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propacetamol

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propacetamol

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Propacetamol is a prodrug form of paracetamol which is formed from esterification of paracetamol, and the carboxylic acid diethylglycine. This has the advantage of making it more water-soluble. It is used in post-operative care and is delivered by I.V. It is given if the patient is unable to take oral or rectally delivered paracetamol and nonsteroidal anti-inflammatory drugs (NSAIDs) are contraindicated. The onset of analgesia from propacetamol is more rapid than paracetamol given orally. 2 grams of propacetamol are equivalent to 1g of paracetamol.

Chemical data

Formula
C14H20N2O3
Molecular weight
264.32 g/mol
IUPAC name
(4-acetamidophenyl) 2-(diethylamino)acetate
SMILES
CCN(CC)CC(=O)OC1=CC=C(C=C1)NC(=O)C
InChIKey
QTGAJCQTLIRCFL-UHFFFAOYSA-N
XLogP
1.1
Polar surface area
58.6 Ų
H-bond donors
1
H-bond acceptors
4
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule
Indications
pain, Fever

via ChEMBL · EBI

Wikidata facts

Mass
264.147393
Has use
medication
Show 5 more facts
chemical formula
C₁₄H₂₀N₂O₃
defined daily dose
6
canonical SMILES
CCN(CC)CC(=O)OC1=CC=C(C=C1)NC(=O)C
subject has role
analgesic
Commons category
Propacetamol
Sources (3)

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Encyclopedic overview

2 sections
Contents
  • See also
  • References

Propacetamol is a prodrug form of paracetamol which is formed from esterification of paracetamol, and the carboxylic acid diethylglycine. This has the advantage of making it more water-soluble. It is used in post-operative care and is delivered by I.V. It is given if the patient is unable to take oral or rectally delivered paracetamol and nonsteroidal anti-inflammatory drugs (NSAIDs) are contraindicated. The onset of analgesia from propacetamol is more rapid than paracetamol given orally. 2 grams of propacetamol are equivalent to 1g of paracetamol.

== See also == Phenacetin

Excerpted from Wikipedia’s “propacetamol” article, available under the CC BY-SA 4.0 licence.

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