MAGL-IN-1

MAGL-IN-1 Suppliers list
Company Name: Shanghai Beckham Medical Technology Co., Ltd  
Tel: 13816613772
Email: huahero21@sina.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 13301690235
Email: Sales@ATKchemical.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com

MAGL-IN-1 manufacturers

  • MAGL-IN-1
  • MAGL-IN-1 pictures
  • $34.00
  • 2026-05-11
  • CAS:2324160-91-8
  • Purity:
  • Supply Ability: 10g
MAGL-IN-1 Basic information
Product Name:MAGL-IN-1
Synonyms:MAGL-IN-1;MAGLIN1,MAGL IN 1;(1-(2-fluoro-5-hydroxybenzoyl)piperidin-4-yl)(4-isopropylphenyl)methanone
CAS:2324160-91-8
MF:C22H24FNO3
MW:369.43
EINECS:
Product Categories:
Mol File:2324160-91-8.mol
MAGL-IN-1 Structure
MAGL-IN-1 Chemical Properties
Boiling point 558.9±50.0 °C(Predicted)
density 1.214±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMF: 25 mg/ml; DMF:PBS (pH 7.2) (1:6): 0.14 mg/ml; DMSO: 20 mg/ml; Ethanol: 2.5 mg/ml
form A crystalline solid
pka9.51±0.18(Predicted)
color White to off-white
Safety Information
MSDS Information
MAGL-IN-1 Usage And Synthesis
DescriptionMAGL inhibitor compound 23 is an inhibitor of monoacylglycerol lipase (MAGL; IC50 = 80 nM).1 It is selective for MAGL over cannabinoid receptor 1 (CB1), CB2, fatty acid amide hydrolase (FAAH), α/β-hydrolase domain-containing protein 6 (ABHD6), and ABHD12 (IC50s = >10 μM). MAGL inhibitor compound 23 inhibits the growth of HCT116, MDA-MB-231, Caov-3, OVCAR-3, and SKOV3 cells (IC50s = 21, 7.9, 25, 57, and 15 μM, respectively) but not MRC5 cells (IC50 = >100 μM). It increases the levels of 2-arachidonoyl glycerol (2-AG; ) in mouse brain and plasma when administered at a dose of 50 mg/kg.
UsesMAGL-IN-1 is a potent, selective, reversible and competitive inhibitor of MAGL, with an IC50 of 80 nM. MAGL-IN-1 exhibits anti-proliferative effects against human breast, colorectal, and ovarian cancer cells. MAGL-IN-1 blocks MAGL in cell-based as well as in vivo assays[1].
in vivo

MAGL (compound 23) (50 mg/kg; a single i.p.) increases the 2-AG level in plasma and brain, and does not alter anandamide (AEA), arachidonic acid and prostaglandin levels in plasma and brain of mice[1].

Animal Model:Male C57BL6 mice, 8-10 weeks old[1]
Dosage:50 mg/kg
Administration:Intraperitoneal injection; once
Result:Increased 2-AG levels in the brain and plasma.
References1. Granchi, C., Lapillo, M., Glasmacher, S., et al. Optimization of a benzoylpiperidine class identifies a highly potent and selective reversible monoacylglycerol lipase (MAGL) inhibitor J. Med. Chem. 62(4),1932-1958(2019).
MAGL-IN-1 Preparation Products And Raw materials
Tag:MAGL-IN-1(2324160-91-8) Related Product Information
1-Acetyl-4-(2,4-difluorobenzoyl)piperidine (2-fluorophenyl)-[3-(4-methoxyphenyl)pyrrolidin-1-yl]methanone N-[[1-(2-fluorobenzoyl)piperidin-4-yl]methyl]-1-(4-fluorophenyl)cyclopropane-1-carboxamide MAGL Inhibitor Compound 23 Methanone, (2-fluoro-4-hydroxyphenyl)-1-piperidinyl- 4-fluoro-3-[(piperidin-1-yl)carbonyl]phenol