6495-46-1

Dioxadrol Chemical Structure
6495-46-1

Chemical Structure

Dioxadrol

  • CAS No.: 6495-46-1
  • Formula:C20H23NO2
  • Molecular Weight:309.40

IUPAC Name: 2-(2,2-diphenyl-1,3-dioxolan-4-yl)piperidine

InChIKey: HGKAMARNFGKMLC-UHFFFAOYSA-N

SMILES: C1(C2OC(C3=CC=CC=C3)(C4=CC=CC=C4)OC2)NCCCC1

Biological Activity: Dioxadrol is an uncompetitive NMDA receptor (PCP binding site) antagonist, with a Ki value of 10.9 nM in pigs. Dioxadrol binds to the phencyclidine (PCP) binding site within the cation channel associated with the NMDA receptor, thereby blocking cation influx. Dioxadrol possesses local anesthetic, spasmolytic and central nervous system activities, including phencyclidine-like dissociative anesthetic properties. Dioxadrol can be used in the research of Alzheimer's disease, Parkinson's disease, Huntington's disease, HIV-associated dementia, multiple sclerosis, amyotrophic lateral sclerosis, neuropathic pain, ischemic stroke, central nervous system trauma, and epilepsy[1].

Cat. No. Product Name Purity Description Pricing
HY-121285
Dioxadrol Dioxadrol is an uncompetitive NMDA receptor (PCP binding site) antagonist, with a Ki value of 10.9 nM in pigs. Dioxadrol binds to the phencyclidine (PCP) binding site within the cation channel associated with the NMDA receptor, thereby blocking cation influx. Dioxadrol possesses local anesthetic, spasmolytic and central nervous system activities, including phencyclidine-like dissociative anesthetic properties. Dioxadrol can be used in the research of Alzheimer's disease, Parkinson's disease, Huntington's disease, HIV-associated dementia, multiple sclerosis, amyotrophic lateral sclerosis, neuropathic pain, ischemic stroke, central nervous system trauma, and epilepsy.
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