Montelukast structure
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Common Name | Montelukast | ||
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CAS Number | 158966-92-8 | Molecular Weight | 586.183 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 750.5±60.0 °C at 760 mmHg | |
Molecular Formula | C35H36ClNO3S | Melting Point | N/A | |
MSDS | N/A | Flash Point | 407.7±32.9 °C |
Use of MontelukastMontelukast is a potent, selective and orally active antagonist of cysteinyl leukotriene receptor 1 (CysLT1). Montelukast can be used for the reseach of asthma and liver injury. Montelukast also has an antioxidant effect in intestinal ischemia-reperfusion injury, and could reduce cardiac damage[1]. |
Name | montelukast |
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Synonym | More Synonyms |
Description | Montelukast is a potent, selective and orally active antagonist of cysteinyl leukotriene receptor 1 (CysLT1). Montelukast can be used for the reseach of asthma and liver injury. Montelukast also has an antioxidant effect in intestinal ischemia-reperfusion injury, and could reduce cardiac damage[1]. |
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Related Catalog | |
Target |
CysLT1 |
In Vitro | Montelukast (5 μM; 1 h) inhibits APAP-induced cell damage[1]. |
In Vivo | Montelukast (3 mg/kg; oral gavage) protects against APAP-induced hepatotoxicity in mice[1]. Montelukast (1 mg/kg; miniosmotic pump administration) reduces the airway remodeling changes observed in OVA-treated mice and blocks the actions of cysteinyl leukotrienes (LT) C4, D4, and E4 mediated by the CysLT1 receptor[2]. Montelukast (1 mg/kg; miniosmotic pump administration) reduces the elevated levels of IL-4 and IL-13 found in the BAL fluid of OVA-treated mice[2]. Animal Model: C57BL/6J mice (8-week-old; 22-25 g) are induced acute hepatic injury[1] Dosage: 3 mg/kg Administration: Oral gavage 1 h after saline or APAP administration Result: Decreased serum levels of alanine transaminase (ALT) and aspartate aminotransferase (AST), and alleviated liver damage. |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 750.5±60.0 °C at 760 mmHg |
Molecular Formula | C35H36ClNO3S |
Molecular Weight | 586.183 |
Flash Point | 407.7±32.9 °C |
Exact Mass | 585.210449 |
PSA | 95.72000 |
LogP | 7.80 |
Vapour Pressure | 0.0±2.6 mmHg at 25°C |
Index of Refraction | 1.678 |
Storage condition | 2-8°C |
Hazard Codes | Xi |
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Precursor 10 | |
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DownStream 2 | |
Cyclopropaneacetic acid, 1-[[[(1R)-1-[3-[(E)-2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]- |
[3H]-Montelukast |
Brondilat (TN) |
Montelukast |
(1-{1-{3(R)-[2-(7-chloro-quinolin-2-yl)-vinyl]-phenyl}-3-[2-(1-hydroxy-1-methyl-ethyl)-phenyl]-propylsulfanylmethyl}-cyclopropyl)-acetic acid |
{1-[({(1R)-1-{3-[(E)-2-(7-Chloroquinolin-2-yl)vinyl]phenyl}-3-[2-(2-hydroxypropan-2-yl)phenyl]propyl}sulfanyl)methyl]cyclopropyl}acetic acid |
Montair |
2-[1-[[(1R)-1-[3-[(E)-2-(7-chloroquinolin-2-yl)ethenyl]phenyl]-3-[2-(2-hydroxypropan-2-yl)phenyl]propyl]sulfanylmethyl]cyclopropyl]acetic acid |
Singular |
[R-(E)]-1-[[[1-[3-[2-(7-Chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]cyclopropaneacetic Acid |
{1-[({(1R)-1-{3-[(E)-2-(7-Chloro-2-quinolinyl)vinyl]phenyl}-3-[2-(2-hydroxy-2-propanyl)phenyl]propyl}sulfanyl)methyl]cyclopropyl}acetic acid |
Montelukast [INN:BAN] |
MFCD05662278 |
Montelukast (INN) |
{1-[({(1R)-1-{3-[(E)-2-(7-chloroquinolin-2-yl)ethenyl]phenyl}-3-[2-(2-hydroxypropan-2-yl)phenyl]propyl}sulfanyl)methyl]cyclopropyl}acetic acid |
[14C]-Montelukast |
UNII-MHM278SD3E |