Echothiophate

Summary

Echothiophate (Phospholine) is an irreversible acetylcholinesterase inhibitor.[1]

Echothiophate
Clinical data
Trade namesPhospholine
Routes of
administration
Topical (eye drops)
ATC code
Identifiers
  • 2-(Diethoxyphosphorylsulfanyl)ethyl-N,N,N-trimethylazanium iodide
CAS Number
  • 6736-03-4 checkY
PubChem CID
  • 10547
DrugBank
  • DB01057 checkY
ChemSpider
  • 10107 checkY
UNII
  • 0F350BVT6S
KEGG
  • D02193 checkY
ChEBI
  • CHEBI:59849 checkY
ChEMBL
  • ChEMBL1201341 ☒N
Chemical and physical data
FormulaC9H23INO3PS
Molar mass383.23 g·mol−1
3D model (JSmol)
  • Interactive image
  • [I-].O=P(OCC)(OCC)SCC[N+](C)(C)C
  • InChI=1S/C9H23NO3PS.HI/c1-6-12-14(11,13-7-2)15-9-8-10(3,4)5;/h6-9H2,1-5H3;1H/q+1;/p-1 checkY
  • Key:OVXQHPWHMXOFRD-UHFFFAOYSA-M checkY
 ☒NcheckY (what is this?)  (verify)

Uses edit

It is used as an ocular antihypertensive in the treatment of open angle glaucoma and, in some cases, accommodative esotropia. It is available under several trade names such as Phospholine Iodide (Wyeth-Ayerst).

Echothiophate binds irreversibly to cholinesterase. Because of the very slow rate at which echothiophate is hydrolyzed by cholinesterase, its effects can last a week or more. Adverse effects include muscle spasm and other systemic effects.

Mechanism of action edit

It covalently binds by its phosphate group to serine group at the active site of the cholinesterase. Once bound, the enzyme is permanently inactive and the cell has to make new enzymes.

Shortage edit

Wyeth Pharmaceuticals stopped manufacturing echothiophate iodide in the US in 2003. After contacting the American Academy of Ophthalmology (AAO), Wyeth rescinded their decision and, according to AAO public relations representative Michelle Stephens, the AAO and Wyeth were in talks for about a year about manufacturing it.[2]

In the meantime, a worldwide shortage of the drug has occurred.[when?][citation needed]

Chemistry edit

Echothiophate is made by reacting diethylchlorophosphoric acid with 2-dimethylaminoethylmercaptan, giving S-(2-dimethylaminoethyl)-O,O-diethylthiophosphate, which is alkylated by methyl iodide, forming echothiophate.[3]

 

References edit

  1. ^ Gabelt BT, Hennes EA, Seeman JL, Tian B, Kaufman PL (August 2004). "H-7 effect on outflow facility after trabecular obstruction following long-term echothiophate treatment in monkeys". Invest. Ophthalmol. Vis. Sci. 45 (8): 2732–6. doi:10.1167/iovs.04-0083. PMID 15277498.
  2. ^ "Eurotimes article: "Echothiophate iodide shortage leaves US specialists struggling to find alternative for acute cases"". Archived from the original on 2006-06-19. Retrieved 2006-08-13.
  3. ^ H.M. Fitch, U.S. patent 2,911,430 (1959)