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    products/biochemicals/ifenprodil-hemitartrate-glun2b-formerly-nr2b-preferring-nmda-antagonist-ab120111.pdf

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Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist (ab120111)

  • Datasheet
  • SDS
  • COA
Submit a review Q&A (1)References (11)

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Chemical Structure - Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist (ab120111)
  • Functional Studies - Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist (ab120111)

Key features and details

  • GluN2B (formerly NR2B)-preferring NMDA antagonist
  • CAS Number: 23210-58-4
  • Soluble in water to 15 mM and in DMSO to 100 mM
  • Form / State: Solid
  • Source: Synthetic

Overview

  • Product name

    Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist
  • Description

    GluN2B (formerly NR2B)-preferring NMDA antagonist
  • Biological description

    Non-competitive NMDA receptor antagonist acting at the polyamine site. Displays GluN2B (formerly NR2B) subunit selectivity. IC50 values are 0.15 μM at NR1/NR2B and >30 μM for NR1/NR2A, NR1/NR2C and NR1/NR2D receptors.

    Also available in simple stock solutions (ab146675) - add 1 ml of water to get an exact, ready-to-use concentration.

  • CAS Number

    23210-58-4
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    erythro-4-(2-(4-Benzylpiperidin-1-yl)-1-hydroxypropyl)phenol hemitartrate
  • Molecular weight

    400.49
  • Molecular formula

    C21H27NO2.0.5C4H6O6
  • PubChem identifier

    656586
  • Storage instructions

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

    Soluble in water to 15 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

    CC(C(C1=CC=C(C=C1)O)O)N2CCC(CC2)CC3=CC=CC=C3.CC(C(C1=CC=C(C=C1)O)O)N2CCC(CC2)CC3=CC=CC=C3.[C@@H]([C@H](C(=O)O)O)(C(=O)O)O
  • 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
    • Biochemicals
    • Product Range
    • Just Add Water
    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Glutamate
    • NMDA
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Glutamate
    • NMDA
    • Polyamine Site
    • Antagonists
    • Biochemicals
    • Research Area
    • Addiction
    • Glutamate
    • NMDA
    • Biochemicals
    • Research Area
    • Addiction
    • Glutamate
    • NMDA
    • Polyamine Site
    • Antagonists
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Glutamate
    • NMDA
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Glutamate
    • NMDA
    • Polyamine Site
    • Antagonists
    • Biochemicals
    • Research Area
    • Depression
    • Glutamate
    • NMDA
    • Biochemicals
    • Research Area
    • Depression
    • Glutamate
    • NMDA
    • Polyamine Site
    • Antagonists
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Glutamate
    • NMDA
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Glutamate
    • NMDA
    • Polyamine Site
    • Antagonists
    • Biochemicals
    • Research Area
    • Parkinson's Disease
    • Glutamate
    • NMDA
    • Biochemicals
    • Research Area
    • Parkinson's Disease
    • Glutamate
    • NMDA
    • Polyamine Site
    • Antagonists
    • Biochemicals
    • Research Area
    • Schizophrenia
    • Glutamate
    • NMDA
    • Biochemicals
    • Research Area
    • Schizophrenia
    • Glutamate
    • NMDA
    • Polyamine Site
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    • Research Area
    • Stroke
    • Glutamate
    • NMDA
    • Biochemicals
    • Research Area
    • Stroke
    • Glutamate
    • NMDA
    • Polyamine Site
    • Antagonists
    • Neuroscience
    • Processes

Associated products

  • Related Products

    • CNQX disodium salt, AMPA / kainate antagonist (ab120044)
    • NBQX disodium salt, AMPA / kainate antagonist (ab120046)
    • QX-314 bromide (N-Ethyllidocaine bromide), Na+ channel blocker (ab120117)
    • DNQX disodium salt, AMPA / kainate antagonist (ab120169)

Images

  • Chemical Structure - Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist (ab120111)
    Chemical Structure - Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist (ab120111)
    2D chemical structure image of ab120111, Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist
  • Functional Studies - Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist (ab120111)
    Functional Studies - Ifenprodil hemitartrate, GluN2B (formerly NR2B)-preferring NMDA antagonist (ab120111)Image from Case DT et al., PLoS One. 2011;6(6):e20756. Fig 4(D).; doi: 10.1371/journal.pone.0020756. Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/
    Median ifenprodil sensitivity from a rat postnatal day 2 (P2) and day 12 (P12) neuron; NMDAR-mediated responses in control (black) and in presence of the GluN2B-preferring antagonist ifenprodil (ab120111, grey).

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 (11)

Publishing research using ab120111? Please let us know so that we can cite the reference in this datasheet.

ab120111 has been referenced in 11 publications.

  • Li Y  et al. Chronic Blockade of NMDAR Subunit 2A in the Hypothalamic Paraventricular Nucleus Alleviates Hypertension through Suppression of MEK/ERK/CREB Pathway. Am J Hypertens N/A:N/A (2021). PubMed: 33856436
  • Taoro-Gonzalez L  et al. Hyperammonemia alters membrane expression of GluA1 and GluA2 subunits of AMPA receptors in hippocampus by enhancing activation of the IL-1 receptor: underlying mechanisms. J Neuroinflammation 15:36 (2018). PubMed: 29422059
  • Yu YJ  et al. Involvement of protein phosphatases in the destabilization of methamphetamine-associated contextual memory. Learn Mem 23:486-93 (2016). PubMed: 27531839
  • Yang Y & Xu-Friedman MA Different pools of glutamate receptors mediate sensitivity to ambient glutamate in the cochlear nucleus. J Neurophysiol 113:3634-45 (2015). PubMed: 25855696
  • Tovar KR  et al. Triheteromeric NMDA receptors at hippocampal synapses. J Neurosci 33:9150-60 (2013). PubMed: 23699525
View all Publications for this product

Customer reviews and Q&As

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Question

Inquiry: hi could you please send me the price details of ifenprodil. Ifenprodil (ab120111) thanks,

Read More

Abcam community

Verified customer

Asked on Feb 26 2013

Answer

Thank you for contacting us.

The price for ab120111 is €45 for 10mg size and €215 for 50 mg size. There will be €39 delivery charges.

I hope this information is helpful to you. Please do not hesitate to contact us if you need any more advice or information.

Read More

Abcam Scientific Support

Answered on Feb 26 2013

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES, NOT FOR USE IN HUMANS"
For licensing inquiries, please contact partnerships@abcam.com

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