Oxeladin

Chemical compound


title: "Oxeladin" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public tags: ["antitussives", "carboxylate-esters", "ethers", "diethylamino-compounds", "sigma-agonists"] description: "Chemical compound" topic_path: "general/antitussives" source: "https://en.wikipedia.org/wiki/Oxeladin" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0

::summary Chemical compound ::

::data[format=table title="Infobox drug"]

FieldValue
Verifiedfieldschanged
verifiedrevid462266955
IUPAC_name2-(2-diethylaminoethoxy)ethyl 2-ethyl-2-phenyl-butanoate
imageOxeladin_skeletal.svg
image_classskin-invert-image
Drugs.com
pregnancy_AU
pregnancy_US
legal_AU
legal_CA
legal_UK
legal_US
CAS_number_Ref
CAS_number468-61-1
ATC_prefixR05
ATC_suffixDB09
PubChem4619
DrugBank_Ref
DrugBankDB04822
ChemSpiderID_Ref
ChemSpiderID4458
UNII_Ref
UNIISNC1080T5Y
KEGG_Ref
KEGGD08310
ChEMBL_Ref
ChEMBL1500276
C20
smilesO=C(OCCOCCN(CC)CC)C(c1ccccc1)(CC)CC
StdInChI_Ref
StdInChI1S/C20H33NO3/c1-5-20(6-2,18-12-10-9-11-13-18)19(22)24-17-16-23-15-14-21(7-3)8-4/h9-13H,5-8,14-17H2,1-4H3
StdInChIKey_Ref
StdInChIKeyIQADUMSPOQKAAO-UHFFFAOYSA-N
::

| Verifiedfields = changed | verifiedrevid = 462266955 | IUPAC_name = 2-(2-diethylaminoethoxy)ethyl 2-ethyl-2-phenyl-butanoate | image = Oxeladin_skeletal.svg | image_class = skin-invert-image

| tradename = | Drugs.com = | pregnancy_AU = | pregnancy_US = | legal_AU = | legal_CA = | legal_UK = | legal_US =

| CAS_number_Ref = | CAS_number = 468-61-1 | ATC_prefix = R05 | ATC_suffix = DB09 | PubChem = 4619 | DrugBank_Ref = | DrugBank = DB04822 | ChemSpiderID_Ref = | ChemSpiderID = 4458 | UNII_Ref = | UNII = SNC1080T5Y | KEGG_Ref = | KEGG = D08310 | ChEMBL_Ref = | ChEMBL = 1500276

| C=20 | H=33 | N=1 | O=3 | smiles = O=C(OCCOCCN(CC)CC)C(c1ccccc1)(CC)CC | StdInChI_Ref = | StdInChI = 1S/C20H33NO3/c1-5-20(6-2,18-12-10-9-11-13-18)19(22)24-17-16-23-15-14-21(7-3)8-4/h9-13H,5-8,14-17H2,1-4H3 | StdInChIKey_Ref = | StdInChIKey = IQADUMSPOQKAAO-UHFFFAOYSA-N

Oxeladin is a cough suppressant. It is a highly potent and effective drug used to treat all types of cough of various etiologies. It is not related to opium or its derivatives, so treatment with oxeladin is free of risk of dependence or addiction. Oxeladin has none of the side effects (such as hypnosis, respiratory depression, tolerance, constipation and analgesia) which are present when common antitussives, such as codeine and its derivatives, are used. It may be used at every age, as well as in patients with heart disease, since it has a high level of safety and a great selectivity to act on the bulbar centre of cough.

Indications

Oxeladin is indicated in all types of cough. Besides its antitussive action, it helps to clear the respiratory tract, since it increases the quantity of secretion and thins bronchial secretion.

Contraindications

Although fetal malformations have not been reported, oxeladin should not be used during the first trimester of pregnancy. Oxeladin is contraindicated in patients with MAOI therapy.

Side effects

Rarely, some patients have reported rash, dizziness, sedation or mild digestive disturbances. These usually disappear on reducing the dosage or interrupting the treatment.

Addiction

Oxeladin differs from common antitussives that cause addiction (such as etilmorphin, codeine or its derivatives) in that there is no evidence of risk of addiction or dependence.

Composition and packaging

Oxeladin is available as drops, syrup and tablets, providing easier ways of management which will be chosen depending on the age and clinical stage.

Drops

Each 1ml (33 drops) contains oxeladin citrate 20 mg. The bottle contains 20ml of solution.

Syrup

Each 100ml contains oxeladin citrate 200 mg. The bottle contains 100ml of syrup.

Tablets

Each tablet contains oxeladin citrate 20 mg. The box contains 20 tablets in blister packs

Dosage

  • Children 2-5yrs: 2.5ml-5ml (17 drops) every 4–6 hours
  • Children 6-12 yrs: 10ml (33 drops), or 1 tablet, every 4–6 hours
  • Children 12 yrs and over and adults: 15ml (50 drops), or 2 tablets, every 4–6 hours

Restrictions in use and availability

Oxeladine formulations were withdrawn from the US, UK and Canadian markets in 1976 due to concerns of potential carcinogenicity. The Drug and Medical Technology Agency of Armenia rejected the registration of oxeladin in July 2000 since studies in Germany have raised similar concerns. (Reference: Communication to WHO, 9 August 2000.)

References

References

  1. (July 1957). "Antitussive and other pharmacological properties of the diethylaminoethoxyethyl ester of alpha alpha-diethylphenylacetic acid, (oxeladin)". The Journal of Pharmacy and Pharmacology.
  2. "Oxeladin - Drug Bank".
  3. "Pharmaceuticals: Restrictions in Use and Availability: Monocomponent products: Oxeladin citrate".

::callout[type=info title="Wikipedia Source"] This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page. ::

antitussivescarboxylate-estersethersdiethylamino-compoundssigma-agonists