MiMeDB: Showing metabocard for Di-trans,poly-cis-undecaprenyl phosphate (MMDBc0030139)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-17 23:55:25 UTC

Update Date

2022-08-31 17:40:02 UTC

Metabolite ID

MMDBc0030139

Metabolite Identification

Common Name

Di-trans,poly-cis-undecaprenyl phosphate

Description

Di-trans,poly-cis-undecaprenyl phosphate is an undecaprenyl phosphate having two (E)- and eight (Z)-double bonds. It is invovled in Peptidoglycan biosynthesis. (KEGG). Escherichia coli and other Gram-negative bacteria utilize the methylerythritol phosphate pathway to synthesize isopentenyl diphosphate and dimethylallyl diphosphate which are the precursors of (2E,6E)-farnesyl diphosphate. The latter compound is a precursor of di-trans,poly-cis-undecaprenyl phosphate, which leads to the biosynthesis of cell wall polymers. Initially (2E,6E)-farnesyl diphosphate is formed by the joining of geranyl diphosphate and isopentenyl diphosphate in a reaction catalyzed by geranyl diphosphate synthase / farnesyl diphosphate synthase encoded by gene ispA. Subsequently multiple units of isopentenyl diphosphate are polymerized to form di-trans,octa-cis-undecaprenyl diphosphate in a series of sequential condensation reactions catalyzed by undecaprenyl diphosphate synthase encoded by gene ispU.

Structure

MOL SDF PDB SMILES InChI

Structure #1
  Mrv0541 02241207102D          

 60 59  0  0  0  0            999 V2000
  -25.1625  -15.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -25.1625  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -22.6875  -12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -20.2125  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.7375   -9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2625   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7875   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3125   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8375   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -23.5125  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -21.0375  -12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.5625  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.0875   -9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6125   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1375   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6625   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1875   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -23.9250  -14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -22.6875  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -21.4500  -12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -20.2125  -12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.9750  -11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.7375  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.5000  -10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2625   -9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0250   -8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7875   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5500   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3125   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0750   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8375   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6000   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -24.7500  -14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -22.2750  -12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -19.8000  -11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.3250  -10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.8500   -8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3750   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9000   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4250   -4.2868    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
   -2.4750   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 P   0  5  0  0  0  0  0  0  0  0  0  0
  1 45  1  0  0  0  0
  2 45  1  0  0  0  0
  3 46  1  0  0  0  0
  4 47  1  0  0  0  0
  5 48  1  0  0  0  0
  6 49  1  0  0  0  0
  7 50  1  0  0  0  0
  8 51  1  0  0  0  0
  9 52  1  0  0  0  0
 10 53  1  0  0  0  0
 11 54  1  0  0  0  0
 12 55  1  0  0  0  0
 13 23  1  0  0  0  0
 13 24  1  0  0  0  0
 25 14  1  4  0  0  0
 14 26  1  0  0  0  0
 27 15  1  4  0  0  0
 15 28  1  0  0  0  0
 29 16  1  4  0  0  0
 16 30  1  0  0  0  0
 31 17  1  4  0  0  0
 17 32  1  0  0  0  0
 33 18  1  4  0  0  0
 18 34  1  0  0  0  0
 35 19  1  4  0  0  0
 19 36  1  0  0  0  0
 37 20  1  4  0  0  0
 20 38  1  0  0  0  0
 39 21  1  4  0  0  0
 21 40  1  0  0  0  0
 41 22  1  4  0  0  0
 22 42  1  0  0  0  0
 23 45  2  0  0  0  0
 24 46  1  0  0  0  0
 25 46  2  0  0  0  0
 26 47  1  0  0  0  0
 27 47  2  0  0  0  0
 28 48  1  0  0  0  0
 29 48  2  0  0  0  0
 30 49  1  0  0  0  0
 31 49  2  0  0  0  0
 32 50  1  0  0  0  0
 33 50  2  0  0  0  0
 34 51  1  0  0  0  0
 35 51  2  0  0  0  0
 36 52  1  0  0  0  0
 37 52  2  0  0  0  0
 38 53  1  0  0  0  0
 39 53  2  0  0  0  0
 40 54  1  0  0  0  0
 41 54  2  0  0  0  0
 42 55  1  0  0  0  0
 43 44  1  4  0  0  0
 43 55  2  0  0  0  0
 44 59  1  0  0  0  0
 56 60  2  0  0  0  0
 57 60  2  0  0  0  0
 58 60  1  0  0  0  0
 59 60  1  0  0  0  0
M  CHG  1  60  -1
M  RAD  1  58   2
M  END

Structure #1
  Mrv0541 02241207102D          

 60 59  0  0  0  0            999 V2000
  -25.1625  -15.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -25.1625  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -22.6875  -12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -20.2125  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.7375   -9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2625   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7875   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3125   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8375   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -23.5125  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -21.0375  -12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.5625  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.0875   -9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6125   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1375   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6625   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1875   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -23.9250  -14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -22.6875  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -21.4500  -12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -20.2125  -12.1460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -18.9750  -11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.7375  -10.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.5000  -10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2625   -9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0250   -8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7875   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5500   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3125   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0750   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8375   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6000   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -24.7500  -14.2894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -22.2750  -12.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -19.8000  -11.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -17.3250  -10.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.8500   -8.5737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3750   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9000   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4250   -4.2868    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
   -2.4750   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 P   0  5  0  0  0  0  0  0  0  0  0  0
  1 45  1  0  0  0  0
  2 45  1  0  0  0  0
  3 46  1  0  0  0  0
  4 47  1  0  0  0  0
  5 48  1  0  0  0  0
  6 49  1  0  0  0  0
  7 50  1  0  0  0  0
  8 51  1  0  0  0  0
  9 52  1  0  0  0  0
 10 53  1  0  0  0  0
 11 54  1  0  0  0  0
 12 55  1  0  0  0  0
 13 23  1  0  0  0  0
 13 24  1  0  0  0  0
 25 14  1  4  0  0  0
 14 26  1  0  0  0  0
 27 15  1  4  0  0  0
 15 28  1  0  0  0  0
 29 16  1  4  0  0  0
 16 30  1  0  0  0  0
 31 17  1  4  0  0  0
 17 32  1  0  0  0  0
 33 18  1  4  0  0  0
 18 34  1  0  0  0  0
 35 19  1  4  0  0  0
 19 36  1  0  0  0  0
 37 20  1  4  0  0  0
 20 38  1  0  0  0  0
 39 21  1  4  0  0  0
 21 40  1  0  0  0  0
 41 22  1  4  0  0  0
 22 42  1  0  0  0  0
 23 45  2  0  0  0  0
 24 46  1  0  0  0  0
 25 46  2  0  0  0  0
 26 47  1  0  0  0  0
 27 47  2  0  0  0  0
 28 48  1  0  0  0  0
 29 48  2  0  0  0  0
 30 49  1  0  0  0  0
 31 49  2  0  0  0  0
 32 50  1  0  0  0  0
 33 50  2  0  0  0  0
 34 51  1  0  0  0  0
 35 51  2  0  0  0  0
 36 52  1  0  0  0  0
 37 52  2  0  0  0  0
 38 53  1  0  0  0  0
 39 53  2  0  0  0  0
 40 54  1  0  0  0  0
 41 54  2  0  0  0  0
 42 55  1  0  0  0  0
 43 44  1  4  0  0  0
 43 55  2  0  0  0  0
 44 59  1  0  0  0  0
 56 60  2  0  0  0  0
 57 60  2  0  0  0  0
 58 60  1  0  0  0  0
 59 60  1  0  0  0  0
M  CHG  1  60  -1
M  RAD  1  58   2
M  END
> <DATABASE_ID>
MMDBc0030139

> <DATABASE_NAME>
MIME

> <SMILES>
CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCO[P-]([O])(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C55H89O4P/c1-45(2)23-13-24-46(3)25-14-26-47(4)27-15-28-48(5)29-16-30-49(6)31-17-32-50(7)33-18-34-51(8)35-19-36-52(9)37-20-38-53(10)39-21-40-54(11)41-22-42-55(12)43-44-59-60(56,57)58/h23,25,27,29,31,33,35,37,39,41,43H,13-22,24,26,28,30,32,34,36,38,40,42,44H2,1-12H3/q-1

> <INCHI_KEY>
DCZTULDWWVSYKM-UHFFFAOYSA-N

> <FORMULA>
C55H89O4P

> <MOLECULAR_WEIGHT>
845.2665

> <EXACT_MASS>
844.649847848

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
108.06195875429212

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
-1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{dioxo[(3,7,11,15,19,23,27,31,35,39,43-undecamethyltetratetraconta-2,6,10,14,18,22,26,30,34,38,42-undecaen-1-yl)oxy]-λ⁵-phosphanuidyl}oxidanyl

> <ALOGPS_LOGP>
9.49

> <JCHEM_LOGP>
15.140699999999999

> <ALOGPS_LOGS>
-6.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_POLAR_SURFACE_AREA>
43.370000000000005

> <JCHEM_REFRACTIVITY>
274.035

> <JCHEM_ROTATABLE_BOND_COUNT>
33

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.36e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{dioxo[(3,7,11,15,19,23,27,31,35,39,43-undecamethyltetratetraconta-2,6,10,14,18,22,26,30,34,38,42-undecaen-1-yl)oxy]-λ⁵-phosphanuidyl}oxidanyl

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Structure #1                                      
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0     -46.970 -28.007   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -46.970 -25.340   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -42.350 -22.673   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -37.730 -20.005   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -33.110 -17.338   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -28.490 -14.671   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -23.870 -12.003   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -19.250  -9.336   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -14.630  -6.668   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -10.010  -4.001   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.390  -1.334   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -43.890 -25.340   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -39.270 -22.673   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -34.650 -20.005   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -30.030 -17.338   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -25.410 -14.671   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -20.790 -12.003   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -16.170  -9.336   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -11.550  -6.668   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.930  -4.001   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -44.660 -26.674   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -42.350 -25.340   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -40.040 -24.006   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -37.730 -22.673   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -35.420 -21.339   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -33.110 -20.005   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -30.800 -18.672   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -28.490 -17.338   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -26.180 -16.004   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -23.870 -14.671   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -21.560 -13.337   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -19.250 -12.003   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -16.940 -10.669   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -14.630  -9.336   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -12.320  -8.002   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -10.010  -6.668   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -7.700  -5.335   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -5.390  -4.001   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -3.080  -2.667   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -46.200 -26.674   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -41.580 -24.006   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -36.960 -21.339   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0     -32.340 -18.672   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0     -27.720 -16.004   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0     -23.100 -13.337   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0     -18.480 -10.669   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0     -13.860  -8.002   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -9.240  -5.335   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -4.620  -2.667   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0       5.390   4.001   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0       5.954   1.897   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0       3.286   3.437   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0       3.850   1.334   0.000  0.00  0.00           O+0
HETATM   60  P   UNK     0       4.620   2.667   0.000  0.00  0.00           P-1
CONECT    1   45                                                            
CONECT    2   45                                                            
CONECT    3   46                                                            
CONECT    4   47                                                            
CONECT    5   48                                                            
CONECT    6   49                                                            
CONECT    7   50                                                            
CONECT    8   51                                                            
CONECT    9   52                                                            
CONECT   10   53                                                            
CONECT   11   54                                                            
CONECT   12   55                                                            
CONECT   13   23   24                                                       
CONECT   14   25   26                                                       
CONECT   15   27   28                                                       
CONECT   16   29   30                                                       
CONECT   17   31   32                                                       
CONECT   18   33   34                                                       
CONECT   19   35   36                                                       
CONECT   20   37   38                                                       
CONECT   21   39   40                                                       
CONECT   22   41   42                                                       
CONECT   23   13   45                                                       
CONECT   24   13   46                                                       
CONECT   25   14   46                                                       
CONECT   26   14   47                                                       
CONECT   27   15   47                                                       
CONECT   28   15   48                                                       
CONECT   29   16   48                                                       
CONECT   30   16   49                                                       
CONECT   31   17   49                                                       
CONECT   32   17   50                                                       
CONECT   33   18   50                                                       
CONECT   34   18   51                                                       
CONECT   35   19   51                                                       
CONECT   36   19   52                                                       
CONECT   37   20   52                                                       
CONECT   38   20   53                                                       
CONECT   39   21   53                                                       
CONECT   40   21   54                                                       
CONECT   41   22   54                                                       
CONECT   42   22   55                                                       
CONECT   43   44   55                                                       
CONECT   44   43   59                                                       
CONECT   45    1    2   23                                                  
CONECT   46    3   24   25                                                  
CONECT   47    4   26   27                                                  
CONECT   48    5   28   29                                                  
CONECT   49    6   30   31                                                  
CONECT   50    7   32   33                                                  
CONECT   51    8   34   35                                                  
CONECT   52    9   36   37                                                  
CONECT   53   10   38   39                                                  
CONECT   54   11   40   41                                                  
CONECT   55   12   42   43                                                  
CONECT   56   60                                                            
CONECT   57   60                                                            
CONECT   58   60                                                            
CONECT   59   44   60                                                       
CONECT   60   56   57   58   59                                             
MASTER        0    0    0    0    0    0    0    0   60    0  118    0
END

Synonyms

Value	Source
Di-trans,poly-cis-undecaprenyl phosphoric acid	Generator

Molecular Formula

C₅₅H₈₉O₄P

Average Mass

845.2665

Monoisotopic Mass

844.649847848

IUPAC Name

{dioxo[(3,7,11,15,19,23,27,31,35,39,43-undecamethyltetratetraconta-2,6,10,14,18,22,26,30,34,38,42-undecaen-1-yl)oxy]-λ⁵-phosphanuidyl}oxidanyl

Traditional Name

{dioxo[(3,7,11,15,19,23,27,31,35,39,43-undecamethyltetratetraconta-2,6,10,14,18,22,26,30,34,38,42-undecaen-1-yl)oxy]-λ⁵-phosphanuidyl}oxidanyl

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCO[P-]([O])(=O)=O

InChI Identifier

InChI=1S/C55H89O4P/c1-45(2)23-13-24-46(3)25-14-26-47(4)27-15-28-48(5)29-16-30-49(6)31-17-32-50(7)33-18-34-51(8)35-19-36-52(9)37-20-38-53(10)39-21-40-54(11)41-22-42-55(12)43-44-59-60(56,57)58/h23,25,27,29,31,33,35,37,39,41,43H,13-22,24,26,28,30,32,34,36,38,40,42,44H2,1-12H3/q-1

InChI Key

DCZTULDWWVSYKM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as polyterpenoids. These are terpenoids consisting of more than eight isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Polyterpenoids

Direct Parent

Polyterpenoids

Alternative Parents

Substituents

Polyterpenoid
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic anion
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.00024 g/L	ALOGPS
logP	9.49	ALOGPS
logP	15.14	ChemAxon
logS	-6.6	ALOGPS
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	43.37 Å²	ChemAxon
Rotatable Bond Count	33	ChemAxon
Refractivity	274.04 m³·mol⁻¹	ChemAxon
Polarizability	108.06 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

Spectra

Spectrum Type	Description	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

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

Metabolic Reactions

Not Available

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
Bacteria	Proteobacteria	1	Human ; Human feces; Human feces; pleural fluid plaque; bal; Human stool	Unknown

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

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

References

Synthesis Reference

Not Available

General References

Keseler IM, Collado-Vides J, Santos-Zavaleta A, Peralta-Gil M, Gama-Castro S, Muniz-Rascado L, Bonavides-Martinez C, Paley S, Krummenacker M, Altman T, Kaipa P, Spaulding A, Pacheco J, Latendresse M, Fulcher C, Sarker M, Shearer AG, Mackie A, Paulsen I, Gunsalus RP, Karp PD: EcoCyc: a comprehensive database of Escherichia coli biology. Nucleic Acids Res. 2011 Jan;39(Database issue):D583-90. doi: 10.1093/nar/gkq1143. Epub 2010 Nov 21. [PubMed:21097882 ]
Kanehisa M, Goto S, Sato Y, Furumichi M, Tanabe M: KEGG for integration and interpretation of large-scale molecular data sets. Nucleic Acids Res. 2012 Jan;40(Database issue):D109-14. doi: 10.1093/nar/gkr988. Epub 2011 Nov 10. [PubMed:22080510 ]

Showing metabocard for Di-trans,poly-cis-undecaprenyl phosphate (MMDBc0030139)

MOL for #<Metabolite:0x00007fecd7980ff0>

3D MOL for #<Metabolite:0x00007fecd7980ff0>

3D SDF for #<Metabolite:0x00007fecd7980ff0>

3D-SDF for #<Metabolite:0x00007fecd7980ff0>

PDB for #<Metabolite:0x00007fecd7980ff0>

3D PDB for #<Metabolite:0x00007fecd7980ff0>

SMILES for #<Metabolite:0x00007fecd7980ff0>

INCHI for #<Metabolite:0x00007fecd7980ff0>

Structure for #<Metabolite:0x00007fecd7980ff0>

3D Structure for #<Metabolite:0x00007fecd7980ff0>