2. Metabolic Enzyme/Protease
  3. MAGL
  4. MAGLi 432

MAGLi 432 is a non-covalent, potent, highly selective, and reversible MAGL inhibitor. MAGLi 432 binds with high affinity to the MAGL active site, with IC50 values of 4.2 nM (human enzyme) and 3.1 nM (mouse enzyme). MAGLi 432 can be used in the research of chronic inflammation, blood–brain barrier dysfunction, neurological disorders such as multiple sclerosis, Alzheimer’s disease and Parkinson’s disease.

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

MAGLi 432 Chemical Structure

MAGLi 432 Chemical Structure

CAS No. : 2361575-20-2

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MAGLi 432 Related Antibodies

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Description

MAGLi 432 is a non-covalent, potent, highly selective, and reversible MAGL inhibitor. MAGLi 432 binds with high affinity to the MAGL active site, with IC50 values of 4.2 nM (human enzyme) and 3.1 nM (mouse enzyme). MAGLi 432 can be used in the research of chronic inflammation, blood–brain barrier dysfunction, neurological disorders such as multiple sclerosis, Alzheimer’s disease and Parkinson’s disease[1].

In Vitro

MAGLi 432 (10 μΜ, 25 min) displays selectivity and potency for MAGL over other serine hydrolases in mouse and human brain lysates[1].
MAGLi 432 (1 μΜ, 6 h) inhibits MAGL activity and robustly enhances 2-AG levels in human NVU cells[1].

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

MAGLi 432 Related Antibodies

Western Blot Analysis[1]

Cell Line: Human BMECs (hCMEC/D3), primary human astrocytes, and pericytes
Concentration: 10 nM, 100 nM, 1 μM and 10 μM
Incubation Time: 6 h
Result: Inhibited MAGL activity in a dose-dependent manner, and increased 2-AG levels in all cell types.
Modulated arachidonic acid levels in a cell specific-manner, with no effect in BMECs, but significant depletion in astrocytes and pericytes.
In Vivo

MAGLi 432 (intraperitoneal injection, 1 mg/kg for 3 consecutive days) inhibits MAGL in the brain and reduces arachidonic acid and PGE2 levels in LPS-induced neuroinflammation, without reducing BBB permeability and inflammatory cytokine expression in the cortex[1].

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

Animal Model: Male CD-1 mice model of LPS-induced neuroinflammation[1]
Dosage: 1 mg/kg for 3 consecutive days
Administration: Intraperitoneal injection
Result: Accumulated ~10-fold more 2-AG than vehicle controls, reducted LPS-induced PGE2.
Increased LCN2 and TNF expression compared to the LPS treatment.
Molecular Weight

463.80

Formula

C22H24BrClN2O2
CAS No.
SMILES

O=C(C1=CC=CC(OC)=C1Br)N2C[C@](CC[C@H](C3=CC=C(Cl)C=C3)C4)([H])N4CC2
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
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MAGLi 432 Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

MAGLi 4322361575-20-2MAGLi432MAGLi-432MAGLMonoacylglycerol lipaseLipase MAGLinflammationBBBAD2-AGNVU cell chronic inflammationneurologicalmultiple sclerosisAlzheimer’s diseaseParkinson’s diseaseInhibitorinhibitorinhibit

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