ChemicalBook >> CAS DataBase List >>488793-85-7

488793-85-7

CAS No.
488793-85-7
Chemical Name:
488793-85-7
Synonyms
ARN272;ARN-272
CBNumber:
CB23145843
Molecular Formula:
C27H20N4O2
Molecular Weight:
432.47
MDL Number:
MOL File:
488793-85-7.mol

488793-85-7 Properties

Boiling point 629.1±55.0 °C(Predicted)
Density 1.357±0.06 g/cm3(Predicted)
pka 8.56±0.30(Predicted)

488793-85-7 price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 11244 ARN272 488793-85-7 1mg $36 2021-12-16 Buy
Cayman Chemical 11244 ARN272 488793-85-7 5mg $150 2021-12-16 Buy
Cayman Chemical 11244 ARN272 488793-85-7 10mg $250 2021-12-16 Buy
Axon Medchem Axon 2941 ARN 272 98% 488793-85-7 25mg $330 2021-12-16 Buy
Axon Medchem Axon 2941 ARN 272 98% 488793-85-7 2x25mg $550 2021-12-16 Buy
Product number Packaging Price Buy
11244 1mg $36 Buy
11244 5mg $150 Buy
11244 10mg $250 Buy
Axon 2941 25mg $330 Buy
Axon 2941 2x25mg $550 Buy

488793-85-7 Chemical Properties,Uses,Production

Uses

ARN 272 is a a competitive antagonist of the interaction of anandamide with FAAH-like anandamide transporter (FLAT), that lacks amidase activity but binds anandamide with low micromolar affinity and facilitates its translocation into cells.

Enzyme inhibitor

This FLAT inhibitor (FW = 432.47 g/mol; CAS 488793-85-7), also named 4-[[4-(4-hydroxy-phenyl)-1-phthalazinyl]amino]-N-phenylbenzamide, targets the FAAH-Like Anandamide Transporter (IC50 = 1.8 μM), a catalytically silent variant of fatty acid amide hydrolase-1 (FAAH-1) that drives anandamide transport. Mode of Action: The intensity and duration of anandamide signaling appear to be controlled by a two-step elimination process, in which the anandamide or an anandamide-like substance is first internalized by neurons and astrocytes through the action of FLAT and then undergoes hydrolysis through the action of the intracellular membrane- bound amidases, FAAH-1 and FAAH-2. ARN-272 attenuates anandamide internalization, thereby reducing its deactivation. ARN272 competitively antagonizes [ 3 H]-anandamide binding to FLAT (IC50 = 1.8 μM) and inhibits [ 3 H]-anandamide accumulation in both FLAT-expressing Hek293 cells (IC50 ≈ 3 μM) and primary cultures of cortical neurons prepared from rats or wild-type mice. By contrast, ARN272 is without significant effect on the residual [ 3 H]-anandamide accumulation observed in cortical transport system may also facilitate the release of this lipid mediator from cells It also exhibits analgesic effects in rodent models of CB1 endocannabinoid receptor-mediated nociceptive and inflammatory pain.

488793-85-7 Preparation Products And Raw materials

Raw materials

Preparation Products

488793-85-7 Suppliers

Global( 9)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Lollane Biological Technology Co.,Ltd. 021-52996696,15000506266 15000506266 China 4153 55
Shanghai Biopharmaleader Co., Ltd. +86 18721201413 sales@biopharmaleader.com China 1720 58
Shanghai hongqu biomedical technology co. LTD 88888888888 hongquchem@qq.com China 5132 58
United States Biological -- sales@advtechind.com United States 6106 58
ARN272 ARN-272