CP-465022 Maleate

Modify Date: 2025-08-26 09:18:33

CP-465022 Maleate Structure
CP-465022 Maleate structure
Common Name CP-465022 Maleate
CAS Number 199656-46-7 Molecular Weight 579.02
Density N/A Boiling Point N/A
Molecular Formula C30H28ClFN4O5 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of CP-465022 Maleate


CP-465022 Maleate is a potent, and selective noncompetitive AMPA receptor antagonist with anticonvulsant activity. CP-465022 is against Kainate-induced response with an IC50 of 25 nM in rat cortical neurons. CP-465022 provides a new tool to investigate the role of AMPA receptors in physiological and pathophysiological processes[1][2].

 Names

Name 3-(2-Chlorophenyl)-2-[(E)-2-{6-[(diethylamino)methyl]-2-pyridinyl}vinyl]-6-fluoro-4(3H)-quinazolinone (2Z)-2-butenedioate (1:1)
Synonym More Synonyms

 CP-465022 Maleate Biological Activity

Description CP-465022 Maleate is a potent, and selective noncompetitive AMPA receptor antagonist with anticonvulsant activity. CP-465022 is against Kainate-induced response with an IC50 of 25 nM in rat cortical neurons. CP-465022 provides a new tool to investigate the role of AMPA receptors in physiological and pathophysiological processes[1][2].
Related Catalog
Target

IC50: 25 nM (rat cortical neurons)[1]

In Vitro CP-465022 (0.0001 μM-10 μM) inhibits kainate-induced response in relatively slow manner and dependents on compound concentration, exhibiting a calculated IC50 of 25 nM and essentially complete inhibition at 3.2 µM[1]. CP-465022 1 µM for 10 min has little effect on peak NMDA-induced currents but reduces current measured at 8 s during NMDA application by 26%.CP-465,022 at 10 µM inhibits peak NMDA-induced currents in cortical neurons by 36% and currents measured at 8 s by 70% d in primary cultures of cortical and cerebellar granule neurons[1]. CP-465022 1 µM for 10 min inhibits peak NMDA currents in cultured rat cerebellar granule neurons with mean inhibition of 19% and NMDA currents measured at 8 s by 45%, similar to what is observed in the cortical neurons[1]. CP-465022 (100 nM -10 µM) has inhibitory effects on Kainate-induced whole-cell currents in voltage-clamped rat hippocampal, 100 nM CP465,022 inhibits kainate currents developed over the course of 200s, 500 nM and 1 µM CP-465,022 nearly complete inhibits this time frame (99.3%)[1].
References

[1]. J T Lazzaro, et al. Functional characterization of CP-465,022, a selective, noncompetitive AMPA receptor antagonist. Neuropharmacology. 2002 Feb;42(2):143-53.

 Chemical & Physical Properties

Molecular Formula C30H28ClFN4O5
Molecular Weight 579.02
Exact Mass 578.173218

 Synonyms

4(3H)-Quinazolinone, 3-(2-chlorophenyl)-2-[(E)-2-[6-[(diethylamino)methyl]-2-pyridinyl]ethenyl]-6-fluoro-, (2Z)-2-butenedioate (1:1)
3-(2-Chlorophenyl)-2-[(E)-2-{6-[(diethylamino)methyl]-2-pyridinyl}vinyl]-6-fluoro-4(3H)-quinazolinone (2Z)-2-butenedioate (1:1)
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here


Get all suppliers and price by the below link:

CP-465022 Maleate suppliers


Price: ¥12500/1 mg

Reference only. check more CP-465022 Maleate price

Related Compounds: More...
CP 465022 HCl
1785666-59-2
cp 162399
154531-78-9
Cp(molybdenum)dinitrosyl(methyl)
57034-48-7
(4S,5R,6S)-3-[6-[(2R)-3-amino-2-hydroxypropyl]-7-methylsulfanylimidazo[5,1-b][1,3]thiazol-6-ium-2-yl]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
770700-40-8
CP 55,940
83003-12-7
cp 16 460
36322-91-5
CP 55,940
83002-04-4
CP 47,497-C6-homolog
70435-06-2
[Cp(CO)3W]2Mg
123118-50-3
N-(2,4-dimethoxyphenyl)-2-(1-(4-fluorophenyl)-4-methyl-7-oxo-1H-pyrazolo[3,4-d]pyridazin-6(7H)-yl)acetamide
942008-95-9
N-(2,5-dimethoxyphenyl)-2-(1-(4-fluorophenyl)-4-methyl-7-oxo-1H-pyrazolo[3,4-d]pyridazin-6(7H)-yl)acetamide
941884-42-0
N-(3,4-dimethoxyphenyl)-2-(1-(4-fluorophenyl)-4-methyl-7-oxo-1H-pyrazolo[3,4-d]pyridazin-6(7H)-yl)acetamide
941973-06-4
N-(benzo[d][1,3]dioxol-5-yl)-2-(1-(4-fluorophenyl)-4-methyl-7-oxo-1H-pyrazolo[3,4-d]pyridazin-6(7H)-yl)acetamide
941915-21-5
N-(2-iodophenyl)-5-[(4-methylphenoxy)methyl]furan-2-carboxamide
890615-21-1
5-(4-chloro-2-nitrophenyl)-2-methyl-N-(4-sulfamoylphenyl)furan-3-carboxamide
890617-00-2
N-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-[1-(4-fluorophenyl)-4-methyl-7-oxo-1H,6H,7H-pyrazolo[3,4-d]pyridazin-6-yl]acetamide
942008-98-2
2-(1-(4-fluorophenyl)-4-methyl-7-oxo-1H-pyrazolo[3,4-d]pyridazin-6(7H)-yl)-N-(3-(trifluoromethyl)phenyl)acetamide
941884-44-2
2-(1-(4-fluorophenyl)-4-methyl-7-oxo-1H-pyrazolo[3,4-d]pyridazin-6(7H)-yl)-N-(4-(trifluoromethyl)phenyl)acetamide
941973-08-6
methyl 4-(2-(1-(4-fluorophenyl)-4-methyl-7-oxo-1H-pyrazolo[3,4-d]pyridazin-6(7H)-yl)acetamido)benzoate
941915-23-7