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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:04:54 UTC

Update Date

2022-03-07 02:54:44 UTC

HMDB ID

HMDB0036016

Secondary Accession Numbers

HMDB36016

Metabolite Identification

Common Name

Mangiferoleanone

Description

Mangiferoleanone 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 Mangiferoleanone.

Structure

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


  Mrv0541 02241216452D          

 31 35  0  0  0  0            999 V2000
   -2.8557   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8557   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1404   -2.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4263   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1404   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111   -2.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027   -1.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027   -0.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7152    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0027    0.7883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7111    0.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4277   -0.8557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389   -0.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8488    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    2.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4277    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5539   -2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4263    0.7911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8557   -0.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  4  5  1  0  0  0  0
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  9 27  1  0  0  0  0
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 17 31  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 29  1  0  0  0  0
 21 30  1  0  0  0  0
M  END

HMDB0036016
     RDKit          3D
Mangiferoleanone
 79 83  0  0  0  0  0  0  0  0999 V2000
   -3.1702    2.7433    0.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1039    1.5900   -0.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3701   -1.3597   -0.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6680    2.8201    0.1682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2709    2.1739   -1.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4307    0.1688   -2.3333 C   0  0  0  0  0  0  0  0  0  0  0  0
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 31 79  1  0
M  END


  Mrv0541 02241216452D          

 31 35  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
HMDB0036016

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(C)CCC2(C)CCC3(C)C(CC(=O)C4C5(C)CCCC(C)(C)C5CCC34C)=C2C1

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O/c1-25(2)14-15-27(5)16-17-29(7)20(21(27)19-25)18-22(31)24-28(6)12-9-11-26(3,4)23(28)10-13-30(24,29)8/h23-24H,9-19H2,1-8H3

> <INCHI_KEY>
MQILTVJSXIHHGW-UHFFFAOYSA-N

> <FORMULA>
C30H48O

> <MOLECULAR_WEIGHT>
424.7015

> <EXACT_MASS>
424.370516158

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
53.029055922090336

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14-icosahydropicen-13-one

> <ALOGPS_LOGP>
7.06

> <JCHEM_LOGP>
7.667043533333333

> <ALOGPS_LOGS>
-6.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.574489301428429

> <JCHEM_PKA_STRONGEST_BASIC>
-7.51477217640865

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
130.7925

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.03e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,7,8,8a,10,11,12,12b,14-dodecahydro-1H-picen-13-one

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0036016
     RDKit          3D
Mangiferoleanone
 79 83  0  0  0  0  0  0  0  0999 V2000
   -3.1702    2.7433    0.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1039    1.5900   -0.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5105    2.1311   -0.3276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6797    1.0163   -1.6352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0886   -0.4205   -1.8112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3701   -1.3597   -0.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4476   -2.2903   -0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922   -2.1048   -1.4937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8997   -1.6836   -1.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6669   -1.4941    0.3459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0818   -2.8284    0.9958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6746   -0.5199    0.8177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8613   -0.4679    0.2993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9273    0.5027    0.7473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2965    0.4310    1.8934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0099    1.0182    1.4447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0338    2.1769    1.2888 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1302    0.1085    1.2485 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4199    0.7259    0.8605 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4602    0.5838    1.9884 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3600    2.2425    0.6312 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6680    2.8201    0.1682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2709    2.1739   -1.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2798    0.6862   -0.8815 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4825    0.1501   -0.1616 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4307    0.1688   -2.3333 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9665    0.2139   -0.4336 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9910   -1.2907   -0.3677 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5174   -1.6249   -0.5926 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7556   -1.2207    0.6759 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2429   -2.2965    1.6759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4830    3.6366   -0.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1788    2.4577   -0.4027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0871    2.9799    1.0673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1806    1.3875    0.1878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6220    3.0735    0.2450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8372    2.2832   -1.3726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5999    1.1203   -1.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2210    1.5898   -2.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7945   -0.7151   -2.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1740   -0.4898   -1.7483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3743   -3.3068   -0.7993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3692   -2.4788    0.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4675   -1.9287   -0.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3658   -1.8867   -2.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4275   -3.2072   -1.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2533   -2.4616   -1.5943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7597   -0.6734   -1.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4804   -2.6565    2.0255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9145   -3.3164    0.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2686   -3.5802    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9217   -0.0540    0.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8414    0.8628    1.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1101   -0.2163    2.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0340    1.1490    2.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3036   -0.1347    2.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0517    1.4667    2.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0367   -0.3352    1.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8212    0.4796    2.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6564    2.4858   -0.1892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1766    2.7627    1.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4238    2.9850    0.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4036    3.8752   -0.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114    2.4414   -1.9476 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2926    2.5329   -1.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3523    0.2364   -0.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3547   -0.9213   -0.0001 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8015    0.7400    0.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9995    0.8889   -2.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9671   -0.7867   -2.3533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4476    0.0238   -2.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2326    0.5667   -1.2246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977   -1.7462   -1.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2650   -1.6933    0.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5110   -2.7307   -0.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223   -1.0799   -1.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1075   -1.8545    2.2681 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4899   -2.4809    2.4689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6788   -3.1715    1.2094 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 14  2  1  0
 30 18  1  0
 13  6  1  0
 27 19  1  0
 30 10  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  7 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
  9 48  1  0
 11 49  1  0
 11 50  1  0
 11 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 18 56  1  0
 20 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  0
 21 61  1  0
 22 62  1  0
 22 63  1  0
 23 64  1  0
 23 65  1  0
 25 66  1  0
 25 67  1  0
 25 68  1  0
 26 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  0
 28 73  1  0
 28 74  1  0
 29 75  1  0
 29 76  1  0
 31 77  1  0
 31 78  1  0
 31 79  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      -5.331  -1.600   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.331  -3.143   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.995  -3.916   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.662  -3.143   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.662  -1.600   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.995  -0.831   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.327  -3.916   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.005  -3.143   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.005  -1.600   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.327  -0.831   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.335  -0.831   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.335   0.705   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.005   1.471   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.327   0.705   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.665  -1.597   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.993  -0.831   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.993   0.705   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.665   1.469   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.318   1.469   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.318   3.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.993   3.761   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.665   3.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.767  -5.253   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.224  -5.253   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.662   1.477   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.662  -0.056   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.005  -0.056   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.335  -2.374   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.594   5.253   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.392   5.253   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.331  -0.067   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   23   24                                             
CONECT    4    3    5    7                                                  
CONECT    5    4    6   10   26                                             
CONECT    6    1    5                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   27                                             
CONECT   10    5    9   14                                                  
CONECT   11    9   12   15   28                                             
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   10   13   25                                                  
CONECT   15   11   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   31                                             
CONECT   18   12   17   22                                                  
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   29   30                                             
CONECT   22   18   21                                                       
CONECT   23    3                                                            
CONECT   24    3                                                            
CONECT   25   14                                                            
CONECT   26    5                                                            
CONECT   27    9                                                            
CONECT   28   11                                                            
CONECT   29   21                                                            
CONECT   30   21                                                            
CONECT   31   17                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

COMPND    HMDB0036016
HETATM    1  C1  UNL     1      -3.170   2.743   0.001  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.104   1.590  -0.295  1.00  0.00           C  
HETATM    3  C3  UNL     1      -5.511   2.131  -0.328  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.680   1.016  -1.635  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.089  -0.420  -1.811  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.370  -1.360  -0.825  1.00  0.00           C  
HETATM    7  C7  UNL     1      -4.448  -2.290  -0.323  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.292  -2.105  -1.494  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.900  -1.684  -1.136  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.667  -1.494   0.346  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.082  -2.828   0.996  1.00  0.00           C  
HETATM   12  C12 UNL     1      -1.675  -0.520   0.818  1.00  0.00           C  
HETATM   13  C13 UNL     1      -2.861  -0.468   0.299  1.00  0.00           C  
HETATM   14  C14 UNL     1      -3.927   0.503   0.747  1.00  0.00           C  
HETATM   15  C15 UNL     1      -1.297   0.431   1.893  1.00  0.00           C  
HETATM   16  C16 UNL     1      -0.010   1.018   1.445  1.00  0.00           C  
HETATM   17  O1  UNL     1      -0.034   2.177   1.289  1.00  0.00           O  
HETATM   18  C17 UNL     1       1.130   0.108   1.249  1.00  0.00           C  
HETATM   19  C18 UNL     1       2.420   0.726   0.860  1.00  0.00           C  
HETATM   20  C19 UNL     1       3.460   0.584   1.988  1.00  0.00           C  
HETATM   21  C20 UNL     1       2.360   2.242   0.631  1.00  0.00           C  
HETATM   22  C21 UNL     1       3.668   2.820   0.168  1.00  0.00           C  
HETATM   23  C22 UNL     1       4.271   2.174  -1.014  1.00  0.00           C  
HETATM   24  C23 UNL     1       4.280   0.686  -0.882  1.00  0.00           C  
HETATM   25  C24 UNL     1       5.482   0.150  -0.162  1.00  0.00           C  
HETATM   26  C25 UNL     1       4.431   0.169  -2.333  1.00  0.00           C  
HETATM   27  C26 UNL     1       2.966   0.214  -0.434  1.00  0.00           C  
HETATM   28  C27 UNL     1       2.991  -1.291  -0.368  1.00  0.00           C  
HETATM   29  C28 UNL     1       1.517  -1.625  -0.593  1.00  0.00           C  
HETATM   30  C29 UNL     1       0.756  -1.221   0.676  1.00  0.00           C  
HETATM   31  C30 UNL     1       1.243  -2.297   1.676  1.00  0.00           C  
HETATM   32  H1  UNL     1      -3.483   3.637  -0.599  1.00  0.00           H  
HETATM   33  H2  UNL     1      -2.179   2.458  -0.403  1.00  0.00           H  
HETATM   34  H3  UNL     1      -3.087   2.980   1.067  1.00  0.00           H  
HETATM   35  H4  UNL     1      -6.181   1.388   0.188  1.00  0.00           H  
HETATM   36  H5  UNL     1      -5.622   3.073   0.245  1.00  0.00           H  
HETATM   37  H6  UNL     1      -5.837   2.283  -1.373  1.00  0.00           H  
HETATM   38  H7  UNL     1      -2.600   1.120  -1.742  1.00  0.00           H  
HETATM   39  H8  UNL     1      -4.221   1.590  -2.414  1.00  0.00           H  
HETATM   40  H9  UNL     1      -3.795  -0.715  -2.837  1.00  0.00           H  
HETATM   41  H10 UNL     1      -5.174  -0.490  -1.748  1.00  0.00           H  
HETATM   42  H11 UNL     1      -4.374  -3.307  -0.799  1.00  0.00           H  
HETATM   43  H12 UNL     1      -4.369  -2.479   0.769  1.00  0.00           H  
HETATM   44  H13 UNL     1      -5.468  -1.929  -0.515  1.00  0.00           H  
HETATM   45  H14 UNL     1      -2.366  -1.887  -2.609  1.00  0.00           H  
HETATM   46  H15 UNL     1      -2.427  -3.207  -1.483  1.00  0.00           H  
HETATM   47  H16 UNL     1      -0.253  -2.462  -1.594  1.00  0.00           H  
HETATM   48  H17 UNL     1      -0.760  -0.673  -1.597  1.00  0.00           H  
HETATM   49  H18 UNL     1      -1.480  -2.657   2.025  1.00  0.00           H  
HETATM   50  H19 UNL     1      -1.915  -3.316   0.455  1.00  0.00           H  
HETATM   51  H20 UNL     1      -0.269  -3.580   0.953  1.00  0.00           H  
HETATM   52  H21 UNL     1      -4.922  -0.054   0.725  1.00  0.00           H  
HETATM   53  H22 UNL     1      -3.841   0.863   1.752  1.00  0.00           H  
HETATM   54  H23 UNL     1      -1.110  -0.216   2.807  1.00  0.00           H  
HETATM   55  H24 UNL     1      -2.034   1.149   2.200  1.00  0.00           H  
HETATM   56  H25 UNL     1       1.304  -0.135   2.374  1.00  0.00           H  
HETATM   57  H26 UNL     1       4.052   1.467   2.172  1.00  0.00           H  
HETATM   58  H27 UNL     1       4.037  -0.335   1.909  1.00  0.00           H  
HETATM   59  H28 UNL     1       2.821   0.480   2.921  1.00  0.00           H  
HETATM   60  H29 UNL     1       1.656   2.486  -0.189  1.00  0.00           H  
HETATM   61  H30 UNL     1       2.177   2.763   1.589  1.00  0.00           H  
HETATM   62  H31 UNL     1       4.424   2.985   0.933  1.00  0.00           H  
HETATM   63  H32 UNL     1       3.404   3.875  -0.168  1.00  0.00           H  
HETATM   64  H33 UNL     1       3.711   2.441  -1.948  1.00  0.00           H  
HETATM   65  H34 UNL     1       5.293   2.533  -1.149  1.00  0.00           H  
HETATM   66  H35 UNL     1       6.352   0.236  -0.882  1.00  0.00           H  
HETATM   67  H36 UNL     1       5.355  -0.921  -0.000  1.00  0.00           H  
HETATM   68  H37 UNL     1       5.802   0.740   0.707  1.00  0.00           H  
HETATM   69  H38 UNL     1       5.000   0.889  -2.937  1.00  0.00           H  
HETATM   70  H39 UNL     1       4.967  -0.787  -2.353  1.00  0.00           H  
HETATM   71  H40 UNL     1       3.448   0.024  -2.799  1.00  0.00           H  
HETATM   72  H41 UNL     1       2.233   0.567  -1.225  1.00  0.00           H  
HETATM   73  H42 UNL     1       3.598  -1.746  -1.173  1.00  0.00           H  
HETATM   74  H43 UNL     1       3.265  -1.693   0.601  1.00  0.00           H  
HETATM   75  H44 UNL     1       1.511  -2.731  -0.670  1.00  0.00           H  
HETATM   76  H45 UNL     1       1.222  -1.080  -1.479  1.00  0.00           H  
HETATM   77  H46 UNL     1       2.107  -1.855   2.268  1.00  0.00           H  
HETATM   78  H47 UNL     1       0.490  -2.481   2.469  1.00  0.00           H  
HETATM   79  H48 UNL     1       1.679  -3.171   1.209  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3    4   14
CONECT    3   35   36   37
CONECT    4    5   38   39
CONECT    5    6   40   41
CONECT    6    7    8   13
CONECT    7   42   43   44
CONECT    8    9   45   46
CONECT    9   10   47   48
CONECT   10   11   12   30
CONECT   11   49   50   51
CONECT   12   13   13   15
CONECT   13   14
CONECT   14   52   53
CONECT   15   16   54   55
CONECT   16   17   17   18
CONECT   18   19   30   56
CONECT   19   20   21   27
CONECT   20   57   58   59
CONECT   21   22   60   61
CONECT   22   23   62   63
CONECT   23   24   64   65
CONECT   24   25   26   27
CONECT   25   66   67   68
CONECT   26   69   70   71
CONECT   27   28   72
CONECT   28   29   73   74
CONECT   29   30   75   76
CONECT   30   31
CONECT   31   77   78   79
END

HMDB0036016
     RDKit          3D
Mangiferoleanone
 79 83  0  0  0  0  0  0  0  0999 V2000
   -3.1702    2.7433    0.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1039    1.5900   -0.2952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5105    2.1311   -0.3276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6797    1.0163   -1.6352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0886   -0.4205   -1.8112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3701   -1.3597   -0.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4476   -2.2903   -0.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922   -2.1048   -1.4937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8997   -1.6836   -1.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6669   -1.4941    0.3459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0818   -2.8284    0.9958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6746   -0.5199    0.8177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8613   -0.4679    0.2993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9273    0.5027    0.7473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2965    0.4310    1.8934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0099    1.0182    1.4447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0338    2.1769    1.2888 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1302    0.1085    1.2485 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4199    0.7259    0.8605 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4602    0.5838    1.9884 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3600    2.2425    0.6312 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6680    2.8201    0.1682 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2709    2.1739   -1.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2798    0.6862   -0.8815 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4825    0.1501   -0.1616 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4307    0.1688   -2.3333 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9665    0.2139   -0.4336 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9910   -1.2907   -0.3677 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5174   -1.6249   -0.5926 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7556   -1.2207    0.6759 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2429   -2.2965    1.6759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4830    3.6366   -0.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1788    2.4577   -0.4027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0871    2.9799    1.0673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1806    1.3875    0.1878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6220    3.0735    0.2450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8372    2.2832   -1.3726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5999    1.1203   -1.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2210    1.5898   -2.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7945   -0.7151   -2.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1740   -0.4898   -1.7483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3743   -3.3068   -0.7993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3692   -2.4788    0.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4675   -1.9287   -0.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3658   -1.8867   -2.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4275   -3.2072   -1.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2533   -2.4616   -1.5943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7597   -0.6734   -1.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4804   -2.6565    2.0255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9145   -3.3164    0.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2686   -3.5802    0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9217   -0.0540    0.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8414    0.8628    1.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1101   -0.2163    2.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0340    1.1490    2.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3036   -0.1347    2.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0517    1.4667    2.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0367   -0.3352    1.9087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8212    0.4796    2.9211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6564    2.4858   -0.1892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1766    2.7627    1.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4238    2.9850    0.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4036    3.8752   -0.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114    2.4414   -1.9476 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2926    2.5329   -1.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3523    0.2364   -0.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3547   -0.9213   -0.0001 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8015    0.7400    0.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9995    0.8889   -2.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9671   -0.7867   -2.3533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4476    0.0238   -2.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2326    0.5667   -1.2246 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977   -1.7462   -1.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2650   -1.6933    0.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5110   -2.7307   -0.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223   -1.0799   -1.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1075   -1.8545    2.2681 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4899   -2.4809    2.4689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6788   -3.1715    1.2094 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 14  2  1  0
 30 18  1  0
 13  6  1  0
 27 19  1  0
 30 10  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  7 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  0
  8 46  1  0
  9 47  1  0
  9 48  1  0
 11 49  1  0
 11 50  1  0
 11 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 18 56  1  0
 20 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  0
 21 61  1  0
 22 62  1  0
 22 63  1  0
 23 64  1  0
 23 65  1  0
 25 66  1  0
 25 67  1  0
 25 68  1  0
 26 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  0
 28 73  1  0
 28 74  1  0
 29 75  1  0
 29 76  1  0
 31 77  1  0
 31 78  1  0
 31 79  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₃₀H₄₈O

Average Molecular Weight

424.7015

Monoisotopic Molecular Weight

424.370516158

IUPAC Name

2,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14-icosahydropicen-13-one

Traditional Name

2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,7,8,8a,10,11,12,12b,14-dodecahydro-1H-picen-13-one

CAS Registry Number

18674-26-5

SMILES

CC1(C)CCC2(C)CCC3(C)C(CC(=O)C4C5(C)CCCC(C)(C)C5CCC34C)=C2C1

InChI Identifier

InChI=1S/C30H48O/c1-25(2)14-15-27(5)16-17-29(7)20(21(27)19-25)18-22(31)24-28(6)12-9-11-26(3,4)23(28)10-13-30(24,29)8/h23-24H,9-19H2,1-8H3

InChI Key

MQILTVJSXIHHGW-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
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: HMDB0036016)
Cell membrane (HMDB: HMDB0036016)

Cellular substructure

Extracellular (HMDB: HMDB0036016)
Membrane (HMDB: HMDB0036016)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036016)

Source

Endogenous

Endogenous (HMDB: HMDB0036016)

Plant

Plant (HMDB: HMDB0036016)

Animal

Animal (HMDB: HMDB0036016)

Exogenous

Food

Food (HMDB: HMDB0036016)

Fruit

Fruits (FooDB: FOOD00871)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0036016)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0036016)

Cellular process

Cell signaling (HMDB: HMDB0036016)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0036016)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0036016)

Nutrient

Nutrient (HMDB: HMDB0036016)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036016)

Emulsifier (HMDB: HMDB0036016)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	223 - 225 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	1.6e-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	0.0003 g/L	ALOGPS
logP	7.06	ALOGPS
logP	7.67	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	15.57	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	130.79 m³·mol⁻¹	ChemAxon
Polarizability	53.03 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]+	196.734	31661259
DarkChem	[M-H]-	191.545	31661259
DeepCCS	[M-2H]-	245.005	30932474
DeepCCS	[M+Na]+	220.234	30932474
AllCCS	[M+H]+	213.9	32859911
AllCCS	[M+H-H2O]+	212.1	32859911
AllCCS	[M+NH4]+	215.6	32859911
AllCCS	[M+Na]+	216.0	32859911
AllCCS	[M-H]-	214.1	32859911
AllCCS	[M+Na-2H]-	215.7	32859911
AllCCS	[M+HCOO]-	217.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Mangiferoleanone	CC1(C)CCC2(C)CCC3(C)C(CC(=O)C4C5(C)CCCC(C)(C)C5CCC34C)=C2C1	2929.8	Standard polar	33892256
Mangiferoleanone	CC1(C)CCC2(C)CCC3(C)C(CC(=O)C4C5(C)CCCC(C)(C)C5CCC34C)=C2C1	3337.7	Standard non polar	33892256
Mangiferoleanone	CC1(C)CCC2(C)CCC3(C)C(CC(=O)C4C5(C)CCCC(C)(C)C5CCC34C)=C2C1	3288.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Mangiferoleanone,1TMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=C2C1)CC(O[Si](C)(C)C)=C1C2(C)CCCC(C)(C)C2CCC13C	3278.2	Semi standard non polar	33892256
Mangiferoleanone,1TMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=C2C1)CC(O[Si](C)(C)C)=C1C2(C)CCCC(C)(C)C2CCC13C	3194.4	Standard non polar	33892256
Mangiferoleanone,1TMS,isomer #2	CC1(C)CCC2(C)CCC3(C)C(=C2C1)C=C(O[Si](C)(C)C)C1C2(C)CCCC(C)(C)C2CCC13C	3278.3	Semi standard non polar	33892256
Mangiferoleanone,1TMS,isomer #2	CC1(C)CCC2(C)CCC3(C)C(=C2C1)C=C(O[Si](C)(C)C)C1C2(C)CCCC(C)(C)C2CCC13C	3146.1	Standard non polar	33892256
Mangiferoleanone,1TBDMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=C2C1)CC(O[Si](C)(C)C(C)(C)C)=C1C2(C)CCCC(C)(C)C2CCC13C	3532.4	Semi standard non polar	33892256
Mangiferoleanone,1TBDMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=C2C1)CC(O[Si](C)(C)C(C)(C)C)=C1C2(C)CCCC(C)(C)C2CCC13C	3486.6	Standard non polar	33892256
Mangiferoleanone,1TBDMS,isomer #2	CC1(C)CCC2(C)CCC3(C)C(=C2C1)C=C(O[Si](C)(C)C(C)(C)C)C1C2(C)CCCC(C)(C)C2CCC13C	3523.5	Semi standard non polar	33892256
Mangiferoleanone,1TBDMS,isomer #2	CC1(C)CCC2(C)CCC3(C)C(=C2C1)C=C(O[Si](C)(C)C(C)(C)C)C1C2(C)CCCC(C)(C)C2CCC13C	3354.8	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Mangiferoleanone GC-MS (Non-derivatized) - 70eV, Positive	splash10-0pbj-0948500000-be6fe69768aa60b1844d	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mangiferoleanone 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 - Mangiferoleanone 10V, Positive-QTOF	splash10-004i-0002900000-f6f0a5b987a356d1c155	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 20V, Positive-QTOF	splash10-0a6r-1958600000-f8358b58c1bc1ce1fa24	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 40V, Positive-QTOF	splash10-052e-2829100000-42742c2a1f0573ba8c4a	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 10V, Negative-QTOF	splash10-00di-0000900000-0dfb20539e9ccb34b85d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 20V, Negative-QTOF	splash10-00di-0000900000-f19ef07e2bc3e5a98a0e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 40V, Negative-QTOF	splash10-0a4l-2149700000-7a823c320f74f448f52e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 10V, Negative-QTOF	splash10-00di-0000900000-ae374dd49287e6271d4c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 20V, Negative-QTOF	splash10-00di-0000900000-ae374dd49287e6271d4c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 40V, Negative-QTOF	splash10-00di-0000900000-ae374dd49287e6271d4c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 10V, Positive-QTOF	splash10-004i-0003900000-21ef1cd92db688b96bd2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 20V, Positive-QTOF	splash10-004i-1105900000-95db7917ce2d193641d7	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mangiferoleanone 40V, Positive-QTOF	splash10-05g3-8955500000-8fbdde14601d0e154751	2021-09-22	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

FDB014833

KNApSAcK ID

C00057177

Chemspider ID

35014066

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131751900

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1853211

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 Mangiferoleanone (HMDB0036016)

MOL for HMDB0036016 (Mangiferoleanone)

3D MOL for HMDB0036016 (Mangiferoleanone)

3D SDF for HMDB0036016 (Mangiferoleanone)

3D-SDF for HMDB0036016 (Mangiferoleanone)

PDB for HMDB0036016 (Mangiferoleanone)

3D PDB for HMDB0036016 (Mangiferoleanone)

SMILES for HMDB0036016 (Mangiferoleanone)

INCHI for HMDB0036016 (Mangiferoleanone)

Structure for HMDB0036016 (Mangiferoleanone)

3D Structure for HMDB0036016 (Mangiferoleanone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra