プランルカスト
- 関
- pranlukast hydrate
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/12/06 09:03:11」(JST)
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Pranlukast
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Systematic (IUPAC) name |
N-[4-oxo-2-(1H-tetrazol-5-yl)-4H-chromen-7-yl]-4-(4-phenylbutoxy)benzamide |
Clinical data |
AHFS/Drugs.com |
International Drug Names |
Pregnancy cat. |
? |
Legal status |
? |
Routes |
Oral |
Pharmacokinetic data |
Metabolism |
Hepatic (mainly CYP3A4)[1] |
Half-life |
1.5 hours[1] |
Identifiers |
CAS number |
103177-37-3 Y |
ATC code |
R03DC02 |
PubChem |
CID 4887 |
DrugBank |
DB01411 |
ChemSpider |
4718 Y |
UNII |
TB8Z891092 Y |
ChEMBL |
CHEMBL21333 Y |
Chemical data |
Formula |
C27H23N5O4 |
Mol. mass |
481.503 g/mol |
SMILES
- O=C(c2ccc(OCCCCc1ccccc1)cc2)Nc5cccc3c5O/C(=C\C3=O)c4nnnn4
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InChI
-
InChI=1S/C27H23N5O4/c33-23-17-24(26-29-31-32-30-26)36-25-21(23)10-6-11-22(25)28-27(34)19-12-14-20(15-13-19)35-16-5-4-9-18-7-2-1-3-8-18/h1-3,6-8,10-15,17H,4-5,9,16H2,(H,28,34)(H,29,30,31,32) Y
Key:NBQKINXMPLXUET-UHFFFAOYSA-N Y
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Y (what is this?) (verify)
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Pranlukast is a cysteinyl leukotriene receptor-1 antagonist. This drug works similarly to Merck & Co.'s Singulair (montelukast). It is widely used in Japan.
Medications of this class, which go under a variety of names according to whether one looks at the American, British or European system of nomenclature, have as their primary function the antagonism of bronchospasm caused, principally in asthmatics, by an allergic reaction to accidentally or inadvertently encountered allergens.
Medications of this group are normally used as an adjunct to the standard therapy of inhaled steroids with inhaled long- and/or short-acting beta-agonists. There are several similar medications in the group; all appear to be equally effective.
References[edit]
- ^ a b Nakade S, Ueda S, Ohno T, Nakayama K, Miyata Y, Yukawa E, Higuchi S (2006). "Population pharmacokinetics of pranlukast hydrate dry syrup in children with allergic rhinitis and bronchial asthma.". Drug Metab Pharmacokinet 21 (2): 133–9. doi:10.2133/dmpk.21.133. PMID 16702733.
Drugs for obstructive airway diseases: asthma/COPD (R03)
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Adrenergics, inhalants |
Short acting β2-agonists |
- Bitolterol
- Carbuterol
- Fenoterol
- Pirbuterol
- Procaterol
- Reproterol
- Rimiterol
- Salbutamol#/Levosalbutamol
- Terbutaline
- Tulobuterol
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Long acting β2-agonists (LABA) |
- Arformoterol
- Bambuterol
- Clenbuterol
- Formoterol
- Olodaterol
- Salmeterol
- Ultra LABA: Indacaterol
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other |
- Epinephrine#
- Hexoprenaline
- Isoprenaline (Isoproterenol)
- Orciprenaline (Metaproterenol)
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Glucocorticoids |
- Beclometasone#
- Betamethasone
- Budesonide
- Ciclesonide
- Flunisolide
- Fluticasone
- Mometasone
- Triamcinolone
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Anticholinergics/
muscarinic antagonist |
- Aclidinium bromide
- Glycopyrronium bromide
- Ipratropium bromide#
- Oxitropium bromide
- Tiotropium bromide
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Mast cell stabilizers |
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Xanthines |
- Acefylline
- Ambuphylline
- Bamifylline
- Doxofylline
- Enprofylline
- Etamiphylline
- Proxyphylline
- Theobromine
- Theophylline/Aminophylline/Choline theophyllinate
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Eicosanoid inhibition |
Leukotriene antagonists |
- Montelukast
- Pranlukast
- Zafirlukast
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Lipoxygenase inhibitor |
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Thromboxane receptor antagonists |
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Non-xanthine PDE4 inhibitors |
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Others/unknown |
- Amlexanox
- Eprozinol
- Fenspiride
- Omalizumab
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Combination products |
- Budesonide/formoterol
- Fluticasone/salmeterol
- Ipratropium bromide/salbutamol
- Mometasone/formoterol
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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anat (n, x, l, c)/phys/devp
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noco (c, p)/cong/tumr, sysi/epon, injr
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proc, drug (R1/2/3/5/6/7)
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UpToDate Contents
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English Journal
- A co-module approach for elucidating drug-disease associations and revealing their molecular basis.
- Zhao S, Li S.SourceMOE Key Laboratory of Bioinformatics and Bioinformatics Division, TNLIST/Department of Automation, Tsinghua University, Beijing, China.
- Bioinformatics (Oxford, England).Bioinformatics.2012 Apr 1;28(7):955-61. Epub 2012 Jan 28.
- MOTIVATION: Understanding how drugs and diseases are associated in the molecular level is of critical importance to unveil disease mechanisms and treatments. Until recently, few studies attempt end to discover important gene modules shared by both drugs and diseases.RESULTS: Here, we propose a novel
- PMID 22285830
- Impact of add-on pranlukast in stable asthma; the additive effect on peripheral airway inflammation.
- Yasui H, Fujisawa T, Inui N, Kato M, Hashimoto D, Enomoto N, Nakamura Y, Shirai T, Suda T, Nakamura H, Chida K.SourceSecond Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan. yassy19781119@yahoo.co.jp
- Respiratory medicine.Respir Med.2012 Apr;106(4):508-14. Epub 2012 Jan 21.
- BACKGOUND: The importance of airway inflammation has been highlighted in the pathophysiology of asthma. Even in controlled asthmatics treated with inhaled corticosteroid (ICS), residual airway inflammation is reported. Systemic therapy with oral leukotriene receptor antagonist, pranlukast, may have
- PMID 22265857
Japanese Journal
- 臨床研究・症例報告 プランルカストが有効であった抗ヒスタミン薬抵抗性慢性特発性蕁麻疹の1男児例
- プランルカスト水和物の経口持続性製剤化を目指した胃内滞留性製剤の設計に関する研究
- 杉原 光,竹内 洋文,スギハラ ヒカル,タケウチ ヒロフミ,Hikaru SUGIHARA,Hirofumi TAKEUCHI
- 岐阜薬科大学紀要 = The annual proceedings of Gifu Pharmaceutical University 63, 1-10, 2014-06-30
- … In a human site-of-absorption study pranlukast hydrate was demonstrated to have extremely poor absorption properties inthe lower gastrointestinal tract. …
- NAID 120005564609
- Cysteinyl leukotriene receptor antagonist regulates allergic airway inflammation in an organ- and cytokine-specific manner
- Kawano Tetsuya,Matsuse Hiroto,Tsuchida Tomoko,Fukahori Susumu,Fukushima Chizu,Nishino Tomoya,Kohno Shigeru
- Medical Science Monitor 20, 297-302, 2014-02-22
- … pranlukast (Prl), an LTRA-treated AS; …
- NAID 120005438870
Related Links
- PRANLUKAST 薬価基準収載 効能・効果、用法・用量、使用上の注意等は裏面の製品DIをご参照下さい。 〈実寸大〉 【禁忌(次の患者には投与しないこと)】 本剤の成分に対し過敏症の既往歴のある患者 気管支喘息・アレルギー性鼻炎 ...
- プランルカスト水和物(Pranlukast hydrate)の検索ならお薬検索QLife(キューライフ)。お医者さんが処方する処方薬と、薬局で買える市販薬(OTC)、の効果と副作用、写真、添付文書、保管方法等を掲載。商品名だけでなく一般名や剤形、色 ...
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