MiMeDB: Showing metabocard for Phylloquinone (MMDBc0033533)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 04:52:32 UTC

Update Date

2022-12-15 22:51:56 UTC

Metabolite ID

MMDBc0033533

Metabolite Identification

Common Name

Phylloquinone

Description

Vitamin K1, also known as phylloquinone or phytonadione, is a polycyclic aromatic ketone, based on 1,4-naphthoquinone, with 2-methyl and 3-phytyl substituents. Vitamin K is a family of phylloquinones that contain a ring of 2-methyl-1,4-naphthoquinone and an isoprenoid side chain. Several forms of vitamin K have been identified: vitamin K1 derived from plants, vitamin K2 (menaquinone) from bacteria and synthetic naphthoquinone provitamins, and vitamin K3 (menadione). Vitamin K1 has only one double bond on the proximal isoprene unit. Vitamin K1 possesses the same type and degree of activity as does naturally-occurring vitamin K, which is necessary for the production via the liver of active prothrombin (factor II), proconvertin (factor VII), plasma thromboplastin component (factor IX), and Stuart factor (factor X). Rich sources of vitamin K1 include green plants, algae, and photosynthetic bacteria. Vitamin K1 has antihemorrhagic and prothrombogenic activity. Vitamin K1 is a fat-soluble vitamin that is stable to air and moisture but decomposes in sunlight. Vitamin K1 is an antidote for coumatetralyl.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652305252111302D          

 33 34  0  0  0  0            999 V2000
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8578   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0012   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7157   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8591   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5736   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0025   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7170   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0025   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
M  END

HMDB0259855
     RDKit          3D
Vitamin K-d7 (5,6,7,8-d4, 2-methyl-d3)
 79 80  0  0  0  0  0  0  0  0999 V2000
    1.8739   -0.2495   -1.5569 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8141    0.7397   -0.8974 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0456    0.7384   -1.3554 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1482    1.5780   -0.9121 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2655    0.7283   -0.3462 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6703    0.8523    0.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0536    1.8325    1.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7700   -0.0070    1.3940 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1339    0.1377    2.5949 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4101   -0.9852    0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4291   -1.7907    0.9630 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0270   -2.7123    0.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6181   -2.8606   -1.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5919   -2.0515   -1.6254 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9915   -1.1198   -0.7785 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9045   -0.2543   -1.2280 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5421   -0.4035   -2.4389 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3985    1.6149    0.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8385    0.9151    1.3804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6161    0.1638    1.4123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7369    0.8274    1.2717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9741    1.5448   -0.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7514   -0.2480    1.5724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1671    0.0664    1.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8589    0.5404    0.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3632    0.7048    0.7212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4806    1.7152    1.8419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1328    1.2200   -0.4467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0931    0.3316   -1.6587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6526   -1.0351   -1.4072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0981   -1.0174   -0.9663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5212   -2.4655   -0.7493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0083   -0.4709   -2.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8710    0.1247   -1.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1944   -0.3105   -2.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0372   -1.2520   -1.1027 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    0.0251   -2.1720 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6112    2.0179   -1.8751 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9304    2.3900   -0.2367 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6964    1.9178    2.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0246    2.8340    1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0777    1.4723    2.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7580   -1.6816    1.9960 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8316   -3.3426    0.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0870   -3.5850   -1.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2196   -2.1141   -2.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4002    2.0476    0.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9212    2.5665   -0.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8126    1.6668    2.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6819    0.1846    1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5922   -0.6805    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124   -0.4472    2.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8742    1.5750    2.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4590    0.8540   -0.7310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5646    2.4754    0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0671    1.9018   -0.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4788   -0.5819    2.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4927   -1.1891    0.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7607   -0.8621    1.8971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3562    0.7703    2.4443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7929   -0.2512   -0.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5404    1.4813   -0.0948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6704   -0.2659    1.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5432    2.0792    1.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3139    1.2771    2.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8658    2.6188    1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6515    2.1945   -0.7476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1614    1.4643   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6368    0.8491   -2.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0438    0.2131   -1.9691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0162   -1.6229   -0.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6460   -1.5669   -2.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2374   -0.4005   -0.0555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6301   -3.1092   -0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2195   -2.8220   -1.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0534   -2.5195    0.2406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6152    0.3947   -2.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9837   -0.2472   -1.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2765   -1.3196   -2.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  3
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  2 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 16  5  1  0
 15 10  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  7 40  1  0
  7 41  1  0
  7 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 22 54  1  0
 22 55  1  0
 22 56  1  0
 23 57  1  0
 23 58  1  0
 24 59  1  0
 24 60  1  0
 25 61  1  0
 25 62  1  0
 26 63  1  0
 27 64  1  0
 27 65  1  0
 27 66  1  0
 28 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 30 72  1  0
 31 73  1  0
 32 74  1  0
 32 75  1  0
 32 76  1  0
 33 77  1  0
 33 78  1  0
 33 79  1  0
M  END


  Mrv1652305252111302D          

 33 34  0  0  0  0            999 V2000
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8578   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0012   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7157   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8591   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5736   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0025   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7170   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0025   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0033533

> <DATABASE_NAME>
MIME

> <SMILES>
CC(C)CCCC(C)CCCC(C)CCCC(C)=CCC1=C(C)C(=O)C2=CC=CC=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H46O2/c1-22(2)12-9-13-23(3)14-10-15-24(4)16-11-17-25(5)20-21-27-26(6)30(32)28-18-7-8-19-29(28)31(27)33/h7-8,18-20,22-24H,9-17,21H2,1-6H3

> <INCHI_KEY>
MBWXNTAXLNYFJB-UHFFFAOYSA-N

> <FORMULA>
C31H46O2

> <MOLECULAR_WEIGHT>
450.707

> <EXACT_MASS>
450.349780721

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
57.07020367874705

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-methyl-3-(3,7,11,15-tetramethylhexadec-2-en-1-yl)-1,4-dihydronaphthalene-1,4-dione

> <ALOGPS_LOGP>
8.48

> <JCHEM_LOGP>
9.696445808333333

> <ALOGPS_LOGS>
-6.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.224343412034619

> <JCHEM_POLAR_SURFACE_AREA>
34.14

> <JCHEM_REFRACTIVITY>
142.9568

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.92e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
vitamin k

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0259855
     RDKit          3D
Vitamin K-d7 (5,6,7,8-d4, 2-methyl-d3)
 79 80  0  0  0  0  0  0  0  0999 V2000
    1.8739   -0.2495   -1.5569 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8141    0.7397   -0.8974 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0456    0.7384   -1.3554 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1482    1.5780   -0.9121 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2655    0.7283   -0.3462 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6703    0.8523    0.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0536    1.8325    1.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7700   -0.0070    1.3940 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1339    0.1377    2.5949 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4101   -0.9852    0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4291   -1.7907    0.9630 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0270   -2.7123    0.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6181   -2.8606   -1.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5919   -2.0515   -1.6254 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9915   -1.1198   -0.7785 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9045   -0.2543   -1.2280 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5421   -0.4035   -2.4389 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3985    1.6149    0.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8385    0.9151    1.3804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6161    0.1638    1.4123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7369    0.8274    1.2717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9741    1.5448   -0.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7514   -0.2480    1.5724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1671    0.0664    1.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8589    0.5404    0.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3632    0.7048    0.7212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4806    1.7152    1.8419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1328    1.2200   -0.4467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0931    0.3316   -1.6587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6526   -1.0351   -1.4072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0981   -1.0174   -0.9663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5212   -2.4655   -0.7493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0083   -0.4709   -2.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8710    0.1247   -1.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1944   -0.3105   -2.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0372   -1.2520   -1.1027 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    0.0251   -2.1720 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6112    2.0179   -1.8751 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9304    2.3900   -0.2367 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6964    1.9178    2.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0246    2.8340    1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0777    1.4723    2.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7580   -1.6816    1.9960 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8316   -3.3426    0.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0870   -3.5850   -1.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2196   -2.1141   -2.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4002    2.0476    0.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9212    2.5665   -0.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8126    1.6668    2.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6819    0.1846    1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5922   -0.6805    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124   -0.4472    2.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8742    1.5750    2.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4590    0.8540   -0.7310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5646    2.4754    0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0671    1.9018   -0.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4788   -0.5819    2.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4927   -1.1891    0.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7607   -0.8621    1.8971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3562    0.7703    2.4443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7929   -0.2512   -0.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5404    1.4813   -0.0948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6704   -0.2659    1.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5432    2.0792    1.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3139    1.2771    2.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8658    2.6188    1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6515    2.1945   -0.7476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1614    1.4643   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6368    0.8491   -2.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0438    0.2131   -1.9691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0162   -1.6229   -0.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6460   -1.5669   -2.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2374   -0.4005   -0.0555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6301   -3.1092   -0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2195   -2.8220   -1.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0534   -2.5195    0.2406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6152    0.3947   -2.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9837   -0.2472   -1.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2765   -1.3196   -2.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  3
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  2 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 16  5  1  0
 15 10  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  7 40  1  0
  7 41  1  0
  7 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 22 54  1  0
 22 55  1  0
 22 56  1  0
 23 57  1  0
 23 58  1  0
 24 59  1  0
 24 60  1  0
 25 61  1  0
 25 62  1  0
 26 63  1  0
 27 64  1  0
 27 65  1  0
 27 66  1  0
 28 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 30 72  1  0
 31 73  1  0
 32 74  1  0
 32 75  1  0
 32 76  1  0
 33 77  1  0
 33 78  1  0
 33 79  1  0
M  END

HEADER    PROTEIN                                 25-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-MAY-21         0                                  
HETATM    1  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.667 -10.780   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.001  -8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.668  -8.470   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.002 -10.780   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.336  -8.470   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.003  -8.470   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.337 -10.780   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.670  -8.470   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.338  -8.470   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      18.671  -9.240   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      20.005  -8.470   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      18.671 -10.780   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4   14                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11    2   13                                                  
CONECT   13   12                                                            
CONECT   14    3   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

COMPND    HMDB0259855
HETATM    1  C1  UNL     1       1.874  -0.250  -1.557  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.814   0.740  -0.897  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.046   0.738  -1.355  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.148   1.578  -0.912  1.00  0.00           C  
HETATM    5  C5  UNL     1       6.266   0.728  -0.346  1.00  0.00           C  
HETATM    6  C6  UNL     1       6.670   0.852   0.899  1.00  0.00           C  
HETATM    7  C7  UNL     1       6.054   1.832   1.818  1.00  0.00           C  
HETATM    8  C8  UNL     1       7.770  -0.007   1.394  1.00  0.00           C  
HETATM    9  O1  UNL     1       8.134   0.138   2.595  1.00  0.00           O  
HETATM   10  C9  UNL     1       8.410  -0.985   0.526  1.00  0.00           C  
HETATM   11  C10 UNL     1       9.429  -1.791   0.963  1.00  0.00           C  
HETATM   12  C11 UNL     1      10.027  -2.712   0.134  1.00  0.00           C  
HETATM   13  C12 UNL     1       9.618  -2.861  -1.180  1.00  0.00           C  
HETATM   14  C13 UNL     1       8.592  -2.052  -1.625  1.00  0.00           C  
HETATM   15  C14 UNL     1       7.991  -1.120  -0.778  1.00  0.00           C  
HETATM   16  C15 UNL     1       6.905  -0.254  -1.228  1.00  0.00           C  
HETATM   17  O2  UNL     1       6.542  -0.404  -2.439  1.00  0.00           O  
HETATM   18  C16 UNL     1       2.398   1.615   0.213  1.00  0.00           C  
HETATM   19  C17 UNL     1       1.838   0.915   1.380  1.00  0.00           C  
HETATM   20  C18 UNL     1       0.616   0.164   1.412  1.00  0.00           C  
HETATM   21  C19 UNL     1      -0.737   0.827   1.272  1.00  0.00           C  
HETATM   22  C20 UNL     1      -0.974   1.545  -0.001  1.00  0.00           C  
HETATM   23  C21 UNL     1      -1.751  -0.248   1.572  1.00  0.00           C  
HETATM   24  C22 UNL     1      -3.167   0.066   1.569  1.00  0.00           C  
HETATM   25  C23 UNL     1      -3.859   0.540   0.344  1.00  0.00           C  
HETATM   26  C24 UNL     1      -5.363   0.705   0.721  1.00  0.00           C  
HETATM   27  C25 UNL     1      -5.481   1.715   1.842  1.00  0.00           C  
HETATM   28  C26 UNL     1      -6.133   1.220  -0.447  1.00  0.00           C  
HETATM   29  C27 UNL     1      -6.093   0.332  -1.659  1.00  0.00           C  
HETATM   30  C28 UNL     1      -6.653  -1.035  -1.407  1.00  0.00           C  
HETATM   31  C29 UNL     1      -8.098  -1.017  -0.966  1.00  0.00           C  
HETATM   32  C30 UNL     1      -8.521  -2.465  -0.749  1.00  0.00           C  
HETATM   33  C31 UNL     1      -9.008  -0.471  -2.045  1.00  0.00           C  
HETATM   34  H1  UNL     1       0.871   0.125  -1.576  1.00  0.00           H  
HETATM   35  H2  UNL     1       2.194  -0.311  -2.647  1.00  0.00           H  
HETATM   36  H3  UNL     1       2.037  -1.252  -1.103  1.00  0.00           H  
HETATM   37  H4  UNL     1       4.288   0.025  -2.172  1.00  0.00           H  
HETATM   38  H5  UNL     1       5.611   2.018  -1.875  1.00  0.00           H  
HETATM   39  H6  UNL     1       4.930   2.390  -0.237  1.00  0.00           H  
HETATM   40  H7  UNL     1       6.696   1.918   2.746  1.00  0.00           H  
HETATM   41  H8  UNL     1       6.025   2.834   1.385  1.00  0.00           H  
HETATM   42  H9  UNL     1       5.078   1.472   2.218  1.00  0.00           H  
HETATM   43  H10 UNL     1       9.758  -1.682   1.996  1.00  0.00           H  
HETATM   44  H11 UNL     1      10.832  -3.343   0.493  1.00  0.00           H  
HETATM   45  H12 UNL     1      10.087  -3.585  -1.833  1.00  0.00           H  
HETATM   46  H13 UNL     1       8.220  -2.114  -2.647  1.00  0.00           H  
HETATM   47  H14 UNL     1       3.400   2.048   0.643  1.00  0.00           H  
HETATM   48  H15 UNL     1       1.921   2.567  -0.099  1.00  0.00           H  
HETATM   49  H16 UNL     1       1.813   1.667   2.254  1.00  0.00           H  
HETATM   50  H17 UNL     1       2.682   0.185   1.708  1.00  0.00           H  
HETATM   51  H18 UNL     1       0.592  -0.681   0.649  1.00  0.00           H  
HETATM   52  H19 UNL     1       0.612  -0.447   2.387  1.00  0.00           H  
HETATM   53  H20 UNL     1      -0.874   1.575   2.125  1.00  0.00           H  
HETATM   54  H21 UNL     1      -1.459   0.854  -0.731  1.00  0.00           H  
HETATM   55  H22 UNL     1      -1.565   2.475   0.199  1.00  0.00           H  
HETATM   56  H23 UNL     1      -0.067   1.902  -0.490  1.00  0.00           H  
HETATM   57  H24 UNL     1      -1.479  -0.582   2.638  1.00  0.00           H  
HETATM   58  H25 UNL     1      -1.493  -1.189   0.991  1.00  0.00           H  
HETATM   59  H26 UNL     1      -3.761  -0.862   1.897  1.00  0.00           H  
HETATM   60  H27 UNL     1      -3.356   0.770   2.444  1.00  0.00           H  
HETATM   61  H28 UNL     1      -3.793  -0.251  -0.428  1.00  0.00           H  
HETATM   62  H29 UNL     1      -3.540   1.481  -0.095  1.00  0.00           H  
HETATM   63  H30 UNL     1      -5.670  -0.266   1.104  1.00  0.00           H  
HETATM   64  H31 UNL     1      -6.543   2.079   1.818  1.00  0.00           H  
HETATM   65  H32 UNL     1      -5.314   1.277   2.840  1.00  0.00           H  
HETATM   66  H33 UNL     1      -4.866   2.619   1.644  1.00  0.00           H  
HETATM   67  H34 UNL     1      -5.652   2.195  -0.748  1.00  0.00           H  
HETATM   68  H35 UNL     1      -7.161   1.464  -0.155  1.00  0.00           H  
HETATM   69  H36 UNL     1      -6.637   0.849  -2.473  1.00  0.00           H  
HETATM   70  H37 UNL     1      -5.044   0.213  -1.969  1.00  0.00           H  
HETATM   71  H38 UNL     1      -6.016  -1.623  -0.747  1.00  0.00           H  
HETATM   72  H39 UNL     1      -6.646  -1.567  -2.403  1.00  0.00           H  
HETATM   73  H40 UNL     1      -8.237  -0.401  -0.055  1.00  0.00           H  
HETATM   74  H41 UNL     1      -7.630  -3.109  -0.638  1.00  0.00           H  
HETATM   75  H42 UNL     1      -9.220  -2.822  -1.524  1.00  0.00           H  
HETATM   76  H43 UNL     1      -9.053  -2.520   0.241  1.00  0.00           H  
HETATM   77  H44 UNL     1      -8.615   0.395  -2.575  1.00  0.00           H  
HETATM   78  H45 UNL     1      -9.984  -0.247  -1.523  1.00  0.00           H  
HETATM   79  H46 UNL     1      -9.276  -1.320  -2.741  1.00  0.00           H  
CONECT    1    2   34   35   36
CONECT    2    3    3   18
CONECT    3    4   37
CONECT    4    5   38   39
CONECT    5    6    6   16
CONECT    6    7    8
CONECT    7   40   41   42
CONECT    8    9    9   10
CONECT   10   11   11   15
CONECT   11   12   43
CONECT   12   13   13   44
CONECT   13   14   45
CONECT   14   15   15   46
CONECT   15   16
CONECT   16   17   17
CONECT   18   19   47   48
CONECT   19   20   49   50
CONECT   20   21   51   52
CONECT   21   22   23   53
CONECT   22   54   55   56
CONECT   23   24   57   58
CONECT   24   25   59   60
CONECT   25   26   61   62
CONECT   26   27   28   63
CONECT   27   64   65   66
CONECT   28   29   67   68
CONECT   29   30   69   70
CONECT   30   31   71   72
CONECT   31   32   33   73
CONECT   32   74   75   76
CONECT   33   77   78   79
END

HMDB0259855
     RDKit          3D
Vitamin K-d7 (5,6,7,8-d4, 2-methyl-d3)
 79 80  0  0  0  0  0  0  0  0999 V2000
    1.8739   -0.2495   -1.5569 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8141    0.7397   -0.8974 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0456    0.7384   -1.3554 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1482    1.5780   -0.9121 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2655    0.7283   -0.3462 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6703    0.8523    0.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0536    1.8325    1.8181 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7700   -0.0070    1.3940 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1339    0.1377    2.5949 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4101   -0.9852    0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4291   -1.7907    0.9630 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0270   -2.7123    0.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6181   -2.8606   -1.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5919   -2.0515   -1.6254 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9915   -1.1198   -0.7785 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9045   -0.2543   -1.2280 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5421   -0.4035   -2.4389 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3985    1.6149    0.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8385    0.9151    1.3804 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6161    0.1638    1.4123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7369    0.8274    1.2717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9741    1.5448   -0.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7514   -0.2480    1.5724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1671    0.0664    1.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8589    0.5404    0.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3632    0.7048    0.7212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4806    1.7152    1.8419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1328    1.2200   -0.4467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0931    0.3316   -1.6587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6526   -1.0351   -1.4072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0981   -1.0174   -0.9663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5212   -2.4655   -0.7493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0083   -0.4709   -2.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8710    0.1247   -1.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1944   -0.3105   -2.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0372   -1.2520   -1.1027 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    0.0251   -2.1720 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6112    2.0179   -1.8751 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9304    2.3900   -0.2367 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6964    1.9178    2.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0246    2.8340    1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0777    1.4723    2.2179 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7580   -1.6816    1.9960 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8316   -3.3426    0.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0870   -3.5850   -1.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2196   -2.1141   -2.6466 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4002    2.0476    0.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9212    2.5665   -0.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8126    1.6668    2.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6819    0.1846    1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5922   -0.6805    0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124   -0.4472    2.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8742    1.5750    2.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4590    0.8540   -0.7310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5646    2.4754    0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0671    1.9018   -0.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4788   -0.5819    2.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4927   -1.1891    0.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7607   -0.8621    1.8971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3562    0.7703    2.4443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7929   -0.2512   -0.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5404    1.4813   -0.0948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6704   -0.2659    1.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5432    2.0792    1.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3139    1.2771    2.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8658    2.6188    1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6515    2.1945   -0.7476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1614    1.4643   -0.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6368    0.8491   -2.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0438    0.2131   -1.9691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0162   -1.6229   -0.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6460   -1.5669   -2.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2374   -0.4005   -0.0555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6301   -3.1092   -0.6377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2195   -2.8220   -1.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0534   -2.5195    0.2406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6152    0.3947   -2.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9837   -0.2472   -1.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2765   -1.3196   -2.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  3
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  2 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 16  5  1  0
 15 10  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  7 40  1  0
  7 41  1  0
  7 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  0
 14 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 22 54  1  0
 22 55  1  0
 22 56  1  0
 23 57  1  0
 23 58  1  0
 24 59  1  0
 24 60  1  0
 25 61  1  0
 25 62  1  0
 26 63  1  0
 27 64  1  0
 27 65  1  0
 27 66  1  0
 28 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 30 72  1  0
 31 73  1  0
 32 74  1  0
 32 75  1  0
 32 76  1  0
 33 77  1  0
 33 78  1  0
 33 79  1  0
M  END

Synonyms

Not Available

Molecular Formula

C₃₁H₄₆O₂

Average Mass

450.707

Monoisotopic Mass

450.349780721

IUPAC Name

2-methyl-3-(3,7,11,15-tetramethylhexadec-2-en-1-yl)-1,4-dihydronaphthalene-1,4-dione

Traditional Name

vitamin k

CAS Registry Number

84-80-0

SMILES

CC(C)CCCC(C)CCCC(C)CCCC(C)=CCC1=C(C)C(=O)C2=CC=CC=C2C1=O

InChI Identifier

InChI=1S/C31H46O2/c1-22(2)12-9-13-23(3)14-10-15-24(4)16-11-17-25(5)20-21-27-26(6)30(32)28-18-7-8-19-29(28)31(27)33/h7-8,18-20,22-24H,9-17,21H2,1-6H3

InChI Key

MBWXNTAXLNYFJB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as vitamin k compounds. These are quinone lipids containing a methylated naphthoquinone ring structure, and vary in the aliphatic side chain attached at the 3-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Quinone and hydroquinone lipids

Direct Parent

Vitamin K compounds

Alternative Parents

Substituents

Diterpenoid
Naphthoquinone
Naphthalene
Aryl ketone
Quinone
Benzenoid
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

a vitamin K (2-METHYL-3-PHYTYL-14-NAPHTHOQUINONE )
an electron-transfer-related quinone (2-METHYL-3-PHYTYL-14-NAPHTHOQUINONE )

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
Water Solubility	5.9e-05 g/L	ALOGPS
logP	8.48	ALOGPS
logP	9.7	ChemAxon
logS	-6.9	ALOGPS
pKa (Strongest Basic)	-7.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	34.14 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	142.96 m³·mol⁻¹	ChemAxon
Polarizability	57.07 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Biological Properties

Cellular Locations

Cytoplasm
Extracellular
Membrane

Biospecimen Locations

Blood
Liver

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Unknown

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Age	Sex	Health Condition	Data Source	Reference
Human	Detected and Quantified	0.00102				Adult (>18 years old)	Female	Normal	HMDB	9109609
Human	Detected and Quantified	0.00106				Adult (>18 years old)	Male	Normal	HMDB	9109609
Human	Detected and Quantified	0.00143				Adult (>18 years old)	Male	Normal	HMDB	9109609
Human	Detected and Quantified	0.00147				Adult (>18 years old)	Female	Normal	HMDB	9109609
Human	Detected and Quantified	0.00049		0.00009	0.0022	Adolescent (13-18 years old)	Both	Normal	HMDB	7657478
Human	Detected and Quantified	0.000500	0.000520			Adult (>18 years old)	Male	Normal	HMDB	12067432
Human	Detected and Quantified	0.000540	0.000560			Adult (>18 years old)	Both	Normal	HMDB	12067432
Human	Detected and Quantified	0.000560	0.000580			Adult (>18 years old)	Female	Normal	HMDB	12067432
Human	Detected and Quantified	0.0011	0.0042			Adult (>18 years old)	Female	Normal	HMDB	15340366
Human	Detected and Quantified	0.00150	0.00219			Adult (>18 years old)	Female	Normal	HMDB	17181887
Human	Detected and Quantified	0.00164	0.00215			Adult (>18 years old)	Both	Normal	HMDB	17181887
Human	Detected and Quantified	0.00180	0.00209			Adult (>18 years old)	Male	Normal	HMDB	17181887
Human	Detected and Quantified	0.0058		0.0020	0.017	Adult (>18 years old)	Both	Normal	HMDB	Geigy Scientific Tables, 8th Rev edition, pp. 130. Edited by C. Lentner, West Cadwell, N.J.: Medical education Div., Ciba-Geigy Corp. Basel, Switzerland c1981-1992.
Human Liver	Detected but not Quantified					Not Specified	Not Specified	Normal	HMDB	34986597

External Links

HMDB ID

HMDB0250298

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4647

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

4812

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Gover PA, Ingram GI, Cork MS, Holland L, Hopkins RP, Callaghan P, Barkhan P, Shearer MJ: Bleeding from self-administration of phenindione: a detailed case study. Br J Haematol. 1976 Aug;33(4):551-64. doi: 10.1111/j.1365-2141.1976.tb03574.x. [PubMed:1009028 ]
Hirauchi K, Sakano T, Nagaoka T, Morimoto A: Simultaneous determination of vitamin K1, vitamin K1 2,3-epoxide and menaquinone-4 in human plasma by high-performance liquid chromatography with fluorimetric detection. J Chromatogr. 1988 Aug 19;430(1):21-9. doi: 10.1016/s0378-4347(00)83130-8. [PubMed:2851012 ]
Shearer MJ, Mallinson CN, Webster GR, Barkhan P: Absorption of tritiated vitamin K1 in patients with fat malabsorption. Gut. 1970 Dec;11(12):1063-4. [PubMed:5511811 ]
Huang Y, Zhang C, Zhang X, Zhang Z: Chemiluminescence analysis of menadione sodium bisulfite and analgin in pharmaceutical preparations and biological fluids. J Pharm Biomed Anal. 1999 Dec;21(4):817-25. doi: 10.1016/s0731-7085(99)00191-0. [PubMed:10701947 ]
Begley GS, Furie BC, Czerwiec E, Taylor KL, Furie GL, Bronstein L, Stenflo J, Furie B: A conserved motif within the vitamin K-dependent carboxylase gene is widely distributed across animal phyla. J Biol Chem. 2000 Nov 17;275(46):36245-9. doi: 10.1074/jbc.M003944200. [PubMed:10893417 ]
Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. doi: 10.1038/35036052. [PubMed:11413487 ]
de Moerloose P, Boehlen F: [Haemostasis. A search for an ideal antithrombotics agent]. Rev Med Suisse. 2005 Jan 5;1(1):35-8. [PubMed:15773196 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. doi: 10.1194/jlr.R600022-JLR200. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. doi: 10.1194/jlr.R700005-JLR200. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Phylloquinone (MMDBc0033533)

MOL for #<Metabolite:0x0000560be28e9d80>

3D MOL for #<Metabolite:0x0000560be28e9d80>

3D SDF for #<Metabolite:0x0000560be28e9d80>

3D-SDF for #<Metabolite:0x0000560be28e9d80>

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3D PDB for #<Metabolite:0x0000560be28e9d80>

SMILES for #<Metabolite:0x0000560be28e9d80>

INCHI for #<Metabolite:0x0000560be28e9d80>

Structure for #<Metabolite:0x0000560be28e9d80>

3D Structure for #<Metabolite:0x0000560be28e9d80>