Identification | More | [Name]
LEUKOTRIENE B4 | [CAS]
71160-24-2 | [Synonyms]
LTB4 LEUKOTRIENE B4 Leukotriene B? LTB4 (Leukotriene B4) VNYSSYRCGWBHLG-AMOLWHMGSA-N Leukotriene B4 MaxSpecStandard leukotriene B4 ethanol solution Leukotriene B4 Lipid Maps MS Standard Leukotriene B - CAS 71160-24-2 - Calbiochem [5S,12R]-DIHYDROXY-[6Z,8E,10E,14Z]-EICOSATETRAENOIC ACID 5,12-DIHYDROXY-[S-[R*,S-(E,Z,Z,E))]-6,8,10,14-EICOSATETRAENOIC ACID 5,12-DIHYDROXY-[S-[R*,S*-(E,Z,Z,E)]]-6,8,10,14-EICOSATETRAENOIC ACID (5S,6Z,8E,10E,12R,14Z)-5,12-dihydroxyicosa-6,8,10,14-tetraenoic acid (5S,12R,6Z,8E,10E,14Z)-5,12-Dihydroxy-6,8,10,14-icosatetraenoic acid (5S,6Z,8E,10E,12R,14Z)-5,12-Dihydroxy-6,8,10,14-icosatetraenoic acid (5S,6Z,8E,10E,12R,14Z)-5,12-DIHYDROXY-6,8,10,14-EICOSATETRAENOIC ACID 5(S), 12(R)-DIHYDROXY-6-CIS-8-TRANS-10-TRANS-14-CIS-EICOSATETRAENOIC ACID 6,8,10,14-Eicosatetraenoic acid, 5,12-dihydroxy-, (5S,6Z,8E,10E,12R,14Z)- | [EINECS(EC#)]
200-578-6 | [Molecular Formula]
C20H32O4 | [MDL Number]
MFCD00135630 | [Molecular Weight]
336.47 | [MOL File]
71160-24-2.mol |
Chemical Properties | Back Directory | [Boiling point ]
536.4±50.0 °C(Predicted) | [density ]
1.040±0.06 g/cm3(Predicted) | [Fp ]
14 °C | [storage temp. ]
−20°C
| [solubility ]
Soluble in ethanol (supplied pre-dissolved in anhydrous ethanol, 50μg/ml) | [form ]
Clear oil | [pka]
4.66±0.10(Predicted) | [color ]
Colorless to light yellow | [CAS DataBase Reference]
71160-24-2(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
F | [Risk Statements ]
R11:Highly Flammable. | [Safety Statements ]
S7:Keep container tightly closed . S16:Keep away from sources of ignition-No smoking . | [RIDADR ]
UN 1170 3/PG 2
| [WGK Germany ]
1
|
Hazard Information | Back Directory | [Description]
Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from arachidonic acid through the 5-LO pathway.1,2,3 It promotes a number of leukocyte functions including aggregation, stimulation of ion fluxes, enhancement of lysosomal enzyme release, superoxide anion production, chemotaxis, and chemokinesis. In subnanomolar ranges (3.9 x 10−10 M), LTB4 causes chemotaxis and chemokinesis in human polymorphonuclear leukocytes.4 At higher concentrations, (1.0 x 10−7 M), LTB4 leads to neutrophil aggregation and degranulation as well as superoxide anion production.4,5 | [Description]
Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from arachidonic acid through the 5-LO pathway.1,2,3 It promotes a number of leukocyte functions including aggregation, stimulation of ion fluxes, enhancement of lysosomal enzyme release, superoxide anion production, chemotaxis, and chemokinesis. In subnanomolar ranges (3.9 x 10−10 M), LTB4 causes chemotaxis and chemokinesis in human polymorphonuclear leukocytes.4 At higher concentrations, (1.0 x 10−7 M), LTB4 leads to neutrophil aggregation and degranulation as well as superoxide anion production.4,5
LTB4 MaxSpec® standard is a quantitative grade standard of LTB4 (Item No. 20110) that has been prepared specifically for mass spectrometry and related applications where quantitative reproducibility is required. The solution has been prepared gravimetrically and is supplied in a deactivated glass ampule sealed under argon. The concentration was verified by comparison to an independently prepared calibration standard. This LTB4 MaxSpec® standard is guaranteed to meet identity, purity, stability, and concentration specifications and is provided with a batch-specific certificate of analysis. Ongoing stability testing is performed to ensure the concentration remains accurate throughout the shelf life of the product. Note: The amount of solution added to the vial is in excess of the listed amount. Therefore, it is necessary to accurately measure volumes for preparation of calibration standards. Follow recommended storage and handling conditions to maintain product quality. | [Uses]
LTB4 (Leukotriene B4) is a potent chemokine with roles in inflammation, immunology, the nervous system, brain and skin. | [Definition]
ChEBI: A leukotriene composed of (6Z,8E,10E,14Z)-icosatetraenoic acid having (5S)- and (12R)-hydroxy substituents. | [Biological Activity]
Potent lipid inflammatory mediator derived from the 5-lipoxygenase pathway of arachidonic acid metabolism. Binds to BLT 1 and BLT 2 receptors and acts as a potent chemotactic agent and activator of leukocytes. Also displays antiviral activity towards DNA viruses and retroviruses.牋. | [Biochem/physiol Actions]
Proinflammatory agent. Stimulates c-Fos and c-Jun proto-oncogene transcription in human monocytes. Stimulates chemotaxis, aggregation, and degranulation of polymorphonuclear leukocytes. | [storage]
Store at -20°C |
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