Date published: 2025-9-6

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Gα s 抑制因子

Common Gα s Inhibitors include, but are not limited to SQ 22536 CAS 17318-31-9, NF449 CAS 627034-85-9, NF 023 CAS 104869-31-0, Nobiletin CAS 478-01-3 and MRS 1754 CAS 264622-58-4.

Gαs inhibitors are a class of chemical compounds specifically designed to target and inhibit the function of the Gαs protein, a crucial component of the heterotrimeric G protein complex involved in signal transduction. Gαs, or the G alpha subunit of the stimulatory G protein, plays a pivotal role in mediating cellular responses to extracellular signals, particularly those transmitted through G protein-coupled receptors (GPCRs). Upon activation by a GPCR, Gαs exchanges GDP for GTP and dissociates from the Gβγ subunits, subsequently activating adenylyl cyclase. This activation leads to the conversion of ATP to cyclic AMP (cAMP), a key secondary messenger that regulates numerous cellular processes, including metabolism, gene expression, and cell growth. By inhibiting Gαs, researchers can block the production of cAMP, effectively disrupting the downstream signaling pathways that rely on this molecule.

In research, Gαs inhibitors are valuable tools for dissecting the complex signaling networks mediated by GPCRs and for understanding the specific contributions of Gαs to various cellular functions. By blocking Gαs activity, scientists can explore how the inhibition affects cAMP levels and the subsequent impact on cellular processes such as energy metabolism, hormone regulation, and ion channel activity. These inhibitors allow researchers to investigate the dynamics of G protein signaling, including the interactions between Gαs and its associated receptors, effectors, and regulatory proteins. Additionally, Gαs inhibitors provide insights into the role of Gαs in physiological and pathological conditions where altered cAMP signaling plays a significant role. Through these studies, the use of Gαs inhibitors enhances our understanding of the molecular mechanisms underlying GPCR signaling, the regulation of secondary messengers like cAMP, and the broader implications of G protein function in cellular communication and homeostasis.

関連項目

Items 1 to 10 of 11 total

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产品名称CAS #产品编号数量价格应用排名

SQ 22536

17318-31-9sc-201572
sc-201572A
5 mg
25 mg
¥1049.00
¥4016.00
13
(1)

SQ 22536是一种腺苷酸环化酶抑制剂,可间接影响Gαs。它通过阻断腺苷酸环化酶活性来抑制cAMP的产生,从而减少Gαs介导的cAMP信号传导和下游效应。

NF449

627034-85-9sc-478179
sc-478179A
sc-478179B
10 mg
25 mg
100 mg
¥2245.00
¥5190.00
¥16686.00
1
(0)

NF449是一种腺苷受体拮抗剂,可抑制Gαs信号传导。它干扰腺苷受体-Gαs偶联,从而减少Gαs介导的cAMP信号传导和下游细胞反应。

NF 023

104869-31-0sc-204124
sc-204124A
10 mg
50 mg
¥1783.00
¥6961.00
1
(1)

NF023是一种非选择性嘌呤受体拮抗剂,可通过干扰嘌呤受体-Gαs耦合来抑制Gαs信号,从而减少Gαs介导的cAMP信号。

Nobiletin

478-01-3sc-202733
10 mg
¥2132.00
2
(0)

Nobiletin是一种天然化合物,据称可以抑制Gαs信号传导和cAMP的产生。它可能与Gαs或Gαs-cAMP途径中的下游成分相互作用,从而降低cAMP水平并影响细胞。

MRS 1754

264622-58-4sc-301174
sc-301174A
5 mg
25 mg
¥2369.00
¥9229.00
1
(0)

MRS 1754 是一种选择性 P2Y6 受体拮抗剂,可间接影响 Gαs。通过阻断 P2Y6 受体-Gαs 耦合,它能减少 Gαs 介导的 cAMP 信号传导和下游细胞反应。

NF 157

104869-26-3sc-204125
sc-204125A
1 mg
5 mg
¥5528.00
¥22564.00
1
(0)

NF157是一种非选择性嘌呤受体拮抗剂,可抑制Gαs信号传导。它干扰嘌呤受体-Gαs偶联,从而减少Gαs介导的cAMP信号传导。

YM 254890

568580-02-9sc-507356
1 mg
¥5641.00
(0)

YM-254890是一种Gq/11蛋白抑制剂,可间接影响Gαs。它可降低Gq/11的活性,从而对Gαs信号产生交叉影响,导致依赖Gαs介导的途径的细胞反应发生变化。

W-7

61714-27-0sc-201501
sc-201501A
sc-201501B
50 mg
100 mg
1 g
¥1839.00
¥3385.00
¥18525.00
18
(1)

W-7 是一种钙调蛋白抑制剂,可能会间接影响 Gαs 信号传导。通过抑制钙调蛋白,它可以调节与 Gαs 相互作用的下游效应物的活性,从而改变 Gαs 介导的信号传导和细胞反应。

Verapamil

52-53-9sc-507373
1 g
¥4140.00
(0)

维拉帕米是一种钙通道阻滞剂,可能间接影响Gαs信号传导。通过降低细胞内钙离子水平,它可以调节Gαs介导的信号传导通路和细胞反应中的下游效应。

SC 19220

19395-87-0sc-203450B
sc-203450C
sc-203450
sc-203450A
1 mg
5 mg
10 mg
50 mg
¥248.00
¥1173.00
¥2076.00
¥8992.00
2
(0)

SC 19220 是一种腺苷酸环化酶抑制剂,可间接影响 Gα。通过抑制腺苷酸环化酶,它可以减少 Gαs 下游的 cAMP 生成,从而改变依赖于 Gαs 介导的 cAMP 信号的细胞反应。