Details
Stereochemistry | RACEMIC |
Molecular Formula | C13H13NO4 |
Molecular Weight | 247.2466 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1N2CCCC2OC3=CC4=C(OCCO4)C=C13
InChI
InChIKey=RQEPVMAYUINZRE-UHFFFAOYSA-N
InChI=1S/C13H13NO4/c15-13-8-6-10-11(17-5-4-16-10)7-9(8)18-12-2-1-3-14(12)13/h6-7,12H,1-5H2
Molecular Formula | C13H13NO4 |
Molecular Weight | 247.2466 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/23999288Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/20839777 | https://www.ncbi.nlm.nih.gov/pubmed/21543522 | https://www.ncbi.nlm.nih.gov/pubmed/10999951 | https://www.ncbi.nlm.nih.gov/pubmed/24550387
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23999288
Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/20839777 | https://www.ncbi.nlm.nih.gov/pubmed/21543522 | https://www.ncbi.nlm.nih.gov/pubmed/10999951 | https://www.ncbi.nlm.nih.gov/pubmed/24550387
CX614 (2H,3H,6aH-pyrrolidino(2,1-3',2')1,3-oxazino(6',5'-5,4)benzo(e)1,4-dioxan-10-one) is a positive allosteric modulator of the AMPA receptor. Chronic treatment of rat hippocampal slices with CX614 gradually reduced levels of glutamate receptor (GluR)1 and GluR2/3 AMPA subunits and of their anchoring proteins synapse-associated protein 97 (SAP97) and glutamate receptor interacting protein 1 (GRIP1). The physiological and toxicological properties of this compound have not been evaluated in humans.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2009 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20839777 |
21.0 µM [EC50] | ||
Target ID: CHEMBL4016 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21543522 |
46.0 µM [EC50] | ||
Target ID: CHEMBL3504 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10999951 |
71.0 µM [EC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21543522
Outside-out membrane patches from transfected HEK293 cells were held under voltage-clamp at a holding potential of _60 mV using an Axopatch 200B amplifier. During recordings, cells were perfused continuously with extracellular control solution containing 20 mM sucrose, 145 mM NaCl, 5.4 mM KCl, 5 mM HEPES, 1 mM MgCl2, 1.8 mM CaCl2, and 0.01 mg/ml phenol red, pH 7.3. Currents were evoked with test solutions containing 10 mM glutamate. Control and test solutions were perfused through quartz tubing. The patch pipette tip was positioned in the control solution stream near the interface between the control and glutamate-containing streams. When modulators were used, they were added to both test and control solutions in the following concentrations: 100 mkM CTZ, 100 mkM CX614, and 10 mkM CMPDA or CMPDB. Modulator stock solutions (10 mM) were dissolved in DMSO before dilution in extracellular solutions; final DMSO concentrations were 0.3 to 1%. When applying glutamate in the absence of modulator, after having perfused modulator through the tubing for a previous patch, we noticed that the steady-state current responses were not completely desensitized.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:50:33 GMT 2023
by
admin
on
Fri Dec 15 16:50:33 GMT 2023
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Record UNII |
87V631480W
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Record Status |
Validated (UNII)
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Record Version |
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CX614
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191744-13-5
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DTXSID30912324
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6451148
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87V631480W
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admin on Fri Dec 15 16:50:33 GMT 2023 , Edited by admin on Fri Dec 15 16:50:33 GMT 2023
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