You Searched For: 3-Methyladenine


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Catalog Number: (76002-048)
Supplier: Enzo Life Sciences
Description: PI3 kinase inhibitor


Supplier: TCI America
Description: 3-Methyladenine, CAS Number: 5142-23-4, Molecular Formula: C6H7N5, Molecular Weight: 149.16, Synonyms: 6-Amino-3-methylpurine, Form: Crystal - Powder, Solid, Color: White - Almost white, Size: 1G
Supplier: MP Biomedicals
Description: 3-Methyladenine, Purity: >99%, CAS No: 5142-23-4, Molecular Formula: C6H7N5, Molecular Weight: 149.2, Solubility: 1 M Sodium Hydroxide or dimethylformamide (10mg/ml-clear, colorless solution), Synonym: 6-amino-3-methylpurine, Appearance: White to off white powder, Size: 100MG

Supplier: Thermo Scientific Chemicals
Description: 3-Methyladenine 90+%

Supplier: APOLLO SCIENTIFIC
Description: 3-Methyladenine

Supplier: Ambeed
Description: 3-Methyl-3H-purin-6-amine, Purity: 98%, CAS Number: 5142-23-4, Appearance: Form: Crystal - Powder/Colour: White - Almost white, Storage: Keep in dark place, Sealed in dry, Room Temperature, Size: 100mg

Supplier: Thermo Scientific Chemicals
Description: A synthetic intermediate and a cell-permeable autophagic sequestration blocker that protects cerebellar granule cells from apoptosis post serum/potassium deprivation
Supplier: Adipogen
Description: Used to inhibit and study the mechanism of autophagy (lysosomal self-degradation) and apoptosis under various conditions. Inhibits autophagy by blocking autophagosome formation via the inhibition of type III Phosphatidylinositol 3-kinases (PI-3K).

Supplier: Adipogen
Description: Potent cell permeable and selective inhibitor of phosphatidyl-inositol 3-kinase (PI3K). Blocks class I, class II and class III PI3Ks, including some downstream targets. Blocks class I PI3K persistently and class III PI3K transiently. Induces autophagy under nutrient-rich conditions and inhibits starvation-induced autophagy due to differential effects on class I versus class III PI3 kinase. Shows some limited Vps34 preference in vitro compared to PtdIns3Kgamma. However, it is typically employed in cellular studies at a concentration of 10 mM, which can inhibit all PtdIns3Ks. Can target other kinases and affect other cellular processes, such as glycogen metabolism, lysosomal acidification, endocytosis and mitochondrial permeability transition. Anticancer compound. Neuroprotective. PKA-activation dependent lipolytic agent. Enhances ATGL-dependent hydrolysis of triacylglycerols.

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