目錄:MedChemExpress LLC>>信號通路>> LV-320 | MCE
CAS | 2449093-46-1 | 分子量 | 520.11 |
---|---|---|---|
分子式 | C??H??ClNO?S? | 供貨周期 | 現(xiàn)貨 |
規(guī)格 | 5 mg | 貨號 | HY-112711 |
應用領域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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產(chǎn)品活性:LV-320 是一種有效且非競爭性的 ATG4B 抑制劑,其 IC50 值為 24.5 μM,Kd 值為 16 μM。 LV-320 抑制 ATG4B 的酶促活性,阻斷細胞自噬,并且在體內(nèi)穩(wěn)定,無毒且有活性。
研究領域:Autophagy | Metabolic Enzyme/Protease
作用靶點:Autophagy | Cathepsin
In Vitro: LV-320 (0-120?µM; SKBR3, MCF7, JIMT1, and MDA-MB-231 cells) treatment results in a dose-dependent increase in endogenous LC3B-II and protein p62 levels in all four cell lines.
LV-320 (120?µM; 48 hours; MDA-MB-231 cells) treatment results in an increase in LC3B-II, indicating that LV-320 blocks autophagic flux.
In Vivo: LV-320 (100-200?mg/kg; oral gavage; three times over two days; GFP-LC3 mice) treatment results in a terminal blood level of 169 µM and a liver level of 104 µM. The expression of GFP-LC3 puncta is significantly greater accumulation in LV-320 treated animals compared to controls. LC3B-II protein is also increased in LV-320-treated animals. The treatment do not cause significant toxicity in mice at either dose.
相關產(chǎn)品:Bioactive Compound Library Plus | Metabolism/Protease Compound Library | Anti-Cancer Compound Library | Autophagy Compound Library | Angiogenesis-Related Compound Library | Targeted Diversity Library | Membrane Protein-targeted Compound Library | Cathepsin X-IN-1 | RO5461111 | Balicatib | MK-0674 | Cathepsin D and E FRET Substrate acetate | L-006235 | CA-074 methyl ester | Ac-Leu-Val-Lys-Aldehyde | Papain | VBY-825 | Cathepsin inhibitor 1 | Z-Arg-Arg-4MβNA triacetate | L-873724 | Cathepsin C-IN-4 | Cathepsin C-IN-3 | Odanacatib | N-CBZ-Phe-Arg-AMC | Cysteine Protease inhibitor | Z-FA-FMK | Relacatib | E-64 | 2-Cyanopyrimidine | Cathepsin C-IN-5 | ALLM | Z-LVG-CHN2 | SID 26681509 quarterhydrate | Gü1303 | Z-WEHD-FMK | GSK-2793660 free base | TSC25
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