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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-24 10:14:15 UTC

Update Date

2021-09-24 10:14:15 UTC

HMDB ID

HMDB0304497

Secondary Accession Numbers

None

Metabolite Identification

Common Name

tetrahydrogeranylgeranyl-PP

Description

3,7,11,15-tetramethylhexadeca-2,14-dien-1-yl (phosphonatooxy)phosphonate belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle. Based on a literature review very few articles have been published on 3,7,11,15-tetramethylhexadeca-2,14-dien-1-yl (phosphonatooxy)phosphonate.

Structure

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


  Mrv1533005141521472D          

 29 28  0  0  0  0            999 V2000
    2.0921    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5237    4.5079    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   13.9362    3.7934    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   13.1112    5.2224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2381    4.9204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2381    5.7454    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   14.2381    6.5704    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   15.0631    5.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4131    5.7454    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   11.3802    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    4.0954    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  4  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 22 25  1  0  0  0  0
 14 26  1  0  0  0  0
 10 27  1  0  0  0  0
  6 28  1  0  0  0  0
  2 29  1  0  0  0  0
M  CHG  3  19  -1  23  -1  25  -1
M  END

HMDB0304497
     RDKit          3D
tetrahydrogeranylgeranyl-PP
 66 65  0  0  0  0  0  0  0  0999 V2000
   -7.8542   -0.7302   -0.9162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2133   -0.5902    0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0085    0.2227    1.4349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0669   -1.0538    0.7907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0767   -1.8481    0.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7005   -1.1623    0.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7299    0.1666   -0.4719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6748    1.2161    0.0386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4085    0.7992   -0.8361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3980    0.9242    0.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8109   -0.4030    0.6676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1768   -1.0959   -0.5368 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3655   -2.4104    0.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0216   -0.2690   -0.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1169   -0.1919    0.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0959    0.8975   -0.4429 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1952    0.9343    0.5217 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7669    0.9690    1.9892 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4317    0.9129    0.2362 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1507    0.8496   -1.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8814    2.0578   -1.0694 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5266    1.9290   -0.9076 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.2590    1.4164   -2.0702 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1613    3.5118   -0.5139 O   0  0  0  0  0  1  0  0  0  0  0  0
    8.8332    0.9536    0.4806 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4139   -0.5294    0.0666 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.3751   -0.8395   -1.3738 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5655   -1.7935    0.8822 O   0  0  0  0  0  1  0  0  0  0  0  0
   11.0389   -0.5940    0.6593 O   0  0  0  0  0  1  0  0  0  0  0  0
   -7.2354   -1.2069   -1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1509    0.2716   -1.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8024   -1.2944   -0.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2986    0.6165    2.1861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4424    1.0928    0.8750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7681   -0.4202    1.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7483   -0.8496    1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9931   -2.8476    0.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3386   -2.0234   -1.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5783   -1.1460    1.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9858   -1.8243   -0.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1686   -0.0400   -1.5595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1239    2.2196   -0.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5560    1.3743   -0.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9032    1.2230    1.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6419    1.8599   -1.1708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9318    0.3530   -1.7220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8411    1.3798    1.1784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5893    1.5901   -0.0606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0265   -0.1843    1.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4518   -1.0863    1.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8694   -1.3297   -1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1040   -2.8698   -0.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7046   -2.3125    1.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5343   -3.1036    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6764    0.7344   -1.2786 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5120   -0.7872   -1.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8452    0.1149    1.0494 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6934   -1.1666    0.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3424    0.8266   -1.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983    1.8595   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7055   -0.1078    2.3174 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8660    1.5281    2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6181    1.4155    2.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1255    0.9267    1.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7681    0.0059   -1.2202 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3872    0.9589   -1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  3
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 15 58  1  0
 16 59  1  0
 16 60  1  0
 18 61  1  0
 18 62  1  0
 18 63  1  0
 19 64  1  0
 20 65  1  0
 20 66  1  0
M  CHG  3  24  -1  28  -1  29  -1
M  END


  Mrv1533005141521472D          

 29 28  0  0  0  0            999 V2000
    2.0921    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5237    4.5079    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   13.9362    3.7934    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   13.1112    5.2224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2381    4.9204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2381    5.7454    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   14.2381    6.5704    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   15.0631    5.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4131    5.7454    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   11.3802    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8066    4.0954    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  4  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 22 25  1  0  0  0  0
 14 26  1  0  0  0  0
 10 27  1  0  0  0  0
  6 28  1  0  0  0  0
  2 29  1  0  0  0  0
M  CHG  3  19  -1  23  -1  25  -1
M  END
> <DATABASE_ID>
HMDB0304497

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(CCCC(C)CCC=C(C)C)CCCC(C)=CCOP([O-])(=O)OP([O-])([O-])=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H40O7P2/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-26-29(24,25)27-28(21,22)23/h9,15,18-19H,6-8,10-14,16H2,1-5H3,(H,24,25)(H2,21,22,23)/p-3

> <INCHI_KEY>
VZBGWADXUJSBTI-UHFFFAOYSA-K

> <FORMULA>
C20H37O7P2

> <MOLECULAR_WEIGHT>
451.458

> <EXACT_MASS>
451.203098267

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.70711283140872

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
-3

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(3,7,11,15-tetramethylhexadeca-2,14-dien-1-yl phosphonato)oxy]phosphonate

> <ALOGPS_LOGP>
5.22

> <JCHEM_LOGP>
6.087606298333334

> <ALOGPS_LOGS>
-4.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.2043406144385607

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7672186921617796

> <JCHEM_POLAR_SURFACE_AREA>
121.78

> <JCHEM_REFRACTIVITY>
115.46799999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.28e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3,7,11,15-tetramethylhexadeca-2,14-dien-1-yl phosphonato)oxyphosphonate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0304497
     RDKit          3D
tetrahydrogeranylgeranyl-PP
 66 65  0  0  0  0  0  0  0  0999 V2000
   -7.8542   -0.7302   -0.9162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2133   -0.5902    0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0085    0.2227    1.4349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0669   -1.0538    0.7907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0767   -1.8481    0.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7005   -1.1623    0.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7299    0.1666   -0.4719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6748    1.2161    0.0386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4085    0.7992   -0.8361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3980    0.9242    0.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8109   -0.4030    0.6676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1768   -1.0959   -0.5368 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3655   -2.4104    0.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0216   -0.2690   -0.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1169   -0.1919    0.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0959    0.8975   -0.4429 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1952    0.9343    0.5217 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7669    0.9690    1.9892 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4317    0.9129    0.2362 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1507    0.8496   -1.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8814    2.0578   -1.0694 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5266    1.9290   -0.9076 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.2590    1.4164   -2.0702 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1613    3.5118   -0.5139 O   0  0  0  0  0  1  0  0  0  0  0  0
    8.8332    0.9536    0.4806 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4139   -0.5294    0.0666 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.3751   -0.8395   -1.3738 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5655   -1.7935    0.8822 O   0  0  0  0  0  1  0  0  0  0  0  0
   11.0389   -0.5940    0.6593 O   0  0  0  0  0  1  0  0  0  0  0  0
   -7.2354   -1.2069   -1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1509    0.2716   -1.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8024   -1.2944   -0.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2986    0.6165    2.1861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4424    1.0928    0.8750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7681   -0.4202    1.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7483   -0.8496    1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9931   -2.8476    0.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3386   -2.0234   -1.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5783   -1.1460    1.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9858   -1.8243   -0.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1686   -0.0400   -1.5595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1239    2.2196   -0.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5560    1.3743   -0.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9032    1.2230    1.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6419    1.8599   -1.1708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9318    0.3530   -1.7220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8411    1.3798    1.1784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5893    1.5901   -0.0606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0265   -0.1843    1.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4518   -1.0863    1.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8694   -1.3297   -1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1040   -2.8698   -0.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7046   -2.3125    1.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5343   -3.1036    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6764    0.7344   -1.2786 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5120   -0.7872   -1.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8452    0.1149    1.0494 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6934   -1.1666    0.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3424    0.8266   -1.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983    1.8595   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7055   -0.1078    2.3174 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8660    1.5281    2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6181    1.4155    2.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1255    0.9267    1.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7681    0.0059   -1.2202 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3872    0.9589   -1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  3
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 15 58  1  0
 16 59  1  0
 16 60  1  0
 18 61  1  0
 18 62  1  0
 18 63  1  0
 19 64  1  0
 20 65  1  0
 20 66  1  0
M  CHG  3  24  -1  28  -1  29  -1
M  END

HEADER    PROTEIN                                 14-MAY-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAY-15         0                                  
HETATM    1  C   UNK     0       3.905   5.335   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.239   6.105   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.573   5.335   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.906   6.105   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.574   6.105   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.907   5.335   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.241   6.105   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.575   5.335   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.908   6.105   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.242   5.335   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.576   6.105   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      19.909   5.335   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.243   6.105   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      22.577   5.335   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      23.910   6.105   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      23.910   7.645   0.000  0.00  0.00           O+0
HETATM   18  P   UNK     0      25.244   8.415   0.000  0.00  0.00           P+0
HETATM   19  O   UNK     0      26.014   7.081   0.000  0.00  0.00           O-1
HETATM   20  O   UNK     0      24.474   9.748   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      26.578   9.185   0.000  0.00  0.00           O+0
HETATM   22  P   UNK     0      26.578  10.725   0.000  0.00  0.00           P+0
HETATM   23  O   UNK     0      26.578  12.265   0.000  0.00  0.00           O-1
HETATM   24  O   UNK     0      28.118  10.725   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      25.038  10.725   0.000  0.00  0.00           O-1
HETATM   26  C   UNK     0      21.243   7.645   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.908   7.645   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.574   7.645   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.239   7.645   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22                                                            
CONECT   26   14                                                            
CONECT   27   10                                                            
CONECT   28    6                                                            
CONECT   29    2                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   56    0
END

COMPND    HMDB0304497
HETATM    1  C1  UNL     1      -7.854  -0.730  -0.916  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.213  -0.590   0.412  1.00  0.00           C  
HETATM    3  C3  UNL     1      -8.009   0.223   1.435  1.00  0.00           C  
HETATM    4  C4  UNL     1      -6.067  -1.054   0.791  1.00  0.00           C  
HETATM    5  C5  UNL     1      -5.077  -1.848   0.010  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.701  -1.162   0.121  1.00  0.00           C  
HETATM    7  C7  UNL     1      -3.730   0.167  -0.472  1.00  0.00           C  
HETATM    8  C8  UNL     1      -4.675   1.216   0.039  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.409   0.799  -0.836  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.398   0.924   0.228  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.811  -0.403   0.668  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.177  -1.096  -0.537  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.365  -2.410   0.011  1.00  0.00           C  
HETATM   14  C14 UNL     1       1.022  -0.269  -0.972  1.00  0.00           C  
HETATM   15  C15 UNL     1       2.117  -0.192   0.042  1.00  0.00           C  
HETATM   16  C16 UNL     1       3.096   0.897  -0.443  1.00  0.00           C  
HETATM   17  C17 UNL     1       4.195   0.934   0.522  1.00  0.00           C  
HETATM   18  C18 UNL     1       3.767   0.969   1.989  1.00  0.00           C  
HETATM   19  C19 UNL     1       5.432   0.913   0.236  1.00  0.00           C  
HETATM   20  C20 UNL     1       6.151   0.850  -1.041  1.00  0.00           C  
HETATM   21  O1  UNL     1       6.881   2.058  -1.069  1.00  0.00           O  
HETATM   22  P1  UNL     1       8.527   1.929  -0.908  1.00  0.00           P  
HETATM   23  O2  UNL     1       9.259   1.416  -2.070  1.00  0.00           O  
HETATM   24  O3  UNL     1       9.161   3.512  -0.514  1.00  0.00           O1-
HETATM   25  O4  UNL     1       8.833   0.954   0.481  1.00  0.00           O  
HETATM   26  P2  UNL     1       9.414  -0.529   0.067  1.00  0.00           P  
HETATM   27  O5  UNL     1       9.375  -0.840  -1.374  1.00  0.00           O  
HETATM   28  O6  UNL     1       8.565  -1.793   0.882  1.00  0.00           O1-
HETATM   29  O7  UNL     1      11.039  -0.594   0.659  1.00  0.00           O1-
HETATM   30  H1  UNL     1      -7.235  -1.207  -1.661  1.00  0.00           H  
HETATM   31  H2  UNL     1      -8.151   0.272  -1.337  1.00  0.00           H  
HETATM   32  H3  UNL     1      -8.802  -1.294  -0.781  1.00  0.00           H  
HETATM   33  H4  UNL     1      -7.299   0.616   2.186  1.00  0.00           H  
HETATM   34  H5  UNL     1      -8.442   1.093   0.875  1.00  0.00           H  
HETATM   35  H6  UNL     1      -8.768  -0.420   1.888  1.00  0.00           H  
HETATM   36  H7  UNL     1      -5.748  -0.850   1.836  1.00  0.00           H  
HETATM   37  H8  UNL     1      -4.993  -2.848   0.531  1.00  0.00           H  
HETATM   38  H9  UNL     1      -5.339  -2.023  -1.031  1.00  0.00           H  
HETATM   39  H10 UNL     1      -3.578  -1.146   1.255  1.00  0.00           H  
HETATM   40  H11 UNL     1      -2.986  -1.824  -0.387  1.00  0.00           H  
HETATM   41  H12 UNL     1      -4.169  -0.040  -1.560  1.00  0.00           H  
HETATM   42  H13 UNL     1      -4.124   2.220  -0.114  1.00  0.00           H  
HETATM   43  H14 UNL     1      -5.556   1.374  -0.646  1.00  0.00           H  
HETATM   44  H15 UNL     1      -4.903   1.223   1.104  1.00  0.00           H  
HETATM   45  H16 UNL     1      -2.642   1.860  -1.171  1.00  0.00           H  
HETATM   46  H17 UNL     1      -1.932   0.353  -1.722  1.00  0.00           H  
HETATM   47  H18 UNL     1      -1.841   1.380   1.178  1.00  0.00           H  
HETATM   48  H19 UNL     1      -0.589   1.590  -0.061  1.00  0.00           H  
HETATM   49  H20 UNL     1       0.027  -0.184   1.374  1.00  0.00           H  
HETATM   50  H21 UNL     1      -1.452  -1.086   1.209  1.00  0.00           H  
HETATM   51  H22 UNL     1      -0.869  -1.330  -1.343  1.00  0.00           H  
HETATM   52  H23 UNL     1       1.104  -2.870  -0.646  1.00  0.00           H  
HETATM   53  H24 UNL     1       0.705  -2.312   1.085  1.00  0.00           H  
HETATM   54  H25 UNL     1      -0.534  -3.104   0.081  1.00  0.00           H  
HETATM   55  H26 UNL     1       0.676   0.734  -1.279  1.00  0.00           H  
HETATM   56  H27 UNL     1       1.512  -0.787  -1.873  1.00  0.00           H  
HETATM   57  H28 UNL     1       1.845   0.115   1.049  1.00  0.00           H  
HETATM   58  H29 UNL     1       2.693  -1.167   0.137  1.00  0.00           H  
HETATM   59  H30 UNL     1       3.342   0.827  -1.492  1.00  0.00           H  
HETATM   60  H31 UNL     1       2.498   1.859  -0.339  1.00  0.00           H  
HETATM   61  H32 UNL     1       3.705  -0.108   2.317  1.00  0.00           H  
HETATM   62  H33 UNL     1       2.866   1.528   2.117  1.00  0.00           H  
HETATM   63  H34 UNL     1       4.618   1.415   2.582  1.00  0.00           H  
HETATM   64  H35 UNL     1       6.126   0.927   1.169  1.00  0.00           H  
HETATM   65  H36 UNL     1       6.768   0.006  -1.220  1.00  0.00           H  
HETATM   66  H37 UNL     1       5.387   0.959  -1.880  1.00  0.00           H  
CONECT    1    2   30   31   32
CONECT    2    3    4    4
CONECT    3   33   34   35
CONECT    4    5   36
CONECT    5    6   37   38
CONECT    6    7   39   40
CONECT    7    8    9   41
CONECT    8   42   43   44
CONECT    9   10   45   46
CONECT   10   11   47   48
CONECT   11   12   49   50
CONECT   12   13   14   51
CONECT   13   52   53   54
CONECT   14   15   55   56
CONECT   15   16   57   58
CONECT   16   17   59   60
CONECT   17   18   19   19
CONECT   18   61   62   63
CONECT   19   20   64
CONECT   20   21   65   66
CONECT   21   22
CONECT   22   23   23   24   25
CONECT   25   26
CONECT   26   27   27   28   29
END

HMDB0304497
     RDKit          3D
tetrahydrogeranylgeranyl-PP
 66 65  0  0  0  0  0  0  0  0999 V2000
   -7.8542   -0.7302   -0.9162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2133   -0.5902    0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0085    0.2227    1.4349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0669   -1.0538    0.7907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0767   -1.8481    0.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7005   -1.1623    0.1214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7299    0.1666   -0.4719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6748    1.2161    0.0386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4085    0.7992   -0.8361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3980    0.9242    0.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8109   -0.4030    0.6676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1768   -1.0959   -0.5368 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3655   -2.4104    0.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0216   -0.2690   -0.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1169   -0.1919    0.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0959    0.8975   -0.4429 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1952    0.9343    0.5217 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7669    0.9690    1.9892 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4317    0.9129    0.2362 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1507    0.8496   -1.0408 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8814    2.0578   -1.0694 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5266    1.9290   -0.9076 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.2590    1.4164   -2.0702 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1613    3.5118   -0.5139 O   0  0  0  0  0  1  0  0  0  0  0  0
    8.8332    0.9536    0.4806 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4139   -0.5294    0.0666 P   0  0  0  0  0  5  0  0  0  0  0  0
    9.3751   -0.8395   -1.3738 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5655   -1.7935    0.8822 O   0  0  0  0  0  1  0  0  0  0  0  0
   11.0389   -0.5940    0.6593 O   0  0  0  0  0  1  0  0  0  0  0  0
   -7.2354   -1.2069   -1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1509    0.2716   -1.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8024   -1.2944   -0.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2986    0.6165    2.1861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4424    1.0928    0.8750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7681   -0.4202    1.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7483   -0.8496    1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9931   -2.8476    0.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3386   -2.0234   -1.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5783   -1.1460    1.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9858   -1.8243   -0.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1686   -0.0400   -1.5595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1239    2.2196   -0.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5560    1.3743   -0.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9032    1.2230    1.1036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6419    1.8599   -1.1708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9318    0.3530   -1.7220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8411    1.3798    1.1784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5893    1.5901   -0.0606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0265   -0.1843    1.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4518   -1.0863    1.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8694   -1.3297   -1.3427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1040   -2.8698   -0.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7046   -2.3125    1.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5343   -3.1036    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6764    0.7344   -1.2786 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5120   -0.7872   -1.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8452    0.1149    1.0494 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6934   -1.1666    0.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3424    0.8266   -1.4925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4983    1.8595   -0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7055   -0.1078    2.3174 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8660    1.5281    2.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6181    1.4155    2.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1255    0.9267    1.1689 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7681    0.0059   -1.2202 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3872    0.9589   -1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  3
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 26 29  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 15 58  1  0
 16 59  1  0
 16 60  1  0
 18 61  1  0
 18 62  1  0
 18 63  1  0
 19 64  1  0
 20 65  1  0
 20 66  1  0
M  CHG  3  24  -1  28  -1  29  -1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3,7,11,15-Tetramethylhexadeca-2,14-dien-1-yl (phosphonatooxy)phosphonic acid	Generator

Chemical Formula

C₂₀H₃₇O₇P₂

Average Molecular Weight

451.458

Monoisotopic Molecular Weight

451.203098267

IUPAC Name

[(3,7,11,15-tetramethylhexadeca-2,14-dien-1-yl phosphonato)oxy]phosphonate

Traditional Name

(3,7,11,15-tetramethylhexadeca-2,14-dien-1-yl phosphonato)oxyphosphonate

CAS Registry Number

Not Available

SMILES

CC(CCCC(C)CCC=C(C)C)CCCC(C)=CCOP([O-])(=O)OP([O-])([O-])=O

InChI Identifier

InChI=1S/C20H40O7P2/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-26-29(24,25)27-28(21,22)23/h9,15,18-19H,6-8,10-14,16H2,1-5H3,(H,24,25)(H2,21,22,23)/p-3

InChI Key

VZBGWADXUJSBTI-UHFFFAOYSA-K

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Acyclic diterpenoids

Alternative Parents

Substituents

Acyclic diterpenoid
Organic pyrophosphate
Isoprenoid phosphate
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic anion
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

a small molecule (CPD-7003 )

Ontology

Not Available

Herbs and Spices (FooDB: FOOD00866)

Nut

Almond (FooDB: FOOD00148)
Brazil nut (FooDB: FOOD00024)
Cashew nut (FooDB: FOOD00011)
Chestnut (FooDB: FOOD00045)
Hazelnut (FooDB: FOOD00376)
Peanut (FooDB: FOOD00016)
Pecan nut (FooDB: FOOD00044)
Pine nut (FooDB: FOOD00138)
Pistachio (FooDB: FOOD00140)
Walnut (FooDB: FOOD00608)
Acorn (FooDB: FOOD00282)
Beech nut (FooDB: FOOD00299)
Butternut (FooDB: FOOD00316)
Chinese chestnut (FooDB: FOOD00331)
European chestnut (FooDB: FOOD00363)
Hickory nut (FooDB: FOOD00377)
Macadamia nut (FooDB: FOOD00525)
Mixed nuts (FooDB: FOOD00771)
Pili nut (FooDB: FOOD00432)
Colorado pinyon (FooDB: FOOD00433)
Black walnut (FooDB: FOOD00093)
Common walnut (FooDB: FOOD00094)
Japanese chestnut (FooDB: FOOD00385)
Common hazelnut (FooDB: FOOD00062)
Macadamia nut (M. tetraphylla) (FooDB: FOOD00225)
Japanese walnut (FooDB: FOOD00240)
Nuts (FooDB: FOOD00869)

Fruit

Pome

Drupe

Apricot (FooDB: FOOD00144)
Prunus (Cherry, Plum) (FooDB: FOOD00143)
Nectarine (FooDB: FOOD00229)
Peach (FooDB: FOOD00149)
European plum (FooDB: FOOD00147)
Sour cherry (FooDB: FOOD00146)
Sweet cherry (FooDB: FOOD00145)
Common chokecherry (FooDB: FOOD00562)
Peach (var.) (FooDB: FOOD00230)

Tropical fruit

Berry

Bilberry (FooDB: FOOD00193)
Rubus (Blackberry, Raspberry) (FooDB: FOOD00160)
Vaccinium (Blueberry, Cranberry, Huckleberry) (FooDB: FOOD00188)
Blackcurrant (FooDB: FOOD00155)
Redcurrant (FooDB: FOOD00156)
Elderberry (FooDB: FOOD00358)
Gooseberry (FooDB: FOOD00157)
Grape (FooDB: FOOD00369)
Lingonberry (FooDB: FOOD00194)
Loganberry (FooDB: FOOD00400)
Strawberry (FooDB: FOOD00083)
Boysenberry (FooDB: FOOD00542)
American cranberry (FooDB: FOOD00192)
Common grape (FooDB: FOOD00204)
Strawberry guava (FooDB: FOOD00482)
Black mulberry (FooDB: FOOD00117)
Red raspberry (FooDB: FOOD00162)
Muscadine grape (FooDB: FOOD00203)
Salmonberry (FooDB: FOOD00456)
Alaska blueberry (FooDB: FOOD00380)
Sea-buckthornberry (FooDB: FOOD00087)
Black elderberry (FooDB: FOOD00166)
Black crowberry (FooDB: FOOD00075)
Black huckleberry (FooDB: FOOD00084)
Mulberry (FooDB: FOOD00116)
Black chokeberry (FooDB: FOOD00136)
Cloudberry (FooDB: FOOD00161)
Black raspberry (FooDB: FOOD00163)
Rowanberry (FooDB: FOOD00176)
Lowbush blueberry (FooDB: FOOD00189)
Sparkleberry (FooDB: FOOD00190)
Highbush blueberry (FooDB: FOOD00191)
Arctic blackberry (FooDB: FOOD00207)
Bayberry (FooDB: FOOD00209)
Elliott's blueberry (FooDB: FOOD00210)
Canada blueberry (FooDB: FOOD00211)
Bog bilberry (FooDB: FOOD00212)
Buffalo currant (FooDB: FOOD00213)
European cranberry (FooDB: FOOD00217)
Deerberry (FooDB: FOOD00218)
Cascade huckleberry (FooDB: FOOD00220)
Oval-leaf huckleberry (FooDB: FOOD00221)
Evergreen huckleberry (FooDB: FOOD00222)
Red huckleberry (FooDB: FOOD00223)
Summer grape (FooDB: FOOD00227)
Fox grape (FooDB: FOOD00228)
Half-highbush blueberry (FooDB: FOOD00248)
Jostaberry (FooDB: FOOD00257)
Sweet rowanberry (FooDB: FOOD00265)
Skunk currant (FooDB: FOOD00267)
Squashberry (FooDB: FOOD00344)
Ohelo berry (FooDB: FOOD00419)
Chinese bayberry (FooDB: FOOD00852)
Saskatoon berry (FooDB: FOOD00884)
Nanking cherry (FooDB: FOOD00885)

Other fruit

Date (FooDB: FOOD00135)
Fig (FooDB: FOOD00081)
Jujube (FooDB: FOOD00388)

Citrus

Grapefruit (FooDB: FOOD00256)
Lemon (FooDB: FOOD00054)
Lime (FooDB: FOOD00053)
Sweet orange (FooDB: FOOD00057)
Mandarin orange (Clementine, Tangerine) (FooDB: FOOD00056)
Persian lime (FooDB: FOOD00543)
Pummelo (FooDB: FOOD00055)
Grapefruit/Pummelo hybrid (FooDB: FOOD00255)
Citrus (FooDB: FOOD00859)

Fruits (FooDB: FOOD00871)

Vegetable

Shoot vegetable

Fruit vegetable

Eggplant (FooDB: FOOD00174)
Avocado (FooDB: FOOD00130)
Groundcherry (FooDB: FOOD00371)
Olive (FooDB: FOOD00121)
Pepper (FooDB: FOOD00040)
Garden tomato (FooDB: FOOD00171)
Mexican groundcherry (FooDB: FOOD00491)
Green bell pepper (FooDB: FOOD00877)
Yellow bell pepper (FooDB: FOOD00878)
Red bell pepper (FooDB: FOOD00880)
Italian sweet red pepper (FooDB: FOOD00881)
Garden tomato (var.) (FooDB: FOOD00173)
Cherry tomato (FooDB: FOOD00172)
Pepper (C. baccatum) (FooDB: FOOD00231)
Pepper (C. chinense) (FooDB: FOOD00232)
Pepper (Capsicum) (FooDB: FOOD00233)
Pepper (C. frutescens) (FooDB: FOOD00428)
Pepper (C. pubescens) (FooDB: FOOD00849)
Orange bell pepper (FooDB: FOOD00879)

Root vegetable

Cabbage

Leaf vegetable

Lettuce (FooDB: FOOD00095)
Swiss chard (FooDB: FOOD00237)
Garden cress (FooDB: FOOD00099)
Endive (FooDB: FOOD00048)
Spinach (FooDB: FOOD00178)
Common beet (FooDB: FOOD00025)
Garland chrysanthemum (FooDB: FOOD00333)
Jute (FooDB: FOOD00389)
Lambsquarters (FooDB: FOOD00394)
New Zealand spinach (FooDB: FOOD00415)
Swamp cabbage (FooDB: FOOD00091)
Rocket salad (ssp.) (FooDB: FOOD00077)
Yautia (FooDB: FOOD00510)
Romaine lettuce (FooDB: FOOD00888)
Rocket salad (FooDB: FOOD00244)
Chicory leaves (FooDB: FOOD00250)
Corn salad (FooDB: FOOD00340)
Malabar spinach (FooDB: FOOD00404)
Ostrich fern (FooDB: FOOD00556)
Green vegetables (FooDB: FOOD00872)

Mushroom

Tuber

Onion-family vegetable

Leek (FooDB: FOOD00007)
Allium (FooDB: FOOD00005)
Wild leek (FooDB: FOOD00396)
Shallot (FooDB: FOOD00243)
Garden onion (FooDB: FOOD00006)
Garden onion (var.) (FooDB: FOOD00226)
Onion-family vegetables (FooDB: FOOD00855)
Green onion (FooDB: FOOD00963)
Red onion (FooDB: FOOD00962)

Other vegetable

Okra (FooDB: FOOD00420)
Horseradish tree (FooDB: FOOD00379)
Sacred lotus (FooDB: FOOD00402)
Tree fern (FooDB: FOOD00797)
Chinese water chestnut (FooDB: FOOD00332)
Nopal (FooDB: FOOD00416)
Carob (FooDB: FOOD00321)
Agave (FooDB: FOOD00563)
Narrowleaf cattail (FooDB: FOOD00564)
Giant butterbur (FooDB: FOOD00314)
Sesbania flower (FooDB: FOOD00469)

Stalk vegetable

Brassica

Brassicas (FooDB: FOOD00857)

Cereal and cereal product

Other bread

Other bread (FooDB: FOOD00269)

Cereal

Cereal product

Dough

Sourdough (FooDB: FOOD00275)

Cereals and cereal products (FooDB: FOOD00858)

Pulse

Bean

Lentil

Lentils (FooDB: FOOD00098)

Pea

Other pulse

White lupine (FooDB: FOOD00403)
Lupine (FooDB: FOOD00104)

Pulses (FooDB: FOOD00867)

Soy

Soy bean (FooDB: FOOD00085)

Soy product

Other soy product (FooDB: FOOD00271)

Abalone (FooDB: FOOD00279)
Conch (FooDB: FOOD00611)

Gourd

Chayote (FooDB: FOOD00325)
Cucumber (FooDB: FOOD00065)
Muskmelon (FooDB: FOOD00064)
Cucurbita (FooDB: FOOD00066)
Watermelon (FooDB: FOOD00052)
Bitter gourd (FooDB: FOOD00115)
Calabash (FooDB: FOOD00318)
Towel gourd (FooDB: FOOD00492)
Winter squash (FooDB: FOOD00283)
Butternut squash (FooDB: FOOD00317)
Wax gourd (FooDB: FOOD00499)
Green zucchini (FooDB: FOOD00875)
Yellow zucchini (FooDB: FOOD00876)
Japanese pumpkin (FooDB: FOOD00886)
Sunburst squash (pattypan squash) (FooDB: FOOD00874)
Tinda (FooDB: FOOD00559)
Horned melon (FooDB: FOOD00761)

Tea

Herbal tea

Greenthread tea (FooDB: FOOD00820)

Cocoa and cocoa product

Cocoa

Cocoa bean (FooDB: FOOD00182)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	5.22	ALOGPS
logP	6.09	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	1.77	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	121.78 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	115.47 m³·mol⁻¹	ChemAxon
Polarizability	47.71 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	215.388	32859911
AllCCS	[M+H-H2O]+	213.309	32859911
AllCCS	[M+Na]+	217.843	32859911
AllCCS	[M+NH4]+	217.297	32859911
AllCCS	[M-H]-	204.245	32859911
AllCCS	[M+Na-2H]-	206.786	32859911
AllCCS	[M+HCOO]-	209.728	32859911
DeepCCS	[M+H]+	198.005	30932474
DeepCCS	[M-H]-	194.745	30932474
DeepCCS	[M-2H]-	229.224	30932474
DeepCCS	[M+Na]+	205.648	30932474

Predicted Kovats Retention Indices

Not Available

Spectra

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB031194

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for tetrahydrogeranylgeranyl-PP (HMDB0304497)

MOL for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

3D MOL for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

3D SDF for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

3D-SDF for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

PDB for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

3D PDB for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

SMILES for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

INCHI for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

Structure for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

3D Structure for HMDB0304497 (tetrahydrogeranylgeranyl-PP)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices