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- W4313570078 endingPage "100147" @default.
- W4313570078 startingPage "100147" @default.
- W4313570078 abstract "Non-steroidal anti-inflammatory drugs (NSAIDs) injure the proximal and distal gut by different mechanisms. While many drugs reduce gastrointestinal injury, no drug directly stimulates mucosal wound healing. Focal adhesion kinase (FAK), a non-receptor tyrosine kinase, induces epithelial sheet migration. We synthesized and evaluated a water-soluble FAK-activating small molecule, M64HCl, with drug-like properties. Monolayer wound closure and Western blots measured migration and FAK phosphorylation in Caco-2 cells, in vitro kinase assays established FAK activation, and pharmacologic tests assessed drug-like properties. 30 mg/kg/day M64HCl was administered in two murine small intestine injury models for 4 days. M64HCl (0.1–1000 nM) dose-dependently increased Caco-2 FAK-Tyr 397 phosphorylation, without activating Pyk2 and accelerated Caco-2 monolayer wound closure. M64HCl dose-responsively activates the FAK kinase domain vs. the non-salt M64, increasing the Vmax of ATP-binding. Pharmacologic tests suggested M64HCl has drug-like properties and is enterally absorbed. M64HCl 25 mg/kg/day continuous infusion promoted healing of ischemic jejunal ulcers and indomethacin-induced small intestinal injury in C57Bl/6 mice. M64HCl-treated mice exhibited smaller ulcers 4 days after ischemic ulcer induction or indomethacin injury. Renal histology and plasma creatinine were normal. Mild hepatic inflammatory changes and ALT elevation were similar among M64HCl-treated mice and controls. M64HCl was concentrated in kidney and gastrointestinal mucosa and functional nephrectomy studies suggested predominantly urinary excretion. Little toxicity was observed in vitro or in single-dose mouse toxicity studies until >1000x higher than effective concentrations. M64HCl, a water-soluble FAK activator, promotes epithelial restitution and intestinal mucosal healing and may be useful to treat gut mucosal injury." @default.
- W4313570078 created "2023-01-06" @default.
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- W4313570078 date "2023-01-01" @default.
- W4313570078 modified "2023-10-15" @default.
- W4313570078 title "A novel drug-like water-soluble small molecule Focal Adhesion Kinase (FAK) activator promotes intestinal mucosal healing" @default.
- W4313570078 cites W1489584806 @default.
- W4313570078 cites W1520620836 @default.
- W4313570078 cites W1964020745 @default.
- W4313570078 cites W1974996455 @default.
- W4313570078 cites W1988158628 @default.
- W4313570078 cites W1999368455 @default.
- W4313570078 cites W2002924275 @default.
- W4313570078 cites W2014283481 @default.
- W4313570078 cites W2017168126 @default.
- W4313570078 cites W2027039192 @default.
- W4313570078 cites W202766920 @default.
- W4313570078 cites W2030617231 @default.
- W4313570078 cites W2031196360 @default.
- W4313570078 cites W2038787794 @default.
- W4313570078 cites W2045549203 @default.
- W4313570078 cites W2055230090 @default.
- W4313570078 cites W2057626906 @default.
- W4313570078 cites W2070555511 @default.
- W4313570078 cites W2094601449 @default.
- W4313570078 cites W2094984846 @default.
- W4313570078 cites W2097535640 @default.
- W4313570078 cites W2098280618 @default.
- W4313570078 cites W2101592854 @default.
- W4313570078 cites W2111130664 @default.
- W4313570078 cites W2118910625 @default.
- W4313570078 cites W2121723262 @default.
- W4313570078 cites W2134782997 @default.
- W4313570078 cites W2136151278 @default.
- W4313570078 cites W2136530078 @default.
- W4313570078 cites W2145926981 @default.
- W4313570078 cites W2150750095 @default.
- W4313570078 cites W2151411980 @default.
- W4313570078 cites W2155151216 @default.
- W4313570078 cites W2155674292 @default.
- W4313570078 cites W2158750799 @default.
- W4313570078 cites W2163546205 @default.
- W4313570078 cites W2167452086 @default.
- W4313570078 cites W2169555754 @default.
- W4313570078 cites W2171451849 @default.
- W4313570078 cites W2194591433 @default.
- W4313570078 cites W2217213811 @default.
- W4313570078 cites W2238829069 @default.
- W4313570078 cites W2314423784 @default.
- W4313570078 cites W2519770441 @default.
- W4313570078 cites W2564618766 @default.
- W4313570078 cites W2607171239 @default.
- W4313570078 cites W2607698451 @default.
- W4313570078 cites W2742440932 @default.
- W4313570078 cites W2748513498 @default.
- W4313570078 cites W2790004381 @default.
- W4313570078 cites W2791120196 @default.
- W4313570078 cites W2792893019 @default.
- W4313570078 cites W2801607015 @default.
- W4313570078 cites W2838257419 @default.
- W4313570078 cites W2897073041 @default.
- W4313570078 cites W2908381102 @default.
- W4313570078 cites W2912967573 @default.
- W4313570078 cites W2926213206 @default.
- W4313570078 cites W2929435396 @default.
- W4313570078 cites W2938524649 @default.
- W4313570078 cites W2980176187 @default.
- W4313570078 cites W2983225545 @default.
- W4313570078 cites W2994847826 @default.
- W4313570078 cites W3011609294 @default.
- W4313570078 cites W3011990562 @default.
- W4313570078 cites W3024117458 @default.
- W4313570078 cites W3033212453 @default.
- W4313570078 cites W3048792538 @default.
- W4313570078 cites W3129757530 @default.
- W4313570078 cites W3131100411 @default.
- W4313570078 cites W3137382409 @default.
- W4313570078 cites W3139050683 @default.
- W4313570078 cites W3153557350 @default.
- W4313570078 cites W3204166386 @default.
- W4313570078 cites W4292878182 @default.
- W4313570078 cites W4302807908 @default.
- W4313570078 cites W4361868330 @default.
- W4313570078 doi "https://doi.org/10.1016/j.crphar.2022.100147" @default.
- W4313570078 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36632414" @default.
- W4313570078 hasPublicationYear "2023" @default.
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