Date published: 2025-9-8

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SNX16激活剂

dNT-1 activators, known chemically as compounds influencing NT5C, play a crucial role in modulating the functional activity of dNT-1, a key enzyme in nucleoside metabolism. These activators primarily act by either serving as substrates for dNT-1 or by modifying the cellular nucleotide environment, thereby influencing the enzyme's activity. Substrates like Adenosine, Inosine, Deoxyadenosine, Deoxyinosine, and Guanosine directly enhance dNT-1's enzymatic activity by serving as necessary components for its metabolic processes. These nucleosides, integral to purine and pyrimidine metabolism, are directly acted upon by dNT-1, facilitating effective nucleotide breakdown and recycling. Furthermore, compounds such as Dipyridamole and Ribavirin influence dNT-1's activity indirectly. Dipyridamole, by inhibiting nucleoside transport, increases the intracellular availability of substrates for dNT-1, while Ribavirin, a guanosine analog, may serve as an alternative substrate, affecting dNT-1's substrate specificity and metabolism.

Additional activators like Pentostatin, Mycophenolate Mofetil, and Allopurinol modulate the nucleotide pool within cells, indirectly enhancing the functional role of dNT-1. Pentostatin, an adenosine deaminase inhibitor, increases adenosine levels, thus potentially enhancing dNT-1's role in adenosine metabolism. Mycophenolate Mofetil, by inhibiting inosine monophosphate dehydrogenase, and Allopurinol, a xanthine oxidase inhibitor, alter purine metabolism pathways, impacting dNT-1's activity. Furthermore, Methotrexate and Fludarabine, through their roles as a dihydrofolate reductase inhibitor and a nucleotide analog, respectively, affect purine synthesis and nucleotide metabolism, thereby indirectly influencing dNT-1 activity.

関連項目

Items 1 to 10 of 11 total

展示:

产品名称CAS #产品编号数量价格应用排名

PMA

16561-29-8sc-3576
sc-3576A
sc-3576B
sc-3576C
sc-3576D
1 mg
5 mg
10 mg
25 mg
100 mg
¥451.00
¥1455.00
¥2369.00
¥5528.00
¥10481.00
119
(6)

PMA是一种二酰基甘油类似物,可激活蛋白激酶C(PKC),后者在囊泡运输中发挥作用。激活PKC可以增强内体循环,SNX16在内体中发挥作用,从而可能提高SNX16的功能活性。

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
¥745.00
¥2471.00
¥4705.00
97
(3)

Wortmannin是一种PI3激酶抑制剂。通过抑制PI3K,它会影响磷脂酰肌醇依赖性信号传导通路,从而改变涉及SNX16的膜运输途径,使其功能增强。

Monensin A

17090-79-8sc-362032
sc-362032A
5 mg
25 mg
¥1715.00
¥5810.00
(1)

莫能菌素是一种离子载体,可破坏内体pH梯度。SNX16与内体膜运输有关;改变内体pH可通过影响内体分选过程来增强SNX16的功能。

Bafilomycin A1

88899-55-2sc-201550
sc-201550A
sc-201550B
sc-201550C
100 µg
1 mg
5 mg
10 mg
¥1083.00
¥2821.00
¥8462.00
¥16111.00
280
(6)

巴夫洛霉素A1是一种液泡型H+-ATP酶的特异性抑制剂。当内体酸化被抑制时,由于内体动力学发生变化,SNX16相关的内体分选活性会增加。

Chlorpromazine

50-53-3sc-357313
sc-357313A
5 g
25 g
¥677.00
¥1218.00
21
(1)

氯丙嗪已知可抑制由衣藻素介导的内吞作用。通过抑制该通路,氯丙嗪可能会增加对SNX16活跃的替代内吞途径的需求,从而增强其功能。

Dynamin Inhibitor I, Dynasore

304448-55-3sc-202592
10 mg
¥982.00
44
(2)

Dynasore 是一种动态蛋白的 GTPase 抑制剂,可阻断凝集素介导的内吞作用。这种抑制作用可能会改变通过 SNX16 所调节途径的流量,从而间接增强其活性。

Nocodazole

31430-18-9sc-3518B
sc-3518
sc-3518C
sc-3518A
5 mg
10 mg
25 mg
50 mg
¥654.00
¥936.00
¥1579.00
¥2730.00
38
(2)

诺考达唑会破坏微管,影响内体和跨高尔基体网络之间的运输,而SNX16参与其中的分类和运输,从而可能增强其功能。

Cytochalasin D

22144-77-0sc-201442
sc-201442A
1 mg
5 mg
¥1636.00
¥4987.00
64
(4)

细胞分裂素D抑制肌动蛋白聚合。肌动蛋白在胞吞作用和囊泡运输中起着关键作用,因此抑制肌动蛋白可以间接增强SNX16的功能,改变内体动力学。

Pitstop 2

1419093-54-1sc-507418
10 mg
¥4062.00
(0)

Pitstop 2 是一种凝集素终止子结构域抑制剂,会影响凝集素介导的内吞作用。这种抑制作用可增强 SNX16 在替代内吞途径中的功能作用。

ML 141

71203-35-5sc-362768
sc-362768A
5 mg
25 mg
¥1512.00
¥5664.00
7
(1)

ML141 是一种 Cdc42 抑制剂;鉴于 Cdc42 参与肌动蛋白聚合和囊泡贩运,抑制 Cdc42 可能会导致更多地依赖 SNX16 介导的途径。