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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:01:20 UTC

Update Date

2022-03-07 02:55:52 UTC

HMDB ID

HMDB0038687

Secondary Accession Numbers

HMDB38687

Metabolite Identification

Common Name

(ent-15beta,16beta)-15,16-Epoxy-3-kauranone

Description

(ent-15beta,16beta)-15,16-Epoxy-3-kauranone is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, (ent-15beta,16beta)-15,16-epoxy-3-kauranone has been detected, but not quantified in, cereals and cereal products. This could make (ent-15beta,16beta)-15,16-epoxy-3-kauranone a potential biomarker for the consumption of these foods.

Structure

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

HMDB0038687
     RDKit          3D
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone
 52 56  0  0  0  0  0  0  0  0999 V2000
   -3.3484    1.0373   -1.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7201    0.6619   -0.0108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0632    1.7963    0.9702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3364   -0.5590    0.5806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5468   -0.6892    0.3778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6279   -1.5733    1.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1625   -1.6920    1.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7578   -0.9241   -0.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4743   -1.6836   -1.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2549    0.4787   -0.0478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6592    1.2500   -1.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7585    1.5844   -0.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4152    0.3975   -0.1571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7467    0.1766   -0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4929   -0.3819    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8889   -1.6841    0.6221 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5033   -1.9836    0.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6873   -0.9242   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2649    0.7695    1.2048 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7499    2.0485    0.4959 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3913    1.2136    2.0732 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7442    0.4511    1.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2131    0.3385   -1.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6535    1.0683   -2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8344    2.0570   -1.3012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9576    1.5608    1.5627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2205    2.0106    1.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2811    2.7366    0.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8174   -1.3363    2.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1791   -2.5524    1.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9825   -2.7759    0.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6187   -1.3797    1.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4153   -1.2451   -1.5942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6351   -2.7465   -1.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7992   -1.7099   -2.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8342    0.8708    0.9235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6175    0.6414   -2.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1829    2.2303   -1.3700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2868    1.9913   -1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5731    2.3875    0.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1625    1.0847   -1.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907   -0.5548   -1.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5645   -0.4354    0.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1078   -1.9180    1.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5558   -2.4510    0.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4300   -2.8940   -0.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9714   -2.3598    1.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8182   -1.0527   -1.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779    2.7553    1.2763 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6421    1.8476   -0.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9536    2.6078    0.0218 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -0.5471    1.8099 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 15 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 10  2  1  0
 18 13  1  0
 22 19  1  0
 18  8  1  0
 22 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 11 37  1  0
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 14 41  1  0
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 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 22 52  1  0
M  END


  Mrv0541 05061310352D          

 22 26  0  0  0  0            999 V2000
    4.1140    3.6566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1565    3.4612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4372    1.0422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0425    1.2439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9409    0.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7355    0.7080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1166    3.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9930    1.5898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2148    1.3161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3282    2.9377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162    1.5029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2548    0.9229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8008    1.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1450    2.4006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2306    2.3293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5188    2.9377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5886    1.8532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7593    1.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1038    2.1149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9232    2.6744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4086    2.3990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  9  8  1  0  0  0  0
 10  7  1  0  0  0  0
 12  5  1  0  0  0  0
 12 11  1  0  0  0  0
 13  7  1  0  0  0  0
 14  6  1  0  0  0  0
 15  8  1  0  0  0  0
 17  1  1  0  0  0  0
 17  2  1  0  0  0  0
 17 13  1  0  0  0  0
 17 15  1  0  0  0  0
 18  3  1  0  0  0  0
 18  9  1  0  0  0  0
 18 13  1  0  0  0  0
 18 14  1  0  0  0  0
 19  4  1  0  0  0  0
 19 12  1  0  0  0  0
 19 16  1  0  0  0  0
 20 10  1  0  0  0  0
 20 11  1  0  0  0  0
 20 14  1  0  0  0  0
 20 16  1  0  0  0  0
 21 15  2  0  0  0  0
 22 16  1  0  0  0  0
 22 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038687

> <DATABASE_NAME>
hmdb

> <SMILES>
CC12OC1C13CC2CCC1C1(C)CCC(=O)C(C)(C)C1CC3

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O2/c1-17(2)13-7-10-20-11-12(19(4)16(20)22-19)5-6-14(20)18(13,3)9-8-15(17)21/h12-14,16H,5-11H2,1-4H3

> <INCHI_KEY>
SVKMTDSTFGJBCS-UHFFFAOYSA-N

> <FORMULA>
C20H30O2

> <MOLECULAR_WEIGHT>
302.451

> <EXACT_MASS>
302.224580204

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
35.16396122520008

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,5,9,14-tetramethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-6-one

> <ALOGPS_LOGP>
3.73

> <JCHEM_LOGP>
4.2240008153333335

> <ALOGPS_LOGS>
-5.62

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.9610891235682

> <JCHEM_PKA_STRONGEST_BASIC>
-4.230309350977825

> <JCHEM_POLAR_SURFACE_AREA>
29.6

> <JCHEM_REFRACTIVITY>
85.94159999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.31e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,5,9,14-tetramethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-6-one

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0038687
     RDKit          3D
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone
 52 56  0  0  0  0  0  0  0  0999 V2000
   -3.3484    1.0373   -1.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7201    0.6619   -0.0108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0632    1.7963    0.9702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3364   -0.5590    0.5806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5468   -0.6892    0.3778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6279   -1.5733    1.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1625   -1.6920    1.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7578   -0.9241   -0.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4743   -1.6836   -1.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2549    0.4787   -0.0478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6592    1.2500   -1.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7585    1.5844   -0.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4152    0.3975   -0.1571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7467    0.1766   -0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4929   -0.3819    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8889   -1.6841    0.6221 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5033   -1.9836    0.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6873   -0.9242   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2649    0.7695    1.2048 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7499    2.0485    0.4959 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3913    1.2136    2.0732 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7442    0.4511    1.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2131    0.3385   -1.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6535    1.0683   -2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8344    2.0570   -1.3012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9576    1.5608    1.5627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2205    2.0106    1.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2811    2.7366    0.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6351   -2.7465   -1.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7992   -1.7099   -2.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8342    0.8708    0.9235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6175    0.6414   -2.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2868    1.9913   -1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5731    2.3875    0.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1625    1.0847   -1.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907   -0.5548   -1.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5645   -0.4354    0.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1078   -1.9180    1.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5558   -2.4510    0.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4300   -2.8940   -0.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9714   -2.3598    1.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8182   -1.0527   -1.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779    2.7553    1.2763 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6421    1.8476   -0.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9536    2.6078    0.0218 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -0.5471    1.8099 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
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 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 15 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 10  2  1  0
 18 13  1  0
 22 19  1  0
 18  8  1  0
 22 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 22 52  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       7.680   6.826   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.625   6.461   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.416   1.946   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.079   2.322   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.623   0.732   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.106   1.322   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.818   5.992   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.320   2.968   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.868   2.457   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.346   5.484   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.204   2.805   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.342   1.723   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.983   4.973   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.228   2.939   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.604   4.481   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.297   4.348   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.435   5.484   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.699   3.459   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.417   3.084   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.927   3.948   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.057   4.992   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.763   4.478   0.000  0.00  0.00           O+0
CONECT    1   17                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   19                                                            
CONECT    5    6   12                                                       
CONECT    6    5   14                                                       
CONECT    7   10   13                                                       
CONECT    8    9   15                                                       
CONECT    9    8   18                                                       
CONECT   10    7   20                                                       
CONECT   11   12   20                                                       
CONECT   12    5   11   19                                                  
CONECT   13    7   17   18                                                  
CONECT   14    6   18   20                                                  
CONECT   15    8   17   21                                                  
CONECT   16   19   20   22                                                  
CONECT   17    1    2   13   15                                             
CONECT   18    3    9   13   14                                             
CONECT   19    4   12   16   22                                             
CONECT   20   10   11   14   16                                             
CONECT   21   15                                                            
CONECT   22   16   19                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   52    0
END

COMPND    HMDB0038687
HETATM    1  C1  UNL     1      -3.348   1.037  -1.323  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.720   0.662  -0.011  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.063   1.796   0.970  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.336  -0.559   0.581  1.00  0.00           C  
HETATM    5  O1  UNL     1      -4.547  -0.689   0.378  1.00  0.00           O  
HETATM    6  C5  UNL     1      -2.628  -1.573   1.356  1.00  0.00           C  
HETATM    7  C6  UNL     1      -1.163  -1.692   1.086  1.00  0.00           C  
HETATM    8  C7  UNL     1      -0.758  -0.924  -0.173  1.00  0.00           C  
HETATM    9  C8  UNL     1      -1.474  -1.684  -1.299  1.00  0.00           C  
HETATM   10  C9  UNL     1      -1.255   0.479  -0.048  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.659   1.250  -1.236  1.00  0.00           C  
HETATM   12  C11 UNL     1       0.758   1.584  -0.743  1.00  0.00           C  
HETATM   13  C12 UNL     1       1.415   0.398  -0.157  1.00  0.00           C  
HETATM   14  C13 UNL     1       2.747   0.177  -0.906  1.00  0.00           C  
HETATM   15  C14 UNL     1       3.493  -0.382   0.322  1.00  0.00           C  
HETATM   16  C15 UNL     1       2.889  -1.684   0.622  1.00  0.00           C  
HETATM   17  C16 UNL     1       1.503  -1.984   0.231  1.00  0.00           C  
HETATM   18  C17 UNL     1       0.687  -0.924  -0.453  1.00  0.00           C  
HETATM   19  C18 UNL     1       3.265   0.770   1.205  1.00  0.00           C  
HETATM   20  C19 UNL     1       3.750   2.049   0.496  1.00  0.00           C  
HETATM   21  O2  UNL     1       2.391   1.214   2.073  1.00  0.00           O  
HETATM   22  C20 UNL     1       1.744   0.451   1.267  1.00  0.00           C  
HETATM   23  H1  UNL     1      -4.213   0.339  -1.487  1.00  0.00           H  
HETATM   24  H2  UNL     1      -2.654   1.068  -2.170  1.00  0.00           H  
HETATM   25  H3  UNL     1      -3.834   2.057  -1.301  1.00  0.00           H  
HETATM   26  H4  UNL     1      -3.958   1.561   1.563  1.00  0.00           H  
HETATM   27  H5  UNL     1      -2.221   2.011   1.645  1.00  0.00           H  
HETATM   28  H6  UNL     1      -3.281   2.737   0.416  1.00  0.00           H  
HETATM   29  H7  UNL     1      -2.817  -1.336   2.446  1.00  0.00           H  
HETATM   30  H8  UNL     1      -3.179  -2.552   1.220  1.00  0.00           H  
HETATM   31  H9  UNL     1      -0.982  -2.776   0.813  1.00  0.00           H  
HETATM   32  H10 UNL     1      -0.619  -1.380   1.975  1.00  0.00           H  
HETATM   33  H11 UNL     1      -2.415  -1.245  -1.594  1.00  0.00           H  
HETATM   34  H12 UNL     1      -1.635  -2.747  -1.037  1.00  0.00           H  
HETATM   35  H13 UNL     1      -0.799  -1.710  -2.205  1.00  0.00           H  
HETATM   36  H14 UNL     1      -0.834   0.871   0.924  1.00  0.00           H  
HETATM   37  H15 UNL     1      -0.618   0.641  -2.136  1.00  0.00           H  
HETATM   38  H16 UNL     1      -1.183   2.230  -1.370  1.00  0.00           H  
HETATM   39  H17 UNL     1       1.287   1.991  -1.626  1.00  0.00           H  
HETATM   40  H18 UNL     1       0.573   2.387   0.032  1.00  0.00           H  
HETATM   41  H19 UNL     1       3.162   1.085  -1.301  1.00  0.00           H  
HETATM   42  H20 UNL     1       2.691  -0.555  -1.704  1.00  0.00           H  
HETATM   43  H21 UNL     1       4.564  -0.435   0.053  1.00  0.00           H  
HETATM   44  H22 UNL     1       3.108  -1.918   1.711  1.00  0.00           H  
HETATM   45  H23 UNL     1       3.556  -2.451   0.107  1.00  0.00           H  
HETATM   46  H24 UNL     1       1.430  -2.894  -0.444  1.00  0.00           H  
HETATM   47  H25 UNL     1       0.971  -2.360   1.160  1.00  0.00           H  
HETATM   48  H26 UNL     1       0.818  -1.053  -1.571  1.00  0.00           H  
HETATM   49  H27 UNL     1       4.178   2.755   1.276  1.00  0.00           H  
HETATM   50  H28 UNL     1       4.642   1.848  -0.146  1.00  0.00           H  
HETATM   51  H29 UNL     1       2.954   2.608   0.022  1.00  0.00           H  
HETATM   52  H30 UNL     1       1.616  -0.547   1.810  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3    4   10
CONECT    3   26   27   28
CONECT    4    5    5    6
CONECT    6    7   29   30
CONECT    7    8   31   32
CONECT    8    9   10   18
CONECT    9   33   34   35
CONECT   10   11   36
CONECT   11   12   37   38
CONECT   12   13   39   40
CONECT   13   14   18   22
CONECT   14   15   41   42
CONECT   15   16   19   43
CONECT   16   17   44   45
CONECT   17   18   46   47
CONECT   18   48
CONECT   19   20   21   22
CONECT   20   49   50   51
CONECT   21   22
CONECT   22   52
END

HMDB0038687
     RDKit          3D
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone
 52 56  0  0  0  0  0  0  0  0999 V2000
   -3.3484    1.0373   -1.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7201    0.6619   -0.0108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0632    1.7963    0.9702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3364   -0.5590    0.5806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5468   -0.6892    0.3778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6279   -1.5733    1.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1625   -1.6920    1.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7578   -0.9241   -0.1733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4743   -1.6836   -1.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2549    0.4787   -0.0478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6592    1.2500   -1.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7585    1.5844   -0.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4152    0.3975   -0.1571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7467    0.1766   -0.9061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4929   -0.3819    0.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8889   -1.6841    0.6221 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5033   -1.9836    0.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6873   -0.9242   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2649    0.7695    1.2048 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7499    2.0485    0.4959 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3913    1.2136    2.0732 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7442    0.4511    1.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2131    0.3385   -1.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6535    1.0683   -2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8344    2.0570   -1.3012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9576    1.5608    1.5627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2205    2.0106    1.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2811    2.7366    0.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8174   -1.3363    2.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1791   -2.5524    1.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9825   -2.7759    0.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6187   -1.3797    1.9747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4153   -1.2451   -1.5942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6351   -2.7465   -1.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7992   -1.7099   -2.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8342    0.8708    0.9235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6175    0.6414   -2.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1829    2.2303   -1.3700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2868    1.9913   -1.6264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5731    2.3875    0.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1625    1.0847   -1.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907   -0.5548   -1.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5645   -0.4354    0.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1078   -1.9180    1.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5558   -2.4510    0.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4300   -2.8940   -0.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9714   -2.3598    1.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8182   -1.0527   -1.5707 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779    2.7553    1.2763 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6421    1.8476   -0.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9536    2.6078    0.0218 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6160   -0.5471    1.8099 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 15 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 10  2  1  0
 18 13  1  0
 22 19  1  0
 18  8  1  0
 22 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  7 32  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 22 52  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(ent-15b,16b)-15,16-Epoxy-3-kauranone	Generator
(ent-15Β,16β)-15,16-epoxy-3-kauranone	Generator

Chemical Formula

C₂₀H₃₀O₂

Average Molecular Weight

302.451

Monoisotopic Molecular Weight

302.224580204

IUPAC Name

5,5,9,14-tetramethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-6-one

Traditional Name

5,5,9,14-tetramethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-6-one

CAS Registry Number

140636-10-8

SMILES

CC12OC1C13CC2CCC1C1(C)CCC(=O)C(C)(C)C1CC3

InChI Identifier

InChI=1S/C20H30O2/c1-17(2)13-7-10-20-11-12(19(4)16(20)22-19)5-6-14(20)18(13,3)9-8-15(17)21/h12-14,16H,5-11H2,1-4H3

InChI Key

SVKMTDSTFGJBCS-UHFFFAOYSA-N

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Oxane
Cyclic ketone
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0038687)
Cell membrane (HMDB: HMDB0038687)

Cellular substructure

Extracellular (HMDB: HMDB0038687)
Membrane (HMDB: HMDB0038687)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038687)

Source

Endogenous

Endogenous (HMDB: HMDB0038687)

Plant

Poaceae (HMDB: HMDB0038687)

Animal

Animal (HMDB: HMDB0038687)

Exogenous

Food

Food (HMDB: HMDB0038687)

Cereal and cereal product

Cereal product

Breakfast cereal (FooDB: FOOD00270)

Cereals and cereal products (FooDB: FOOD00858)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0038687)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0038687)

Cellular process

Cell signaling (HMDB: HMDB0038687)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0038687)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0038687)

Nutrient

Nutrient (HMDB: HMDB0038687)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038687)

Emulsifier (HMDB: HMDB0038687)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	134 - 136 °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	0.00073 g/L	ALOGPS
logP	3.73	ALOGPS
logP	4.22	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	19.96	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	29.6 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	85.94 m³·mol⁻¹	ChemAxon
Polarizability	35.16 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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]+	169.694	31661259
DarkChem	[M-H]-	166.759	31661259
DeepCCS	[M-2H]-	204.826	30932474
DeepCCS	[M+Na]+	180.053	30932474
AllCCS	[M+H]+	176.8	32859911
AllCCS	[M+H-H2O]+	173.9	32859911
AllCCS	[M+NH4]+	179.6	32859911
AllCCS	[M+Na]+	180.4	32859911
AllCCS	[M-H]-	184.3	32859911
AllCCS	[M+Na-2H]-	184.3	32859911
AllCCS	[M+HCOO]-	184.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone	CC12OC1C13CC2CCC1C1(C)CCC(=O)C(C)(C)C1CC3	2902.0	Standard polar	33892256
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone	CC12OC1C13CC2CCC1C1(C)CCC(=O)C(C)(C)C1CC3	2245.1	Standard non polar	33892256
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone	CC12OC1C13CC2CCC1C1(C)CCC(=O)C(C)(C)C1CC3	2481.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone,1TMS,isomer #1	CC1(C)C(O[Si](C)(C)C)=CCC2(C)C1CCC13CC(CCC21)C1(C)OC31	2430.9	Semi standard non polar	33892256
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone,1TMS,isomer #1	CC1(C)C(O[Si](C)(C)C)=CCC2(C)C1CCC13CC(CCC21)C1(C)OC31	2397.5	Standard non polar	33892256
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone,1TBDMS,isomer #1	CC1(C)C(O[Si](C)(C)C(C)(C)C)=CCC2(C)C1CCC13CC(CCC21)C1(C)OC31	2667.8	Semi standard non polar	33892256
(ent-15beta,16beta)-15,16-Epoxy-3-kauranone,1TBDMS,isomer #1	CC1(C)C(O[Si](C)(C)C(C)(C)C)=CCC2(C)C1CCC13CC(CCC21)C1(C)OC31	2586.4	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone GC-MS (Non-derivatized) - 70eV, Positive	splash10-006t-1490000000-8c7d34e177ccb101435c	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 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 - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 10V, Positive-QTOF	splash10-0udi-0139000000-df08a5544cf1b89815a7	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 20V, Positive-QTOF	splash10-0udr-1392000000-bef8b0f20d218db9e875	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 40V, Positive-QTOF	splash10-029f-9730000000-98b1ed3de81f04367f7c	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 10V, Negative-QTOF	splash10-0udi-0019000000-321b591167711101826a	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 20V, Negative-QTOF	splash10-0udi-1019000000-72749b42ef110acad8eb	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 40V, Negative-QTOF	splash10-00ku-5190000000-aa802ba146526f73e557	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 10V, Positive-QTOF	splash10-0udi-0029000000-bc9dbc3f9d11ec4d40cf	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 20V, Positive-QTOF	splash10-0f79-0965000000-d3a399454ecbd02d095b	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 40V, Positive-QTOF	splash10-0uy0-1920000000-91a79bb3b18ba7ed8a37	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 10V, Negative-QTOF	splash10-0udi-0009000000-16d58525184e918518fa	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 20V, Negative-QTOF	splash10-0udi-0009000000-16d58525184e918518fa	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (ent-15beta,16beta)-15,16-Epoxy-3-kauranone 40V, Negative-QTOF	splash10-0udi-0059000000-455bf58967105e7e4497	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB018091

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752427

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

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 (ent-15beta,16beta)-15,16-Epoxy-3-kauranone (HMDB0038687)

MOL for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

3D MOL for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

3D SDF for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

3D-SDF for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

PDB for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

3D PDB for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

SMILES for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

INCHI for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

Structure for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

3D Structure for HMDB0038687 ((ent-15beta,16beta)-15,16-Epoxy-3-kauranone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra