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Chemical Structure
Chemical Structure
Chemical Structure

(-)-Bicuculline methiodide [40709-69-1]

Research Use Only
CDX-B0240
Chemodex
CAS Number40709-69-1
Product group Chemicals
Estimated Purity>95%
Molecular Weight509.29
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    (-)-Bicuculline methiodide [40709-69-1]
  • Delivery Days Customer
    10
  • ADR Class
    6.1
  • CAS Number
    40709-69-1
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Hazard Information
    Danger,Excepted quantity
  • Molecular Formula
    C21H20INO6
  • Molecular Weight
    509.29
  • Scientific Description
    (-)-Bicuculline methiodide is the N-methylated water-soluble derivative of the widely-employed ionotropic GABAA receptor antagonist (+)-Bicuculline. This prototypic, competitive GABAA receptor antagonist displaces GABA from the agonist binding site to prevent receptor activation. It also acts as a negative allosteric inhibitor of channel opening to inhibit GABAA receptor activation by anaesthetic agents. Additionally it shows activity at SK calcium-activated potassium channels, nicotinic acetylcholine receptors and acetylcholinesterase. This compound reversibly and competitively blocks GABAA receptor mediated currents and is widely used to isolate glutamate receptor mediated EPSCs (excitatory postsynaptic potentials). - Chemical. CAS: 40709-69-1. Formula: C21H20INO6. MW: 509.29. (-)-Bicuculline methiodide is the N-methylated water-soluble derivative of the widely-employed ionotropic GABAA receptor antagonist (+)-Bicuculline. This prototypic, competitive GABAA receptor antagonist displaces GABA from the agonist binding site to prevent receptor activation. It also acts as a negative allosteric inhibitor of channel opening to inhibit GABAA receptor activation by anaesthetic agents. Additionally it shows activity at SK calcium-activated potassium channels, nicotinic acetylcholine receptors and acetylcholinesterase. This compound reversibly and competitively blocks GABAA receptor mediated currents and is widely used to isolate glutamate receptor mediated EPSCs (excitatory postsynaptic potentials).
  • SMILES
    C[N+]1(C)[C@@]([C@@]2([H])C(C=CC3=C4OCO3)=C4C(O2)=O)([H])C5=CC6=C(OCO6)C=C5CC1.[I-]
  • Storage Instruction
    2°C to 8°C,RT
  • UN Number
    1544
  • UNSPSC
    12352200