5,7-Dichlorokynurenic acid

SKU:BHB21300120
Overview
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5,7-Dichlorokynurenic acid (CAS 131123-76-7) is an NMDA receptor antagonist acting at the glycine site1. Supplied as Lyophilized powder (purity >98%, solubility 200 mM in DMSO. Centrifuge all product preparations before use (10 000 X g fo...). Commonly used in Neuroscience studies, including binding assays and second-messenger readouts.
Target NMDA receptor
Cas No 131123-76-7
concentration 0.5-20 µM.
purity >98%
Molecular Formula C10H5Cl2NO3.
Form Lyophilized powder.
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size (4) - 10 mg, 100 mg, 25 mg, 50 mg; Quantity: 1
  • Lead time: typically ships in 1-2 business days; timing may vary by selected option.
  • Storage: Before reconstitution: The product is shipped as a lyophilized powder at room temperature. Upon receipt, store the product at -20°C. Protect from moisture. After reconstitution: The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods (up to 6 months), small aliquots should be stored at -20°C. We do not recommend storing the product in working solutions for longer than a few days. Avoid multiple freeze-thaw cycles. Storage of solutions: Up to four weeks at 4°C or three months at -20°C.
  • Shipping: Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Options selector
Catalog no. Size Quantity
D-190-10MG-1 10 mg
D-190-100MG-1 100 mg
D-190-25MG-1 25 mg
D-190-50MG-1 50 mg
Field Specification
Activity
  • Antagonist
Cas No. 131123-76-7
Concentration 0.5-20 µM.
Form Lyophilized powder.
Product Type
  • Biochemicals
  • Small Molecules
Purity >98%
Reconstitution 200 mM in DMSO. Centrifuge all product preparations before use (10 000 X g for 1 min).
Shipping Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
Solubility 200 mM in DMSO. Centrifuge all product preparations before use (10 000 X g for 1 min).
Source Synthetic
Storage Before reconstitution: The product is shipped as a lyophilized powder at room temperature. Upon receipt, store the product at -20°C. Protect from moisture. After reconstitution: The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods (up to 6 months), small aliquots should be stored at -20°C. We do not recommend storing the product in working solutions for longer than a few days. Avoid multiple freeze-thaw cycles. Storage of solutions: Up to four weeks at 4°C or three months at -20°C.
Target NMDA receptor

Product details

  • Chemical name: 5,7-dichloro-4-oxo-1H-quinoline-2-carboxylic acid.
  • Also known as: 5,7-DCKA
  • CAS number: 131123-76-7
  • Molecular formula: C10H5Cl2NO3.
  • Purity: >98%
  • Concentration: 0.5-20 µM.
  • Form: Lyophilized powder.
  • Solubility: 200 mM in DMSO. Centrifuge all product preparations before use (10 000 X g for 1 min).
  • Reconstitution: 200 mM in DMSO. Centrifuge all product preparations before use (10 000 X g for 1 min).
  • Shipping: Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
  • Target: NMDA receptors
  • Source: Synthetic
  • Activity: 5,7-Dichlorokynurenic acid is an NMDA receptor antagonist acting at the glycine site1.
  • Alternative names: 5,7-DCKA

Scientific background

5,7-Dichlorokynurenic acid (5,7-DCKA), is a derivative of kynurenic acid, an extremely potent excitatory amino acid receptor antagonist of N-methyl-D-aspartate (NMDA) receptors. 5,7-DCKA binds with high affinity to a strychnine-insensitive glycine binding site located on the NMDA receptor. This site is considered to be used as a therapeutic target for acute focal ischemia. The compound exhibits strong selectivity for binding to GluN1 subunit over GluN3A1,2 with an IC50 value of 79 nM in rat cortical and hippocampal membranes4.Small concentrations of 5,7-DCKA have the ability to inhibit several processes including NMDA-stimulated elevation of cytosolic calcium in cultured hippocampal neurons, cGMP accumulation in cerebellar slices, and norepinephrine release from hippocampal regions1.Several different studies have demonstrated potent anticonvulsant features of 5,7-DCKA when the compound is administrated intra-cerebroventricularly directly to the brain1.NMDA receptors play an important role in a variety of cellular processes and brain functions such as synaptic plasticity, addiction and stroke. They mediate several physiological functions including learning and memory formation; they play a role in glutamate excitotoxicity and are involved in many neurodegenerative conditions including Alzheimer's disease.

Lead time: 1-2 Business Days

Country of origin: Israel/IL

Applications key

Application key: FC- Flow cytometry, IFC- Indirect flow cytometry, IHC- Immunohistochemistry,LCI- Live cell imaging, Calcium imaging assay,Cell survival assay, Electrophysiology, Neurite outgrowth assay.

Bioassay tested: Yes

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  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
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