CNQX - Moligand™, ≥98% , Antagonist of GluA1;Antagonist of GluA2;GluA3;GluA4, CAS No.115066-14-3, Antagonist of GluA1;Antagonist of GluA2;GluA3;GluA4

CAS: 115066-14-3 Cat. No.: C131944 Peso molecular: 232.15 Número EC: 878-456-2
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
6-cyano-7-nitro-1,4-dihydroquinoxaline-2,3-dione | BRD-K53545112-304-01-6 | EX-A5681 | GTPL5475 | 6-CYANO-7-NITROQUINOXALINE-2,3-DIONE | [3H]CNQX | CNQX | 6-Quinoxalinecarbonitrile,1,2,3,4-tetrahydro-7-nitro-2,3-dioxo- | Biomol-NT_000200 | BRD-K19438463-0
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1mg
C131944-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

26,90US$

40,90US$
Guardar 14,00 US$ (34.23%)
5mg
C131944-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

69,90US$

104,90US$
Guardar 35,00 US$ (33.37%)
25mg
C131944-25mg
2

144,90US$

217,90US$
Guardar 73,00 US$ (33.50%)
100mg
C131944-100mg
3

340,90US$

511,90US$
Guardar 171,00 US$ (33.40%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
6-cyano-7-nitro-1, 4-dihydroquinoxaline-2, 3-dione | BRD-K53545112-304-01-6 | EX-A5681 | GTPL5475 | 6-CYANO-7-NITROQUINOXALINE-2, 3-DIONE | [3H]CNQX | CNQX | 6-Quinoxalinecarbonitrile, 1, 2, 3, 4-tetrahydro-7-nitro-2, 3-dioxo- | Biomol-NT_000200 | BRD-K19438463-0
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Potent, competitive AMPA/kainate glutamate receptor antagonist.Potent, competitive AMPA / kainate receptor antagonist. Also antagonist at NMDA receptor glycine site.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Tipo de acción
ANTAGONIST
Mecanismo de acción
Antagonist of GluA1;Antagonist of GluA2;GluA3;GluA4
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504762687
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504762687
Sonrisas canónicasC1=C(C(=CC2=C1NC(=O)C(=O)N2)[N+](=O)[O-])C#N
IUPAC Name7-nitro-2,3-dioxo-1,4-dihydroquinoxaline-6-carbonitrile
InChIKeyRPXVIAFEQBNEAX-UHFFFAOYSA-N
INCHI1S/C9H4N4O4/c10-3-4-1-5-6(2-7(4)13(16)17)12-9(15)8(14)11-5/h1-2H,(H,11,14)(H,12,15)
Isómeros SMILES C1=C(C(=CC2=C1NC(=O)C(=O)N2)[N+](=O)[O-])C#N
WGK Alemania 3
CAS alternativo 115066-14-3
Términos de entrada MeSH 1,4-dihydro-2,3-dihydroxy-7-nitro-6-quinoxalinecarbonitrile;6 Cyano 2,3 dihydroxy 7 nitroquinoxaline;6 Cyano 7 nitroquinoxaline 2,3 dione;6-Cyano-2,3-dihydroxy-7-nitroquinoxaline;6-Cyano-7-nitroquinoxaline-2,3-dione;CNQX;FG 9065;FG-9065;FG9065
Peso molecular 232.15
Reaxy-Rn 5821072
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5821072&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseDiazanaphthalenes
SubclassBenzodiazines
Intermediate Tree Nodes Not available
Direct ParentQuinoxalines
Alternative Parents Nitroaromatic compounds  Pyrazines  Benzenoids  Heteroaromatic compounds  Lactams  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Nitriles  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Quinoxaline - Nitroaromatic compound - Pyrazine - Benzenoid - Heteroaromatic compound - Lactam - C-nitro compound - Organic nitro compound - Carbonitrile - Nitrile - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organooxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as quinoxalines. These are compounds containing a quinoxaline moiety, a bicyclic heterocycle made up of a benzene ring fused to a pyrazine ring.
External Descriptors quinoxaline derivative
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
GRIA4 Tclin Glutamate receptor 4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA2 Tclin Glutamate receptor 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA3 Tclin Glutamate receptor 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA1 Tclin Glutamate receptor 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIA4 Tclin Glutamate receptor ionotropic AMPA (265 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Impa1 Inositol monophosphatase 1 (16203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeFechaArticulo
H1624071Certificate of AnalysisNov 06, 2025 C131944
H2528028Certificate of AnalysisSep 10, 2025 C131944
A2213363Certificate of AnalysisJul 14, 2025 C131944
A2213378Certificate of AnalysisJul 14, 2025 C131944
A2213380Certificate of AnalysisJul 14, 2025 C131944
A2509194Certificate of AnalysisApr 24, 2024 C131944
A2509193Certificate of AnalysisApr 23, 2024 C131944
Propiedades químicas y físicas
Sensibilidadlight sensitive
Peso molecular232.150 g/mol
XLogP30.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass232.023 Da
Monoisotopic Mass232.023 Da
Topological Polar Surface Area128.000 Ų
Heavy Atom Count17
Formal Charge0
Complexity434.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Huijun Li, Xin Xu, Jiwei Wang, Xuefeng Han, Zhouqing Xu.  (2021)  A Robust PVDF-Assisted Composite Membrane for Tetracycline Degradation in Emulsion and Oil-Water Separation.  Nanomaterials,  11  (12): (3201).  [PMID:34947550] [10.3390/nano11123201]
2. Shuling Shen, Junjie Wang, Zhujun Wu, Zheng Du, Zhihong Tang, Junhe Yang.  (2020)  Graphene Quantum Dots with High Yield and High Quality Synthesized from Low Cost Precursor of Aphanitic Graphite.  Nanomaterials,  10  (2): (375).  [PMID:32098041] [10.3390/nano10020375]
3. Zhicheng Wang, Shuping Nie, Ru Xia, Yang Lv, Ming Cao, Ming Chen, Qiannian Dong, Lifen Su, Peng Chen, Bin Yang, Jibin Miao, Zhengzhi Zheng, Jiasheng Qian.  (2018)  Preparation of the Yellow-Colored Aluminum Pigments with Double-Layer Structure Using a Crosslinked Copolymeric Dye.  Polymers,  10  (10): (1097).  [PMID:30961022] [10.3390/polym10101097]
4. Juan Li, Zhen Li, Yanbo Liu, Yijing Li, Yanqiong Wu, Anne Manyande, Zhixiao Li, Hongbing Xiang.  (2024)  Lysophosphatidylcholine induced by fat transplantation regulates hyperalgesia by affecting the dysfunction of ACC perineuronal nets.  iScience,      [PMID:39640595] [10.1016/j.isci.2024.111274]
5. Huanhuan Gao, Hui Liu, Peihui Xu, Jianzhong Liu.  (2024)  Micro-explosion-induced combustion and agglomeration characteristics in composite propellants with fluorinated graphene.  ACTA ASTRONAUTICA,      [PMID:] [10.1016/j.actaastro.2024.09.050]
6. Wei Du, Xiaomin Zhang, Songze Li, Xin Xie.  (2024)  Novel Perspective on Sevoflurane-Induced Cognitive Dysfunction: Implications of Neuronal SIRPα and Microglial Synaptic Remodeling.  ACS Chemical Neuroscience,      [PMID:39644326] [10.1021/acschemneuro.4c00485]
Calculadoras de soluciones
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