ChemicalBook > CAS DataBase List > JZL 184

JZL 184

Product Name
JZL 184
CAS No.
1101854-58-3
Chemical Name
JZL 184
Synonyms
CS-815;CS-1861;JZL 184;JZL-184; JZL 184;JZL 184 JZL184 JZL-184;JZL184 (with 15% inorganics);MAGL Inhibitor III, JZL184 - CAS 1101854-58-3 - Calbiochem;4-Nitrophenyl 4-[bis(1,3-benzodioxol-5-yl)(hydroxy)Methyl]-1-piperidinecarboxylate;4-Nitrophenyl 4-(bis(benzo[d][1,3]dioxol-5-yl)(hydroxy)methyl)piperidine-1-carboxylate;4-[Bis(1,3-benzodioxol-5-yl)hydroxymethyl]-1-piperidinecarboxylic acid 4-nitrophenyl ester
CBNumber
CB12535677
Molecular Formula
C27H24N2O9
Formula Weight
520.49
MOL File
1101854-58-3.mol
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JZL 184 Property

Melting point:
116-120°C
Boiling point:
706.4±60.0 °C(Predicted)
Density 
1.467±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Soluble in DMSO (up to 25 mg/ml).
form 
White to off-white solid
pka
13.32±0.29(Predicted)
color 
light yellow to yellow-green
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months
CAS DataBase Reference
1101854-58-3
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Safety

RIDADR 
UN 2811 6.1 / PGIII
HS Code 
29349990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

Precautionary statements

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
475741
Product name
MAGL Inhibitor III, JZL184 - CAS 1101854-58-3 - Calbiochem<br />The MAGL Inhibitor III, JZL184, also referenced under CAS 1101854-58-3, controls the biological activity of MAGL.
Packaging
10mg
Price
$159
Updated
2024/03/01
Sigma-Aldrich
Product number
J3455
Product name
JZL 184 hydrate
Purity
≥97% (HPLC)
Packaging
5MG
Price
$170
Updated
2023/06/20
Cayman Chemical
Product number
13158
Product name
JZL 184
Purity
≥97%
Packaging
5mg
Price
$44
Updated
2024/03/01
Cayman Chemical
Product number
13158
Product name
JZL 184
Purity
≥97%
Packaging
10mg
Price
$74
Updated
2024/03/01
Cayman Chemical
Product number
13158
Product name
JZL 184
Purity
≥97%
Packaging
50mg
Price
$299
Updated
2024/03/01
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JZL 184 Chemical Properties,Usage,Production

Description

Endocannabinoids such as 2-arachidonoyl glycerol (2-AG) and arachidonoyl ethanolamide (AEA) are biologically active lipids that are involved in a number of synaptic processes including activation of cannabinoid receptors. Monoacylglycerol lipase (MAGL) is a serine hydrolase responsible for the hydrolysis of 2-AG to arachidonic acid and glycerol, thus terminating its biological function. JZL 184 is a potent and selective inhibitor of monoacylglycerol lipase (MAGL) that displays IC50 values of 8 nM and 4 μM for inhibition of MAGL and fatty acid amide hydrolase in mouse brain membranes, respectively. When administered to mice at 16 mg/kg, intraperitoneally, JZL 184 reduces MAGL activity by 85%, elevates brain 2-AG levels by 8-fold, and elicits analgesic activity in a variety of pain assays that qualitatively mimics direct central cannabinoid (CB1) agonists.

Uses

JZL 184 hydrate has been used as an inhibitor of monoacylglycerol lipase to study its effect on human osteoblast differentiation and proliferation and postsynaptic neurons.

Uses

JZL184 is a strong and selective inhibitor of Monoglyceride Lipase.

Definition

ChEBI: 4-[bis(1,3-benzodioxol-5-yl)-hydroxymethyl]-1-piperidinecarboxylic acid (4-nitrophenyl) ester is a member of benzodioxoles.

Biochem/physiol Actions

JZL184 selectively inhibits MAGL, the enzyme predominantly responsible for the degradation of the endocannabinoid 2-arachidonoylglycerol (2-AG). Anandamide and 2-AG are the two endogenous endocannabinoids that activate the cannabinoid receptors CB1 and CB2. Anandamide is predominantly metabolized by fatty acid amide hydrolase (FAAH), whereas monoacylglycerol lipase (MAGL) is thought to be the enzyme primarily responsible for the degradation of 2-AG. It is difficult to separate the activities of the two because most currently available inhibitors of MAGL are not selective, and also inhibit FAAH or other enzymes. JZL 184 is the first selective inhibitor of MAGL with nanomolar portency and over 200-fold selectivity for MAGL vs FAAH. When administered to mice, JZL184 increased levels of 2-arachidonoylglycerol in the brain by about 8-fold, with no effect on levels of anandamide.

storage

Store at -20°C

References

1) Long et al. (2009), Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects; Nat. Chem. Biol.,5 37 2) Pan et al. (2009), Blockade of 2-arachidonoylglycerol hydrolysis by selective monoacylglycerol lipase inhibitor 4-nitrophenyl 4-(dibenzo[d][1,3]dioxol-5-yl(hydroxyl)methyl)piperidine-1-carboxylate (JZL 184) enhances retrograde endocannabinoid signaling; J. Pharmacol. Exp. Ther., 331 591 3) Kinsey et al. (2009), Blockade of endocannabinoid-degrading enzymes attenuates neuropathic pain; J. Pharmacol. Exp. Ther., 330 902

JZL 184 Preparation Products And Raw materials

Raw materials

Preparation Products

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JZL 184 Suppliers

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View Lastest Price from JZL 184 manufacturers

Career Henan Chemical Co
Product
JZL 184 1101854-58-3
Price
US $1.00/g
Min. Order
1g
Purity
99.99%
Supply Ability
200kg
Release date
2019-12-23

1101854-58-3, JZL 184Related Search:


  • JZL 184 JZL184 JZL-184
  • JZL 184
  • 4-Nitrophenyl 4-[bis(1,3-benzodioxol-5-yl)(hydroxy)Methyl]-1-piperidinecarboxylate
  • 4-[Bis(1,3-benzodioxol-5-yl)hydroxymethyl]-1-piperidinecarboxylic acid 4-nitrophenyl ester
  • 1-Piperidinecarboxylic acid, 4-[bis(1,3-benzodioxol-5-yl)hydroxymethyl]-, 4-nitrophenyl ester
  • 4-[Bis(1,3-benzodioxol-5-yl)hydroxymethyl]-1-piperidinecarboxylic acid 4-nitrophenyl ester JZL 184
  • MAGL Inhibitor III, JZL184 - CAS 1101854-58-3 - Calbiochem
  • JZL-184; JZL 184
  • CS-815
  • CS-1861
  • JZL 184 ?JZL184 ?JZL-184 ?(4-Nitrophenyl) 4-[bis(1,3-benzodioxol-5-yl)-hydroxymethyl]piperidine-1-carboxylate
  • 1-Piperidinecarboxylicacid,4-Chemicalbook[bis(1,3-benzodioxol-5-yl)hydroxymethyl]-,4-nitrophenylester
  • JZL184 (with 15% inorganics)
  • 4-Nitrophenyl 4-(bis(benzo[d][1,3]dioxol-5-yl)(hydroxy)methyl)piperidine-1-carboxylate
  • 1101854-58-3
  • Inhibitors