IndraLab

Statements


1 | 1 11

reach
"Among Abl kinase inhibitors, KW-2449 and Tozasertib [41] only targeted RIPK1, while GNF-7, Ponatinib and DCC-2036 were shown to inhibit both RIPK1 and RIPK3 [33,40,42] ."

reach
"Ponatinib and pazopanib, which were found could inhibit RIP1 and RIP3, has been approved by Food and Drug Administration (FDA) as chemotherapeutics in clinical treatment [22] ."

reach
"Interestingly, some US Food and Drug Administration-approved anticancer drugs, including ponatinib and pazopanib, can inhibit RIPK1; these drugs would be better prospects in further clinical studies (Fauster et al., 2015)."

eidos
"In addition , the activity of RIPK1 , an NSP12 interactor which is associated with apoptosis , necroptosis , and inflammatory pathways , is predicted to be inhibited by ponatinib and pazopanib ."

reach
"They found that ponatinib can inhibit dual activity of RIPK1 and RIPK3 in vitro, which may limit its clinic application considering the safety."

reach
"Ponatinib has been shown to inhibit both RIP1 and RIP3 via direct binding [XREF_BIBR, XREF_BIBR]."

reach
"Two receptor tyrosine kinase inhibitors, Pazopanib and Ponatinib were confirmed to block cell necroptosis by targeting RIPK1, but failed to apply in clinic trails due to cardiotoxicity ( Fauster et al[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

reach
"This is highlighted by the fact that both ponatinib and sorafenib are also inhibitors of RIPK1, limiting their development as therapies for necroptotic diseases.HTS efforts have also identified other putative type I and II RIPK3 inhibitor scaffolds (Figure 13)."

reach
"Furthermore, ponatinib and pazopanib are expected to suppress the activity of receptor-interacting serine/threonine protein kinase 1 (RIPK1), a SARS-CoV-2 NSP12 interactor linked to apoptosis, necroptosis, and inflammatory processes [167]."

reach
"Leveraging this similarity, they explored the RIPK1 inhibitory activity of a range of ABL kinase inhibitors and confirmed that ponatinib efficiently inhibited RIPK1, consistent with Superti-Furga G's [MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

reach
"Ponatinib inhibits RIPK1 (38) and RIPK3 (39) and is a US Food and Drug Administration-approved drug for the treatment of acute lymphoid leukemia and chronic myeloid leukemia."

reach
"Ponatinib and DCC-2036 were shown to inhibit both RIPK1 and RIPK3 [30,32] , while Tozasertib only targeted RIPK1 to inhibit necroptosis [45] ."