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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:04:58 UTC

Update Date

2022-03-07 02:54:44 UTC

HMDB ID

HMDB0036017

Secondary Accession Numbers

HMDB36017

Metabolite Identification

Common Name

Mangiferursanone

Description

Mangiferursanone belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review a small amount of articles have been published on Mangiferursanone.

Structure

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


  Mrv0541 02241215022D          

 31 35  0  0  0  0            999 V2000
   -2.5013   -1.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5013   -0.8382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7865   -2.0751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0719   -1.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0719   -0.8382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7865   -0.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3573   -0.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.2160   -2.0751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1 13  2  0  0  0  0
  2  6  1  0  0  0  0
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 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

HMDB0036017
     RDKit          3D
Mangiferursanone
 81 85  0  0  0  0  0  0  0  0999 V2000
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 31 81  1  0
M  END


  Mrv0541 02241215022D          

 31 35  0  0  0  0            999 V2000
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 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036017

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1CCC2(C)CCC3(C)C(CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C2C1C

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O/c1-19-11-14-27(5)17-18-29(7)21(25(27)20(19)2)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h19-23,25H,9-18H2,1-8H3

> <INCHI_KEY>
YEVQBJVJPQFPNE-UHFFFAOYSA-N

> <FORMULA>
C30H50O

> <MOLECULAR_WEIGHT>
426.7174

> <EXACT_MASS>
426.386166222

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
53.98927913924217

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,4,6a,6b,8a,11,12,14b-octamethyl-docosahydropicen-3-one

> <ALOGPS_LOGP>
6.25

> <JCHEM_LOGP>
8.359219997666667

> <ALOGPS_LOGS>
-7.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.96217044236992

> <JCHEM_PKA_STRONGEST_BASIC>
-7.47088496448267

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
130.30849999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.78e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,4,6a,6b,8a,11,12,14b-octamethyl-hexadecahydropicen-3-one

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036017
     RDKit          3D
Mangiferursanone
 81 85  0  0  0  0  0  0  0  0999 V2000
   -6.1252   -0.2339    2.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0978   -0.2998    0.9028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9463   -1.7358    0.5249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6873   -2.0588   -0.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0902   -0.7988   -0.8107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0620   -0.3578   -1.8946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7978   -1.1652   -1.5492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1616    0.1264   -1.9395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7033    1.0011   -0.7934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3829    2.3547   -1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4033    0.5710    0.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6767   -0.4156    1.3055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7457   -0.7036    0.8804 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3817    0.6514    0.6350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8119    0.4668    0.7868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9584   -0.2009    2.1700 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7407    1.6414    0.8259 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1979    1.2772    1.0624 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6143    0.4188   -0.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6119    0.7115   -0.6957 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7422   -0.7496   -0.3439 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1588   -1.8592    0.5863 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1170   -1.2210   -1.7573 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2961   -0.4351   -0.3257 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9517    0.2692   -1.6246 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4684    0.5074   -1.7708 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7806    1.1619   -0.6251 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040    2.6833   -0.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8550    0.2789    0.2302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7397    0.2383    1.3973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4323   -0.5548    2.5951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1420   -0.0498    1.5729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9598    0.6420    2.6912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2264   -1.1902    2.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4728    0.3625    0.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8753   -2.0319   -0.0282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9817   -2.3561    1.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0078   -2.6702   -1.1161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717   -2.6844    0.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1997    0.7523   -1.8724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6704   -0.5601   -2.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0254   -0.9060   -1.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2197   -1.9150   -1.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1276   -1.6333   -2.5295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0535    0.6020   -2.4968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4786    0.0880   -2.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8425    2.8293   -0.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2756    2.1814   -1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7597    2.9693   -1.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4355    1.5255    1.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5375   -0.0802    2.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1903   -1.3970    1.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7770   -1.3691    0.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1965   -1.2936    1.6970 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040    1.3147    1.4694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7801    0.2341    2.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0885    0.0699    2.8468 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655   -1.2639    2.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5174    2.3729    1.6313 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8722    2.1336   -0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7442    2.2748    0.9945 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4773    0.8980    2.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1005   -2.3157    0.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4950   -1.4719    1.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4412   -2.6815    0.6578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2387   -0.3845   -2.4521 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4912   -2.0453   -2.0996 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1546   -1.6527   -1.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -1.4225   -0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5835    1.1105   -1.8866 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2058   -0.4996   -2.4241 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3360    1.0106   -2.7462 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0721   -0.5551   -1.7820 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1114    3.1524   -0.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2415    3.1262   -1.5125 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7535    2.9919    0.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1915    1.2261   -0.3147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0047    1.2762    1.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2531   -1.6371    2.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3989   -0.5614    3.2023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7269   -0.0855    3.3117 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 11 29  1  0
 29 30  1  0
 30 31  1  0
 30  2  1  0
 29  5  1  0
 27  9  1  0
 27 14  1  0
 24 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  6 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
 10 47  1  0
 10 48  1  0
 10 49  1  0
 11 50  1  0
 12 51  1  0
 12 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  0
 16 56  1  0
 16 57  1  0
 16 58  1  0
 17 59  1  0
 17 60  1  0
 18 61  1  0
 18 62  1  0
 22 63  1  0
 22 64  1  0
 22 65  1  0
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 23 67  1  0
 23 68  1  0
 24 69  1  0
 25 70  1  0
 25 71  1  0
 26 72  1  0
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 28 74  1  0
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 29 77  1  0
 30 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.669  -3.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.669  -1.565   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.335  -3.874   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.001  -3.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.001  -1.565   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.335  -0.795   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.667  -0.795   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.667  -1.565   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.667  -3.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.667  -3.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.937  -5.362   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.105  -5.208   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -6.003  -3.874   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.667   0.744   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.001  -0.795   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.001   0.744   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.667   1.513   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.667  -0.026   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.001  -0.026   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.335   1.513   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.669   0.744   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.669  -0.795   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.335  -1.565   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.335   3.053   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.003   1.513   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.003   3.053   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.669   3.823   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.669   5.362   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.001   3.823   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.003  -0.026   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.001  -2.334   0.000  0.00  0.00           C+0
CONECT    1    2    3   13                                                  
CONECT    2    1    6                                                       
CONECT    3    1    4   11   12                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   19                                             
CONECT    6    2    5                                                       
CONECT    7    5    8   14                                                  
CONECT    8    7    9   15   18                                             
CONECT    9    8   10                                                       
CONECT   10    4    9                                                       
CONECT   11    3                                                            
CONECT   12    3                                                            
CONECT   13    1                                                            
CONECT   14    7   17                                                       
CONECT   15    8   16   23   31                                             
CONECT   16   15   17   20                                                  
CONECT   17   14   16                                                       
CONECT   18    8                                                            
CONECT   19    5                                                            
CONECT   20   16   21   24                                                  
CONECT   21   20   22   25   30                                             
CONECT   22   21   23                                                       
CONECT   23   15   22                                                       
CONECT   24   20   27   29                                                  
CONECT   25   21   26                                                       
CONECT   26   25   27                                                       
CONECT   27   24   26   28                                                  
CONECT   28   27                                                            
CONECT   29   24                                                            
CONECT   30   21                                                            
CONECT   31   15                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

COMPND    HMDB0036017
HETATM    1  C1  UNL     1      -6.125  -0.234   2.032  1.00  0.00           C  
HETATM    2  C2  UNL     1      -5.098  -0.300   0.903  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.946  -1.736   0.525  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.687  -2.059  -0.217  1.00  0.00           C  
HETATM    5  C5  UNL     1      -3.090  -0.799  -0.811  1.00  0.00           C  
HETATM    6  C6  UNL     1      -4.062  -0.358  -1.895  1.00  0.00           C  
HETATM    7  C7  UNL     1      -1.798  -1.165  -1.549  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.162   0.126  -1.939  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.703   1.001  -0.793  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.383   2.355  -1.141  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.403   0.571   0.491  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.677  -0.416   1.305  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.746  -0.704   0.880  1.00  0.00           C  
HETATM   14  C14 UNL     1       1.382   0.651   0.635  1.00  0.00           C  
HETATM   15  C15 UNL     1       2.812   0.467   0.787  1.00  0.00           C  
HETATM   16  C16 UNL     1       2.958  -0.201   2.170  1.00  0.00           C  
HETATM   17  C17 UNL     1       3.741   1.641   0.826  1.00  0.00           C  
HETATM   18  C18 UNL     1       5.198   1.277   1.062  1.00  0.00           C  
HETATM   19  C19 UNL     1       5.614   0.419  -0.073  1.00  0.00           C  
HETATM   20  O1  UNL     1       6.612   0.711  -0.696  1.00  0.00           O  
HETATM   21  C20 UNL     1       4.742  -0.750  -0.344  1.00  0.00           C  
HETATM   22  C21 UNL     1       5.159  -1.859   0.586  1.00  0.00           C  
HETATM   23  C22 UNL     1       5.117  -1.221  -1.757  1.00  0.00           C  
HETATM   24  C23 UNL     1       3.296  -0.435  -0.326  1.00  0.00           C  
HETATM   25  C24 UNL     1       2.952   0.269  -1.625  1.00  0.00           C  
HETATM   26  C25 UNL     1       1.468   0.507  -1.771  1.00  0.00           C  
HETATM   27  C26 UNL     1       0.781   1.162  -0.625  1.00  0.00           C  
HETATM   28  C27 UNL     1       1.004   2.683  -0.554  1.00  0.00           C  
HETATM   29  C28 UNL     1      -2.855   0.279   0.230  1.00  0.00           C  
HETATM   30  C29 UNL     1      -3.740   0.238   1.397  1.00  0.00           C  
HETATM   31  C30 UNL     1      -3.432  -0.555   2.595  1.00  0.00           C  
HETATM   32  H1  UNL     1      -7.142  -0.050   1.573  1.00  0.00           H  
HETATM   33  H2  UNL     1      -5.960   0.642   2.691  1.00  0.00           H  
HETATM   34  H3  UNL     1      -6.226  -1.190   2.564  1.00  0.00           H  
HETATM   35  H4  UNL     1      -5.473   0.362   0.119  1.00  0.00           H  
HETATM   36  H5  UNL     1      -5.875  -2.032  -0.028  1.00  0.00           H  
HETATM   37  H6  UNL     1      -4.982  -2.356   1.467  1.00  0.00           H  
HETATM   38  H7  UNL     1      -4.008  -2.670  -1.116  1.00  0.00           H  
HETATM   39  H8  UNL     1      -2.972  -2.684   0.310  1.00  0.00           H  
HETATM   40  H9  UNL     1      -4.200   0.752  -1.872  1.00  0.00           H  
HETATM   41  H10 UNL     1      -3.670  -0.560  -2.932  1.00  0.00           H  
HETATM   42  H11 UNL     1      -5.025  -0.906  -1.860  1.00  0.00           H  
HETATM   43  H12 UNL     1      -1.220  -1.915  -1.061  1.00  0.00           H  
HETATM   44  H13 UNL     1      -2.128  -1.633  -2.529  1.00  0.00           H  
HETATM   45  H14 UNL     1      -2.053   0.602  -2.497  1.00  0.00           H  
HETATM   46  H15 UNL     1      -0.479   0.088  -2.805  1.00  0.00           H  
HETATM   47  H16 UNL     1      -1.843   2.829  -0.282  1.00  0.00           H  
HETATM   48  H17 UNL     1      -2.276   2.181  -1.825  1.00  0.00           H  
HETATM   49  H18 UNL     1      -0.760   2.969  -1.806  1.00  0.00           H  
HETATM   50  H19 UNL     1      -1.436   1.525   1.111  1.00  0.00           H  
HETATM   51  H20 UNL     1      -0.537  -0.080   2.381  1.00  0.00           H  
HETATM   52  H21 UNL     1      -1.190  -1.397   1.271  1.00  0.00           H  
HETATM   53  H22 UNL     1       0.777  -1.369   0.023  1.00  0.00           H  
HETATM   54  H23 UNL     1       1.197  -1.294   1.697  1.00  0.00           H  
HETATM   55  H24 UNL     1       1.004   1.315   1.469  1.00  0.00           H  
HETATM   56  H25 UNL     1       3.780   0.234   2.775  1.00  0.00           H  
HETATM   57  H26 UNL     1       2.088   0.070   2.847  1.00  0.00           H  
HETATM   58  H27 UNL     1       3.166  -1.264   2.112  1.00  0.00           H  
HETATM   59  H28 UNL     1       3.517   2.373   1.631  1.00  0.00           H  
HETATM   60  H29 UNL     1       3.872   2.134  -0.187  1.00  0.00           H  
HETATM   61  H30 UNL     1       5.744   2.275   0.995  1.00  0.00           H  
HETATM   62  H31 UNL     1       5.477   0.898   2.021  1.00  0.00           H  
HETATM   63  H32 UNL     1       6.101  -2.316   0.158  1.00  0.00           H  
HETATM   64  H33 UNL     1       5.495  -1.472   1.589  1.00  0.00           H  
HETATM   65  H34 UNL     1       4.441  -2.682   0.658  1.00  0.00           H  
HETATM   66  H35 UNL     1       5.239  -0.385  -2.452  1.00  0.00           H  
HETATM   67  H36 UNL     1       4.491  -2.045  -2.100  1.00  0.00           H  
HETATM   68  H37 UNL     1       6.155  -1.653  -1.628  1.00  0.00           H  
HETATM   69  H38 UNL     1       2.761  -1.422  -0.346  1.00  0.00           H  
HETATM   70  H39 UNL     1       3.583   1.111  -1.887  1.00  0.00           H  
HETATM   71  H40 UNL     1       3.206  -0.500  -2.424  1.00  0.00           H  
HETATM   72  H41 UNL     1       1.336   1.011  -2.746  1.00  0.00           H  
HETATM   73  H42 UNL     1       1.072  -0.555  -1.782  1.00  0.00           H  
HETATM   74  H43 UNL     1       0.111   3.152  -0.027  1.00  0.00           H  
HETATM   75  H44 UNL     1       1.241   3.126  -1.512  1.00  0.00           H  
HETATM   76  H45 UNL     1       1.754   2.992   0.172  1.00  0.00           H  
HETATM   77  H46 UNL     1      -3.192   1.226  -0.315  1.00  0.00           H  
HETATM   78  H47 UNL     1      -4.005   1.276   1.771  1.00  0.00           H  
HETATM   79  H48 UNL     1      -3.253  -1.637   2.442  1.00  0.00           H  
HETATM   80  H49 UNL     1      -4.399  -0.561   3.202  1.00  0.00           H  
HETATM   81  H50 UNL     1      -2.727  -0.086   3.312  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3   30   35
CONECT    3    4   36   37
CONECT    4    5   38   39
CONECT    5    6    7   29
CONECT    6   40   41   42
CONECT    7    8   43   44
CONECT    8    9   45   46
CONECT    9   10   11   27
CONECT   10   47   48   49
CONECT   11   12   29   50
CONECT   12   13   51   52
CONECT   13   14   53   54
CONECT   14   15   27   55
CONECT   15   16   17   24
CONECT   16   56   57   58
CONECT   17   18   59   60
CONECT   18   19   61   62
CONECT   19   20   20   21
CONECT   21   22   23   24
CONECT   22   63   64   65
CONECT   23   66   67   68
CONECT   24   25   69
CONECT   25   26   70   71
CONECT   26   27   72   73
CONECT   27   28
CONECT   28   74   75   76
CONECT   29   30   77
CONECT   30   31   78
CONECT   31   79   80   81
END

HMDB0036017
     RDKit          3D
Mangiferursanone
 81 85  0  0  0  0  0  0  0  0999 V2000
   -6.1252   -0.2339    2.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0978   -0.2998    0.9028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9463   -1.7358    0.5249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6873   -2.0588   -0.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0902   -0.7988   -0.8107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0620   -0.3578   -1.8946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7978   -1.1652   -1.5492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1616    0.1264   -1.9395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7033    1.0011   -0.7934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3829    2.3547   -1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4033    0.5710    0.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6767   -0.4156    1.3055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7457   -0.7036    0.8804 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3817    0.6514    0.6350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8119    0.4668    0.7868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9584   -0.2009    2.1700 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7407    1.6414    0.8259 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1979    1.2772    1.0624 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6143    0.4188   -0.0732 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6119    0.7115   -0.6957 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7422   -0.7496   -0.3439 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1588   -1.8592    0.5863 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1170   -1.2210   -1.7573 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2961   -0.4351   -0.3257 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9517    0.2692   -1.6246 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4684    0.5074   -1.7708 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7806    1.1619   -0.6251 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040    2.6833   -0.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8550    0.2789    0.2302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7397    0.2383    1.3973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4323   -0.5548    2.5951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1420   -0.0498    1.5729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9598    0.6420    2.6912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2264   -1.1902    2.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4728    0.3625    0.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8753   -2.0319   -0.0282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9817   -2.3561    1.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0078   -2.6702   -1.1161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717   -2.6844    0.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1997    0.7523   -1.8724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6704   -0.5601   -2.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0254   -0.9060   -1.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2197   -1.9150   -1.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1276   -1.6333   -2.5295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0535    0.6020   -2.4968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4786    0.0880   -2.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8425    2.8293   -0.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2756    2.1814   -1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7597    2.9693   -1.8063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4355    1.5255    1.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5375   -0.0802    2.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1903   -1.3970    1.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7770   -1.3691    0.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1965   -1.2936    1.6970 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040    1.3147    1.4694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7801    0.2341    2.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0885    0.0699    2.8468 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655   -1.2639    2.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5174    2.3729    1.6313 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8722    2.1336   -0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7442    2.2748    0.9945 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4773    0.8980    2.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1005   -2.3157    0.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4950   -1.4719    1.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4412   -2.6815    0.6578 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2387   -0.3845   -2.4521 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4912   -2.0453   -2.0996 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1546   -1.6527   -1.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -1.4225   -0.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5835    1.1105   -1.8866 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2058   -0.4996   -2.4241 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3360    1.0106   -2.7462 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0721   -0.5551   -1.7820 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1114    3.1524   -0.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2415    3.1262   -1.5125 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7535    2.9919    0.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1915    1.2261   -0.3147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0047    1.2762    1.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2531   -1.6371    2.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3989   -0.5614    3.2023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7269   -0.0855    3.3117 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 11 29  1  0
 29 30  1  0
 30 31  1  0
 30  2  1  0
 29  5  1  0
 27  9  1  0
 27 14  1  0
 24 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  6 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
 10 47  1  0
 10 48  1  0
 10 49  1  0
 11 50  1  0
 12 51  1  0
 12 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  0
 16 56  1  0
 16 57  1  0
 16 58  1  0
 17 59  1  0
 17 60  1  0
 18 61  1  0
 18 62  1  0
 22 63  1  0
 22 64  1  0
 22 65  1  0
 23 66  1  0
 23 67  1  0
 23 68  1  0
 24 69  1  0
 25 70  1  0
 25 71  1  0
 26 72  1  0
 26 73  1  0
 28 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 30 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₃₀H₅₀O

Average Molecular Weight

426.7174

Monoisotopic Molecular Weight

426.386166222

IUPAC Name

4,4,6a,6b,8a,11,12,14b-octamethyl-docosahydropicen-3-one

Traditional Name

4,4,6a,6b,8a,11,12,14b-octamethyl-hexadecahydropicen-3-one

CAS Registry Number

114717-95-2

SMILES

CC1CCC2(C)CCC3(C)C(CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C2C1C

InChI Identifier

InChI=1S/C30H50O/c1-19-11-14-27(5)17-18-29(7)21(25(27)20(19)2)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h19-23,25H,9-18H2,1-8H3

InChI Key

YEVQBJVJPQFPNE-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Cyclic ketone
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0036017)
Cell membrane (HMDB: HMDB0036017)

Cellular substructure

Extracellular (HMDB: HMDB0036017)
Membrane (HMDB: HMDB0036017)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036017)

Source

Endogenous

Endogenous (HMDB: HMDB0036017)

Plant

Plant (HMDB: HMDB0036017)

Animal

Animal (HMDB: HMDB0036017)

Exogenous

Food

Food (HMDB: HMDB0036017)

Fruit

Fruits (FooDB: FOOD00871)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0036017)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0036017)

Cellular process

Cell signaling (HMDB: HMDB0036017)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0036017)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0036017)

Nutrient

Nutrient (HMDB: HMDB0036017)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036017)

Emulsifier (HMDB: HMDB0036017)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	236 - 238 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	7.3e-05 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.8e-05 g/L	ALOGPS
logP	6.25	ALOGPS
logP	8.36	ChemAxon
logS	-7.4	ALOGPS
pKa (Strongest Acidic)	19.96	ChemAxon
pKa (Strongest Basic)	-7.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	130.31 m³·mol⁻¹	ChemAxon
Polarizability	53.99 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	202.871	31661259
DarkChem	[M-H]-	197.131	31661259
DeepCCS	[M-2H]-	242.803	30932474
DeepCCS	[M+Na]+	218.031	30932474
AllCCS	[M+H]+	213.2	32859911
AllCCS	[M+H-H2O]+	211.3	32859911
AllCCS	[M+NH4]+	214.8	32859911
AllCCS	[M+Na]+	215.3	32859911
AllCCS	[M-H]-	210.4	32859911
AllCCS	[M+Na-2H]-	212.2	32859911
AllCCS	[M+HCOO]-	214.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Mangiferursanone	CC1CCC2(C)CCC3(C)C(CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C2C1C	2928.2	Standard polar	33892256
Mangiferursanone	CC1CCC2(C)CCC3(C)C(CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C2C1C	3422.0	Standard non polar	33892256
Mangiferursanone	CC1CCC2(C)CCC3(C)C(CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C2C1C	3412.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Mangiferursanone,1TMS,isomer #1	CC1CCC2(C)CCC3(C)C(CCC4C5(C)CC=C(O[Si](C)(C)C)C(C)(C)C5CCC43C)C2C1C	3387.9	Semi standard non polar	33892256
Mangiferursanone,1TMS,isomer #1	CC1CCC2(C)CCC3(C)C(CCC4C5(C)CC=C(O[Si](C)(C)C)C(C)(C)C5CCC43C)C2C1C	3133.2	Standard non polar	33892256
Mangiferursanone,1TBDMS,isomer #1	CC1CCC2(C)CCC3(C)C(CCC4C5(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C5CCC43C)C2C1C	3611.8	Semi standard non polar	33892256
Mangiferursanone,1TBDMS,isomer #1	CC1CCC2(C)CCC3(C)C(CCC4C5(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C5CCC43C)C2C1C	3339.5	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Mangiferursanone GC-MS (Non-derivatized) - 70eV, Positive	splash10-03dj-0119500000-a05a67b057f96269be9b	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mangiferursanone GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 10V, Positive-QTOF	splash10-004i-0011900000-45cbb0692d3e9cc13cb2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 20V, Positive-QTOF	splash10-056r-0129500000-1d6ece959b79636240ae	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 40V, Positive-QTOF	splash10-0a6s-2229200000-0d10d3543c04ce0d23aa	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 10V, Negative-QTOF	splash10-004i-0000900000-ee422d8c76ca8300f467	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 20V, Negative-QTOF	splash10-004i-0000900000-241aac206326bdaeb59a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 40V, Negative-QTOF	splash10-052f-5009600000-15b9f5c01186691e1412	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 10V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 20V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 40V, Negative-QTOF	splash10-00fr-0000900000-ef06d46de462a12081e7	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 10V, Positive-QTOF	splash10-004i-0001900000-9e2e1567d25a8cffc1fd	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 20V, Positive-QTOF	splash10-0a6r-0390300000-f66760419f2f5dc79f60	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferursanone 40V, Positive-QTOF	splash10-03dr-2970100000-98ecd6e608cf715b604b	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

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

FDB014834

KNApSAcK ID

C00056506

Chemspider ID

35014067

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

77227632

PDB ID

Not Available

ChEBI ID

175456

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1853221

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Mangiferursanone (HMDB0036017)

MOL for HMDB0036017 (Mangiferursanone)

3D MOL for HMDB0036017 (Mangiferursanone)

3D SDF for HMDB0036017 (Mangiferursanone)

3D-SDF for HMDB0036017 (Mangiferursanone)

PDB for HMDB0036017 (Mangiferursanone)

3D PDB for HMDB0036017 (Mangiferursanone)

SMILES for HMDB0036017 (Mangiferursanone)

INCHI for HMDB0036017 (Mangiferursanone)

Structure for HMDB0036017 (Mangiferursanone)

3D Structure for HMDB0036017 (Mangiferursanone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra