From Wikipedia, the free encyclopedia
Mr. Ibrahem/Montelukast
Clinical data
Trade namesSingulair, others
AHFS/ Drugs.com Monograph
MedlinePlus a600014
License data
Pregnancy
category
Routes of
administration
By mouth
Drug class Leukotriene receptor antagonist
Legal status
Legal status
Pharmacokinetic data
Bioavailability63–73%
Protein binding99%
Metabolism Liver ( CYP2C8-major, CYP3A4 and CYP2C9-minor) [2]
Elimination half-life2.7–5.5 hours
ExcretionBiliary
Identifiers
  • (R,E)-2-(1-((1-(3-(2-(7-Chloroquinolin-2-yl)vinyl)phenyl)-3-(2-(2-hydroxypropan-2-yl)phenyl)propylthio)methyl)cyclopropyl)acetic acid
Chemical and physical data
FormulaC35H36ClNO3S
Molar mass586.19 g·mol−1
3D model ( JSmol)
Melting point145 to 148 °C (293 to 298 °F)
  • O=C(O)CC1(CC1)CS[C@@H](c2cccc(c2)\C=C\c3nc4cc(Cl)ccc4cc3)CCc5ccccc5C(O)(C)C
  • InChI=1S/C35H36ClNO3S/c1-34(2,40)30-9-4-3-7-25(30)13-17-32(41-23-35(18-19-35)22-33(38)39)27-8-5-6-24(20-27)10-15-29-16-12-26-11-14-28(36)21-31(26)37-29/h3-12,14-16,20-21,32,40H,13,17-19,22-23H2,1-2H3,(H,38,39)/b15-10+/t32-/m1/s1 checkY
  • Key:UCHDWCPVSPXUMX-TZIWLTJVSA-N checkY
   (verify)

Montelukast, sold under the brand name Singulair among others, is a medication used in the maintenance treatment of asthma. [3] It is generally less preferred for this use than inhaled corticosteroids. [3] It is not useful for acute asthma attacks. [3] Other uses include allergic rhinitis and hives of long duration. [3] For allergic rhinitis it is a second line treatment. [5] It is taken by mouth. [3]

Common side effects include abdominal pain, cough, and headache. [3] Severe side effects may include allergic reactions, such as anaphylaxis and eosinophilia. [3] Use in pregnancy appears to be safe. [3] Montelukast is in the leukotriene receptor antagonist family of medications. [3] It works by blocking the action of leukotriene D4 in the lungs resulting in decreased inflammation and relaxation of smooth muscle. [3]

Montelukast was approved for medical use in the United States in 1998. [3] It is available as a generic medication. [6] In the United States, the wholesale cost per dose is less than 0.15 USD as of 2018. [7] In 2017, it was the 16th most commonly prescribed medication in the United States, with more than 31 million prescriptions. [8] [9]

References

  1. ^ a b "Montelukast (Singulair) Use During Pregnancy". Drugs.com. 13 December 2019. Archived from the original on 7 August 2019. Retrieved 4 March 2020.
  2. ^ "Montelukast 10 mg film coated tablets - Summary of Product Characteristics (SmPC) - (eMC)". Archived from the original on 23 December 2018. Retrieved 23 December 2018.
  3. ^ a b c d e f g h i j k l m "Montelukast Sodium Monograph for Professionals". Drugs.com. AHFS. Archived from the original on 7 June 2019. Retrieved 23 December 2018.
  4. ^ Cite error: The named reference WHO2020DDD was invoked but never defined (see the help page).
  5. ^ Grainger, J.; Drake-Lee, A. (2006). "Montelukast in allergic rhinitis: a systematic review and meta-analysis". Clinical Otolaryngology. 31 (5). Wiley: 360–367. doi: 10.1111/j.1749-4486.2006.01276.x. ISSN  0307-7772. PMID  17014443. regarded as second line therapy. When used, montelukast should be used in combination with an antihistamine.
  6. ^ British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 269. ISBN  9780857113382.
  7. ^ "NADAC as of 2018-12-19". Centers for Medicare and Medicaid Services. Archived from the original on 19 December 2018. Retrieved 22 December 2018.
  8. ^ "The Top 300 of 2020". ClinCalc. Archived from the original on 12 February 2021. Retrieved 4 March 2020.
  9. ^ "Montelukast - Drug Usage Statistics". ClinCalc. 23 December 2019. Archived from the original on 11 April 2020. Retrieved 11 April 2020.
From Wikipedia, the free encyclopedia
Mr. Ibrahem/Montelukast
Clinical data
Trade namesSingulair, others
AHFS/ Drugs.com Monograph
MedlinePlus a600014
License data
Pregnancy
category
Routes of
administration
By mouth
Drug class Leukotriene receptor antagonist
Legal status
Legal status
Pharmacokinetic data
Bioavailability63–73%
Protein binding99%
Metabolism Liver ( CYP2C8-major, CYP3A4 and CYP2C9-minor) [2]
Elimination half-life2.7–5.5 hours
ExcretionBiliary
Identifiers
  • (R,E)-2-(1-((1-(3-(2-(7-Chloroquinolin-2-yl)vinyl)phenyl)-3-(2-(2-hydroxypropan-2-yl)phenyl)propylthio)methyl)cyclopropyl)acetic acid
Chemical and physical data
FormulaC35H36ClNO3S
Molar mass586.19 g·mol−1
3D model ( JSmol)
Melting point145 to 148 °C (293 to 298 °F)
  • O=C(O)CC1(CC1)CS[C@@H](c2cccc(c2)\C=C\c3nc4cc(Cl)ccc4cc3)CCc5ccccc5C(O)(C)C
  • InChI=1S/C35H36ClNO3S/c1-34(2,40)30-9-4-3-7-25(30)13-17-32(41-23-35(18-19-35)22-33(38)39)27-8-5-6-24(20-27)10-15-29-16-12-26-11-14-28(36)21-31(26)37-29/h3-12,14-16,20-21,32,40H,13,17-19,22-23H2,1-2H3,(H,38,39)/b15-10+/t32-/m1/s1 checkY
  • Key:UCHDWCPVSPXUMX-TZIWLTJVSA-N checkY
   (verify)

Montelukast, sold under the brand name Singulair among others, is a medication used in the maintenance treatment of asthma. [3] It is generally less preferred for this use than inhaled corticosteroids. [3] It is not useful for acute asthma attacks. [3] Other uses include allergic rhinitis and hives of long duration. [3] For allergic rhinitis it is a second line treatment. [5] It is taken by mouth. [3]

Common side effects include abdominal pain, cough, and headache. [3] Severe side effects may include allergic reactions, such as anaphylaxis and eosinophilia. [3] Use in pregnancy appears to be safe. [3] Montelukast is in the leukotriene receptor antagonist family of medications. [3] It works by blocking the action of leukotriene D4 in the lungs resulting in decreased inflammation and relaxation of smooth muscle. [3]

Montelukast was approved for medical use in the United States in 1998. [3] It is available as a generic medication. [6] In the United States, the wholesale cost per dose is less than 0.15 USD as of 2018. [7] In 2017, it was the 16th most commonly prescribed medication in the United States, with more than 31 million prescriptions. [8] [9]

References

  1. ^ a b "Montelukast (Singulair) Use During Pregnancy". Drugs.com. 13 December 2019. Archived from the original on 7 August 2019. Retrieved 4 March 2020.
  2. ^ "Montelukast 10 mg film coated tablets - Summary of Product Characteristics (SmPC) - (eMC)". Archived from the original on 23 December 2018. Retrieved 23 December 2018.
  3. ^ a b c d e f g h i j k l m "Montelukast Sodium Monograph for Professionals". Drugs.com. AHFS. Archived from the original on 7 June 2019. Retrieved 23 December 2018.
  4. ^ Cite error: The named reference WHO2020DDD was invoked but never defined (see the help page).
  5. ^ Grainger, J.; Drake-Lee, A. (2006). "Montelukast in allergic rhinitis: a systematic review and meta-analysis". Clinical Otolaryngology. 31 (5). Wiley: 360–367. doi: 10.1111/j.1749-4486.2006.01276.x. ISSN  0307-7772. PMID  17014443. regarded as second line therapy. When used, montelukast should be used in combination with an antihistamine.
  6. ^ British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 269. ISBN  9780857113382.
  7. ^ "NADAC as of 2018-12-19". Centers for Medicare and Medicaid Services. Archived from the original on 19 December 2018. Retrieved 22 December 2018.
  8. ^ "The Top 300 of 2020". ClinCalc. Archived from the original on 12 February 2021. Retrieved 4 March 2020.
  9. ^ "Montelukast - Drug Usage Statistics". ClinCalc. 23 December 2019. Archived from the original on 11 April 2020. Retrieved 11 April 2020.

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