MiMeDB: Showing metabocard for 1-Diphosinositol pentakisphosphate (MMDBc0047836)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 15:45:08 UTC

Update Date

2022-09-01 01:59:36 UTC

Metabolite ID

MMDBc0047836

Metabolite Identification

Common Name

1-Diphosinositol pentakisphosphate

Description

1-Diphosinositol pentakisphosphate, also known as 3-PP-ip5 or 1-(trihydrogen diphosphate), belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety. 1-Diphosinositol pentakisphosphate is an extremely strong acidic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02251208052D          

 40 40  0  0  1  0            999 V2000
   12.6206  -12.4415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3351  -12.0290    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   14.0496  -11.6165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7476  -12.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9226  -11.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0976  -11.3145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.6851  -12.0290    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.0976  -12.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6851  -13.4580    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   10.9706  -13.0455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3996  -13.8705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2726  -14.1724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8601  -12.0290    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4476  -12.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6226  -12.7434    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    9.6226  -11.9184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6226  -13.5685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7976  -12.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4476  -11.3145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6226  -11.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2101  -10.6000    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    9.9245  -10.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4956  -11.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7976   -9.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2101   -9.1711    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    9.9245   -9.5836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4956   -8.7586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6226   -8.4566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8601  -10.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4476   -9.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8601   -9.1711    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   11.5745   -9.5836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1456   -8.7586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2726   -8.4566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6851  -10.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.0976   -9.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9226   -9.8856    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   12.9226  -10.7106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9226   -9.0606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7476   -9.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  2  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  6 35  1  0  0  0  0
  7  8  1  1  0  0  0
  7 13  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  2  0  0  0  0
 13 14  1  6  0  0  0
 13 19  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  2  0  0  0  0
 19 20  1  1  0  0  0
 19 29  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  2  0  0  0  0
 29 30  1  1  0  0  0
 29 35  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
 31 34  2  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  2  0  0  0  0
M  END


  Mrv0541 02251208052D          

 40 40  0  0  1  0            999 V2000
   12.6206  -12.4415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3351  -12.0290    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   14.0496  -11.6165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7476  -12.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9226  -11.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0976  -11.3145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.6851  -12.0290    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.0976  -12.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6851  -13.4580    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   10.9706  -13.0455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3996  -13.8705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2726  -14.1724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8601  -12.0290    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4476  -12.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6226  -12.7434    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    9.6226  -11.9184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6226  -13.5685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7976  -12.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4476  -11.3145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6226  -11.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2101  -10.6000    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    9.9245  -10.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4956  -11.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7976   -9.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2101   -9.1711    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    9.9245   -9.5836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4956   -8.7586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6226   -8.4566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8601  -10.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4476   -9.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8601   -9.1711    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   11.5745   -9.5836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1456   -8.7586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2726   -8.4566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6851  -10.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.0976   -9.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9226   -9.8856    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   12.9226  -10.7106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9226   -9.0606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7476   -9.8856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  2  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  6 35  1  0  0  0  0
  7  8  1  1  0  0  0
  7 13  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  2  0  0  0  0
 13 14  1  6  0  0  0
 13 19  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  2  0  0  0  0
 19 20  1  1  0  0  0
 19 29  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  2  0  0  0  0
 29 30  1  1  0  0  0
 29 35  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
 31 34  2  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  2  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0047836

> <DATABASE_NAME>
MIME

> <SMILES>
OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(=O)OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C6H19O27P7/c7-34(8,9)27-1-2(28-35(10,11)12)4(30-37(16,17)18)6(32-40(25,26)33-39(22,23)24)5(31-38(19,20)21)3(1)29-36(13,14)15/h1-6H,(H,25,26)(H2,7,8,9)(H2,10,11,12)(H2,13,14,15)(H2,16,17,18)(H2,19,20,21)(H2,22,23,24)/t1-,2-,3+,4-,5-,6-/m0/s1

> <INCHI_KEY>
UPHPWXPNZIOZJL-PTQMNWPWSA-N

> <FORMULA>
C6H19O27P7

> <MOLECULAR_WEIGHT>
740.0152

> <EXACT_MASS>
739.827700986

> <JCHEM_ACCEPTOR_COUNT>
20

> <JCHEM_AVERAGE_POLARIZABILITY>
47.47997283057903

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(1S,2S,3R,4S,5R,6R)-3-{[hydroxy(phosphonooxy)phosphoryl]oxy}-2,4,5,6-tetrakis(phosphonooxy)cyclohexyl]oxy}phosphonic acid

> <ALOGPS_LOGP>
0.35

> <JCHEM_LOGP>
-4.945204319

> <ALOGPS_LOGS>
-1.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-12

> <JCHEM_PKA>
0.5803373082352428

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.1432035931677449

> <JCHEM_POLAR_SURFACE_AREA>
447.0900000000001

> <JCHEM_REFRACTIVITY>
111.88529999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.40e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2S,3R,4S,5R,6R)-3-{[hydroxy(phosphonooxy)phosphoryl]oxy}-2,4,5,6-tetrakis(phosphonooxy)cyclohexyl]oxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-FEB-12         0                                  
HETATM    1  O   UNK     0      23.558 -23.224   0.000  0.00  0.00           O+0
HETATM    2  P   UNK     0      24.892 -22.454   0.000  0.00  0.00           P+0
HETATM    3  O   UNK     0      26.226 -21.684   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      25.662 -23.788   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      24.122 -21.120   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      22.582 -21.120   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.812 -22.454   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      22.582 -23.788   0.000  0.00  0.00           O+0
HETATM    9  P   UNK     0      21.812 -25.122   0.000  0.00  0.00           P+0
HETATM   10  O   UNK     0      20.478 -24.352   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      23.146 -25.892   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      21.042 -26.455   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      20.272 -22.454   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      19.502 -23.788   0.000  0.00  0.00           O+0
HETATM   15  P   UNK     0      17.962 -23.788   0.000  0.00  0.00           P+0
HETATM   16  O   UNK     0      17.962 -22.248   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      17.962 -25.328   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      16.422 -23.788   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      19.502 -21.120   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      17.962 -21.120   0.000  0.00  0.00           O+0
HETATM   21  P   UNK     0      17.192 -19.787   0.000  0.00  0.00           P+0
HETATM   22  O   UNK     0      18.526 -19.017   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      15.858 -20.557   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      16.422 -18.453   0.000  0.00  0.00           O+0
HETATM   25  P   UNK     0      17.192 -17.119   0.000  0.00  0.00           P+0
HETATM   26  O   UNK     0      18.526 -17.889   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      15.858 -16.349   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      17.962 -15.786   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      20.272 -19.787   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      19.502 -18.453   0.000  0.00  0.00           O+0
HETATM   31  P   UNK     0      20.272 -17.119   0.000  0.00  0.00           P+0
HETATM   32  O   UNK     0      21.606 -17.889   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      18.938 -16.349   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      21.042 -15.786   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      21.812 -19.787   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      22.582 -18.453   0.000  0.00  0.00           O+0
HETATM   37  P   UNK     0      24.122 -18.453   0.000  0.00  0.00           P+0
HETATM   38  O   UNK     0      24.122 -19.993   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      24.122 -16.913   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      25.662 -18.453   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7   35                                                  
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9                                                            
CONECT   13    7   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15                                                            
CONECT   19   13   20   29                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25                                                            
CONECT   29   19   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31                                                            
CONECT   35    6   29   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39   40                                             
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   37                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   80    0
END

Synonyms

Value	Source
(1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentakis(phosphonooxy)cyclohexyl trihydrogen diphosphate	ChEBI
3-PP-IP5	ChEBI
(1S,2S,3R,4S,5S,6S)-2,3,4,5,6-Pentakis(phosphonooxy)cyclohexyl trihydrogen diphosphoric acid	Generator
1-Diphosinositol pentakisphosphoric acid	Generator
1-(Trihydrogen diphosphate)	HMDB
D-Myo-inositol, 2,3,4,5,6-pentakis(dihydrogen phosphate)	HMDB
Diphospho-myo-inositol pentakisphosphate	HMDB

Molecular Formula

C₆H₁₉O₂₇P₇

Average Mass

740.0152

Monoisotopic Mass

739.827700986

IUPAC Name

{[(1S,2S,3R,4S,5R,6R)-3-{[hydroxy(phosphonooxy)phosphoryl]oxy}-2,4,5,6-tetrakis(phosphonooxy)cyclohexyl]oxy}phosphonic acid

Traditional Name

[(1S,2S,3R,4S,5R,6R)-3-{[hydroxy(phosphonooxy)phosphoryl]oxy}-2,4,5,6-tetrakis(phosphonooxy)cyclohexyl]oxyphosphonic acid

CAS Registry Number

Not Available

SMILES

OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(=O)OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O

InChI Identifier

InChI=1S/C6H19O27P7/c7-34(8,9)27-1-2(28-35(10,11)12)4(30-37(16,17)18)6(32-40(25,26)33-39(22,23)24)5(31-38(19,20)21)3(1)29-36(13,14)15/h1-6H,(H,25,26)(H2,7,8,9)(H2,10,11,12)(H2,13,14,15)(H2,16,17,18)(H2,19,20,21)(H2,22,23,24)/t1-,2-,3+,4-,5-,6-/m0/s1

InChI Key

UPHPWXPNZIOZJL-PTQMNWPWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as inositol phosphates. Inositol phosphates are compounds containing a phosphate group attached to an inositol (or cyclohexanehexol) moiety.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Inositol phosphates

Alternative Parents

Substituents

Inositol phosphate
Organic pyrophosphate
Monoalkyl phosphate
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Organic oxide
Hydrocarbon derivative
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

myo-inositol pentakisphosphate (CHEBI:62922 )

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
Water Solubility	14 g/L	ALOGPS
logP	0.35	ALOGPS
logP	-4.9	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	0.14	ChemAxon
Physiological Charge	-12	ChemAxon
Hydrogen Acceptor Count	20	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	447.09 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	111.89 m³·mol⁻¹	ChemAxon
Polarizability	47.48 Å³	ChemAxon
Number of Rings	1	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	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-056v-3500129000-92e02f48f80539fd2ebb	2017-11-06	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-01ox-2200039500-ca3324ec34611cb741e8	2016-09-14	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-01ox-1100019100-a4bf41f87596bb42e4aa	2016-09-14	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-03dl-3200592000-718743d53ee9b1a54936	2016-09-14	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-002r-4100001900-58fc5d06ef574febc5fc	2016-09-14	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-056r-9300013300-99dcc5e94c530a9c5edd	2016-09-14	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9000000000-7891e87bda74c3a75d76	2016-09-14	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

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; Human saliva	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

HMDB0012494

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB029100

KNApSAcK ID

Not Available

Chemspider ID

26332921

KEGG Compound ID

C11174

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

62922

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Wishart DS, Li C, Marcu A, Badran H, Pon A, Budinski Z, Patron J, Lipton D, Cao X, Oler E, Li K, Paccoud M, Hong C, Guo AC, Chan C, Wei W, Ramirez-Gaona M: PathBank: a comprehensive pathway database for model organisms. Nucleic Acids Res. 2020 Jan 8;48(D1):D470-D478. doi: 10.1093/nar/gkz861. [PubMed:31602464 ]

Showing metabocard for 1-Diphosinositol pentakisphosphate (MMDBc0047836)

MOL for #<Metabolite:0x00007fece0009568>

3D MOL for #<Metabolite:0x00007fece0009568>

3D SDF for #<Metabolite:0x00007fece0009568>

3D-SDF for #<Metabolite:0x00007fece0009568>

PDB for #<Metabolite:0x00007fece0009568>

3D PDB for #<Metabolite:0x00007fece0009568>

SMILES for #<Metabolite:0x00007fece0009568>

INCHI for #<Metabolite:0x00007fece0009568>

Structure for #<Metabolite:0x00007fece0009568>

3D Structure for #<Metabolite:0x00007fece0009568>