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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
Structure of CX614

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

HIDE SMILES / InChI

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 ( + / - )

Description
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.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
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 Fri Dec 15 16:50:33 UTC 2023
Edited
by admin
on Fri Dec 15 16:50:33 UTC 2023
Record UNII
87V631480W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CX614
Common Name English
BDP 37
Code English
CX-614
Code English
2H,3H,6AH-PYRROLIDINO(2,1-3',2')1,3-OXAZINO(6',5'-5,4)BENZO(E)1,4-DIOXAN-10-ONE
Common Name English
CX 614
Code English
11H-1,4-DIOXINO(2,3-G)PYRROLO(2,1-B)(1,3)BENZOXAZIN-11-ONE, 2,3,6A,7,8,9-HEXAHYDRO-
Common Name English
LID-37
Code English
(±)-CX 614
Common Name English
BDP-37
Code English
LID 37
Code English
Code System Code Type Description
WIKIPEDIA
CX614
Created by admin on Fri Dec 15 16:50:33 UTC 2023 , Edited by admin on Fri Dec 15 16:50:33 UTC 2023
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CAS
191744-13-5
Created by admin on Fri Dec 15 16:50:33 UTC 2023 , Edited by admin on Fri Dec 15 16:50:33 UTC 2023
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EPA CompTox
DTXSID30912324
Created by admin on Fri Dec 15 16:50:33 UTC 2023 , Edited by admin on Fri Dec 15 16:50:33 UTC 2023
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PUBCHEM
6451148
Created by admin on Fri Dec 15 16:50:33 UTC 2023 , Edited by admin on Fri Dec 15 16:50:33 UTC 2023
PRIMARY
FDA UNII
87V631480W
Created by admin on Fri Dec 15 16:50:33 UTC 2023 , Edited by admin on Fri Dec 15 16:50:33 UTC 2023
PRIMARY