Structure Database (LMSD)

Common Name
Menaquinone-10
Systematic Name
2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-3-methylnaphthalene-1,4-dione
Synonyms
  • MK-10
LM ID
LMPR02030047
Formula
C61H88O2
Exact Mass
Calculate m/z
852.678432
Status
Curated
Show lipids differing only in stereochemistry/bond geometry

Classification

Category
Main Class
Sub Class
Prenol Lipids [PR]
Quinones and hydroquinones [PR02]
Vitamin K [PR0203]

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Prevotella melaninogenica (#28132)
Bacteroidia (#200643)
Biosynthetic precursors of vitamin K as growth promoters for Bacteroides melaninogenicus.,
J Bacteriol, 1973
Pubmed ID: 4745437
Bos (#9903)
Mammalia (#40674)
Characterization of vitamin K from bovine liver.,
J Lipid Res, 1968
Pubmed ID: 4295867

String Representations

InChiKey (Click to copy)
OCQQATZYCNAKQB-UQUNHUMXSA-N
InChi (Click to copy)
InChI=1S/C61H88O2/c1-46(2)24-15-25-47(3)26-16-27-48(4)28-17-29-49(5)30-18-31-50(6)32-19-33-51(7)34-20-35-52(8)36-21-37-53(9)38-22-39-54(10)40-23-41-55(11)44-45-57-56(12)60(62)58-42-13-14-43-59(58)61(57)63/h13-14,24,26,28,30,32,34,36,38,40,42-44H,15-23,25,27,29,31,33,35,37,39,41,45H2,1-12H3/b47-26+,48-28+,49-30+,50-32+,51-34+,52-36+,53-38+,54-40+,55-44+
SMILES (Click to copy)
C1(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)/CC/C=C(\C)/C)C(=O)C2=C(C=CC=C2)C(=O)C=1C

Other Databases

PubChem CID
9988135
PDB ID
A1L8Q

Calculated Physicochemical Properties

Heavy Atoms 63
Rings 2
Aromatic Rings 1
Rotatable Bonds 29
Van der Waals Molecular Volume 1003.58
Topological Polar Surface Area 34.14
Hydrogen Bond Donors
Hydrogen Bond Acceptors 2
logP 19.28
Molar Refractivity 278.77

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Created at
2nd Jul 2025
Updated at
2nd Jul 2025