Basic information
- Standard SMILES
Cc1cc(C(C)(C)C)cc(C)c1CC1=NCCN1- InChIKey
HUCJFAOMUPXHDK-UHFFFAOYSA-N- Molecular formula
- C16H24N2
- Average molar mass
- 244.37 g/mol
- Monoisotopic mass
- 244.19394877
Overview
Xylometazoline is an alkylbenzene.
Names & identifiers
- Preferred name
- Xylometazoline
- IUPAC
- 2-[(4-tert-butyl-2,6-dimethylphenyl)methyl]-4,5-dihydro-1H-imidazole
- English name
- 2-(4-TERT-BUTYL-2,6-DIMETHYL-BENZYL)-4,5-DIHYDRO-1H-IMIDAZOLE
- Molecular formula
- C16H24N2
- Molecular weight
- 244.38
Names & synonyms
Show more names
Database identifiers
- CAS
526-36-3- PubChem CID
- 5709
- DTXSID
DTXSID8046957- ChEMBL
CHEMBL312448- ChEBI
CHEBI:10082- UNII
- WPY40FTH8K
- EC Number
- 208-390-6
- Nikkaji
- J6.660E
Properties
Computed structural properties
- XLogP
- 3.2
- Topological polar surface area
- 24.4 Ų
- Hydrogen bond donors
- 1
- Hydrogen bond acceptors
- 1
- Rotatable bonds
- 3
- Heavy atoms
- 18
- Formal charge
- 0
- Complexity
- 302
Experimental & physicochemical properties
Drugs
Pharmaceuticals -> Listed in ZINC15
Pharmaceutical
Pharmaceuticals
Human Drugs
Breast Feeding; Lactation; Milk, Human; Adrenergic alpha-Agonists; Sympathomimetics; Nasal Decongestants
Pharmaceuticals
Ear, nose and throat medicines [c]
Melting Point
317-329
131 - 133 °C
Collision Cross Section
161.58 Ų [M+Na]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]
170.4 Ų [M+H]+ [CCS Type: TW; Method: Major Mix IMS/Tof Calibration Kit (Waters)]
Physicochemical properties
- Melting point
- 131 · 131-133°
- Boiling point
- 394.2 · 394.2±21.0 °C(Predicted)
- Density
- 1 · 1.00±0.1 g/cm3(Predicted)
- storage temp.
- -20 °C · Store at -20°C
- solubility
- 49 mg/mL · DMSO: 49 mg/mL (200.51 mM);Ethanol: 49 mg/mL (200.51 mM)
- pka
- 10.6 · pKa 10.6±0.1(H2O t = 22.0) (Uncertain)
- Water Solubility
- Water: Insoluble
- InChI
- InChI=1S/C16H24N2/c1-11-8-13(16(3,4)5)9-12(2)14(11)10-15-17-6-7-18-15/h8-9H,6-7,10H2,1-5H3,(H,17,18)
- InChIKey
- HUCJFAOMUPXHDK-UHFFFAOYSA-N
- SMILES
- C1(CC2=C(C)C=C(C(C)(C)C)C=C2C)NCCN=1
- CAS DataBase Reference
- 526 · 526-36-3
- EWG's Food Scores
- 1 · 1
- FDA UNII
- 40 FTH8K · WPY40FTH8K
- ATC code
- 1 AA07,R01AB06,S01GA03,S01GA53 · R01AA07,R01AB06,S01GA03,S01GA53
- Toxicity
- 50 oral · LD50 oral in mouse: 215mg/kg
Safety & regulation
Hazard information
Toxicology
Drug Induced Liver Injury
Drug-Induced Liver Injury Severity and Toxicity (DILIst)
Xylometazoline
DILI Positive
DOI:10.1016/j.drudis.2019.09.022
Safety data
- Toxicity
- LD50 oral in mouse: 215mg/kg
Chemistry & industry
Pharmacology
ATC Code
R01AA07
R - Respiratory system
R - Respiratory system
S - Sensory organs
QR - Respiratory system
QR - Respiratory system
Pharmacodynamics
Xylometazoline is a sympathomimetic agent that causes vasoconstriction of the nasal mucosa. In one study comprising subjects with nasal congestion associated with the common cold, the median time of onset of subjective relief of nasal congestion was about 1.7 minutes and the time of subjective peak relief of nasal congestion was 30 minutes. Previous studies reported rebound swelling, rebound nasal congestion, rhinitis medicamentosa, and shorter duration of decongestant effect from the long-term use of xylometazoline in healthy volunteers, suggesting that the drug is most effective if used temporarily. An early _in vitro_ study demonstrated xylometazoline to exert anti-oxidant actions, where it inhibited microsomal lipid peroxidation and mediated hydroxyl radical scavenging activity. This suggests that xylometazoline has a beneficial effect against oxidants, which play a role in tissue damage in inflammation.
Mechanism of Action
Nasal congestion is caused by various etiologies, such as rhinosinusitis and allergic or non-allergic rhinitis, leading to congestion of the venous sinusoids lining the nasal mucosa. Activation of α-adrenergic receptors leads to vasoconstriction of the blood vessels of the nasal mucosa and resumption of nasal airflow. As the most abundantly expressed in the human nasal mucosa, α<sub>1A</sub>- and α<sub>2B</sub>-adrenoceptors may play the most important role in vasoconstriction of the human nasal mucosa. Xylometazoline is a more selective agonist at α<sub>2B</sub>-adrenoceptors, with affinity at α<sub>1A</sub>-, α<sub>2A</sub>-, α<sub>2C</sub>-, α<sub>1B</sub>-, and α<sub>1D</sub>-adrenoceptors. Xylometazoline decreases nasal resistance during inspiration and expiration and increases the volume of nasal airflow. Compared to [oxymetazoline], another imidazoline nasal decongestant, xylometazoline had a slightly faster onset of action although they had a similar duration of action. In one study, subjects with nasal congestion reported relief of earache and sore throat in addition to nasal decongestion: it is speculated that oxymetazoline mediates this effect by causing vasoconstriction of the nasal mucosa that contains the venous sinuses and nasal decongestion allows breathing through the nose, providing relief from sore throat caused by mouth breathing that dries and irritates the throat.
MeSH Pharmacological Classification
Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS.
A class of drugs that act by selective inhibition of calcium influx through cellular membranes.
Drugs designed to treat inflammation of the nasal passages, generally the result of an infection (more often than not the common cold) or an allergy related condition, e.g., hay fever. The inflammation involves swelling of the mucous membrane that lines the nasal passages and results in inordinate mucus production. The primary class of nasal decongestants are vasoconstrictor agents. (From PharmAssist, The Family Guide to Health and Medicine, 1993)
Drugs used to cause dilation of the blood vessels.
Absorption, Distribution and Excretion
No information is available on xylometazoline pharmacokinetics.
No information is available on xylometazoline pharmacokinetics.
No information is available on xylometazoline pharmacokinetics.
No information is available on xylometazoline pharmacokinetics.
Uses & manufacturing
Applications
UsesAdrenergic (vasoconstrictor).
UsesXylometazoline is used for rhinitis, laryngitis, sinusitis, inflammation of antrum of Highmore, and allergic illnesses of the nasal cavity and throat.
Suppliers45 total
Additional notes
DefinitionChEBI: Xylometazoline is an alkylbenzene.
Related reactions
Linked notes
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