7 Results for "

autolysosome

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "autolysosome" in MCE Product Catalog:

Cat. No.: HY-174806
CAS No.: 889662-19-5
Synonyms: 7-(β-D-Galactopyranosyloxy)-4-phenylchromen-2-one
Research Areas:  

Neurological Disease

Y040-7904 is a mitophagy activator. Y040-7904 enhances mitophagy by promoting mitochondria transport to autophagosomes and the fusion of autophagosomes with autolysosomes. Y040-7904 induces mitophagy through the SIRT1/FoxO3 pathway. Y040-7904 upregulates the levels of Parkin, PINK1, and LC3II/I. Y040-7904 reduces amyloid-β () accumulation in both in vitro and in vivo models of Alzheimer’s disease.
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Cat. No.: HY-146307
CAS No.: 2445565-58-0
Target:  

TrxR

Research Areas:  

Cancer

TrxR-IN-3 (Compound 2c) is a potent inhibitor of TrxR. TrxR-IN-3 exhibits potent antiproliferative activities against five human cancer cell lines, especially against breast tumor cells. TrxR-IN-3 increases ROS levels and resulted in marked apoptosis by regulating apoptosis-related proteins expressed in the breast cancer cells. TrxR-IN-3 also triggers the formation of autophagosomes and autolysosomes by promoting the expression of LC3-II and Beclin-1 and diminishing the expression of LC3-I and p62 proteins .
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Cat. No.: HY-111137
CAS No.: 916890-10-3
Synonyms: XC-302 free base
Target:  

Akt

Research Areas:  

Cancer

Puquitinib (XC-302 free base) is a multi-target inhibitor with the activity of inducing autophagy in nasopharyngeal carcinoma cells by inhibiting the PI3K/AKT/mTOR signaling pathway. Puquitinib was able to inhibit the proliferation of CNE-2 cells, showing a dose-dependent antiproliferative effect. Puquitinib induced the formation of autophagosomes and autolysosomes in CNE-2 cells, which were observed by fluorescence microscopy and electron microscopy. Puquitinib promoted the formation of LC3-II and increased the expression of beclin 1, while reducing the level of p62. Puquitinib inhibited the PI3K/AKT/mTOR pathway by reducing the expression of p-AKT and p-mTOR. Puquitinib also induced apoptosis in CNE-2 cells, and when autophagy was inhibited, the apoptosis rate was reduced, which means that autophagy may interact with apoptosis to induce cell death .
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Cat. No.: HY-186251
CAS No.: 1401032-35-6
Target:  

Autophagy

Research Areas:  

Cancer

C18-Pyr-Cer is a chemically modified synthetic ceramide analog. C18-Pyr-Cer directly interacts with MAP1LC3B-II. C18-Pyr-Cer induces autophagy, targets autolysosomes to mitochondria, and mediates lethal autophagy in cancer cells. C18-Pyr-Cer can be used in the research of head and neck squamous cell carcinoma .
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Cat. No.: HY-D3087
CAS No.: 1966158-27-9
Target:  

Fluorescent Dye

Research Areas:  

Cancer

Lyso-OC is a two-photon fluorescent probe that enables real-time monitoring of autophagy through ultrasensitive detection of lysosomal polarity changes. Lyso-OC possesses a coumarin (HY-N0709) solvatochromic group and a morpholine lysosome-targeting group, allowing selective lysosomal localization in living cells. Lyso-OC emits strong fluorescence in low-polarity lysosomes, whereas in high-polarity autolysosomes formed during autophagy, its fluorescence intensity decreases and the emission peak shifts by approximately 30 nm. For two-photon detection, the excitation/emission wavelengths of Lyso-OC are 760/490-550 nm, and its one-photon excitation wavelength is 375 nm. Lyso-OC can be used in cancer-related research .
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Cat. No.: HY-184160
Research Areas:  

Cancer

Mcl1 Degrader-1 is an autophagy-targeting chimera (AUTAC) that selectively degrades the Mcl1 protein. Mcl1 Degrader-1 mediates K63 ubiquitination of Mcl1 via TRAF6/UBC13, transports it to autolysosomes for degradation through p62/SQSTM1, and activates Beclin1-dependent autophagy. Mcl1 Degrader-1 can be used in studies related to multiple myeloma and non-small cell lung cancer .
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Cat. No.: HY-181936
CAS No.: 3126601-01-9
Target:  

Atg4 Autophagy

Research Areas:  

Cancer

Atg4B activator-1 (Compound 16a) is an allosteric, selective, and orally active ATG4B activator with a Kd of 0.2199 μM. Atg4B activator-1 binds to the allosteric pocket of ATG4B and induces conformational changes. Atg4B activator-1 induces Autophagy. Atg4B activator-1 inhibits the proliferation and migration of triple-negative breast cancer cells. Atg4B activator-1 can be used in studies related to triple-negative breast cancer .
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