17(S)-HpDoHE
- Product Name
- 17(S)-HpDoHE
- CAS No.
- 123673-33-6
- Chemical Name
- 17(S)-HpDoHE
- Synonyms
- 17(S)-HpDHA;17(S)-HpDoHE;BNHQALRBDJVUQB-YTQNUIGOSA-N;17(S)-HpDHA(solution in ethanol);17(S)-hydroperoxy-4(E),7(Z),10(Z),13(Z),15(Z),19(Z)-DHA;17(S)-hydroperoxy-4(E),7(Z),10(Z),13(Z),15(Z),19(Z)-Docosahexaenoic acid;4,7,10,13,15,19-Docosahexaenoic acid, 17-hydroperoxy-, (4Z,7Z,10Z,13Z,15E,17S,19Z)-
- CBNumber
- CB12589933
- Molecular Formula
- C22H32O4
- Formula Weight
- 360.49
- MOL File
- 123673-33-6.mol
17(S)-HpDoHE Property
- storage temp.
- Store at -20°C
- solubility
- DMF: Miscible; DMSO: Miscible; Ethanol: Miscible; PBS (pH 7.2): 0.8 mg/ml
N-Bromosuccinimide Price
- Product number
- 13185
- Product name
- 17(S)-HpDHA
- Purity
- ≥98%
- Packaging
- 25μg
- Price
- $129
- Updated
- 2024/03/01
- Product number
- 13185
- Product name
- 17(S)-HpDHA
- Purity
- ≥98%
- Packaging
- 50μg
- Price
- $241
- Updated
- 2024/03/01
- Product number
- 13185
- Product name
- 17(S)-HpDHA
- Purity
- ≥98%
- Packaging
- 100μg
- Price
- $455
- Updated
- 2024/03/01
- Product number
- 13185
- Product name
- 17(S)-HpDHA
- Purity
- ≥98%
- Packaging
- 250μg
- Price
- $947
- Updated
- 2024/03/01
17(S)-HpDoHE Chemical Properties,Usage,Production
Description
17(S)-
Uses
17(S)-HpDHA is the main 15-Lipoxygenase (LOX) isoenzyme: h15-LOX-1 and h15-LOX-2 and docosahexaenoic acid (DHA). product. 17(S)-HpDHA negatively regulates epoxide synthesis via allosteric regulation. 17(S)-HpDHA also inhibits platelet aggregation with an EC50 of approximately 1 μM[1].
Definition
ChEBI: (4Z,7Z,10Z,13Z,15E,17S,19Z)-17-hydroperoxydocosahexaenoic acid is a docosanoid that is (4Z,7Z,10Z,13Z,15E,19Z)-docosahexaenoic acid carrying a hydroperoxy substituent at position 17S. It has a role as a mouse metabolite. It is a docosanoid, a long-chain fatty acid and a hydroperoxy polyunsaturated fatty acid. It is functionally related to an all-cis-docosa-4,7,10,13,16,19-hexaenoic acid. It is a conjugate acid of a (4Z,7Z,10Z,13Z,15E,17S,19Z)-17-hydroperoxydocosahexaenoate.
References
[1] Tsai WC, et al. In Vitro Biosynthetic Pathway Investigations of Neuroprotectin D1 (NPD1) and Protectin DX (PDX) by Human 12-Lipoxygenase, 15-Lipoxygenase-1, and 15-Lipoxygenase-2. Biochemistry. 2021 Jun 8;60(22):1741-1754. DOI:10.1021/acs.biochem.0c00931
17(S)-HpDoHE Preparation Products And Raw materials
Raw materials
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