bind to specific sites on the connexin 46 protein, preventing it from forming functional gap junctions or blocking the channels once they are formed. This inhibition can disrupt intercellular communication and alter the homeostatic balance maintained by gap junctions in tissues expressing connexin 46. The study of connexin 46 inhibitors provides valuable insights into the mechanisms of gap junction regulation and the role of connexin 46 in cellular communication and tissue homeostasis. By understanding how these inhibitors affect connexin 46 function, researchers can explore the broader implications of gap junction modulation on cellular processes, including ion transport, metabolic coordination, and overall tissue health. Research into these inhibitors thus contributes to a deeper understanding of the physiological and biochemical pathways influenced by gap junctions and connexin 46 specifically.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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2-APB | 524-95-8 | sc-201487 sc-201487A | 20 mg 100 mg | ¥305.00 ¥587.00 | 37 | |
影响细胞内钙离子水平,从而间接调节连接蛋白的功能。 | ||||||
Mefenamic acid | 61-68-7 | sc-205380 sc-205380A | 25 g 100 g | ¥1173.00 ¥2302.00 | 6 | |
与氟灭酸类似,可破坏间隙连接。 | ||||||
Quinidine | 56-54-2 | sc-212614 | 10 g | ¥1151.00 | 3 | |
奎宁的立体异构体,也能抑制间隙连接的通信。 | ||||||
Carbenoxolone disodium | 7421-40-1 | sc-203868 sc-203868A sc-203868B sc-203868C | 1 g 5 g 10 g 25 g | ¥508.00 ¥2223.00 ¥3960.00 ¥8563.00 | 1 | |
卡苯磺酸是一种甘草亭酸衍生物,通过阻断间隙连接的细胞间通信来抑制连接蛋白43。它与连接蛋白结合并干扰通道孔的形成。非特异性间隙连接阻断剂。能抑制连接蛋白介导的间隙连接的细胞间通信。 | ||||||
18 β-Glycyrrhetinic Acid | 471-53-4 | sc-205573B sc-205573 sc-205573A sc-205573C sc-205573D | 1 g 5 g 10 g 25 g 100 g | ¥316.00 ¥609.00 ¥959.00 ¥1455.00 ¥3531.00 | 3 | |
18α-甘草亭酸与卡苯磺酸类似,是甘草亭酸的衍生物。它通过阻断间隙连接沟通、影响通道孔的形成来抑制连接蛋白。另一种非特异性间隙连接抑制剂。可减少涉及连接蛋白的间隙连接沟通。 | ||||||
1-Heptanol | 111-70-6 | sc-237561 | 100 ml | ¥1252.00 | ||
庚醇是一种脂肪醇,通过阻断间隙连接的细胞间通信来抑制连接蛋白43。这种非特异性抑制剂会影响细胞膜的脂质双层,破坏间隙连接通道的功能。 | ||||||
1-Octanol | 111-87-5 | sc-255858 | 1 ml | ¥508.00 | ||
辛醇的作用与庚醇类似。它是一种脂肪醇,会破坏细胞膜的脂质双层,从而抑制间隙连接通道的功能,包括连接蛋白的功能。 | ||||||
Quinine | 130-95-0 | sc-212616 sc-212616A sc-212616B sc-212616C sc-212616D | 1 g 5 g 10 g 25 g 50 g | ¥869.00 ¥1151.00 ¥1839.00 ¥3915.00 ¥6329.00 | 1 | |
奎宁是一种天然生物碱,可抑制连接蛋白。它通过与通道孔相互作用来阻断间隙连接的细胞间沟通,从而阻止离子和小分子的交换。一种可非特异性抑制间隙连接沟通的生物碱。 | ||||||
Probenecid | 57-66-9 | sc-202773 sc-202773A sc-202773B sc-202773C | 1 g 5 g 25 g 100 g | ¥305.00 ¥429.00 ¥1106.00 ¥3069.00 | 28 | |
丙磺舒是一种尿酸排泄剂,可抑制连接蛋白43。它阻断半通道,破坏细胞间通讯。已知可阻断某些连接蛋白半通道,并可能间接影响连接蛋白59。 | ||||||
Lanthanum(III) chloride | 10099-58-8 | sc-257661 | 10 g | ¥993.00 | ||
氯化镧是一种间隙连接阻断剂,通过与通道孔相互作用抑制连接蛋白。它阻止离子和其他小分子的交换,破坏间隙连接通讯。 |