A vitamin K2 analog
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Menaquinone 9

Item No. 18242

Technical Information
Formal Name
2-methyl-3-[(2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethyl-2,6,10,14,18,22,26,30,34-hexatriacontanonaen-1-yl]-1,4-naphthalenedione
CAS Number
523-39-7
Synonyms
  • MK-9
  • Vitamin K2(45)
Molecular Formula
C56H80O2
Formula Weight
Purity
≥95%
A crystalline solid
Chloroform: 100 mg/ml
λmax
249, 270, 315 nm
SMILES
O=C1C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/C)=C(C)C(C2=CC=CC=C21)=O
InChi Code
InChI=1S/C56H80O2/c1-42(2)22-14-23-43(3)24-15-25-44(4)26-16-27-45(5)28-17-29-46(6)30-18-31-47(7)32-19-33-48(8)34-20-35-49(9)36-21-37-50(10)40-41-52-51(11)55(57)53-38-12-13-39-54(53)56(52)58/h12-13,22,24,26,28,30,32,34,36,38-40H,14-21,23,25,27,29,31,3
InChi Key
WCRXHNIUHQUASO-UVZVDVBNSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Menaquinone 9 (MK-9) is a vitamin K2 analog that has been found in various bacteria, including E. coli.1,2 MK-9 is UV-sensitive and binds to soluble nitrate reductase, a component of the bacterial electron transport chain.1 In vivo, MK-9 increases plasma prothrombin concentration in vitamin K-deficient rats.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Craciun, A.M., Groenen-van Dooren, M.M., Thijssen, H.H., et alInduction of prothrombin synthesis by K-vitamins compared in vitamin K-deficient and in brodifacoum-treated rats. Biochim. Biophys. Acta 1380(1), 75-81 (1998).

    2. Brito, F., DeMoss, J.A., and Dubourdieu, M. Isolation and identification of menaquinone-9 from purified nitrate reductase of Escherichia coli. J. Bacteriol. 177(13), 3728-3735 (1995).