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    products/biochemicals/cyclothiazide-ampa-receptor-desensitisation-inhibitor-ab120061.pdf

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Cyclothiazide, AMPA receptor desensitisation inhibitor (ab120061)

  • Datasheet
  • SDS
  • COA
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Chemical Structure - Cyclothiazide, AMPA receptor desensitisation inhibitor (ab120061)
  • Cellular activation - Cyclothiazide, AMPA receptor desensitisation inhibitor (ab120061)

Key features and details

  • AMPA receptor desensitisation inhibitor
  • CAS Number: 2259-96-3
  • Soluble in ethanol to 25 mM and in DMSO to 100 mM
  • Form / State: Solid
  • Source: Synthetic

Overview

  • Product name

    Cyclothiazide, AMPA receptor desensitisation inhibitor
  • Description

    AMPA receptor desensitisation inhibitor
  • Biological description

    Positive allosteric modulator of AMPA receptors. Produces a fast inhibition of AMPA receptor desensitization and a much slower potentiation of the AMPA current. Also available in Kit: Ionotropic agonists (ab120323).

  • CAS Number

    2259-96-3
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    6-Chloro-3,4-dihydro-3-(norbornen-5-yl)-2H-1,2,4-benzothiadiazine-7-sulfonamide-1,1-dioxide
  • Molecular weight

    389.87
  • Molecular formula

    C14H16ClN3O4S2
  • PubChem identifier

    2910
  • Storage instructions

    Store at +4°C. Store under desiccating conditions. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in ethanol to 25 mM and in DMSO to 100 mM
  • Handling

    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.

    Refer to SDS for further information

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    NS(=O)(=O)c4cc1c(NC(NS1(=O)=O)C3CC2C=CC3C2)cc4Cl
  • Source

    Synthetic

  • Research areas

    • Neuroscience
    • Neurotransmitter
    • Amino Acids
    • Glutamate
    • Neuroscience
    • Neurotransmission
    • Receptors / Channels
    • GPCR
    • Glutamate Receptors
    • Neuroscience
    • Neurotransmission
    • Receptors / Channels
    • Ligand-Gated Ion Channels
    • AMPA / Kainate
    • Signal Transduction
    • Signaling Pathway
    • G Protein Signaling
    • GPCR
    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Glutamate
    • AMPA & Kainate
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Glutamate
    • AMPA & Kainate
    • Allosteric modulators
    • Biochemicals
    • Research Area
    • Addiction
    • Glutamate
    • AMPA & Kainate
    • Biochemicals
    • Research Area
    • Addiction
    • Glutamate
    • AMPA & Kainate
    • Allosteric modulators
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Glutamate
    • AMPA & Kainate
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Glutamate
    • AMPA & Kainate
    • Allosteric modulators
    • Biochemicals
    • Research Area
    • Depression
    • Glutamate
    • AMPA & Kainate
    • Biochemicals
    • Research Area
    • Depression
    • Glutamate
    • AMPA & Kainate
    • Allosteric modulators
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Glutamate
    • AMPA & Kainate
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Glutamate
    • AMPA & Kainate
    • Allosteric modulators
    • Biochemicals
    • Research Area
    • Parkinson's Disease
    • Glutamate
    • AMPA & Kainate
    • Biochemicals
    • Research Area
    • Parkinson's Disease
    • Glutamate
    • AMPA & Kainate
    • Allosteric modulators
    • Biochemicals
    • Research Area
    • Schizophrenia
    • Glutamate
    • AMPA & Kainate
    • Biochemicals
    • Research Area
    • Schizophrenia
    • Glutamate
    • AMPA & Kainate
    • Allosteric modulators
    • Biochemicals
    • Research Area
    • Stroke
    • Glutamate
    • AMPA & Kainate
    • Biochemicals
    • Research Area
    • Stroke
    • Glutamate
    • AMPA & Kainate
    • Allosteric modulators

Associated products

  • Related Products

    • Ionotropic Agonists Kit (ab120323)

Images

  • Chemical Structure - Cyclothiazide, AMPA receptor desensitisation inhibitor (ab120061)
    Chemical Structure - Cyclothiazide, AMPA receptor desensitisation inhibitor (ab120061)
    2D chemical structure image of ab120061, Cyclothiazide, AMPA receptor desensitisation inhibitor
  • Cellular activation - Cyclothiazide, AMPA receptor desensitisation inhibitor (ab120061)
    Cellular activation - Cyclothiazide, AMPA receptor desensitisation inhibitor (ab120061)Image from Case DT, et al. Plos One, 6(6), e20756. Fig S4,; doi: 10.1371/journal.pone.0020756
    To determine the capability of VCN-LSO synapses to support repetitive activity in the developing circuit, we added cyclothiazide to the perfusate to prevent AMPAR desensitization and measured responses to 50 Hz pulse-train stimuli delivered to the ventral acoustic stria. A. Representative responses to 50 Hz pulse-trains in P2, P5, and P9 cells; responses to the first five pulses only are shown. Greater paired-pulse depression between pulse 1 and 2 is evident in the youngest cell than in the older cells.

Protocols

To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

Click here to view the general protocols

Datasheets and documents

  • SDS download

  • Datasheet download

    Download
  • COA

References (18)

Publishing research using ab120061? Please let us know so that we can cite the reference in this datasheet.

ab120061 has been referenced in 18 publications.

  • Huang Y  et al. GIRK1-mediated inwardly rectifying potassium current suppresses the epileptiform burst activities and the potential antiepileptic effect of ML297. Biomed Pharmacother 101:362-370 (2018). PubMed: 29499411
  • Nguyen-Minh VT  et al. Electrophysiological Excitability and Parallel Fiber Synaptic Properties of Zebrin-Positive and -Negative Purkinje Cells in Lobule VIII of the Mouse Cerebellar Slice. Front Cell Neurosci 12:513 (2018). PubMed: 30670950
  • Droste D  et al. Ca2+-permeable AMPA receptors in mouse olfactory bulb astrocytes. Sci Rep 7:44817 (2017). PubMed: 28322255
  • Winland CD  et al. Inflammation alters AMPA-stimulated calcium responses in dorsal striatal D2 but not D1 spiny projection neurons. Eur J Neurosci 46:2519-2533 (2017). PubMed: 28921719
  • Han W  et al. Ferric Chelate Reductase 1 Like Protein (FRRS1L) Associates with Dynein Vesicles and Regulates Glutamatergic Synaptic Transmission. Front Mol Neurosci 10:402 (2017). PubMed: 29276473
View all Publications for this product

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