RASL12 Inhibitors are a class of chemical compounds designed to target Ras-like protein family member 12 (RASL12), a member of the Ras superfamily of proteins. RASL12 is likely implicated in cellular signaling pathways that govern a host of cellular activities, akin to other members of the Ras family. Given its likely role in intracellular signal transduction, this protein could influence a wide range of cellular functions such as growth, differentiation, and survival. The inhibitors in this class are tailored to modulate the expression or activity of RASL12 through various mechanisms. For instance, compounds like Manumycin A and Salirasib aim to inhibit RASL12 by directly targeting Ras family proteins or their interactions with cellular components. Others like Lonafarnib and Tipifarnib focus on post-translational modifications of RASL12, affecting its cellular localization and function.
The chemical structures of these inhibitors are diverse, reflecting the multiple mechanisms by which they can act on RASL12. Some, like Zoledronic Acid and Trametinib, disrupt processes downstream of RASL12, such as prenylation or MAPK pathway signaling, affecting the protein's activity indirectly. Other compounds like Imatinib, Sorafenib, and Sunitinib target multiple kinases that interact with Ras proteins, thereby affecting RASL12 indirectly through these interactions. It's important to note that the specificity and extent of these compounds' effects on RASL12 are not yet fully characterized and would require further experimental validation to confirm their mechanisms of action. Overall, RASL12 Inhibitors are a class of compounds that target a protein with significance in cellular signaling.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Manumycin A | 52665-74-4 | sc-200857 sc-200857A | 1 mg 5 mg | $215.00 $622.00 | 5 | |
Manumycin A could inhibit RASL12 by targeting Ras family proteins and disrupting their activity. | ||||||
Farnesyl thiosalicylic acid | 162520-00-5 | sc-205322 sc-205322A | 1 mg 5 mg | $60.00 $80.00 | 15 | |
Farnesyl thiosalicylic acid could bind to RASL12 and disrupt its interaction with other cellular components. | ||||||
Lonafarnib | 193275-84-2 | sc-482730 sc-482730A | 5 mg 10 mg | $173.00 $234.00 | ||
Lonafarnib may inhibit RASL12 by blocking farnesyltransferase, an enzyme that modifies Ras proteins. | ||||||
Tipifarnib | 192185-72-1 | sc-364637 | 10 mg | $720.00 | ||
Tipifarnib could inhibit the post-translational modification of RASL12, affecting its localization. | ||||||
Zoledronic acid, anhydrous | 118072-93-8 | sc-364663 sc-364663A | 25 mg 100 mg | $90.00 $251.00 | 5 | |
Zoledronic Acid, anhydrous may inhibit the prenylation of RASL12, disrupting its membrane association. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
Imatinib may inhibit RASL12 by targeting multiple tyrosine kinases that interact with Ras proteins. | ||||||
Trametinib | 871700-17-3 | sc-364639 sc-364639A sc-364639B | 5 mg 10 mg 1 g | $112.00 $163.00 $928.00 | 19 | |
Trametinib could inhibit the MAPK pathway, downstream of RASL12, affecting its signaling activity. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
Sorafenib could inhibit RASL12 by targeting Raf kinases, which are downstream effectors of Ras. | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | $150.00 $920.00 | 5 | |
Sunitinib, Free Base may inhibit RASL12 by affecting multiple receptor tyrosine kinases in the Ras pathway. | ||||||
Gefitinib | 184475-35-2 | sc-202166 sc-202166A sc-202166B sc-202166C | 100 mg 250 mg 1 g 5 g | $62.00 $112.00 $214.00 $342.00 | 74 | |
Gefitinib could inhibit RASL12 by targeting the EGFR tyrosine kinase, which interacts with Ras. | ||||||