Comparison

3-Methyladenine

Item no. CS-5207-100mg
Manufacturer ChemScene
Amount 100mg
Category
Type Molecules
Specific against other
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Similar products 5142-23-4
Available
Alternative Names
3-MA
CAS
5142-23-4
Purity
>98%
Formula
C6H7N5
MWt
149.15
Solubility
H2O : 4 mg/mL (26.82 mM; Need ultrasonic); DMSO : 22.14 mg/mL (148.44 mM; Need ultrasonic)
Clinical Information
No Development Reported
Pathway
PI3K/Akt/mTOR; Autophagy; Autophagy; Metabolic Enzyme/Protease
Target
PI3K; Autophagy; Mitophagy; Endogenous Metabolite
Biological Activity
3-Methyladenine is a PI3K inhibitor. 3-Methyladenine is a widely used inhibitor of autophagy via its inhibitory effect on class III PI3K. IC50 & Target: IC50: 25 uM (Vps34), 60 uM (PI3Kgamma)[1] In Vitro: 3-Methyladenine (0-10 mM; 0-48 hours) induces caspase-dependent cell death in HeLa cells in a time-and dose-dependent manner[2].
3-Methyladenine (5 mM; 24 hours) suppresses autophagy in HeLa cells under both glucose-free conditions and normal conditions[2].
3-Methyladenine (5 mM; 0-48 hours) suppresses conversion of LC3-I to LC3-II (autophagy markers) between 12hours and 48 hours, confirms the inhibitory effects on autophagy[2].
3-Methyladenine induces cell death is independent of autophagy inhibition[2].
3-Methyladenine significantly shortens the duration of nocodazole-induced-prometaphase arrest[2].
In Vivo: 3-Methyladenine (1.5?mg/100?g; intraperitoneal injection; 3-24?hours) treatment alleviates sodium taurocholate-induced severe acute pancreatitis (SAP) in rats at both 12 hours and 24?hours[3].
3-Methyladenine inhibits autophagy of pancreatic acinar cells in sodium taurocholate-tnduced SAP[3].
3-Methyladenine also shows inhibitory effects on PI3K/Akt signaling pathway and NF-kappaB signaling pathway in sodium taurocholate-induced SAP[3].

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All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100mg
Available: In stock
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