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NAGLY

NAGLY Structure
CAS No.
179113-91-8
Chemical Name:
NAGLY
Synonyms
NAGLY;NAGly, CID 5283389;Arachidonyl Glycine;ARACHIDONOYL GLYCINE;N-ARACHIDONYL GLYCINE;N-ARACHIDONOYL GLYCINE;N Arachidonylglycine,NArachidonylglycine;N-Arachidonoyl glycine (solution in ethanol);N-(1-OXO-5Z,8Z,11Z,14Z-EICOSATETRAENYL)GLYCINE;Glycine, N-[(5Z,8Z,11Z,14Z)-1-oxo-5,8,11,14-eicosatetraen-1-yl]-
CBNumber:
CB0232490
Molecular Formula:
C22H35NO3
Molecular Weight:
361.52
MOL File:
179113-91-8.mol
Modify Date:
2023/6/30 15:45:59

NAGLY Properties

Boiling point 560.9±50.0 °C(Predicted)
Density 0.985±0.06 g/cm3(Predicted)
storage temp. −20°C
solubility DMSO: >5 mg/mL, soluble
form waxy solid
pka 3.58±0.10(Predicted)
color off-white
Sensitive Air Sensitive
Stability Stable for 2 years from date of purchase as supplied. Product is subject to oxidation. Solutions in degassed DMSO may be stored at -20°C for up to 1 month.

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H315-H319-H336-H351
Precautionary statements  P201-P302+P352-P305+P351+P338-P308+P313
Safety Statements  22-24/25
WGK Germany  3
NFPA 704
3
0 0

NAGLY Chemical Properties,Uses,Production

Description

Arachidonoyl glycine (N-arachidonyl glycine; NAGly) has been isolated from cell cultures treated with arachidonoyl ethanolamide (AEA; anandamide), from extracts of mammalian brain, and has also been synthesized as an analog of AEA for structure/activity testing. NAGly may be produced endogenously via oxidation of AEA, or by transacylation of arachidonoyl CoA. NAGly is reported to have analgesic activities in whole animal experiments. Since it seems to be a very poor ligand for the CB1 receptor, these effects are probably mediated via other signaling pathways.

Uses

Arachidonoyl glycine (N-arachidonyl glycine; NAGly) has been isolated from cell cultures treated with arachidonoyl ethanolamide (AEA; anandamide), from extracts of mammalian brain, and has also been synthesized as an analog of AEA for structure/activity testing. NAGly may be produced endogenously via oxidation of AEA, or by transacylation of arachidonoyl CoA. NAGly is reported to have analgesic activities in whole animal experiments. Since it seems to be a very poor ligand for the CB1 receptor, these effects are probably mediated via other signaling pathways.[Cayman Chemical]

Biological Activity

Endogenous anandamide-like compound. Lacks affinity for CB 1 receptors (K i > 10 μ M), VR1 receptors (EC 50 > 10 μ M) and anandamide transporters (IC 50 > 50 μ M) but causes hot-plate analgesia in mice when given orally, and suppresses tonic inflammatory pain. Also endogenous GlyT2 inhibitor.

NAGLY Preparation Products And Raw materials

Raw materials

Preparation Products

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TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
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Nantong QuanYi Biotechnology Co., Ltd 0513-66337626 18051384581 China 4552 58 Inquiry
Cayman Chemical Company (800) 364-9897 United States 6618 81 Inquiry
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Shenzhen Regent Biochemical Technology Co., Ltd. 0755-0755-85201366 18938635012 China 9304 58 Inquiry
N-ARACHIDONOYL GLYCINE N-ARACHIDONYL GLYCINE NAGLY N-(1-OXO-5Z,8Z,11Z,14Z-EICOSATETRAENYL)GLYCINE ARACHIDONOYL GLYCINE N-Arachidonoyl glycine (solution in ethanol) Glycine, N-[(5Z,8Z,11Z,14Z)-1-oxo-5,8,11,14-eicosatetraen-1-yl]- Arachidonyl Glycine NAGly, CID 5283389 N Arachidonylglycine,NArachidonylglycine 179113-91-8 Cannabinoid receptor