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17(S)-HDoHE manufacturers
- 17(S)-HDHA
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- $1970.00
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2026-07-27
- CAS:92693-03-3
- Purity:
- Supply Ability: 10g
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| | 17(S)-HDoHE Basic information |
| Product Name: | 17(S)-HDoHE | | Synonyms: | 17(S)-HDoHE;SWTYBBUBEPPYCX-YTQNUIGOSA-N;4,7,10,13,15,19-Docosahexaenoic acid, 17-hydroxy-, (4Z,7Z,10Z,13Z,15E,17S,19Z)-;17(S)-hydroxy-4(Z),7(Z),10(Z),13(Z),15(E),19(Z)-docosahexaenoic acid;17(S)HDHA,17(S) HDHA;17(S)-Hydroxy-4(Z),7(Z),10(Z),13(Z),15(E),19(Z)-DHA;17(S)-HDHA(solution in ethanol);17(S)-HDHA | | CAS: | 92693-03-3 | | MF: | C22H32O3 | | MW: | 344.49 | | EINECS: | | | Product Categories: | | | Mol File: | 92693-03-3.mol |  |
| | 17(S)-HDoHE Chemical Properties |
| Boiling point | 505.091±50.00 °C(Press: 760.00 Torr)(predicted) | | density | 0.996±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | storage temp. | Store at -20°C | | solubility | DMF: Miscible; DMSO: Miscible; Ethanol: Miscible; PBS (pH 7.2): 0.8 mg/ml | | pka | 4.581±0.10(predicted) | | form | ethanol solution | | InChIKey | SWTYBBUBEPPYCX-YTQNUIGOSA-N | | SMILES | CC/C=C\C[C@H](O)/C=C/C=C\C/C=C\C/C=C\C/C=C\CCC(O)=O |
| WGK Germany | WGK 1 | | Storage Class | 3 - Flammable liquids | | Hazard Classifications | Eye Irrit. 2 Flam. Liq. 2 |
| | 17(S)-HDoHE Usage And Synthesis |
| Description | 17(S)-HDHA is a hydroxy fatty acid formed from docosahexaenoic acid (DHA; ) by 15-lipoxygenase (15-LO) and is a precursor to 17(S)-resolvins.1,2 17(S)-HDHA inhibits platelet 12-LO (IC50 = 0.4 μM).2 It inhibits TNF-α-induced expression of IL1B in a human glial cell line (IC50 = ~0.5 nM).1 17(S)-HDHA (100 nM) inhibits NOD-, LRR-, and pyrin domain-containing protein 3 (NLRP3) inflammasome formation induced by homocysteine in podocytes.3 | | Uses | 17(S)-HDHA is a pro-resolving mediator (SPM). 17(S)-HDHA slightly activats PPARγ, PPARα and PPARδ[1]. | | Definition | ChEBI: 17(S)-HDoHE is a polyunsaturated fatty acid that is (4Z,7Z,10Z,13Z,15E,19Z)-docosa-4,7,10,13,15,19-hexaenoic acid carrying a hydroxy substituent at the 17S-position. It is a metabolite of docosahexaenoic acid in human blood and mouse brain, and serves as a precursor to 17(S)-resolvins. It has a role as a mouse metabolite, an animal metabolite and a human xenobiotic metabolite. It is an enantiomer of a 17(R)-HDoHE. | | References | 1. Hong, S., Gronert, K., Devchand, P.R., et al. Novel docosatrienes and 17S-resolvins generated from docosahexaenoic acid in murine brain, human blood, and glial cells. Autacoids in anti-inflammation J. Biol. Chem. 278(17),14677-14687(2003). 2. Mitchell, P.D., Hallam, C., Hemsley, P.E., et al. Inhibition of platelet 12-lipoxygenase by hydroxy-fatty acids Biochem. Soc. Trans. 12,839-841(1984). 3. Li, G., Chen, Z., Bhat, O.M., et al. NLRP3 inflammasome as a novel target for docosahexaenoic acid metabolites to abrogate glomerular injury J. Lipid Res. 58(6),1080-1090(2017). |
| | 17(S)-HDoHE Preparation Products And Raw materials |
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