2525175-25-9
Chemical Structure
12-HETE-d8
- CAS No.: 2525175-25-9
- Formula:C20H24D8O3
- Molecular Weight:328.52
IUPAC Name: (1-(butyl-2,2,3,3,4,4,4-d7)-6-hydroxy-1H-indol-3-yl)(naphthalen-1-yl)methanone
InChIKey: ZNHVWPKMFKADKW-FDBBORNLSA-N
SMILES: CCCCC/C([2H])=C(CC([2H])(/C([2H])=C/C([2H])=C(C/C([2H])=C(CCCC(O)=O)/[2H])/[2H])O)/[2H]
Biological Activity:
12-HETE-d8 is the deuterium labeled 12-HETE. 12-HETE, a major metabolic product of arachidonic acid using 12-LOX catalysis, inhibits cell apoptosis in a dose-dependent manner. 12-HETE promotes the activation and nuclear translocation of NF-κB through the integrin-linked kinase (ILK) pathway[1].12-HETE has both anti-thrombotic and pro-thrombotic effects[2]. 12-HETE is a neuromodulator[3].
The product specifications provided below refer solely to the active content of 12-HETE-d8.
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12-HETE-d8 | 98.03% | 12-HETE-d8 is the deuterium labeled 12-HETE. 12-HETE, a major metabolic product of arachidonic acid using 12-LOX catalysis, inhibits cell apoptosis in a dose-dependent manner. 12-HETE promotes the activation and nuclear translocation of NF-κB through the integrin-linked kinase (ILK) pathway.12-HETE has both anti-thrombotic and pro-thrombotic effects. 12-HETE is a neuromodulator. The product specifications provided below refer solely to the active content of 12-HETE-d8. |
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12-HETE | 95.70% | 12-HETE, a major metabolic product of arachidonic acid using 12-LOX catalysis, inhibits cell apoptosis in a dose-dependent manner. 12-HETE promotes the activation and nuclear translocation of NF-κB through the integrin-linked kinase (ILK) pathway.12-HETE has both anti-thrombotic and pro-thrombotic effects. 12-HETE is a neuromodulator. The product specifications provided below refer solely to the active content of 12-HETE. |
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Similarity Score 1.00
HY-1126538(S)-HETE -
Similarity Score 1.00
HY-112653A(±)8-HETE -
Similarity Score 1.00
HY-1204608(R)-HETE -
Similarity Score 1.00
HY-12302312(S)-HETE-d8 -
Similarity Score 1.00
HY-12440412(R)-HETE -
Similarity Score 1.00
HY-124404A12(S)-HETE -
Similarity Score 0.97
HY-113943S9(S)-HETE-d8 -
Similarity Score 0.97
HY-143677S(±)11-HETE-d8 -
Similarity Score 0.97
HY-11345311(R)-HETE -
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief]
- [2]. Qian Liu, et al. 12-HETE facilitates cell survival by activating the integrin-linked kinase/NF-κB pathway in ovarian cancer. Cancer Manag Res. 2018 Nov 16;10:5825-5838. [Content Brief]
- [3]. Benedetta Porro, et al. Analysis, physiological and clinical significance of 12-HETE: a neglected platelet-derived 12-lipoxygenase product. J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Aug 1;964:26-40. [Content Brief]
