14,15-LEUKOTRIENE C4
- Product Name14,15-LEUKOTRIENE C4
- CAS75290-60-7
- CBNumberCB0196624
- MFC30H47N3O9S
- MW625.77
- MDL NumberMFCD00211501
- MOL File75290-60-7.mol
Chemical Properties
| storage temp. | Store at -20°C |
| solubility | DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 1 mg/ml; PBS (pH 7.2): 100 μg/ml |
| form | Liquid. |
14,15-LEUKOTRIENE C4 Price
| Product number | Packaging | Price | Product description | Buy |
|---|---|---|---|---|
| Cayman Chemical 10011360 | 25μg | $127 | 14,15-Leukotriene C4 ≥95% |
Buy |
| Cayman Chemical 10011360 | 50μg | $236 | 14,15-Leukotriene C4 ≥95% |
Buy |
| Cayman Chemical 10011360 | 100μg | $447 | 14,15-Leukotriene C4 ≥95% |
Buy |
| TRC L330368 | 25μg | $125 | 14,15-LeukotrieneC4 |
Buy |
14,15-LEUKOTRIENE C4 Chemical Properties,Usage,Production
Description
Leukotrienes (LTs) are a group of acute inflammatory mediators derived from arachidonic acid in leukocytes. The majority of these metabolites are formed through the 5-Uses
14,15-Leukotriene C4 is an acute inflammatory mediator.References
[1] M LUO T G B S Lee. Leukotriene synthesis by epithelial cells.[J]. Histology and histopathology, 2003, 18 2: 587-595. DOI: 10.14670/hh-18.587[2] C. YOKOYAMA. Arachidonate 12-lipoxygenase purified from porcine leukocytes by immunoaffinity chromatography and its reactivity with hydroperoxyeicosatetraenoic acids.[J]. The Journal of Biological Chemistry, 1986, 61 1: 16714-16721. DOI: 10.1016/s0021-9258(18)66623-2
[3] R. BRYANT. Leukotriene formation by a purified reticulocyte lipoxygenase enzyme. Conversion of arachidonic acid and 15-hydroperoxyeicosatetraenoic acid to 14, 15-leukotriene A4.[J]. The Journal of Biological Chemistry, 1985, 43 1: 3548-3555. DOI: 10.1016/s0021-9258(19)83657-8
[4] STINA FELTENMARK. Eoxins are proinflammatory arachidonic acid metabolites produced via the 15-lipoxygenase-1 pathway in human eosinophils and mast cells.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2008: 680-685. DOI: 10.1073/pnas.0710127105
[5] SAILESH S. Sheep Uterus Dual Lipoxygenase in the Synthesis of 14,15-Leukotrienes[J]. Archives of biochemistry and biophysics, 1994, 315 2: Pages 362-368. DOI: 10.1006/abbi.1994.1512
[6] J M DRAZEN. Contractile activities of structural analogs of leukotrienes C and D: necessity of a hydrophobic region.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1981, 78 5: 3195-3198. DOI: 10.1073/pnas.78.5.3195
[7] A SALA. Contractile and binding activities of structural analogues of LTC4 in the longitudinal muscle of guinea-pig ileum.[J]. Eicosanoids, 1990, 3 2: 105-110.
Preparation Products And Raw materials
14,15-LEUKOTRIENE C4 Suppliers
Global(31)Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| tp@aladdinsci.com | United States | 52923 | 58 | ||
| 021-65675885 18964387627 |
info@efebio.com | China | 9803 | 58 | |
| 400-9205774 | sales@glpbio.cn | China | 6777 | 58 | |
| 18818260767 | sales@chemegen.com | China | 11218 | 58 | |
| 021-58432009 400-005-6266 |
marketing@energy-chemical.com | China | 44918 | 58 | |
| 021-69985186 13611928337 |
3427709316@qq.com | China | 7982 | 58 | |
| 15002134094 | marketing@targetmol.cn | China | 29387 | 58 | |
| 800-364-9897 | sales@caymanchem.com | China | 6838 | 58 | |
| Enzo Biochem Inc. 13797054060 |
Enzoname@qq.com | China | 6174 | 58 | |
| 021-60936350 | scbt@scbt.com | China | 6594 | 58 |
75290-60-7, 14,15-LEUKOTRIENE C4Related Search
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