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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 02:17:14 UTC

Update Date

2022-03-07 02:56:42 UTC

HMDB ID

HMDB0040711

Secondary Accession Numbers

HMDB40711

Metabolite Identification

Common Name

16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid

Description

16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 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 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid.

Structure

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

  Mrv0541 05061312042D          

 34 38  0  0  0  0            999 V2000
    0.9557   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8742   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3627    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2812    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0014    2.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1492    2.0948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2684    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  9  8  1  0  0  0  0
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 31 22  2  0  0  0  0
 32 23  1  0  0  0  0
 33 24  2  0  0  0  0
 34 24  1  0  0  0  0
M  END

HMDB0040711
     RDKit          3D
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid
 78 82  0  0  0  0  0  0  0  0999 V2000
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 34 78  1  0
M  END

  Mrv0541 05061312042D          

 34 38  0  0  0  0            999 V2000
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 27 21  1  0  0  0  0
 28  6  1  0  0  0  0
 28 13  1  0  0  0  0
 28 21  1  0  0  0  0
 29  7  1  0  0  0  0
 29 17  1  0  0  0  0
 29 18  1  0  0  0  0
 29 28  1  0  0  0  0
 30 15  1  0  0  0  0
 30 19  1  0  0  0  0
 30 23  1  0  0  0  0
 30 24  1  0  0  0  0
 31 22  2  0  0  0  0
 32 23  1  0  0  0  0
 33 24  2  0  0  0  0
 34 24  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0040711

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(C)CCC2(C(O)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC34C)C2C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H44O4/c1-25(2)14-15-30(24(33)34)19(16-25)18-8-9-21-27(5)12-11-22(31)26(3,4)20(27)10-13-28(21,6)29(18,7)17-23(30)32/h8,11-12,19-21,23,32H,9-10,13-17H2,1-7H3,(H,33,34)

> <INCHI_KEY>
DFSIQVYXMRYQGI-UHFFFAOYSA-N

> <FORMULA>
C30H44O4

> <MOLECULAR_WEIGHT>
468.668

> <EXACT_MASS>
468.323959896

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
54.503969593741544

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,12a,12b,13,14b-octadecahydropicene-4a-carboxylic acid

> <ALOGPS_LOGP>
5.79

> <JCHEM_LOGP>
5.9253735616666665

> <ALOGPS_LOGS>
-5.55

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.670591037715084

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.622190204205517

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0579672617894813

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
135.41099999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.32e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,7,8,8a,12b,13,14b-decahydro-1H-picene-4a-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0040711
     RDKit          3D
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid
 78 82  0  0  0  0  0  0  0  0999 V2000
   -4.5660    0.3611   -2.9733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5155    0.1225   -1.4503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6685   -0.8386   -1.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6828    1.4545   -0.7996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6481    1.7369    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2911    0.5444    1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5631    0.0771    1.7269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5910    0.7591    1.6186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6081   -1.1139    2.4315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3936    1.0092    2.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9465    2.1772    2.7382 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9628    1.1473    1.8751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3824   -0.0218    1.1284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0294   -1.0477    2.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3030   -0.7263    0.2508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7863   -1.6180   -0.5852 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811   -1.8919   -0.6274 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3594   -0.5356   -0.6378 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8124   -0.6948   -0.8893 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066   -0.4933   -2.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2758   -2.0718   -0.6107 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4006   -2.3939    0.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3303   -1.3634    0.4895 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2105   -1.6855    1.3194 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1177   -0.0202   -0.0734 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8517    0.1454   -1.3487 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7372    0.9633    0.9333 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6559    0.2732   -0.0855 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2036    0.0519    1.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8890    0.7289    1.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9067    0.4006    0.4118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5660    1.7442   -0.2642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7481   -0.5244    0.2568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787   -0.4949   -1.1992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5324   -0.6602   -3.4295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6490    0.9066   -3.2419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4939    0.8523   -3.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3740   -1.6406   -0.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9754   -1.3938   -2.1040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5741   -0.2941   -0.8521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5454    2.3009   -1.5589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7300    1.5918   -0.4799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7229    2.0877   -0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0199    2.5809    0.8873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7053   -1.1618    3.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4841    0.2681    3.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5349    2.9830    2.3422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8487    2.0455    1.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3473    1.3390    2.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9869   -1.4115    2.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7034   -1.9182    2.2255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1402   -0.6016    3.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4255   -2.1765   -1.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8853   -2.3593   -1.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0158   -2.5868    0.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9222   -0.1215   -1.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6244    0.4642   -2.5694 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1064   -0.3651   -2.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5547   -1.3651   -2.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6731   -2.8975   -0.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6769   -3.4392    0.1772 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7027   -0.6367   -2.1017 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7580    1.1837   -1.7578 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9528    0.0778   -1.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9459    0.4886    1.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7246    1.3439    0.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1012    1.8834    1.0137 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4253    1.2914   -0.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9174    0.5930    2.0560 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2652   -0.9898    1.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5014    0.5143    2.5346 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1152    1.8389    1.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8536    2.6096    0.3360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4309    1.7414   -0.7009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2490    1.8268   -1.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2588   -1.4968    0.6380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2757   -1.5510   -1.5915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4258    0.0932   -1.7602 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
  7  8  2  0
  7  9  1  0
  6 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 15 33  1  0
 33 34  1  0
 34  2  1  0
 33  6  1  0
 31 13  1  0
 31 18  1  0
 28 19  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  3 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  9 45  1  0
 10 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 14 50  1  0
 14 51  1  0
 14 52  1  0
 16 53  1  0
 17 54  1  0
 17 55  1  0
 18 56  1  0
 20 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  0
 22 61  1  0
 26 62  1  0
 26 63  1  0
 26 64  1  0
 27 65  1  0
 27 66  1  0
 27 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 30 72  1  0
 32 73  1  0
 32 74  1  0
 32 75  1  0
 33 76  1  0
 34 77  1  0
 34 78  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       1.784  -1.090   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.499  -2.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.744   3.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.458   2.630   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.931  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336   4.262   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.745   3.910   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.851  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.391  -0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.701   3.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.011  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.471  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.161   3.437   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.461   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.231   2.104   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.771  -0.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.081   3.437   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.081   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.541   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.471   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.161   0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.781   0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.541   3.437   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.781   3.382   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.231  -0.564   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.011   2.104   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.701   0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.391   2.104   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.851   2.104   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.771   2.104   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      16.321   0.770   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       5.211   4.661   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       3.730   4.749   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       2.461   3.437   0.000  0.00  0.00           O+0
CONECT    1   25                                                            
CONECT    2   25                                                            
CONECT    3   26                                                            
CONECT    4   26                                                            
CONECT    5   27                                                            
CONECT    6   28                                                            
CONECT    7   29                                                            
CONECT    8    9   18                                                       
CONECT    9    8   21                                                       
CONECT   10   13   20                                                       
CONECT   11   12   22                                                       
CONECT   12   11   27                                                       
CONECT   13   10   28                                                       
CONECT   14   15   25                                                       
CONECT   15   14   30                                                       
CONECT   16   19   25                                                       
CONECT   17   23   29                                                       
CONECT   18    8   19   29                                                  
CONECT   19   16   18   30                                                  
CONECT   20   10   26   27                                                  
CONECT   21    9   27   28                                                  
CONECT   22   11   26   31                                                  
CONECT   23   17   30   32                                                  
CONECT   24   30   33   34                                                  
CONECT   25    1    2   14   16                                             
CONECT   26    3    4   20   22                                             
CONECT   27    5   12   20   21                                             
CONECT   28    6   13   21   29                                             
CONECT   29    7   17   18   28                                             
CONECT   30   15   19   23   24                                             
CONECT   31   22                                                            
CONECT   32   23                                                            
CONECT   33   24                                                            
CONECT   34   24                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

COMPND    HMDB0040711
HETATM    1  C1  UNL     1      -4.566   0.361  -2.973  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.515   0.123  -1.450  1.00  0.00           C  
HETATM    3  C3  UNL     1      -5.668  -0.839  -1.186  1.00  0.00           C  
HETATM    4  C4  UNL     1      -4.683   1.454  -0.800  1.00  0.00           C  
HETATM    5  C5  UNL     1      -3.648   1.737   0.247  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.291   0.544   1.102  1.00  0.00           C  
HETATM    7  C7  UNL     1      -4.563   0.077   1.727  1.00  0.00           C  
HETATM    8  O1  UNL     1      -5.591   0.759   1.619  1.00  0.00           O  
HETATM    9  O2  UNL     1      -4.608  -1.114   2.432  1.00  0.00           O  
HETATM   10  C8  UNL     1      -2.394   1.009   2.230  1.00  0.00           C  
HETATM   11  O3  UNL     1      -2.947   2.177   2.738  1.00  0.00           O  
HETATM   12  C9  UNL     1      -0.963   1.147   1.875  1.00  0.00           C  
HETATM   13  C10 UNL     1      -0.382  -0.022   1.128  1.00  0.00           C  
HETATM   14  C11 UNL     1      -0.029  -1.048   2.233  1.00  0.00           C  
HETATM   15  C12 UNL     1      -1.303  -0.726   0.251  1.00  0.00           C  
HETATM   16  C13 UNL     1      -0.786  -1.618  -0.585  1.00  0.00           C  
HETATM   17  C14 UNL     1       0.681  -1.892  -0.627  1.00  0.00           C  
HETATM   18  C15 UNL     1       1.359  -0.536  -0.638  1.00  0.00           C  
HETATM   19  C16 UNL     1       2.812  -0.695  -0.889  1.00  0.00           C  
HETATM   20  C17 UNL     1       3.107  -0.493  -2.397  1.00  0.00           C  
HETATM   21  C18 UNL     1       3.276  -2.072  -0.611  1.00  0.00           C  
HETATM   22  C19 UNL     1       4.401  -2.394   0.006  1.00  0.00           C  
HETATM   23  C20 UNL     1       5.330  -1.363   0.490  1.00  0.00           C  
HETATM   24  O4  UNL     1       6.211  -1.685   1.319  1.00  0.00           O  
HETATM   25  C21 UNL     1       5.118  -0.020  -0.073  1.00  0.00           C  
HETATM   26  C22 UNL     1       5.852   0.145  -1.349  1.00  0.00           C  
HETATM   27  C23 UNL     1       5.737   0.963   0.933  1.00  0.00           C  
HETATM   28  C24 UNL     1       3.656   0.273  -0.086  1.00  0.00           C  
HETATM   29  C25 UNL     1       3.204   0.052   1.363  1.00  0.00           C  
HETATM   30  C26 UNL     1       1.889   0.729   1.494  1.00  0.00           C  
HETATM   31  C27 UNL     1       0.907   0.401   0.412  1.00  0.00           C  
HETATM   32  C28 UNL     1       0.566   1.744  -0.264  1.00  0.00           C  
HETATM   33  C29 UNL     1      -2.748  -0.524   0.257  1.00  0.00           C  
HETATM   34  C30 UNL     1      -3.179  -0.495  -1.199  1.00  0.00           C  
HETATM   35  H1  UNL     1      -4.532  -0.660  -3.429  1.00  0.00           H  
HETATM   36  H2  UNL     1      -3.649   0.907  -3.242  1.00  0.00           H  
HETATM   37  H3  UNL     1      -5.494   0.852  -3.271  1.00  0.00           H  
HETATM   38  H4  UNL     1      -5.374  -1.641  -0.460  1.00  0.00           H  
HETATM   39  H5  UNL     1      -5.975  -1.394  -2.104  1.00  0.00           H  
HETATM   40  H6  UNL     1      -6.574  -0.294  -0.852  1.00  0.00           H  
HETATM   41  H7  UNL     1      -4.545   2.301  -1.559  1.00  0.00           H  
HETATM   42  H8  UNL     1      -5.730   1.592  -0.480  1.00  0.00           H  
HETATM   43  H9  UNL     1      -2.723   2.088  -0.258  1.00  0.00           H  
HETATM   44  H10 UNL     1      -4.020   2.581   0.887  1.00  0.00           H  
HETATM   45  H11 UNL     1      -4.705  -1.162   3.440  1.00  0.00           H  
HETATM   46  H12 UNL     1      -2.484   0.268   3.044  1.00  0.00           H  
HETATM   47  H13 UNL     1      -2.535   2.983   2.342  1.00  0.00           H  
HETATM   48  H14 UNL     1      -0.849   2.046   1.244  1.00  0.00           H  
HETATM   49  H15 UNL     1      -0.347   1.339   2.776  1.00  0.00           H  
HETATM   50  H16 UNL     1       0.987  -1.411   2.176  1.00  0.00           H  
HETATM   51  H17 UNL     1      -0.703  -1.918   2.226  1.00  0.00           H  
HETATM   52  H18 UNL     1      -0.140  -0.602   3.247  1.00  0.00           H  
HETATM   53  H19 UNL     1      -1.426  -2.176  -1.260  1.00  0.00           H  
HETATM   54  H20 UNL     1       0.885  -2.359  -1.637  1.00  0.00           H  
HETATM   55  H21 UNL     1       1.016  -2.587   0.125  1.00  0.00           H  
HETATM   56  H22 UNL     1       0.922  -0.122  -1.615  1.00  0.00           H  
HETATM   57  H23 UNL     1       3.624   0.464  -2.569  1.00  0.00           H  
HETATM   58  H24 UNL     1       2.106  -0.365  -2.912  1.00  0.00           H  
HETATM   59  H25 UNL     1       3.555  -1.365  -2.863  1.00  0.00           H  
HETATM   60  H26 UNL     1       2.673  -2.897  -0.933  1.00  0.00           H  
HETATM   61  H27 UNL     1       4.677  -3.439   0.177  1.00  0.00           H  
HETATM   62  H28 UNL     1       5.703  -0.637  -2.102  1.00  0.00           H  
HETATM   63  H29 UNL     1       5.758   1.184  -1.758  1.00  0.00           H  
HETATM   64  H30 UNL     1       6.953   0.078  -1.085  1.00  0.00           H  
HETATM   65  H31 UNL     1       5.946   0.489   1.896  1.00  0.00           H  
HETATM   66  H32 UNL     1       6.725   1.344   0.558  1.00  0.00           H  
HETATM   67  H33 UNL     1       5.101   1.883   1.014  1.00  0.00           H  
HETATM   68  H34 UNL     1       3.425   1.291  -0.393  1.00  0.00           H  
HETATM   69  H35 UNL     1       3.917   0.593   2.056  1.00  0.00           H  
HETATM   70  H36 UNL     1       3.265  -0.990   1.664  1.00  0.00           H  
HETATM   71  H37 UNL     1       1.501   0.514   2.535  1.00  0.00           H  
HETATM   72  H38 UNL     1       2.115   1.839   1.560  1.00  0.00           H  
HETATM   73  H39 UNL     1       0.854   2.610   0.336  1.00  0.00           H  
HETATM   74  H40 UNL     1      -0.431   1.741  -0.701  1.00  0.00           H  
HETATM   75  H41 UNL     1       1.249   1.827  -1.172  1.00  0.00           H  
HETATM   76  H42 UNL     1      -3.259  -1.497   0.638  1.00  0.00           H  
HETATM   77  H43 UNL     1      -3.276  -1.551  -1.591  1.00  0.00           H  
HETATM   78  H44 UNL     1      -2.426   0.093  -1.760  1.00  0.00           H  
CONECT    1    2   35   36   37
CONECT    2    3    4   34
CONECT    3   38   39   40
CONECT    4    5   41   42
CONECT    5    6   43   44
CONECT    6    7   10   33
CONECT    7    8    8    9
CONECT    9   45
CONECT   10   11   12   46
CONECT   11   47
CONECT   12   13   48   49
CONECT   13   14   15   31
CONECT   14   50   51   52
CONECT   15   16   16   33
CONECT   16   17   53
CONECT   17   18   54   55
CONECT   18   19   31   56
CONECT   19   20   21   28
CONECT   20   57   58   59
CONECT   21   22   22   60
CONECT   22   23   61
CONECT   23   24   24   25
CONECT   25   26   27   28
CONECT   26   62   63   64
CONECT   27   65   66   67
CONECT   28   29   68
CONECT   29   30   69   70
CONECT   30   31   71   72
CONECT   31   32
CONECT   32   73   74   75
CONECT   33   34   76
CONECT   34   77   78
END

HMDB0040711
     RDKit          3D
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid
 78 82  0  0  0  0  0  0  0  0999 V2000
   -4.5660    0.3611   -2.9733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5155    0.1225   -1.4503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6685   -0.8386   -1.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6828    1.4545   -0.7996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6481    1.7369    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2911    0.5444    1.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5631    0.0771    1.7269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5910    0.7591    1.6186 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6081   -1.1139    2.4315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3936    1.0092    2.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9465    2.1772    2.7382 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9628    1.1473    1.8751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3824   -0.0218    1.1284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0294   -1.0477    2.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3030   -0.7263    0.2508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7863   -1.6180   -0.5852 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811   -1.8919   -0.6274 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3594   -0.5356   -0.6378 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8124   -0.6948   -0.8893 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1066   -0.4933   -2.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2758   -2.0718   -0.6107 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4006   -2.3939    0.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3303   -1.3634    0.4895 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2105   -1.6855    1.3194 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1177   -0.0202   -0.0734 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8517    0.1454   -1.3487 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7372    0.9633    0.9333 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6559    0.2732   -0.0855 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2036    0.0519    1.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8890    0.7289    1.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9067    0.4006    0.4118 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5660    1.7442   -0.2642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7481   -0.5244    0.2568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787   -0.4949   -1.1992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5324   -0.6602   -3.4295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6490    0.9066   -3.2419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4939    0.8523   -3.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3740   -1.6406   -0.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9754   -1.3938   -2.1040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5741   -0.2941   -0.8521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5454    2.3009   -1.5589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7300    1.5918   -0.4799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7229    2.0877   -0.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0199    2.5809    0.8873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7053   -1.1618    3.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4841    0.2681    3.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5349    2.9830    2.3422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8487    2.0455    1.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3473    1.3390    2.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9869   -1.4115    2.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7034   -1.9182    2.2255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1402   -0.6016    3.2470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4255   -2.1765   -1.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8853   -2.3593   -1.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0158   -2.5868    0.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9222   -0.1215   -1.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6244    0.4642   -2.5694 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1064   -0.3651   -2.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5547   -1.3651   -2.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6731   -2.8975   -0.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6769   -3.4392    0.1772 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7027   -0.6367   -2.1017 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7580    1.1837   -1.7578 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9528    0.0778   -1.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9459    0.4886    1.8965 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7246    1.3439    0.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1012    1.8834    1.0137 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4253    1.2914   -0.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9174    0.5930    2.0560 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2652   -0.9898    1.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5014    0.5143    2.5346 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1152    1.8389    1.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8536    2.6096    0.3360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4309    1.7414   -0.7009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2490    1.8268   -1.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2588   -1.4968    0.6380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2757   -1.5510   -1.5915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4258    0.0932   -1.7602 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
  7  8  2  0
  7  9  1  0
  6 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 15 33  1  0
 33 34  1  0
 34  2  1  0
 33  6  1  0
 31 13  1  0
 31 18  1  0
 28 19  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  3 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  9 45  1  0
 10 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 14 50  1  0
 14 51  1  0
 14 52  1  0
 16 53  1  0
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 17 55  1  0
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 20 57  1  0
 20 58  1  0
 20 59  1  0
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 22 61  1  0
 26 62  1  0
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 27 65  1  0
 27 66  1  0
 27 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 30 72  1  0
 32 73  1  0
 32 74  1  0
 32 75  1  0
 33 76  1  0
 34 77  1  0
 34 78  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
16b-16-Hydroxy-3-oxo-1,12-oleanadien-28-Oate	Generator
16b-16-Hydroxy-3-oxo-1,12-oleanadien-28-Oic acid	Generator
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-Oate	Generator
16Β-16-hydroxy-3-oxo-1,12-oleanadien-28-Oate	Generator
16Β-16-hydroxy-3-oxo-1,12-oleanadien-28-Oic acid	Generator
5-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,12a,12b,13,14b-octadecahydropicene-4a-carboxylate	HMDB

Chemical Formula

C₃₀H₄₄O₄

Average Molecular Weight

468.668

Monoisotopic Molecular Weight

468.323959896

IUPAC Name

5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,12a,12b,13,14b-octadecahydropicene-4a-carboxylic acid

Traditional Name

5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,7,8,8a,12b,13,14b-decahydro-1H-picene-4a-carboxylic acid

CAS Registry Number

77625-72-0

SMILES

CC1(C)CCC2(C(O)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC34C)C2C1)C(O)=O

InChI Identifier

InChI=1S/C30H44O4/c1-25(2)14-15-30(24(33)34)19(16-25)18-8-9-21-27(5)12-11-22(31)26(3,4)20(27)10-13-28(21,6)29(18,7)17-23(30)32/h8,11-12,19-21,23,32H,9-10,13-17H2,1-7H3,(H,33,34)

InChI Key

DFSIQVYXMRYQGI-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
Beta-hydroxy acid
Cyclohexenone
Hydroxy acid
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Alcohol
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0040711)

Source

Endogenous

Endogenous (HMDB: HMDB0040711)

Plant

Plant (HMDB: HMDB0040711)

Animal

Animal (HMDB: HMDB0040711)

Exogenous

Food

Food (HMDB: HMDB0040711)

Fruit

Fruits (FooDB: FOOD00871)

Beverage

Alcoholic beverage

Alcoholic beverages (FooDB: FOOD00854)

Exogenous (HMDB: HMDB0040711)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0040711)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0040711)

Lipid metabolism pathway (HMDB: HMDB0040711)

Cellular process

Cell signaling (HMDB: HMDB0040711)

Biochemical process

Lipid transport (HMDB: HMDB0040711)

Role

Biological role

Energy source (HMDB: HMDB0040711)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0040711)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	175 - 177 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0013 g/L	ALOGPS
logP	5.79	ALOGPS
logP	5.93	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	4.62	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	135.41 m³·mol⁻¹	ChemAxon
Polarizability	54.5 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	209.211	31661259
DarkChem	[M-H]-	204.05	31661259
DeepCCS	[M-2H]-	247.196	30932474
DeepCCS	[M+Na]+	222.621	30932474
AllCCS	[M+H]+	215.6	32859911
AllCCS	[M+H-H2O]+	213.9	32859911
AllCCS	[M+NH4]+	217.2	32859911
AllCCS	[M+Na]+	217.6	32859911
AllCCS	[M-H]-	216.8	32859911
AllCCS	[M+Na-2H]-	218.6	32859911
AllCCS	[M+HCOO]-	220.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid	CC1(C)CCC2(C(O)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC34C)C2C1)C(O)=O	3864.6	Standard polar	33892256
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid	CC1(C)CCC2(C(O)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC34C)C2C1)C(O)=O	3476.5	Standard non polar	33892256
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid	CC1(C)CCC2(C(O)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC34C)C2C1)C(O)=O	3918.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid,1TMS,isomer #1	CC1(C)CCC2(C(=O)O)C(O[Si](C)(C)C)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC43C)C2C1	3921.3	Semi standard non polar	33892256
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid,1TMS,isomer #2	CC1(C)CCC2(C(=O)O[Si](C)(C)C)C(O)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC43C)C2C1	3824.0	Semi standard non polar	33892256
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid,2TMS,isomer #1	CC1(C)CCC2(C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC43C)C2C1	3788.7	Semi standard non polar	33892256
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid,1TBDMS,isomer #1	CC1(C)CCC2(C(=O)O)C(O[Si](C)(C)C(C)(C)C)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC43C)C2C1	4144.1	Semi standard non polar	33892256
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid,1TBDMS,isomer #2	CC1(C)CCC2(C(=O)O[Si](C)(C)C(C)(C)C)C(O)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC43C)C2C1	4069.3	Semi standard non polar	33892256
16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid,2TBDMS,isomer #1	CC1(C)CCC2(C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)CC3(C)C(=CCC4C5(C)C=CC(=O)C(C)(C)C5CCC43C)C2C1	4243.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0ik9-2248900000-99a3fb5e8f6a454608ee	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid GC-MS (2 TMS) - 70eV, Positive	splash10-0002-1110190000-0974f6b6fd125009c3f2	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 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 - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 10V, Positive-QTOF	splash10-0uxr-0000900000-c42135f8730aca5a04bf	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 20V, Positive-QTOF	splash10-0pir-1001900000-c9828329823412426945	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 40V, Positive-QTOF	splash10-0uea-5269700000-1ef0a39d4ce0f9c435bd	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 10V, Negative-QTOF	splash10-01b9-0000900000-c6a5c0b60b362c18ddbe	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 20V, Negative-QTOF	splash10-05fr-0000900000-b403bbcd6985b0b3bb7c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 40V, Negative-QTOF	splash10-0a4i-1001900000-e060833edca78d0d57ef	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 10V, Positive-QTOF	splash10-014i-0000900000-65a10e5d13d11f3be4c7	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 20V, Positive-QTOF	splash10-0udi-0509200000-3da3a6536ec4ccbbb925	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 40V, Positive-QTOF	splash10-0zg0-3942000000-f483d6b5169d507028d6	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 10V, Negative-QTOF	splash10-014i-0000900000-873e7cf5c69fd6054c8e	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 20V, Negative-QTOF	splash10-0600-0000900000-74736ea48b826cc486d1	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid 40V, Negative-QTOF	splash10-0a4i-0000900000-ad1b66e46ee32c8ed107	2021-09-25	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

FDB020515

KNApSAcK ID

Not Available

Chemspider ID

35015009

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752914

PDB ID

Not Available

ChEBI ID

168172

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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 16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid (HMDB0040711)

MOL for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D MOL for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D SDF for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D-SDF for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

PDB for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D PDB for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

SMILES for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

INCHI for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

Structure for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

3D Structure for HMDB0040711 (16beta-16-Hydroxy-3-oxo-1,12-oleanadien-28-oic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra