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Product Name:13(R)-hydroxy-9(Z),11(E)-octadecadienoic acid
CAS:10219-69-9
Purity:98+% Package:100ug
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Alfa Chemistry
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Product Name:13(R)-hydroxy-9(Z),11(E)-octadecadienoic acid
CAS:10219-69-9
Purity:98%+ Package:1g;10g;100g;1KG;5KG
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
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Product Name:13(R)-HODE
CAS:10219-69-9
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
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MedBioPharmaceutical Technology Inc
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Product Name:13(R)-HODE
CAS:10219-69-9
Purity:98% Package:50ug (solution); 100ug (solution); 25ug (solution); 250ug (solution) Remarks:Medbio
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| | 13(R)-HODE Basic information |
| Product Name: | 13(R)-HODE | | Synonyms: | 13(R)-HODE;13R-HYDROXY-9Z,11E-OCTADECADIENOIC ACID;(R,9Z,11E)-13-Hydroxy-9,11-octadecadienoic acid;Coriolic acid;(R-(E,Z))-13-Hydroxy-9,11-octadecadienoic acid;9,11-Octadecadienoic acid, 13-hydroxy-, (R-(E,Z))-;13(R)-hydroxy-9,11-octadienoic acid;HNICUWMFWZBIFP-PIHGWCCBSA-N | | CAS: | 10219-69-9 | | MF: | C18H32O3 | | MW: | 296.44 | | EINECS: | | | Product Categories: | | | Mol File: | 10219-69-9.mol |  |
| | 13(R)-HODE Chemical Properties |
| Boiling point | 422.7±20.0 °C(Predicted) | | density | 0.970±0.06 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 50 mg/ml; PBS pH 7.2: 1 mg/ml | | pka | 4.78±0.10(Predicted) |
| | 13(R)-HODE Usage And Synthesis |
| Description | 13(R)-HODE is the opposite enantiomer of the 13(S)-HODE produced when linoleic acid is incubated with soybean lipoxygenase. The presence of 13(R)-HODE in the supernatants and membranes of cultured bovine endothelial cells has been attributed to COX metabolism.1 13(R)-HODE is a weak (IC50 = 2.7 μM) inhibitor of U-46619-induced platelet aggregation.2 | | Definition | ChEBI: 13(R)-HODE is a 13-HODE in which the stereocentre at position 13 has S-configuration. It is a conjugate acid of a 13(R)-HODE(1-). | | References | 1. Baer, A.N., Costello, P.B., and Green, F.A. Stereospecificity of the hydroxyeicosatetraenoic and hydroxyoctadecadienoic acids produced by cultured bovine endothelial cells Biochim. Biophys. Acta 1085(1),45-52(1991).
2. Lagarde, M., Boutillon, M.M., Guichardant, M., et al. Further studies on the anti-thromboxane A2 activity of monohydroxylated fatty acids Biochem. Pharmacol. 38,1863-1864(1989). |
| | 13(R)-HODE Preparation Products And Raw materials |
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