Lipoxygenase
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Lipoxygenases (LOXs) are dioxygenases that catalyze the formation of corresponding hydroperoxides from polyunsaturated fatty acids such as linoleic acid and arachidonic acid. Thre are six LOX isoforms have been found in the humans and mice. 5-Lipoxygenase (5-LOX) is a distinct isoform playing an important role in asthma and inflammation. 5-LOX causes the constriction of bronchioles in response to cysteinyl leukotrienes such as LTC4, thus leading to asthma. 5-LOX also induces neutrophilic inflammation by its recruitment in response to LTB4. 12-Lipoxygenase (12-LOX) is an isoform expressed in epithelial cells and myeloid cells including platelets. 12-LOX can be found in the epithelial cells of the skin. 12-LOX is a potential target for novel anti-platelet therapeutics.15-Lipoxygenase (15-LOX) is expressed in epithelial cells and leukocytes, has different substrate specificity in the humans and mice.15-LOX-1 is a target of nonsteroidal anti-inflammatory drug-induced apoptosis in colorectal cancer cells.
Products Related to Lipoxygenase(264)
- GC4989415(S)-HETE-d8 ethyl esterPurity: >99.00%
An internal standard for the quantification of 15(S)-HETE ethyl ester
- GC52105MontelukastCAS: 158966-92-8Purity: >99.00%
Montelukast (MK0476 free base) is a potent, selective and orally active antagonist of cysteinyl leukotriene receptor 1 (CysLT1).
- GC524135-Aminosalicylic Acid-d7Purity: >99.00%
An internal standard for the quantification of 5-aminosalicylic acid
- GC62040Cinnamyl-3,4-dihydroxy-α-cyanocinnamateCAS: 132465-11-3Purity: >99.50%
Cinnamyl-3,4-dihydroxy-α-cyanocinnamate (CDC) is a potent 12/15-Lipoxygenases (LO) inhibitor.
- GC640783-O-Acetyl-11-hydroxy-beta-boswellic acidCAS: 146019-25-2Purity: >98.00%
3-O-Acetyl-11-hydroxy-beta-boswellic acid is a potent 5-lipoxygenase (5-LO) inhibitor.
- GC660315-LOX-IN-1CAS: 55040-82-9Purity: >98.00%
5-LOX-IN-1 (compound 2b) is an inhibitor of human 5-Lipoxygenase (5-LOX) with an IC50 value of 2.3 μM. 5-LOX-IN-1 can be used for the research of inflammation.
- GC68641ALOX15-IN-1Purity: >98.00%
ALOX15-IN-1 (compound 8b) is an effective and selective inhibitor of rabbit and human ALOX15 linoleate oxygenase activity, with IC50 values of 0.04 μM for ALOX15 homologous substrate linoleic acid (LA) and 2.06 μM for arachidonic acid (AA).
- GC69434MasoprocolCAS: 27686-84-6Purity: >99.00%
Masoprocol (meso-Nordihydroguaiaretic acid) is an effective and orally active inhibitor of lipoxygenase. Masoprocol has shown anti-hyperglycemic activity by reducing glucose levels and liver triglyceride concentrations in the body. It has potential for researching type II diabetes.
- GC70263TebufeloneCAS: 112018-00-5Purity: >99.00%
Tebufelone (NE-11740), a nonsteroidal anti-inflammatory drug (NSAID), is a selective dual COX-2/5-lipoxygenase inhibitor.
- GC70448MLS000545091CAS: 322666-76-2Purity: >99.00%
MLS000545091 is a potent and selective lipoxygenase-2 (LOX-2) inhibitor with an IC50 value of 2.6 μM for h15-LOX-2.
- GC797065-LOX-IN-9CAS: 2668-47-5Purity: >98.00%
5-LOX-IN-9 is a 5-lipoxygenase and cyclooxygenase inhibitor, with an IC 50 of 0.2 pM against guinea pig 5-LOX and an IC 50 of 0.7 pM against bovine COX.
- GC79757ALOX5 stabilizer-1 TFAPurity: >98.00%
ALOX5 stabilizer-1 TFA is an arachidonate 5-lipoxygenase ( ALOX5 ) stabilizer with a K d of 7.26 μM.
- GC81543GPX4-IN-19CAS: 3102894-57-2Purity: >99.00%
GPX4-IN-19 is an effective GPX4 inhibitor ( IC 50 = 0.311 μM), covalently binds to the Sec 46 site of GPX4.
- GC9065212-oxo-9(Z)-Dodecenoic AcidCAS: 60485-39-4Purity: >95.00%
A metabolite of linoleic acid and linolenic acid
- GC91594LYS-006 (hydrochloride)CAS: 2619563-79-8Purity: >98.00%
LYS-006 is an inhibitor of leukotriene A4 (LTA4) hydrolase.
- GC91613FerroLOXIN-1CAS: 2773428-48-9Purity: >90.00%
FerroLOXIN-1 is an inhibitor of the 15-lipoxygenase-2 (15-LO-2) and phosphatidylethanolamine-binding protein 1 (PEBP1) catalytic complex.
- GN10792Caffeic acidCAS: 331-39-5Purity: >98.50%
Caffeic acid is a hydroxycinnamic acid polyphenol compound with antioxidant activity. Caffeic acid is an inhibitor of TRPV1 ion channel and 5-lipoxygenase.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC49894 | 15(S)-HETE-d8 ethyl ester | - | >99.00% | |
An internal standard for the quantification of 15(S)-HETE ethyl ester | ||||
| GC52105 | Montelukast | 158966-92-8 | >99.00% | |
Montelukast (MK0476 free base) is a potent, selective and orally active antagonist of cysteinyl leukotriene receptor 1 (CysLT1). | ||||
| GC52413 | 5-Aminosalicylic Acid-d7 | - | >99.00% | |
An internal standard for the quantification of 5-aminosalicylic acid | ||||
| GC61180 | Phenidone | 92-43-3 | >98.00% | |
Phenidone, an orally active dual inhibitor of cyclooxygenase (COX) and lipoxygenase (LOX), ameliorates rat paralysis in experimental autoimmune encephalomyelitis. | ||||
| GC62040 | Cinnamyl-3,4-dihydroxy-α-cyanocinnamate | 132465-11-3 | >99.50% | |
Cinnamyl-3,4-dihydroxy-α-cyanocinnamate (CDC) is a potent 12/15-Lipoxygenases (LO) inhibitor. | ||||
| GC64078 | 3-O-Acetyl-11-hydroxy-beta-boswellic acid | 146019-25-2 | >98.00% | |
3-O-Acetyl-11-hydroxy-beta-boswellic acid is a potent 5-lipoxygenase (5-LO) inhibitor. | ||||
| GC64621 | 4-Nitrocatechol | 3316-09-4 | >98% | |
4-Nitrocatechol is a potent lipoxygenase inhibitor. | ||||
| GC66031 | 5-LOX-IN-1 | 55040-82-9 | >98.00% | |
5-LOX-IN-1 (compound 2b) is an inhibitor of human 5-Lipoxygenase (5-LOX) with an IC50 value of 2.3 μM. 5-LOX-IN-1 can be used for the research of inflammation. | ||||
| GC68641 | ALOX15-IN-1 | - | >98.00% | |
ALOX15-IN-1 (compound 8b) is an effective and selective inhibitor of rabbit and human ALOX15 linoleate oxygenase activity, with IC50 values of 0.04 μM for ALOX15 homologous substrate linoleic acid (LA) and 2.06 μM for arachidonic acid (AA). | ||||
| GC69335 | KKII5 | 6381-55-1 | >98.00% | |
KKII5 is an effective lipoxygenase LOX-1 inhibitor with an IC50 of 19 μM. KKII5 inhibits lipid peroxidation. | ||||
| GC69434 | Masoprocol | 27686-84-6 | >99.00% | |
Masoprocol (meso-Nordihydroguaiaretic acid) is an effective and orally active inhibitor of lipoxygenase. Masoprocol has shown anti-hyperglycemic activity by reducing glucose levels and liver triglyceride concentrations in the body. It has potential for researching type II diabetes. | ||||
| GC70263 | Tebufelone | 112018-00-5 | >99.00% | |
Tebufelone (NE-11740), a nonsteroidal anti-inflammatory drug (NSAID), is a selective dual COX-2/5-lipoxygenase inhibitor. | ||||
| GC70448 | MLS000545091 | 322666-76-2 | >99.00% | |
MLS000545091 is a potent and selective lipoxygenase-2 (LOX-2) inhibitor with an IC50 value of 2.6 μM for h15-LOX-2. | ||||
| GC72794 | Flobufen | 112344-52-2 | - | |
Flobufen (VUFB 16066) is a non-steroidal anti-inflammatory agent and cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) inhibitor agent. | ||||
| GC74159 | MK-0731 | 845256-65-7 | >99.00% | |
MK-0731 is a selective, non-competitive and allosteric kinesin spindle protein (KSP) inhibitor with an IC50 of 2.2 nM and a pKa of 7.6. | ||||
| GC79706 | 5-LOX-IN-9 | 2668-47-5 | >98.00% | |
5-LOX-IN-9 is a 5-lipoxygenase and cyclooxygenase inhibitor, with an IC 50 of 0.2 pM against guinea pig 5-LOX and an IC 50 of 0.7 pM against bovine COX. | ||||
| GC79757 | ALOX5 stabilizer-1 TFA | - | >98.00% | |
ALOX5 stabilizer-1 TFA is an arachidonate 5-lipoxygenase ( ALOX5 ) stabilizer with a K d of 7.26 μM. | ||||
| GC81543 | GPX4-IN-19 | 3102894-57-2 | >99.00% | |
GPX4-IN-19 is an effective GPX4 inhibitor ( IC 50 = 0.311 μM), covalently binds to the Sec 46 site of GPX4. | ||||
| GC90533 | (-)-Pinoresinol | 81446-29-9 | >95.00% | |
A lignan with diverse biological activities | ||||
| GC90652 | 12-oxo-9(Z)-Dodecenoic Acid | 60485-39-4 | >95.00% | |
A metabolite of linoleic acid and linolenic acid | ||||
| GC91594 | LYS-006 (hydrochloride) | 2619563-79-8 | >98.00% | |
LYS-006 is an inhibitor of leukotriene A4 (LTA4) hydrolase. | ||||
| GC91613 | FerroLOXIN-1 | 2773428-48-9 | >90.00% | |
FerroLOXIN-1 is an inhibitor of the 15-lipoxygenase-2 (15-LO-2) and phosphatidylethanolamine-binding protein 1 (PEBP1) catalytic complex. | ||||
| GN10269 | Wedelolactone | 524-12-9 | >99.50% | |
| GN10792 | Caffeic acid | 331-39-5 | >98.50% | |
Caffeic acid is a hydroxycinnamic acid polyphenol compound with antioxidant activity. Caffeic acid is an inhibitor of TRPV1 ion channel and 5-lipoxygenase. | ||||
