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Vitamin K1 2,3-epoxide
[CAS# 25486-55-9]

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Identification
Classification Chemical reagent >> Organic reagent >> Epoxide
Name Vitamin K1 2,3-epoxide
Synonyms (2,3-Epoxyphytyl)menaquinone
Molecular Structure CAS # 25486-55-9, Vitamin K1 2,3-epoxide, (2,3-Epoxyphytyl)menaquinone
Molecular Formula C31H46O3
Molecular Weight 466.69
CAS Registry Number 25486-55-9
EC Number 247-022-9
SMILES CC(C)CCCC(C)CCCC(C)CCC/C(=C/CC12C(=O)C3=CC=CC=C3C(=O)C1(O2)C)/C
Properties
Density 1.0±0.1 g/cm3 Calc.*
Boiling point 561.1±50.0 ºC 760 mmHg (Calc.)*
Flash point 233.8±30.2 ºC (Calc.)*
Index of refraction 1.523 (Calc.)*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319    Details
Precautionary Statements P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313    Details
SDS Available
up Discovory and Applicatios
Vitamin K1 2,3-epoxide is a biologically important compound formed as a result of the vitamin K cycle, a critical biochemical pathway involved in blood coagulation. It is a metabolic derivative of phylloquinone (vitamin K1) generated during the carboxylation of specific glutamate residues on vitamin K–dependent proteins.

The discovery of vitamin K and its metabolic cycle dates back to the 1930s and 1940s, when researchers identified its essential role in blood clotting. During this process, vitamin K1 acts as a cofactor for the enzyme γ-glutamyl carboxylase, which catalyzes the post-translational modification of glutamate residues to γ-carboxyglutamate (Gla) on coagulation factors such as prothrombin (factor II), factor VII, factor IX, and factor X. This reaction is essential for enabling these proteins to bind calcium and function effectively in the coagulation cascade.

In the carboxylation reaction, vitamin K1 undergoes oxidation and is converted into vitamin K1 2,3-epoxide. To sustain the cycle, this epoxide form must be reduced back to the active hydroquinone form of vitamin K1 through two sequential reduction steps. These reactions are catalyzed by vitamin K epoxide reductase (VKOR) enzymes. The VKOR complex reduces the epoxide to vitamin K quinone and then to the hydroquinone form, which can again serve as a cofactor for carboxylase enzymes.

The vitamin K1 epoxide form itself does not possess biological activity in coagulation but is crucial as an intermediate in the regeneration of active vitamin K1. The proper functioning of this cycle ensures a continuous supply of vitamin K1 in its active form, thereby maintaining the activation of coagulation proteins.

Clinically, the significance of vitamin K1 2,3-epoxide is closely related to the mechanism of action of anticoagulant drugs such as warfarin. Warfarin inhibits the VKOR enzyme, thereby blocking the reduction of vitamin K1 2,3-epoxide back to the active form. This disruption leads to a decrease in the carboxylation of clotting factors, resulting in an anticoagulant effect. Measurement of vitamin K1 2,3-epoxide levels in plasma has been explored in some clinical studies to assess warfarin activity or vitamin K status.

The accumulation of vitamin K1 2,3-epoxide may occur during anticoagulant therapy or in cases of vitamin K deficiency, which can affect the efficiency of blood coagulation. However, under normal physiological conditions, the vitamin K cycle operates efficiently, and the epoxide form is rapidly converted back to active vitamin K1.

In summary, vitamin K1 2,3-epoxide is a key intermediate in the vitamin K cycle formed during the γ-carboxylation of clotting factors. While it lacks direct biological activity, its presence and reconversion are essential for maintaining the active pool of vitamin K1 and ensuring the proper functioning of the coagulation system.

References

2014. Recent trends in the metabolism and cell biology of vitamin K with special reference to vitamin K cycling and MK-4 biosynthesis. Journal of Lipid Research, 55(3).
DOI: 10.1194/jlr.r045559

2011. Functional study of the vitamin K cycle in mammalian cells. Blood, 117(10).
DOI: 10.1182/blood-2010-08-304303

2014. Rapid, high performance method for the determination of vitamin K(1), menaquinone-4 and vitamin K(1) 2,3-epoxide in human serum and plasma using liquid chromatography-hybrid quadrupole linear ion trap mass spectrometry. Journal of chromatography. A, 1338.
DOI: 10.1016/j.chroma.2014.02.065
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