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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-23 21:49:33 UTC

Update Date

2021-09-23 21:49:34 UTC

HMDB ID

HMDB0302925

Secondary Accession Numbers

None

Metabolite Identification

Common Name

beta-Amyrenone

Description

Beta-amyrenone is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Beta-amyrenone is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amyrenone can be found in rosemary and shea tree, which makes beta-amyrenone a potential biomarker for the consumption of these food products.

Structure

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


  Mrv0541 02241223402D          

 31 35  0  0  0  0            999 V2000
    1.7867    1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7867    0.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

HMDB0302925
     RDKit          3D
beta-Amyrenone
 79 83  0  0  0  0  0  0  0  0999 V2000
    4.9627   -1.3922   -1.8390 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv0541 02241223402D          

 31 35  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
HMDB0302925

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C2C1

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h9,21-23H,10-19H2,1-8H3

> <INCHI_KEY>
LIIFBMGUDSHTOU-UHFFFAOYSA-N

> <FORMULA>
C30H48O

> <MOLECULAR_WEIGHT>
424.7015

> <EXACT_MASS>
424.370516158

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
53.522130228759416

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
7.66

> <JCHEM_LOGP>
7.966668539999999

> <ALOGPS_LOGS>
-6.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.95829272986144

> <JCHEM_PKA_STRONGEST_BASIC>
-7.4708850131330315

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
131.08499999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.15e-05 g/l

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

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0302925
     RDKit          3D
beta-Amyrenone
 79 83  0  0  0  0  0  0  0  0999 V2000
    4.9627   -1.3922   -1.8390 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0686   -1.0616   -0.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9569   -2.0258    0.3400 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5026    0.3837   -0.2592 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7719    1.1491    0.8163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2746    1.2209    0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0407    2.4846   -0.2398 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5180    1.3325    1.8518 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1611    0.7865    2.0143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6450   -0.1418    0.9341 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9248   -1.5570    1.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4489   -0.0015   -0.2783 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8977    0.2071   -1.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5687    0.3283   -1.6587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3043    0.7171   -0.4129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7568    0.7281   -0.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2281    2.1889   -0.5721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0353    0.2198   -2.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4854    0.3352   -2.5144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1964   -0.6543   -1.6188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8468   -1.5733   -2.0301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0027   -0.3661   -0.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9612    0.7930    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5284   -1.5237    0.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936   -0.0856    0.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9555   -1.3832    0.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4557   -1.4581    0.4453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8403   -0.1207    0.7666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4288    0.3051    2.0785 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9164    0.0047   -0.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6551   -1.1448    0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8591   -0.4597   -2.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1641   -2.1317   -2.0509 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9617   -1.8203   -2.1344 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4030   -2.9768    0.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1525   -1.6476    1.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8773   -2.2310   -0.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4332    0.9307   -1.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    0.3703    0.0407 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9857    0.7535    1.8323 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2269    2.1715    0.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5534    2.4270   -1.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5046    3.3406    0.3193 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9688    2.6878   -0.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2187    0.9375    2.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5245    2.4399    2.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4445    1.6221    2.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1552    0.2782    3.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8503   -2.3265    0.6974 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2005   -1.7610    2.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8926   -1.6075    2.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5182    0.2983   -2.3270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8674   -0.5416   -2.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6507    1.2382   -2.3360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9037    1.7501   -0.1585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9122    2.3088    0.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6311    2.5767   -1.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3611    2.8699   -0.3172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4746    0.7276   -2.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8619   -0.8841   -2.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9098    1.3259   -2.4678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5586   -0.0410   -3.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9869    0.3180    0.0770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8425    1.1536    1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9657    1.5530   -0.6698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2562   -1.3629    1.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6574   -1.4632    0.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2836   -2.5016    0.2412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8051    0.5865    1.1246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3359   -2.1213   -0.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2847   -1.8444    1.5303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1386   -2.3040    1.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1690   -1.7118   -0.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2184   -0.4183    2.4650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7452    0.2640    2.9539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7760    1.3579    2.0801 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3573    0.2521   -1.2576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2577   -2.1425    0.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9590   -0.9361    1.3629 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
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 12 30  1  0
 30 31  1  0
 31  2  1  0
 30  6  1  0
 28 10  1  0
 28 15  1  0
 25 16  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
 13 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 17 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  0
 19 62  1  0
 23 63  1  0
 23 64  1  0
 23 65  1  0
 24 66  1  0
 24 67  1  0
 24 68  1  0
 25 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  0
 27 73  1  0
 29 74  1  0
 29 75  1  0
 29 76  1  0
 30 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       3.335   3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.335   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.001   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.666   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.666   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.666  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.666  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.002   3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.002   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.667   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.002   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.667  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.335  -1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.001  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.001  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.666  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.666  -3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.001  -3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.002  -3.850   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.667  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.667  -1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.333  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.001  -1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.001   0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.323  -5.030   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.333  -3.850   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.344  -5.030   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.679   5.030   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.667   3.850   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.658   5.030   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.436  -2.874   0.000  0.00  0.00           C+0
CONECT    1    2   29                                                       
CONECT    2    1    3   10                                                  
CONECT    3    2    4   14                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6   14   16   31                                             
CONECT    8    9   29                                                       
CONECT    9    8   10                                                       
CONECT   10    2    9   11   12                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14    3    7   13   15                                             
CONECT   15   14                                                            
CONECT   16    7   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   23   26                                                  
CONECT   19   20                                                            
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23    6   18   22   24                                             
CONECT   24   23                                                            
CONECT   25   26                                                            
CONECT   26   18   20   25   27                                             
CONECT   27   26                                                            
CONECT   28   29                                                            
CONECT   29    1    8   28   30                                             
CONECT   30   29                                                            
CONECT   31    7                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

COMPND    HMDB0302925
HETATM    1  C1  UNL     1       4.963  -1.392  -1.839  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.069  -1.062  -0.368  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.957  -2.026   0.340  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.503   0.384  -0.259  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.772   1.149   0.816  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.275   1.221   0.601  1.00  0.00           C  
HETATM    7  C7  UNL     1       3.041   2.485  -0.240  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.518   1.333   1.852  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.161   0.786   2.014  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.645  -0.142   0.934  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.925  -1.557   1.482  1.00  0.00           C  
HETATM   12  C12 UNL     1       1.449  -0.002  -0.278  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.898   0.207  -1.444  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.569   0.328  -1.659  1.00  0.00           C  
HETATM   15  C15 UNL     1      -1.304   0.717  -0.413  1.00  0.00           C  
HETATM   16  C16 UNL     1      -2.757   0.728  -0.694  1.00  0.00           C  
HETATM   17  C17 UNL     1      -3.228   2.189  -0.572  1.00  0.00           C  
HETATM   18  C18 UNL     1      -3.035   0.220  -2.106  1.00  0.00           C  
HETATM   19  C19 UNL     1      -4.485   0.335  -2.514  1.00  0.00           C  
HETATM   20  C20 UNL     1      -5.196  -0.654  -1.619  1.00  0.00           C  
HETATM   21  O1  UNL     1      -5.847  -1.573  -2.030  1.00  0.00           O  
HETATM   22  C21 UNL     1      -5.003  -0.366  -0.208  1.00  0.00           C  
HETATM   23  C22 UNL     1      -5.961   0.793   0.117  1.00  0.00           C  
HETATM   24  C23 UNL     1      -5.528  -1.524   0.649  1.00  0.00           C  
HETATM   25  C24 UNL     1      -3.594  -0.086   0.237  1.00  0.00           C  
HETATM   26  C25 UNL     1      -2.956  -1.383   0.573  1.00  0.00           C  
HETATM   27  C26 UNL     1      -1.456  -1.458   0.445  1.00  0.00           C  
HETATM   28  C27 UNL     1      -0.840  -0.121   0.767  1.00  0.00           C  
HETATM   29  C28 UNL     1      -1.429   0.305   2.078  1.00  0.00           C  
HETATM   30  C29 UNL     1       2.916   0.005  -0.234  1.00  0.00           C  
HETATM   31  C30 UNL     1       3.655  -1.145   0.285  1.00  0.00           C  
HETATM   32  H1  UNL     1       4.859  -0.460  -2.440  1.00  0.00           H  
HETATM   33  H2  UNL     1       4.164  -2.132  -2.051  1.00  0.00           H  
HETATM   34  H3  UNL     1       5.962  -1.820  -2.134  1.00  0.00           H  
HETATM   35  H4  UNL     1       5.403  -2.977   0.465  1.00  0.00           H  
HETATM   36  H5  UNL     1       6.153  -1.648   1.366  1.00  0.00           H  
HETATM   37  H6  UNL     1       6.877  -2.231  -0.230  1.00  0.00           H  
HETATM   38  H7  UNL     1       5.433   0.931  -1.205  1.00  0.00           H  
HETATM   39  H8  UNL     1       6.570   0.370   0.041  1.00  0.00           H  
HETATM   40  H9  UNL     1       4.986   0.753   1.832  1.00  0.00           H  
HETATM   41  H10 UNL     1       5.227   2.172   0.812  1.00  0.00           H  
HETATM   42  H11 UNL     1       3.553   2.427  -1.206  1.00  0.00           H  
HETATM   43  H12 UNL     1       3.505   3.341   0.319  1.00  0.00           H  
HETATM   44  H13 UNL     1       1.969   2.688  -0.297  1.00  0.00           H  
HETATM   45  H14 UNL     1       3.219   0.938   2.659  1.00  0.00           H  
HETATM   46  H15 UNL     1       2.524   2.440   2.121  1.00  0.00           H  
HETATM   47  H16 UNL     1       0.444   1.622   2.094  1.00  0.00           H  
HETATM   48  H17 UNL     1       1.155   0.278   3.018  1.00  0.00           H  
HETATM   49  H18 UNL     1       0.850  -2.326   0.697  1.00  0.00           H  
HETATM   50  H19 UNL     1       0.200  -1.761   2.338  1.00  0.00           H  
HETATM   51  H20 UNL     1       1.893  -1.607   2.022  1.00  0.00           H  
HETATM   52  H21 UNL     1       1.518   0.298  -2.327  1.00  0.00           H  
HETATM   53  H22 UNL     1      -0.867  -0.542  -2.198  1.00  0.00           H  
HETATM   54  H23 UNL     1      -0.651   1.238  -2.336  1.00  0.00           H  
HETATM   55  H24 UNL     1      -0.904   1.750  -0.158  1.00  0.00           H  
HETATM   56  H25 UNL     1      -3.912   2.309   0.308  1.00  0.00           H  
HETATM   57  H26 UNL     1      -3.631   2.577  -1.504  1.00  0.00           H  
HETATM   58  H27 UNL     1      -2.361   2.870  -0.317  1.00  0.00           H  
HETATM   59  H28 UNL     1      -2.475   0.728  -2.887  1.00  0.00           H  
HETATM   60  H29 UNL     1      -2.862  -0.884  -2.075  1.00  0.00           H  
HETATM   61  H30 UNL     1      -4.910   1.326  -2.468  1.00  0.00           H  
HETATM   62  H31 UNL     1      -4.559  -0.041  -3.535  1.00  0.00           H  
HETATM   63  H32 UNL     1      -6.987   0.318   0.077  1.00  0.00           H  
HETATM   64  H33 UNL     1      -5.842   1.154   1.137  1.00  0.00           H  
HETATM   65  H34 UNL     1      -5.966   1.553  -0.670  1.00  0.00           H  
HETATM   66  H35 UNL     1      -5.256  -1.363   1.704  1.00  0.00           H  
HETATM   67  H36 UNL     1      -6.657  -1.463   0.630  1.00  0.00           H  
HETATM   68  H37 UNL     1      -5.284  -2.502   0.241  1.00  0.00           H  
HETATM   69  H38 UNL     1      -3.805   0.586   1.125  1.00  0.00           H  
HETATM   70  H39 UNL     1      -3.336  -2.121  -0.203  1.00  0.00           H  
HETATM   71  H40 UNL     1      -3.285  -1.844   1.530  1.00  0.00           H  
HETATM   72  H41 UNL     1      -1.139  -2.304   1.042  1.00  0.00           H  
HETATM   73  H42 UNL     1      -1.169  -1.712  -0.603  1.00  0.00           H  
HETATM   74  H43 UNL     1      -2.218  -0.418   2.465  1.00  0.00           H  
HETATM   75  H44 UNL     1      -0.745   0.264   2.954  1.00  0.00           H  
HETATM   76  H45 UNL     1      -1.776   1.358   2.080  1.00  0.00           H  
HETATM   77  H46 UNL     1       3.357   0.252  -1.258  1.00  0.00           H  
HETATM   78  H47 UNL     1       3.258  -2.142   0.128  1.00  0.00           H  
HETATM   79  H48 UNL     1       3.959  -0.936   1.363  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3    4   31
CONECT    3   35   36   37
CONECT    4    5   38   39
CONECT    5    6   40   41
CONECT    6    7    8   30
CONECT    7   42   43   44
CONECT    8    9   45   46
CONECT    9   10   47   48
CONECT   10   11   12   28
CONECT   11   49   50   51
CONECT   12   13   13   30
CONECT   13   14   52
CONECT   14   15   53   54
CONECT   15   16   28   55
CONECT   16   17   18   25
CONECT   17   56   57   58
CONECT   18   19   59   60
CONECT   19   20   61   62
CONECT   20   21   21   22
CONECT   22   23   24   25
CONECT   23   63   64   65
CONECT   24   66   67   68
CONECT   25   26   69
CONECT   26   27   70   71
CONECT   27   28   72   73
CONECT   28   29
CONECT   29   74   75   76
CONECT   30   31   77
CONECT   31   78   79
END

HMDB0302925
     RDKit          3D
beta-Amyrenone
 79 83  0  0  0  0  0  0  0  0999 V2000
    4.9627   -1.3922   -1.8390 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0686   -1.0616   -0.3676 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9569   -2.0258    0.3400 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5026    0.3837   -0.2592 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7719    1.1491    0.8163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2746    1.2209    0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0407    2.4846   -0.2398 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5180    1.3325    1.8518 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1611    0.7865    2.0143 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6450   -0.1418    0.9341 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9248   -1.5570    1.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4489   -0.0015   -0.2783 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8977    0.2071   -1.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5687    0.3283   -1.6587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3043    0.7171   -0.4129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7568    0.7281   -0.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2281    2.1889   -0.5721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0353    0.2198   -2.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4854    0.3352   -2.5144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1964   -0.6543   -1.6188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8468   -1.5733   -2.0301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0027   -0.3661   -0.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9612    0.7930    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5284   -1.5237    0.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936   -0.0856    0.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9555   -1.3832    0.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4557   -1.4581    0.4453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8403   -0.1207    0.7666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4288    0.3051    2.0785 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9164    0.0047   -0.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6551   -1.1448    0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8591   -0.4597   -2.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1641   -2.1317   -2.0509 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9617   -1.8203   -2.1344 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4030   -2.9768    0.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1525   -1.6476    1.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8773   -2.2310   -0.2297 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4332    0.9307   -1.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    0.3703    0.0407 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9857    0.7535    1.8323 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2269    2.1715    0.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5534    2.4270   -1.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5046    3.3406    0.3193 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9688    2.6878   -0.2971 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2187    0.9375    2.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5245    2.4399    2.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4445    1.6221    2.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1552    0.2782    3.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8503   -2.3265    0.6974 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2005   -1.7610    2.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8926   -1.6075    2.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5182    0.2983   -2.3270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8674   -0.5416   -2.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6507    1.2382   -2.3360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9037    1.7501   -0.1585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9122    2.3088    0.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6311    2.5767   -1.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3611    2.8699   -0.3172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4746    0.7276   -2.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8619   -0.8841   -2.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9098    1.3259   -2.4678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5586   -0.0410   -3.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9869    0.3180    0.0770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8425    1.1536    1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9657    1.5530   -0.6698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2562   -1.3629    1.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6574   -1.4632    0.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2836   -2.5016    0.2412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8051    0.5865    1.1246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3359   -2.1213   -0.2032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2847   -1.8444    1.5303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1386   -2.3040    1.0421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1690   -1.7118   -0.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2184   -0.4183    2.4650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7452    0.2640    2.9539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7760    1.3579    2.0801 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3573    0.2521   -1.2576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2577   -2.1425    0.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9590   -0.9361    1.3629 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
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 12 30  1  0
 30 31  1  0
 31  2  1  0
 30  6  1  0
 28 10  1  0
 28 15  1  0
 25 16  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
 13 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 17 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  0
 19 62  1  0
 23 63  1  0
 23 64  1  0
 23 65  1  0
 24 66  1  0
 24 67  1  0
 24 68  1  0
 25 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  0
 27 73  1  0
 29 74  1  0
 29 75  1  0
 29 76  1  0
 30 77  1  0
 31 78  1  0
 31 79  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
b-Amyrenone	Generator
Β-amyrenone	Generator

Chemical Formula

C₃₀H₄₈O

Average Molecular Weight

424.7015

Monoisotopic Molecular Weight

424.370516158

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CCC34C)C2C1

InChI Identifier

InChI=1S/C30H48O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h9,21-23H,10-19H2,1-8H3

InChI Key

LIIFBMGUDSHTOU-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

Not Available

Rosemary (FooDB: FOOD00159)

Oilseed crop

Shea tree (FooDB: FOOD00775)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	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
logP	7.66	ALOGPS
logP	7.97	ChemAxon
logS	-6.8	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	131.08 m³·mol⁻¹	ChemAxon
Polarizability	53.52 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
AllCCS	[M+H]+	215.772	32859911
AllCCS	[M+H-H2O]+	213.942	32859911
AllCCS	[M+Na]+	217.938	32859911
AllCCS	[M+NH4]+	217.456	32859911
AllCCS	[M-H]-	213.968	32859911
AllCCS	[M+Na-2H]-	215.576	32859911
AllCCS	[M+HCOO]-	217.5	32859911
DeepCCS	[M-2H]-	247.159	30932474
DeepCCS	[M+Na]+	222.387	30932474

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
beta-Amyrenone,1TMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CC=C(O[Si](C)(C)C)C(C)(C)C5CCC43C)C2C1	3348.6	Semi standard non polar	33892256
beta-Amyrenone,1TMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CC=C(O[Si](C)(C)C)C(C)(C)C5CCC43C)C2C1	3169.8	Standard non polar	33892256
beta-Amyrenone,1TMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CC=C(O[Si](C)(C)C)C(C)(C)C5CCC43C)C2C1	3337.0	Standard polar	33892256
beta-Amyrenone,1TBDMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C5CCC43C)C2C1	3584.5	Semi standard non polar	33892256
beta-Amyrenone,1TBDMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C5CCC43C)C2C1	3370.4	Standard non polar	33892256
beta-Amyrenone,1TBDMS,isomer #1	CC1(C)CCC2(C)CCC3(C)C(=CCC4C5(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C5CCC43C)C2C1	3477.9	Standard polar	33892256

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 10V, Positive-QTOF	splash10-004i-0011900000-53b648ad9a86f21667b4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 20V, Positive-QTOF	splash10-05r0-0239500000-1d3ef1fc7a2f232377e5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 40V, Positive-QTOF	splash10-1000-1229100000-5072502379fdb4ed7101	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 10V, Negative-QTOF	splash10-00di-0000900000-abf011b5b8820b80ba71	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 20V, Negative-QTOF	splash10-00di-0000900000-82263737858271c74e9c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 40V, Negative-QTOF	splash10-052f-6009700000-19a335d06219d020eaf0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 10V, Positive-QTOF	splash10-004i-0003900000-14de0215ba41189489c9	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 20V, Positive-QTOF	splash10-0a6r-0390300000-e31687656738f61e837b	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 40V, Positive-QTOF	splash10-052r-1950000000-d8682d00a763128bcac3	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 10V, Negative-QTOF	splash10-00di-0000900000-ae374dd49287e6271d4c	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 20V, Negative-QTOF	splash10-00di-0000900000-ae374dd49287e6271d4c	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Amyrenone 40V, Negative-QTOF	splash10-00di-0000900000-ae374dd49287e6271d4c	2021-10-21	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

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

FDB006919

KNApSAcK ID

Not Available

Chemspider ID

532684

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

612782

PDB ID

Not Available

ChEBI ID

Not Available

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

Not Available

Showing metabocard for beta-Amyrenone (HMDB0302925)

MOL for HMDB0302925 (beta-Amyrenone)

3D MOL for HMDB0302925 (beta-Amyrenone)

3D SDF for HMDB0302925 (beta-Amyrenone)

3D-SDF for HMDB0302925 (beta-Amyrenone)

PDB for HMDB0302925 (beta-Amyrenone)

3D PDB for HMDB0302925 (beta-Amyrenone)

SMILES for HMDB0302925 (beta-Amyrenone)

INCHI for HMDB0302925 (beta-Amyrenone)

Structure for HMDB0302925 (beta-Amyrenone)

3D Structure for HMDB0302925 (beta-Amyrenone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

MS/MS Spectra