Rasarfin
目录号 : GC63647Rasarfin 是 Ras 和 ARF6 的双抑制剂。
Cas No.:674359-73-0
Sample solution is provided at 25 µL, 10mM.
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Rasarfin is a dual Ras and ARF6 inhibitor[1].
Rasarfin also potently inhibits agonist-induced ERK1/2 signaling by GPCRs, and MAPK and Akt signaling by EGFR, as well as prevents cancer cell proliferation[1].Rasarfin blocks GPCR internalization through inhibition of ARF6[1].Rasarfin treatment results in a dose-dependent reduction in MDA-MB-231 cells[1]. Rasarfin inhibits the recruitment of the clathrin adaptor AP-2 to β-arrestin2 and receptor internalization, both processes that require active ARF6[1].
[1]. Jenna Giubilaro, et al. Discovery of a dual Ras and ARF6 inhibitor from a GPCR endocytosis screen. Nat Commun. 2021 Aug 3;12(1):4688.
Cas No. | 674359-73-0 | SDF | |
分子式 | C23H24ClN3O3 | 分子量 | 425.91 |
溶解度 | 储存条件 | Store at -20°C | |
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1 mg | 5 mg | 10 mg | |
1 mM | 2.3479 mL | 11.7396 mL | 23.4791 mL |
5 mM | 0.4696 mL | 2.3479 mL | 4.6958 mL |
10 mM | 0.2348 mL | 1.174 mL | 2.3479 mL |
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Discovery of a dual Ras and ARF6 inhibitor from a GPCR endocytosis screen
Nat Commun 2021 Aug 3;12(1):4688.PMID:34344896DOI:PMC8333425
Internalization and intracellular trafficking of G protein-coupled receptors (GPCRs) play pivotal roles in cell responsiveness. Dysregulation in receptor trafficking can lead to aberrant signaling and cell behavior. Here, using an endosomal BRET-based assay in a high-throughput screen with the prototypical GPCR angiotensin II type 1 receptor (AT1R), we sought to identify receptor trafficking inhibitors from a library of ~115,000 small molecules. We identified a novel dual Ras and ARF6 inhibitor, which we named Rasarfin, that blocks agonist-mediated internalization of AT1R and other GPCRs. Rasarfin also potently inhibits agonist-induced ERK1/2 signaling by GPCRs, and MAPK and Akt signaling by EGFR, as well as prevents cancer cell proliferation. In silico modeling and in vitro studies reveal a unique binding modality of Rasarfin within the SOS-binding domain of Ras. Our findings unveil a class of dual small G protein inhibitors for receptor trafficking and signaling, useful for the inhibition of oncogenic cellular responses.