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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H37NO5S
Molecular Weight 439.609
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 4
Charge 0

SHOW SMILES / InChI
Structure of LEUKOTRIENE E4

SMILES

CCCCC\C=C/C\C=C/C=C/C=C/[C@@H](SC[C@H](N)C(O)=O)[C@@H](O)CCCC(O)=O

InChI

InChIKey=OTZRAYGBFWZKMX-FRFVZSDQSA-N
InChI=1S/C23H37NO5S/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-21(30-18-19(24)23(28)29)20(25)15-14-17-22(26)27/h6-7,9-13,16,19-21,25H,2-5,8,14-15,17-18,24H2,1H3,(H,26,27)(H,28,29)/b7-6-,10-9-,12-11+,16-13+/t19-,20-,21+/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of the leukotriene receptor antagonist MK-0679 on baseline pulmonary function in aspirin sensitive asthmatic subjects.
1993 Dec
Characterization of the leukotriene D4 receptor in dimethylsulphoxide-differentiated U937 cells: comparison with the leukotriene D4 receptor in human lung and guinea-pig lung.
1993 Feb 15
A controlled trial of the effect of the 5-lipoxygenase inhibitor, zileuton, on lung inflammation produced by segmental antigen challenge in human beings.
1996 Feb
Identification and characterization of two cysteinyl-leukotriene high affinity binding sites with receptor characteristics in human lung parenchyma.
1998 Apr
Pharmacology of leukotriene receptor antagonists.
1998 Jun
Leukotriene C4 is a tight-binding inhibitor of microsomal glutathione transferase-1. Effects of leukotriene pathway modifiers.
1999 Jan 22
Anti-inflammatory effects of zileuton in a subpopulation of allergic asthmatics.
2000 Apr
Molecular cloning and characterization of a second human cysteinyl leukotriene receptor: discovery of a subtype selective agonist.
2000 Dec
Molecular cloning and functional characterization of murine cysteinyl-leukotriene 1 (CysLT(1)) receptors.
2001 Nov 1
Urinary metabolites of histamine and leukotrienes before and after placebo-controlled challenge with ASA and food additives in chronic urticaria patients.
2002 Dec
Receptor preferences of cysteinyl-leukotrienes in the guinea pig lung parenchyma.
2002 Feb 1
[Study on relationship between leukotrienes and exercise-induced asthma].
2002 Jan 10
Leukotrienes mediate murine bronchopulmonary hyperreactivity, inflammation, and part of mucosal metaplasia and tissue injury induced by recombinant murine interleukin-13.
2003 Apr
The cysteinyl-leukotriene D4 induces cytosolic Ca2+ elevation and contraction of the human detrusor muscle.
2003 Aug
Leukotrienes mediate part of Ova-induced lung effects in mice via EGFR.
2003 Oct
Hypersensitivity to aspirin: common eicosanoid alterations in urticaria and asthma.
2004 Apr
Leukotriene E(4)-induced persistent eosinophilia and airway obstruction are reversed by zafirlukast in patients with asthma.
2005 Feb
The recently identified P2Y-like receptor GPR17 is a sensor of brain damage and a new target for brain repair.
2008
Differential signaling of cysteinyl leukotrienes and a novel cysteinyl leukotriene receptor 2 (CysLT₂) agonist, N-methyl-leukotriene C₄, in calcium reporter and β arrestin assays.
2011 Feb
Identification of GPR99 protein as a potential third cysteinyl leukotriene receptor with a preference for leukotriene E4 ligand.
2013 Apr 19
Cyclooxygenase-1 serves a vital hepato-protective function in chemically induced acute liver injury.
2015 Feb
Name Type Language
LEUKOTRIENE E4
MI  
Common Name English
(5S,6R,7E,9E,11Z,14Z)-6-(2-AMINO-2-CARBOXYETHYL)SULFANYL-5-HYDROXYICOSA-7,9,11,14-TETRAENOIC ACID
Systematic Name English
LEUKOTRIENE E
Common Name English
LEUKOTRIENE E4 [MI]
Common Name English
LTE4
Common Name English
LTE-4
Common Name English
Classification Tree Code System Code
LOINC 33344-3
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
NCI_THESAURUS C608
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
LOINC 33343-5
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
Code System Code Type Description
MESH
D017999
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY
FDA UNII
8EYT8ATL7G
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY
PUBCHEM
5280879
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY
CHEBI
57462
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY
CHEBI
15650
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY
MERCK INDEX
m6777
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C129009
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY
WIKIPEDIA
LEUKOTRIENE E4
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID20897510
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY
CAS
75715-89-8
Created by admin on Fri Dec 15 15:54:24 GMT 2023 , Edited by admin on Fri Dec 15 15:54:24 GMT 2023
PRIMARY