- Signaling Pathways
- Autophagy
- Autophagy
Autophagy
Autophagy is a conserved cellular degradation and recycling process in the lysosome. In mammalian cells, there are three primary types of autophagy: microautophagy, macroautophagy, and chaperone-mediated autophagy (CMA). Microphagy captures cargoes by means of invaginations or protrusions of the lysosomal membrane directly, CMA uses chaperones to identify cargo proteins and then unfolds and transfers them into the lysosomal, while macroautophagy sequesters cargo by autophagosomes-de novo synthesized of double-membrane vesicles-and subsequently transport it to the lysosome.
Macroautophagy is the best studied and it occurs at a low level constitutively and can also be further induced under stress conditions, such as nutrient or energy starvation with a salient feature of autophagy protein degradation. Stress-induced macrophagy plays an important role in protein catabolism with another key protein degradation pathway, the ubiquitin–proteasome system (UPS).
As the study progressed, autophagy gains its importance under basal, nutrient-rich conditions, and is now recognized as a critical housekeeping pathway in catabolism of diverse cellular constituents, such as protein aggregates (aggrephagy), lipid droplets (lipophagy), iron complex (Ferritinophagy) and carbohydrate. Except for macromolecules, autophagy can also target several organelles and structures, such as mitochondria (mitophagy), peroxisome (pexophagy), endoplasmic reticulum (reticulophagy or ER-phagy), ribosome (ribophagy), spermatozoon-inherited organelles following fertilization (allophagy), secretory granules within pancreatic cells (zymophagy) and intracellular pathogens (xenophagy).
Autophagy and its dysfunction are associated with a variety of human pathologies, including ageing, cancer, neurodegenerative disease, heart disease and metabolic diseases, such as diabetes. Plenty of drugs and natural products are involved in autophagy modulation through multiple signaling pathways. Small molecules that can regulate autophagy seem to have great potential to intervene such diseases in animal models or clinical courses.
All Product Categories
-
Autophagy Inhibitors
(488)
View all products
-
Autophagy Agonists
(6)
View all products
-
Autophagy Activators
(124)
View all products
-
Autophagy Modulators
(59)
View all products
-
Autophagy Chemicals
(2)
View all products
-
Autophagy Inducers
(2220)
View all products
-
Autophagy Controls
(5)
View all products
-
Autophagy Ligand
(1)
View all products
-
Autophagy 관련 제품 (3441)
관련 제품 (3441)
-
Antibodies (31)
-
Autophagy Signaling Pathway
-
CUR5g
0 ImagesCUR5g is a potent autophagy inhibitor. CUR5g selectively inhibits autophagosome degradation in cancer cells by blocking autophagosome-lysosome fusion. CUR5g blocks the recruitment of STX17 to autophagosomes via a UVRAG-dependent mechanism, resulting in the inability of autophagosomes to fuse with lysosomes. CUR5g improves the anticancer effect of Cisplatin (HY-17394) against A549 cells both in vitro and in vivo. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
FAAH inhibitor 1
0 ImagesSynonyms: Benzothiazole analog 3FAAH inhibitor 1 (compound 3) is a selective reversible FAAH inhibitor. FAAH inhibitor 1 has no off-target activity with respect to other serine hydrolases. FAAH inhibitor 1 is exclusively specific against FAAH in rat brain with an IC50 value of 18 nM and had no missing protein bands in all the other tissues. FAAH inhibitor 1 can be used for neurological disorders research. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Deutenzalutamide-d3
0 ImagesCat. No.: HY-70002SCAS No.: 1443331-82-5Synonyms: Enzalutamide-d3; MDV3100-d3Deutenzalutamide (Enzalutamide-d3) is a developed deuterium labeled Enzalutamide (MDV3100). Enzalutamide is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Felodipine-d3
0 ImagesFelodipine-d3 is the deuterium labeled Felodipine. Felodipine, a dihydropyridine, is a potent, vasoselective calcium channel antagonist. Felodipine lowers blood pressure (BP) by selective action on vascular smooth muscle, especially in the resistance vessels. Felodipine, an anti-hypertensive agent, induces autophagy. Felodipine can cross the blood-brain barrier. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Theophylline-d6
0 ImagesSynonyms: 1,3-Dimethylxanthine-d6; Theo-24-d6Theophylline-d6 is the deuterium labeled Theophylline. Theophylline is a nonselective phosphodiesterase (PDE) inhibitor, adenosine receptor blocker, and histone deacetylase (HDAC) activator. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Fludrocortisone acetate (Standard)
0 ImagesSynonyms: 9α-Fludrocortisone acetate(Standard); 9α-Fluorcortisol acetate (Standard)Fludrocortisone acetate (Standard) is the analytical standard of Fludrocortisone acetate. This product is intended for research and analytical applications. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Thalidomide-O-C6-azide
0 ImagesThalidomide-O-C6-azide is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide (HY-14658) based cereblon ligand and a linker used in PROTAC technology. Thalidomide-O-C6-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Fenofibrate-d6
0 ImagesFenofibrate-d6 is the deuterium labeled Fenofibrate. Fenofibrate is a selective PPARα agonist with an EC50 of 30 μM. Fenofibrate also inhibits human cytochrome P450 isoforms, with IC50s of 0.2, 0.7, 9.7, 4.8 and 142.1 μM for CYP2C19, CYP2B6, CYP2C9, CYP2C8, and CYP3A4, respectively. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
TSPO ligand-1
0 ImagesTSPO ligand-1 is the ligand of AUTAC4 (HY-134640) that can be used in the synthesis of PROTACs. TSPO ligand-1 is a mitochondrial outer membrane transmembrane structural domain protein can bind to AUTAC4 and regulate mitochondrial autophagy to promote targeted mitochondrial renewal. TSPO ligand-1 is also involved in the transport of cholesterol from the outer to inner mitochondrial membrane and serves as a sensitive biomarker of brain injury and neurodegeneration. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Autophagy inducer 7
0 ImagesAutophagy inducer 7 (Compound SSA) is an Autophagy and Apoptosis inducer. Autophagy inducer 7 activates autophagy by inhibiting Akt/mTOR signaling and the expression of downstream proteins. Autophagy inducer 7 suppresses DNA synthesis and causes a G0-G1 cell-cycle arrest. Autophagy inducer 7 inhibits tumor cell growth. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
- LC3in-C42
-
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Apigenin-d5
0 ImagesCat. No.: HY-N1201SCAS No.: 263711-74-6Apigenin-d5 is a deuterated labeled Apigenin. Apigenin (4',5,7-Trihydroxyflavone) is a competitive CYP2C9 inhibitor with a Ki of 2 μM. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Dox-btn2
0 ImagesSynonyms: Biotin Labeled DoxorubicinDox-btn2 is a biotin labeled Doxorubicin (HY-15142A), with a biotin label at the point of conjugation to doxorubicin at 3'-NH2. Dox-btn2 can be used for cell imaging. While Doxorubicin is mainly accumulated in the nucleus, while Dox-btn2 is mainly located in the cytoplasm. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Sildenafil citrate (Standard)
0 ImagesSynonyms: UK-92480 citrate (Standard)Sildenafil (citrate) (Standard) is the analytical standard of Sildenafil (citrate). This product is intended for research and analytical applications. Sildenafil citrate is a potent phosphodiesterase type 5 (PDE5) inhibitor with IC50 of 5.22 nM. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
- ARN5187 trihydrochloride
-
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Physalin A
0 ImagesPhysalin A is a biologically active withanolide. Physalin A shows anti-inflammatory, antifibrotic and ameliorative effects on autophagy in models of disc degeneration. Physalin A has antitumor activity and can induce apoptosis, ROS production and G2/M phase cell cycle arrest. Besides. Physalin A can significantly increase the activity of quinone reductase and increase the expression of detoxifying enzymesc. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Bilobalide (Standard)
0 ImagesSynonyms: (-)-Bilobalide (Standard)Bilobalide (Standard) is the analytical standard of Bilobalide. This product is intended for research and analytical applications. Bilobalide, a sesquiterpene trilactone constituent of Ginkgo biloba, inhibits the NMDA-induced efflux of choline with an IC50 value of 2.3 μM. Bilobalide prevents apoptosis through activation of the PI3K/Akt pathway in SH-SY5Y cells. Exerts protective and trophic effects on neurons. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Dasatinib (Standard)
0 ImagesSynonyms: BMS-354825 (Standard)Dasatinib (Standard) is the analytical standard of Dasatinib. This product is intended for research and analytical applications. Dasatinib (BMS-354825) is a highly potent, ATP competitive, orally active dual Src/Bcr-Abl inhibitor with potent antitumor activity. The Kis are 16 pM and 30 pM for Src and Bcr-Abl, respectively. Dasatinib inhibits Bcr-Abl and Src with IC50s of <1.0 nM and 0.5 nM, respectively. Dasatinib also induces apoptosis and autophagy. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
PD98059 (Standard)
0 ImagesPD98059 (Standard) is the analytical standard of PD98059. This product is intended for research and analytical applications. PD98059 is a potent and selective MEK inhibitor with an IC50 of 5 µM. PD98059 binds to the inactive form of MEK, thereby preventing the activation of MEK1 (IC50 of 2-7 µM) and MEK2 (IC50 of 50 µM) by upstream kinases. PD98059 is a ERK1/2 signaling inhibitor. PD98059 is a ligand for the aryl hydrocarbon receptor (AHR), and suppresses TCDD binding (IC50 of 4 μM) and AHR transformation (IC50 of 1 μM). PD98059 also inhibits Mycobacterium bovis Bacillus CalmetteGuerin (BCG)-induced autophagy. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
-
Rapamycin-13C,d3
0 ImagesCat. No.: HY-10219S1Synonyms: Sirolimus-13C,d3; AY-22989-13C,d3 NSC 226080-13C,d3Rapamycin-13C,d3 (Sirolimus-13C,d3) is the 13C, deuterated-labeled Rapamycin (HY-10219). Rapamycin (Sirolimus; AY 22989) is a potent and specific blood-brain barrier-transmissible mTOR inhibitor with an IC50 of 0.1 nM in HEK293 cells. Rapamycin is a molecular glue that binds FKBP12 and mTOR proteins together, thereby inhibiting mTOR kinase activity. Rapamycin binds to FKBP12 and specifically acts as an allosteric inhibitor of mTORC1. Rapamycin is an autophagy activator, an immunosuppressant. -
loading...Please select quantity견적 받기
August 31
-
Please select quantity
August 31
견적 받기
loading... -
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results
No matching results