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Miotine

From Wikipedia, the free encyclopedia
Miotine
Names
IUPAC name
[3-[1-(Dimethylamino)ethyl]phenyl]N-methylcarbamate
Other names
AR-28[1]
T-1843[1]
Identifiers
3D model (JSmol)
ChemSpider
KEGG
UNII
  • InChI=1S/C12H18N2O2/c1-9(14(3)4)10-6-5-7-11(8-10)16-12(15)13-2/h5-9H,1-4H3,(H,13,15) ☒N
    Key: KQOUPMYYRQWZLI-UHFFFAOYSA-N ☒N
  • InChI=1/C12H18N2O2/c1-9(14(3)4)10-6-5-7-11(8-10)16-12(15)13-2/h5-9H,1-4H3,(H,13,15)
    Key: KQOUPMYYRQWZLI-UHFFFAOYAX
  • CC(C1=CC(=CC=C1)OC(=O)NC)N(C)C
Properties
C12H18N2O2
Molar mass222.288 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Miotine is ananticholinesterase drug. Miotine was the first syntheticcarbamate that was used clinically.[2]

Unlike the miotine analogneostigmine, it doesn't have a quaternaryammonium group to give it a permanent positive charge. It can exist as an unchargedfree base which could allow it to cross theblood–brain barrier and cause unwantedcentral nervous system (CNS) side effects.[3]

Miotine equilibrium
Miotine equilibrium

See also

[edit]

References

[edit]
  1. ^abChemical Warfare Agents, and Related Chemical Problems. Parts I-II. 1958.
  2. ^"Archived copy"(PDF). Archived fromthe original(PDF) on 2009-05-09. Retrieved2008-01-04.{{cite web}}: CS1 maint: archived copy as title (link)
  3. ^"An introduction to drugs,their action and discovery"(PDF).


Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
Enhancers


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