[CAS NO. 5142-23-4]  3-Methyladenine

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PRODUCTS SPECIFICATIONS [5142-23-4]

Store
Catalog
AS016753
Brand
Arctom Scientific
CAS
5142-23-4

DESCRIPTION [5142-23-4]

Overview

MDLMFCD00010531
Molecular Weight149.15
Molecular FormulaC6H7N5
SMILESNC1=C2N=CN=C2N(C)C=N1

For research use only. We do not sell to patients.

458 Publications Citing Use of MCE


Summary

3-Methyladenine (3-MA) is a PI3K inhibitor. 3-Methyladenine is a widely used inhibitor of autophagy via its inhibitory effect on class III PI3K [1] .


IC50 & Target

PtdIns3Kγ

60 μM (IC 50 , Cell Assay)

Vps34

25 μM (IC 50 , Cell Assay)

Autophagy

Mitophagy

Human Endogenous Metabolite


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] .
Note:
The recommended concentration of 3-MA is approximately 0.5-10 mM in cell culture. DMSO stock solution is not recommended. We suggest that you can weigh out the amount of 3-MA you required before your experiment. Then please dissolve it in medium and sterilize with a 0.22 μm filter.

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay [2]

Cell Line: HeLa cells
Concentration: 0 mM, 2.5 mM or 5 mM, 10 mM
Incubation Time: 0 hour, 24 hours and 48 hours
Result: Decreased cell viability in a time-and dose-dependent manner, and was associated with caspase-3 activation.

Cell Autophagy Assay [2]

Cell Line: HeLa cells
Concentration: 5 mM
Incubation Time: 24 hours
Result: Suppressed autophagy in HeLa cells under both glucose-free conditions and normal conditions.

Western Blot Analysis [2]

Cell Line: HeLa cells
Concentration: 5 mM
Incubation Time: 0 hour, 12 hours, 24 hours and 48 hours
Result: Suppressed conversion of LC3-I to LC3-II between 12 hours and 48 hours.

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-κB signaling pathway in sodium taurocholate-induced SAP [3] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 10–12 weeks Specific pathogen free- (SPF-) grade healthy male Sprague-Dawley (SD) rats (250–290 g) [3]
Dosage: 1.5 mg/100 g (1000 μM)
Administration: Intraperitoneal injection
Result: Alleviated Sodium Taurocholate-Induced SAP.

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

H 2 O : 5 mg/mL ( 33.52 mM ; Need ultrasonic)

DMSO : 8.33 mg/mL ( 55.85 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 6.7047 mL 33.5233 mL 67.0466 mL
5 mM 1.3409 mL 6.7047 mL 13.4093 mL
10 mM 0.6705 mL 3.3523 mL 6.7047 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: PBS

    Solubility: 4 mg/mL (26.82 mM); Clear solution; Need ultrasonic

* All of the co-solvents are available by MCE.


Synonyms

3H-Purin-6-amine, 3-methyl-
Adenine, 3-methyl-
3-Methyl-3H-purin-6-amine
3-Methyladenine
N3-Methyladenine
6-Amino-3-methylpurine
3-Methyl-6-aminopurine
NSC 66389
3-Methyl-3H-purin-6-ylamine
3-Methylpurin-6-amine