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Autophagy

Autophagy is an intracellular catabolic mechanism. In certain stressful situations, lysosomes degrade degenerated, damaged, aged or non-functional cells, organelles and biomolecules such as proteins and nucleic acids to achieve cellular protection and organelles from cell damage. Autophagy is achieved by forming a bilayer membrane structure in the cytoplasm that wraps the material to be removed and transports it to the lysosome for degradation. In multicellular organisms, newly formed autophagic vesicles form autophagic endosomes by fusing with vesicles in different stages of the endocytic lysosomal pathway, such as early endosomes and late endosomes, before fusing with lysosomes, a process known as autophagic vesicle maturation. Abnormalities in autophagosome maturation, which is precisely regulated by cellular trophic state and stress signaling pathways, lead to the accumulation of large amounts of damaged organelles and toxic protein aggregates in cells.
Cat. No. Product name
BP12758 KU-55933
KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor.
BP12759 Atropine sulfate monohydrate
Atropine sulfate monohydrate, the sulfate salt of atropine, is a competitive muscarinic acetylcholine receptor antagonist.
BP12760 Megestrol acetate
Megestrol acetate is a progestogen with actions and uses similar to those of the progestogens in general. Megestrol acetate also has anti-androgenic properties. It is given by mouth in the palliative treatment or as an adjunct to other therapy in endometrial carcinoma and in breast cancer. Megestrol acetate has been approved to treat anorexia and cachexia.
BP12761 Niacin
Niacin is a water-soluble vitamin belonging to the vitamin B family, which occurs in many animal and plant tissues, with antihyperlipidemic activity. Niacin is converted to its active form niacinamide, which is a component of the coenzymes nicotinamide adenine dinucleotide (NAD) and its phosphate form, NADP.
BP12762 TWS119
TWS119 is a GSK-3β inhibitor; capable of inducing neuronal differentiation
BP12763 Binimetinib
Binimetinib (MEK162, ARRY-162, ARRY-438162) is an orally available inhibitor of MEK1/2 (IC50: 12 nM) in a cell-free assay.
BP12764 Sinomenine hydrochloride
Sinomenine hydrochloride is extracted from Sinomenium Acutum Rehderett Wilson.
BP12765 Bromhexine hydrochloride
Bromhexine hydrochloride is a mucolytic agent used in the treatment of respiratory disorders associated with viscid or excessive mucus.
BP12766 Schisandrin B
Schisandrin B has an antioxidant effect on rodent liver and heart.
BP12767 Schizandrin A
BP12768 Procainamide hydrochloride
Procainamide Hydrochloride is the hydrochloride salt form of procainamide, an amide derivative exhibiting class 1A antiarrhythmic property and analog of procaine. Procainamide hydrochloride reversibly binds to and blocks activated (open) voltage-gated sodium channels, thereby blocks the influx of sodium ions into the cell, which leads to an increase in threshold for excitation and inhibit depolarization during phase 0 of the action potential.
BP12769 Oxaliplatin
Oxaliplatin inhibits DNA synthesis by conforming DNA adducts.
BP12770 TOMATIDINE HYDROCHLORIDE
A steriodal alkaloid structurally similar to Cyclopamine but does not inhibit hedgehog pathway. May be used as a negative control for Cyclopamine and KAAD-Cyclopamine. Tomatidine protects against muscle atrophy and boosting muscle growth.
BP12771 Sulfacetamide sodium monohydrate
Sulfacetamide sodium monohydrate is a sulfonamide antibiotic. It has been investigated for the treatment of rosacea and pityriasis versicolor.
BP12772 Dimethyl fumarate
Dimethyl fumarate, a fumarate derivative, is used as antiinflammatory and immunomodulatory agent.
BP12773 Turofexorate Isopropyl
Turofexorate Isopropyl (XL335) is a potent, selective, and orally bioavailable FXR agonist with EC50 of 4 nM
BP12774 Berberine chloride
Berberine hydrochloride is an alkaloid from Hydrastis canadensis L., Berberidaceae and also found in many other plants. It is relatively toxic to parenterally but has been used orally for various fungal and parasitic infections and an anti-diarrheal.
BP12775 Oxidopamine hydrobromide
Oxidopamine hydrobromide is a neurotransmitter dopamine antagonist.
BP12776 Sulfanilamide
Sulfanilamide can competitively inhibit bacterial enzyme dihydropteroate synthetase with IC50 of 320 μM.
BP12777 Tozasertib
MK-0457 is a pan-Aurora kinase inhibitor (Kis: 0.6/18/4.6 nM for Aurora A/Aurora B/Aurora C). It shows selectivity against more than 190 different kinases.
KU-55933
BP12758
KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor.
Atropine sulfate monohydrate
BP12759
Atropine sulfate monohydrate, the sulfate salt of atropine, is a competitive muscarinic acetylcholine receptor antagonist.
Megestrol acetate
BP12760
Megestrol acetate is a progestogen with actions and uses similar to those of the progestogens in general. Megestrol acetate also has anti-androgenic properties. It is given by mouth in the palliative treatment or as an adjunct to other therapy in endometrial carcinoma and in breast cancer. Megestrol acetate has been approved to treat anorexia and cachexia.
Niacin
BP12761
Niacin is a water-soluble vitamin belonging to the vitamin B family, which occurs in many animal and plant tissues, with antihyperlipidemic activity. Niacin is converted to its active form niacinamide, which is a component of the coenzymes nicotinamide adenine dinucleotide (NAD) and its phosphate form, NADP.
TWS119
BP12762
TWS119 is a GSK-3β inhibitor; capable of inducing neuronal differentiation
Binimetinib
BP12763
Binimetinib (MEK162, ARRY-162, ARRY-438162) is an orally available inhibitor of MEK1/2 (IC50: 12 nM) in a cell-free assay.
Sinomenine hydrochloride
BP12764
Sinomenine hydrochloride is extracted from Sinomenium Acutum Rehderett Wilson.
Bromhexine hydrochloride
BP12765
Bromhexine hydrochloride is a mucolytic agent used in the treatment of respiratory disorders associated with viscid or excessive mucus.
Schisandrin B
BP12766
Schisandrin B has an antioxidant effect on rodent liver and heart.
Schizandrin A
BP12767
Procainamide hydrochloride
BP12768
Procainamide Hydrochloride is the hydrochloride salt form of procainamide, an amide derivative exhibiting class 1A antiarrhythmic property and analog of procaine. Procainamide hydrochloride reversibly binds to and blocks activated (open) voltage-gated sodium channels, thereby blocks the influx of sodium ions into the cell, which leads to an increase in threshold for excitation and inhibit depolarization during phase 0 of the action potential.
Oxaliplatin
BP12769
Oxaliplatin inhibits DNA synthesis by conforming DNA adducts.
TOMATIDINE HYDROCHLORIDE
BP12770
A steriodal alkaloid structurally similar to Cyclopamine but does not inhibit hedgehog pathway. May be used as a negative control for Cyclopamine and KAAD-Cyclopamine. Tomatidine protects against muscle atrophy and boosting muscle growth.
Sulfacetamide sodium monohydrate
BP12771
Sulfacetamide sodium monohydrate is a sulfonamide antibiotic. It has been investigated for the treatment of rosacea and pityriasis versicolor.
Dimethyl fumarate
BP12772
Dimethyl fumarate, a fumarate derivative, is used as antiinflammatory and immunomodulatory agent.
Turofexorate Isopropyl
BP12773
Turofexorate Isopropyl (XL335) is a potent, selective, and orally bioavailable FXR agonist with EC50 of 4 nM
Berberine chloride
BP12774
Berberine hydrochloride is an alkaloid from Hydrastis canadensis L., Berberidaceae and also found in many other plants. It is relatively toxic to parenterally but has been used orally for various fungal and parasitic infections and an anti-diarrheal.
Oxidopamine hydrobromide
BP12775
Oxidopamine hydrobromide is a neurotransmitter dopamine antagonist.
Sulfanilamide
BP12776
Sulfanilamide can competitively inhibit bacterial enzyme dihydropteroate synthetase with IC50 of 320 μM.
Tozasertib
BP12777
MK-0457 is a pan-Aurora kinase inhibitor (Kis: 0.6/18/4.6 nM for Aurora A/Aurora B/Aurora C). It shows selectivity against more than 190 different kinases.