Xylometazoline

HCID 5709CAS 526-36-3

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

xylometazoline526-36-3XylomethazolineOtrivenXilometazolina2-[(4-tert-butyl-2,6-dimethylphenyl)methyl]-4,5-dihydro-1H-imidazoleXylometazolinumBalminilWPY40FTH8K2-(4-tert-Butyl-2,6-dimethylbenzyl)-2-imidazoline1H-Imidazole, 2-((4-(1,1-dimethylethyl)-2,6-dimethylphenyl)methyl)-4,5-dihydro-DTXSID8046957
Show more names
OtrixOtrivinBa-11391OtrivineRhinoxilinAKOS BBS-00000259XYLOMETAZOLINEANDITSHYDROCHLORIDE
1H-Imidazole, 2-[[4-(1,1-dimethylethyl)-2,6-dimethylphenyl]methyl]-4,5-dihydro-stasNasanOtrivin MentolNasentropfen ALNasenspray AL2-((4-tert-butyl-2,6-dimethylphenyl)methyl)-4,5-dihydro-1H-imidazoleNasenSpray ratiopharm

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

Experimental & physicochemical properties

Drugs · 3 items

Pharmaceuticals -> Listed in ZINC15

Pharmaceutical

Pharmaceuticals

LogP3.2
Human Drugs · 3 items

Breast Feeding; Lactation; Milk, Human; Adrenergic alpha-Agonists; Sympathomimetics; Nasal Decongestants

Pharmaceuticals

Ear, nose and throat medicines [c]

Melting Point · 2 items

317-329

131 - 133 °C

Physical DescriptionSolid
Collision Cross Section · 2 items

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)

Safety & regulation

Hazard information

Regulatory InformationChemical: 1H-Imidazole, 2-[[4-(1,1-dimethylethyl)-2,6-dimethylphenyl]methyl]-4,5-dihydro-
Other Safety InformationIMAP assessments - 1H-Imidazole, 2-[[4-(1,1-dimethylethyl)-2,6-dimethylphenyl]methyl]-4,5-dihydro-: Environment tier I assessment

Toxicology

Drug Induced Liver Injury · 4 items

Drug-Induced Liver Injury Severity and Toxicity (DILIst)

Xylometazoline

DILI Positive

DOI:10.1016/j.drudis.2019.09.022

Effects During Pregnancy and Lactation◉ Summary of Use during Lactation

Safety data

Toxicity
LD50 oral in mouse: 215mg/kg

Chemistry & industry

Pharmacology

ATC Code · 6 items

R01AA07

R - Respiratory system

R - Respiratory system

S - Sensory organs

QR - Respiratory system

QR - Respiratory system

Protein BindingNo information is available on xylometazoline pharmacokinetics.
Pharmacodynamics · 1 item

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 · 1 item

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.

Biological Half-LifeNo information is available on xylometazoline pharmacokinetics.
Metabolism/MetabolitesNo information is available on xylometazoline pharmacokinetics.

Uses & manufacturing

UsesUse (kg; approx.) in Germany (2009): >250
Use ClassificationPharmaceuticals

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

陕西缔都医药有限责任公司029-81124775 17791530730 · [email protected]
江苏瑞点药业有限公司15896106238 · [email protected]
武汉英诺医药科技有限公司+86-027-59232304 15387063101 · [email protected]
广州朗欧生物科技有限公司15876533741 · [email protected]
江苏智芯廷科技有限公司18221391031 · [email protected]

Additional notes

DefinitionChEBI: Xylometazoline is an alkylbenzene.

Related reactions

4 records

Linked notes

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