35474-99-8 Usage
Description
1-MONOARACHIDIN, a derivative of 2-Arachidonoylglycerol (A765050), is a significant endocannabinoid that plays a crucial role in the endocannabinoid system. It possesses the ability to inhibit synaptic transmission through its action on presynaptic cannabinoid CB1 receptors, making it a promising candidate for various therapeutic applications.
Uses
Used in Pharmaceutical Industry:
1-MONOARACHIDIN is used as a therapeutic agent for managing various conditions related to the endocannabinoid system. Its ability to inhibit synaptic transmission via cannabinoid CB1 receptors makes it a potential candidate for treating neurological disorders, pain management, and other conditions influenced by the endocannabinoid system.
Used in Research Applications:
1-MONOARACHIDIN serves as an important research tool in studying the endocannabinoid system and its role in various physiological and pathological processes. It aids researchers in understanding the mechanisms of action, signaling pathways, and potential therapeutic targets within the system.
Used in Drug Development:
1-MONOARACHIDIN is utilized in the development of novel drugs targeting the endocannabinoid system. Its interaction with cannabinoid CB1 receptors provides insights into the design and synthesis of new drug candidates that can modulate the system for therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 35474-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,7 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35474-99:
(7*3)+(6*5)+(5*4)+(4*7)+(3*4)+(2*9)+(1*9)=138
138 % 10 = 8
So 35474-99-8 is a valid CAS Registry Number.
InChI:InChI=1/C23H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-23(26)27-21-22(25)20-24/h6-7,9-10,12-13,15-16,22,24-25H,2-5,8,11,14,17-21H2,1H3/b7-6-,10-9-,13-12-,16-15-
35474-99-8Relevant articles and documents
Simplified chemical and radiochemical synthesis of 2-arachidonoyl-glycerol, an endogenous ligand of cannabinoid receptors
Cartoni, Antonella,Margonelli, Andrea,Angelini, Giancarlo,Finazzi-Agrò, Alessandro,Maccarrone, Mauro
, p. 2723 - 2726 (2004)
Endocannabinoids have emerged as a new class of lipid mediators, with manifold roles in the central nervous system and in the periphery. Several studies have identified 2-arachidonoyl-glycerol (2-AG) as a major endogenous agonist of cannabinoid receptors. Here, the chemical synthesis of 2-AG is reported, along with the synthesis of its tritium-labeled derivative. These unlabeled and radiolabeled compounds are suitable tools for unravelling some metabolic routes and biological activities of 2-AG in various cells and tissues.