ロイコトリエンD4
- 関
- leukotriene D、LTD4
- 同
- LTD4
WordNet
- the 4th letter of the Roman alphabet (同)d
PrepTutorEJDIC
- deuteriumの化学記号
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/06/13 21:02:32」(JST)
[Wiki en表示]
Leukotriene D4 |
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Identifiers |
CAS number |
73836-78-9 Y |
PubChem |
5280878 |
MeSH |
Leukotriene+D4 |
ChEMBL |
CHEMBL288943 N |
Jmol-3D images |
Image 1 |
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CCCCC\C=C/C\C=C/C=C/C=C/[C@@H](SC[C@H](N)C(=O)NCC(=O)O)[C@@H](O)CCCC(=O)O
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Properties |
Molecular formula |
C25H40N2O6S |
Molar mass |
496.661 g/mol |
N (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
Infobox references |
Leukotriene D4 is one of the leukotrienes. Its functions in the body are bronchoconstriction, vasoconstriction, contraction of smooth muscle, and increasing vascular permeability. Other leukotrienes that function in a similar manner are leukotrienes C4 and E4. Pharmacological agents that inhibit the function of these leukotrienes are leukotriene receptor antagonists (e.g. Zafirlukast, montelukast) and are useful for asthmatic individuals.
Eicosanoid synthesis. (Leukotrienes at right.)
Autacoids, unsaturated fatty acids: Eicosanoids
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Precursor |
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Prostanoids |
Prostaglandins (PG) and
analogues |
Precursor |
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Active |
D/J |
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E/F |
- E2 (Dinoprostone): Enprostil
- Sulprostone
- E1 (Alprostadil): Misoprostol
- Gemeprost
- F2α (Dinoprost): Bimatoprost
- Carboprost
- Latanoprost
- Tafluprost
- Travoprost
- Unoprostone
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I |
- I2 (Prostacyclin/Epoprostenol): Beraprost
- Iloprost
- Treprostinil
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Thromboxanes (TX) |
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Leukotrienes (LT) |
Precursor |
- Arachidonic acid 5-hydroperoxide
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Initial |
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SRS-A |
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Nonclassic |
- Lipoxins (A4, B4)
- Virodhamine
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By function |
- vasoconstriction
- vasodilation
- platelets: induce
- inhibit
- leukocytes: induce
- inhibit
- labor stimulation:
- PGE2 (Dinoprostone)
- PGF2α (Dinoprost)
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mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m
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k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon
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m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)
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- biochemical families: carbohydrates
- alcohols
- glycoproteins
- glycosides
- lipids
- eicosanoids
- fatty acids / intermediates
- phospholipids
- sphingolipids
- steroids
- nucleic acids
- constituents / intermediates
- proteins
- amino acids / intermediates
- tetrapyrroles / intermediates
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UpToDate Contents
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English Journal
- Leukotriene receptor antagonist as a novel tocolytic in an in vitro model of human uterine contractility.
- Corriveau S1, Rousseau E2, Blouin S3, Pasquier JC4.Author information 1Obstetrics and Gynecology, CHUS, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada; Physiology and Biophysics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.2Physiology and Biophysics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.3Obstetrics and Gynecology, CHUS, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.4Obstetrics and Gynecology, CHUS, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada. Electronic address: Jean-Charles.Pasquier@usherbrooke.ca.AbstractOBJECTIVE: This study analyzed the ability of montelukast, a cysteinyl-leukotrienes receptor antagonist and anti-inflammatory agent, to produce a consistent tocolytic effect alone or in combination with nifedipine, a calcium (Ca2+) channel blocker currently used in clinical practice.
- European journal of obstetrics, gynecology, and reproductive biology.Eur J Obstet Gynecol Reprod Biol.2014 Mar 12. pii: S0301-2115(14)00114-6. doi: 10.1016/j.ejogrb.2014.02.042. [Epub ahead of print]
- OBJECTIVE: This study analyzed the ability of montelukast, a cysteinyl-leukotrienes receptor antagonist and anti-inflammatory agent, to produce a consistent tocolytic effect alone or in combination with nifedipine, a calcium (Ca2+) channel blocker currently used in clinical practice.STUDY DESIGN: Ut
- PMID 24735655
- The inflammatory mediator leukotriene D₄ induces subcellular β-catenin translocation and migration of colon cancer cells.
- Salim T1, Sand-Dejmek J2, Sjölander A3.Author information 1Division of Cell and Experimental Pathology, Department of Laboratory Medicine, Lund University, Clinical Research Center, ;Skåne University Hospital, Malmö, Sweden.2Division of Cell and Experimental Pathology, Department of Laboratory Medicine, Lund University, Clinical Research Center, ;Skåne University Hospital, Malmö, Sweden; Section of Surgery, Department of Clinical Sciences, Lund University, Skåne University Hospital, Malmö, Sweden; Bayer HealthCare, Pharmaceuticals Medical Affairs, Solna, Sweden.3Division of Cell and Experimental Pathology, Department of Laboratory Medicine, Lund University, Clinical Research Center, ;Skåne University Hospital, Malmö, Sweden. Electronic address: anita.sjolander@med.lu.se.AbstractThe abnormal activation of the Wnt/β-catenin pathway frequently occurs in colorectal cancer. The nuclear translocation of β-catenin activates the transcription of target genes that promote cell proliferation, survival, and invasion. The pro-inflammatory mediator leukotriene D4 (LTD4) exerts its effects through the CysLT1 receptor. We previously reported an upregulation of CysLT1R in patients with colon cancer, suggesting the importance of leukotrienes in colon cancer. The aim of this study was to investigate the impact of LTD4 on Wnt/β-catenin signaling and its effects on proliferation and migration of colon cancer cells. LTD4 stimulation led to an increase in β-catenin expression, β-catenin nuclear translocation and the subsequent transcription of MYC and CCND1. Furthermore, LTD4 significantly reduced the expression of E-cadherin and β-catenin at the plasma membrane and increased the migration and proliferation of HCT116 colon cancer cells. The effects of LTD4 can be blocked by the inhibition of CysLT1R. Furthermore, LTD4 induced the inhibition of glycogen synthase kinase 3 (GSK)-3β activity, indicating a crosstalk between the G-protein-coupled receptor CysLT1 and the Wnt/β-catenin pathway. In conclusion, LTD4, which can be secreted from macrophages and leukocytes in the tumor microenvironment, induces β-catenin translocation and the activation of β-catenin target genes, resulting in the increased proliferation and migration of colon cancer cells.
- Experimental cell research.Exp Cell Res.2014 Feb 15;321(2):255-66. doi: 10.1016/j.yexcr.2013.10.021. Epub 2013 Nov 5.
- The abnormal activation of the Wnt/β-catenin pathway frequently occurs in colorectal cancer. The nuclear translocation of β-catenin activates the transcription of target genes that promote cell proliferation, survival, and invasion. The pro-inflammatory mediator leukotriene D4 (LTD4) exerts its ef
- PMID 24211746
- Leukotriene D4 inhalation challenge for predicting short-term efficacy of montelukast: a pilot study.
- Guan WJ1, Shi X, Zheng JP, Gao Y, Jiang CY, Xie YQ, Liu QX, Zhu Z, Guo E, An JY, Yu XX, Liu WT, Zhong NS.Author information 1State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, First Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou, Guangdong, China.AbstractINTRODUCTION: The convenient measure to predict efficacy of leukotriene receptor antagonist is lacking.
- The clinical respiratory journal.Clin Respir J.2014 Feb 8. doi: 10.1111/crj.12117. [Epub ahead of print]
- INTRODUCTION: The convenient measure to predict efficacy of leukotriene receptor antagonist is lacking.OBJECTIVES: To determine if leukotriene D4 inhalation challenge predicts short-term efficacy of montelukast in asthma.METHODS: In this open-labelled 28-day trial, 45 patients with asthma were alloc
- PMID 24506412
Japanese Journal
- ロイコトリエン(B4,C4,D4,E4) (広範囲 血液・尿化学検査 免疫学的検査(第7版・4)その数値をどう読むか) -- (プロスタノイド,サイトカイン,増殖因子,ケモカイン)
- Pharmacological Analysis of Antigen-Induced Late Airway Response in Rats(Pharmacology)
- MIYAGAWA Naoki,IWASAKI Hidenori,KATO Toshinobu,TANAKA Masaru,SHIBATA Tsutomu,WAKITANI Korekiyo
- Biological & pharmaceutical bulletin 32(3), 394-398, 2009-03-01
- … In this study, the pharmacological properties of rat ovalbumin (OVA)-induced LAR and effects of the clinically used anti-asthmatic drugs salbutamol (β_2-agonist), ketotifen (antihista-mine), pranlukast (anti-leukotriene C_4/D_4/E_4), and prednisolone (steroid) were examined. … Although β_2-agonist, antihistamine, and anti-leukotriene C_4/D_4/E_4 exhibited no effects on rat LAR, steroid attenuated LAR and decreased eosinophil number in BALF. …
- NAID 110007122727
Related Links
- The first CysLT metabolite of LTC 4 . ... LTD 4 LTD 4 is one of the constituents of slow-reacting substance of anaphylaxis (SRS-A) produced by the metabolism of LTC 4 by γ-glutamyl transpeptidase. 1,2 It is the first cysteinyl-leukotriene metabolite of LTC ...
- Leukotriene D4 (LTD-4) is one of the leukotrienes. Its function main in the body is to induce the contraction of smooth muscle, resulting in bronchoconstriction and vasoconstriction. It also increases vascular permeability. LTD-4 is ...
Related Pictures
★リンクテーブル★
[★]
ロイコトリエンD
- 関
- leukotriene D4、LTD4
[★]
[★]
ロイコトリエン LT
[★]
ロイコトリエン LT