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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:49:49 UTC

Update Date

2022-03-07 02:55:01 UTC

HMDB ID

HMDB0036665

Secondary Accession Numbers

HMDB36665

Metabolite Identification

Common Name

Blumealactone A

Description

Blumealactone A belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Based on a literature review a small amount of articles have been published on Blumealactone A.

Structure

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


  Mrv0541 05061309162D          

 26 28  0  0  0  0            999 V2000
    0.3232    4.1336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6513    3.1545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8558   -1.4343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116    2.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8643    0.9460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2312    3.3137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5277   -0.4553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2837   -0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1364    0.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8953    2.8242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9477   -0.6145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3919    1.8081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1316    1.0253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7037   -0.2841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7956    0.5357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3756    0.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7115    1.1844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8034    2.0043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2169    1.8024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0445    0.8541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3678   -0.7737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0024    2.1814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7064    2.4665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4664    1.0160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4675    1.5148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0474    1.6740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  8  7  1  0  0  0  0
  9  7  1  0  0  0  0
 10  2  1  0  0  0  0
 10  6  2  0  0  0  0
 11  3  1  0  0  0  0
 11  8  1  0  0  0  0
 12  4  2  0  0  0  0
 13 12  1  0  0  0  0
 14 11  1  0  0  0  0
 15 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 13  1  0  0  0  0
 17 16  1  0  0  0  0
 18 10  1  0  0  0  0
 19 12  1  0  0  0  0
 20  5  1  0  0  0  0
 20  9  1  0  0  0  0
 20 17  1  0  0  0  0
 21 14  1  0  0  0  0
 22 18  2  0  0  0  0
 23 19  2  0  0  0  0
 24 15  1  0  0  0  0
 24 19  1  0  0  0  0
 25 16  1  0  0  0  0
 25 18  1  0  0  0  0
 26 17  1  0  0  0  0
 26 20  1  0  0  0  0
M  END

HMDB0036665
     RDKit          3D
Blumealactone A
 54 56  0  0  0  0  0  0  0  0999 V2000
    1.4452   -2.7529    0.9334 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2528   -2.1996    1.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7602   -2.5580    2.0336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6082   -2.9334    3.2098 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9584   -2.3780    1.3572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8331   -1.2126    0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7959   -1.3511   -0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4747   -2.5992   -0.5489 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8989   -0.3313   -0.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6216   -0.4002   -1.8998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4741    1.0791   -0.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3119    1.5264   -1.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3260    2.4260   -0.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7787    2.2906    0.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2944    3.6214    1.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1895    1.4150    1.8580 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0160    1.1295    1.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3156    0.1145    0.2698 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7038   -0.1970    0.3467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6429    0.1996   -0.5927 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2375    0.8716   -1.5776 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0488   -0.1218   -0.4894 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0079    0.3193   -1.5279 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5015   -0.8148    0.5340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9666   -1.1551    0.6495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4091   -1.1440    0.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1565   -2.4713    0.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7384   -3.5175    1.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2605   -0.4298    1.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2631   -1.3946   -1.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8665   -3.2889   -0.8915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6143   -0.6495    0.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8925   -0.4786   -2.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2419   -1.3357   -1.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2798    0.4722   -2.0177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4144    1.1813    0.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3916    1.7005   -0.4967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9051    0.6052   -1.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7278    2.0608   -1.9450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7707    3.4739   -0.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4676    2.5149   -1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673    4.3075    1.5557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1360    3.4337    2.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5221    4.0009    0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8365    1.2834    2.0688 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2867    0.6980   -0.7177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6635    0.0689   -2.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1461    1.4177   -1.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9905   -0.1632   -1.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7981   -1.1263    1.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2100   -1.8438   -0.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1170   -1.6086    1.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5786   -0.2280    0.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3207   -1.5266   -0.8498 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 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  2  0
 24 25  1  0
 18 26  1  0
 26  2  1  0
 26  6  1  0
 17 14  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  7 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 15 42  1  0
 15 43  1  0
 15 44  1  0
 17 45  1  0
 18 46  1  0
 23 47  1  0
 23 48  1  0
 23 49  1  0
 24 50  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 26 54  1  0
M  END


  Mrv0541 05061309162D          

 26 28  0  0  0  0            999 V2000
    0.3232    4.1336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6513    3.1545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8558   -1.4343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116    2.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8643    0.9460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2312    3.3137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5277   -0.4553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2837   -0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1364    0.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8953    2.8242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9477   -0.6145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3919    1.8081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1316    1.0253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7037   -0.2841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7956    0.5357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3756    0.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7115    1.1844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8034    2.0043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2169    1.8024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0445    0.8541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3678   -0.7737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0024    2.1814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7064    2.4665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4664    1.0160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4675    1.5148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0474    1.6740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  8  7  1  0  0  0  0
  9  7  1  0  0  0  0
 10  2  1  0  0  0  0
 10  6  2  0  0  0  0
 11  3  1  0  0  0  0
 11  8  1  0  0  0  0
 12  4  2  0  0  0  0
 13 12  1  0  0  0  0
 14 11  1  0  0  0  0
 15 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 13  1  0  0  0  0
 17 16  1  0  0  0  0
 18 10  1  0  0  0  0
 19 12  1  0  0  0  0
 20  5  1  0  0  0  0
 20  9  1  0  0  0  0
 20 17  1  0  0  0  0
 21 14  1  0  0  0  0
 22 18  2  0  0  0  0
 23 19  2  0  0  0  0
 24 15  1  0  0  0  0
 24 19  1  0  0  0  0
 25 16  1  0  0  0  0
 25 18  1  0  0  0  0
 26 17  1  0  0  0  0
 26 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036665

> <DATABASE_NAME>
hmdb

> <SMILES>
C\C=C(/C)C(=O)OC1C2OC2(C)CCCC(C)C(O)C2OC(=O)C(=C)C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O6/c1-6-10(2)18(22)25-16-13-12(4)19(23)24-15(13)14(21)11(3)8-7-9-20(5)17(16)26-20/h6,11,13-17,21H,4,7-9H2,1-3,5H3/b10-6+

> <INCHI_KEY>
ZMXFZZOCUKHAFO-UXBLZVDNSA-N

> <FORMULA>
C20H28O6

> <MOLECULAR_WEIGHT>
364.4327

> <EXACT_MASS>
364.188588628

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
39.182281409570145

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradecan-2-yl (2E)-2-methylbut-2-enoate

> <ALOGPS_LOGP>
2.70

> <JCHEM_LOGP>
3.3476976373333334

> <ALOGPS_LOGS>
-3.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.762343152018158

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.2157170183058685

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2735816322894733

> <JCHEM_POLAR_SURFACE_AREA>
85.36

> <JCHEM_REFRACTIVITY>
94.38789999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.60e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradecan-2-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0036665
     RDKit          3D
Blumealactone A
 54 56  0  0  0  0  0  0  0  0999 V2000
    1.4452   -2.7529    0.9334 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2528   -2.1996    1.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7602   -2.5580    2.0336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6082   -2.9334    3.2098 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9584   -2.3780    1.3572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8331   -1.2126    0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7959   -1.3511   -0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4747   -2.5992   -0.5489 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8989   -0.3313   -0.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6216   -0.4002   -1.8998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4741    1.0791   -0.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3119    1.5264   -1.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3260    2.4260   -0.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7787    2.2906    0.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2944    3.6214    1.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1895    1.4150    1.8580 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0160    1.1295    1.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3156    0.1145    0.2698 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7038   -0.1970    0.3467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6429    0.1996   -0.5927 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2375    0.8716   -1.5776 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0488   -0.1218   -0.4894 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0079    0.3193   -1.5279 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5015   -0.8148    0.5340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9666   -1.1551    0.6495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4091   -1.1440    0.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1565   -2.4713    0.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7384   -3.5175    1.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2605   -0.4298    1.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2631   -1.3946   -1.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8665   -3.2889   -0.8915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6143   -0.6495    0.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8925   -0.4786   -2.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2419   -1.3357   -1.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2798    0.4722   -2.0177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4144    1.1813    0.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3916    1.7005   -0.4967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9051    0.6052   -1.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7278    2.0608   -1.9450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7707    3.4739   -0.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4676    2.5149   -1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673    4.3075    1.5557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1360    3.4337    2.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5221    4.0009    0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8365    1.2834    2.0688 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2867    0.6980   -0.7177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6635    0.0689   -2.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1461    1.4177   -1.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9905   -0.1632   -1.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7981   -1.1263    1.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2100   -1.8438   -0.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1170   -1.6086    1.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5786   -0.2280    0.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3207   -1.5266   -0.8498 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 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  2  0
 24 25  1  0
 18 26  1  0
 26  2  1  0
 26  6  1  0
 17 14  1  0
  1 27  1  0
  1 28  1  0
  6 29  1  0
  7 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 15 42  1  0
 15 43  1  0
 15 44  1  0
 17 45  1  0
 18 46  1  0
 23 47  1  0
 23 48  1  0
 23 49  1  0
 24 50  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 26 54  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       0.603   7.716   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.082   5.888   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.464  -2.677   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.568   4.627   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.613   1.766   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.432   6.186   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.985  -0.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.396  -0.233   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.255   0.064   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.671   5.272   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.636  -1.147   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.465   3.375   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.979   1.914   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.047  -0.530   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.218   1.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.568   1.297   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.328   2.211   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.500   3.741   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.005   3.364   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.083   1.594   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.287  -1.444   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -0.004   4.072   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       6.919   4.604   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.471   1.897   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       2.739   2.828   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.088   3.125   0.000  0.00  0.00           O+0
CONECT    1    6                                                            
CONECT    2   10                                                            
CONECT    3   11                                                            
CONECT    4   12                                                            
CONECT    5   20                                                            
CONECT    6    1   10                                                       
CONECT    7    8    9                                                       
CONECT    8    7   11                                                       
CONECT    9    7   20                                                       
CONECT   10    2    6   18                                                  
CONECT   11    3    8   14                                                  
CONECT   12    4   13   19                                                  
CONECT   13   12   15   16                                                  
CONECT   14   11   15   21                                                  
CONECT   15   13   14   24                                                  
CONECT   16   13   17   25                                                  
CONECT   17   16   20   26                                                  
CONECT   18   10   22   25                                                  
CONECT   19   12   23   24                                                  
CONECT   20    5    9   17   26                                             
CONECT   21   14                                                            
CONECT   22   18                                                            
CONECT   23   19                                                            
CONECT   24   15   19                                                       
CONECT   25   16   18                                                       
CONECT   26   17   20                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

COMPND    HMDB0036665
HETATM    1  C1  UNL     1       1.445  -2.753   0.933  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.253  -2.200   1.024  1.00  0.00           C  
HETATM    3  C3  UNL     1      -0.760  -2.558   2.034  1.00  0.00           C  
HETATM    4  O1  UNL     1      -0.608  -2.933   3.210  1.00  0.00           O  
HETATM    5  O2  UNL     1      -1.958  -2.378   1.357  1.00  0.00           O  
HETATM    6  C4  UNL     1      -1.833  -1.213   0.559  1.00  0.00           C  
HETATM    7  C5  UNL     1      -2.796  -1.351  -0.600  1.00  0.00           C  
HETATM    8  O3  UNL     1      -3.475  -2.599  -0.549  1.00  0.00           O  
HETATM    9  C6  UNL     1      -3.899  -0.331  -0.556  1.00  0.00           C  
HETATM   10  C7  UNL     1      -4.622  -0.400  -1.900  1.00  0.00           C  
HETATM   11  C8  UNL     1      -3.474   1.079  -0.240  1.00  0.00           C  
HETATM   12  C9  UNL     1      -2.312   1.526  -1.024  1.00  0.00           C  
HETATM   13  C10 UNL     1      -1.326   2.426  -0.435  1.00  0.00           C  
HETATM   14  C11 UNL     1      -0.779   2.291   0.898  1.00  0.00           C  
HETATM   15  C12 UNL     1      -0.294   3.621   1.528  1.00  0.00           C  
HETATM   16  O4  UNL     1      -1.190   1.415   1.858  1.00  0.00           O  
HETATM   17  C13 UNL     1       0.016   1.130   1.302  1.00  0.00           C  
HETATM   18  C14 UNL     1       0.316   0.114   0.270  1.00  0.00           C  
HETATM   19  O5  UNL     1       1.704  -0.197   0.347  1.00  0.00           O  
HETATM   20  C15 UNL     1       2.643   0.200  -0.593  1.00  0.00           C  
HETATM   21  O6  UNL     1       2.237   0.872  -1.578  1.00  0.00           O  
HETATM   22  C16 UNL     1       4.049  -0.122  -0.489  1.00  0.00           C  
HETATM   23  C17 UNL     1       5.008   0.319  -1.528  1.00  0.00           C  
HETATM   24  C18 UNL     1       4.501  -0.815   0.534  1.00  0.00           C  
HETATM   25  C19 UNL     1       5.967  -1.155   0.650  1.00  0.00           C  
HETATM   26  C20 UNL     1      -0.409  -1.144   0.218  1.00  0.00           C  
HETATM   27  H1  UNL     1       2.156  -2.471   0.188  1.00  0.00           H  
HETATM   28  H2  UNL     1       1.738  -3.518   1.628  1.00  0.00           H  
HETATM   29  H3  UNL     1      -2.260  -0.430   1.206  1.00  0.00           H  
HETATM   30  H4  UNL     1      -2.263  -1.395  -1.574  1.00  0.00           H  
HETATM   31  H5  UNL     1      -2.866  -3.289  -0.891  1.00  0.00           H  
HETATM   32  H6  UNL     1      -4.614  -0.649   0.230  1.00  0.00           H  
HETATM   33  H7  UNL     1      -3.893  -0.479  -2.709  1.00  0.00           H  
HETATM   34  H8  UNL     1      -5.242  -1.336  -1.861  1.00  0.00           H  
HETATM   35  H9  UNL     1      -5.280   0.472  -2.018  1.00  0.00           H  
HETATM   36  H10 UNL     1      -3.414   1.181   0.850  1.00  0.00           H  
HETATM   37  H11 UNL     1      -4.392   1.701  -0.497  1.00  0.00           H  
HETATM   38  H12 UNL     1      -1.905   0.605  -1.543  1.00  0.00           H  
HETATM   39  H13 UNL     1      -2.728   2.061  -1.945  1.00  0.00           H  
HETATM   40  H14 UNL     1      -1.771   3.474  -0.515  1.00  0.00           H  
HETATM   41  H15 UNL     1      -0.468   2.515  -1.171  1.00  0.00           H  
HETATM   42  H16 UNL     1      -1.167   4.307   1.556  1.00  0.00           H  
HETATM   43  H17 UNL     1       0.136   3.434   2.518  1.00  0.00           H  
HETATM   44  H18 UNL     1       0.522   4.001   0.878  1.00  0.00           H  
HETATM   45  H19 UNL     1       0.836   1.283   2.069  1.00  0.00           H  
HETATM   46  H20 UNL     1       0.287   0.698  -0.718  1.00  0.00           H  
HETATM   47  H21 UNL     1       4.664   0.069  -2.553  1.00  0.00           H  
HETATM   48  H22 UNL     1       5.146   1.418  -1.395  1.00  0.00           H  
HETATM   49  H23 UNL     1       5.990  -0.163  -1.401  1.00  0.00           H  
HETATM   50  H24 UNL     1       3.798  -1.126   1.285  1.00  0.00           H  
HETATM   51  H25 UNL     1       6.210  -1.844  -0.181  1.00  0.00           H  
HETATM   52  H26 UNL     1       6.117  -1.609   1.633  1.00  0.00           H  
HETATM   53  H27 UNL     1       6.579  -0.228   0.552  1.00  0.00           H  
HETATM   54  H28 UNL     1      -0.321  -1.527  -0.850  1.00  0.00           H  
CONECT    1    2    2   27   28
CONECT    2    3   26
CONECT    3    4    4    5
CONECT    5    6
CONECT    6    7   26   29
CONECT    7    8    9   30
CONECT    8   31
CONECT    9   10   11   32
CONECT   10   33   34   35
CONECT   11   12   36   37
CONECT   12   13   38   39
CONECT   13   14   40   41
CONECT   14   15   16   17
CONECT   15   42   43   44
CONECT   16   17
CONECT   17   18   45
CONECT   18   19   26   46
CONECT   19   20
CONECT   20   21   21   22
CONECT   22   23   24   24
CONECT   23   47   48   49
CONECT   24   25   50
CONECT   25   51   52   53
CONECT   26   54
END

HMDB0036665
     RDKit          3D
Blumealactone A
 54 56  0  0  0  0  0  0  0  0999 V2000
    1.4452   -2.7529    0.9334 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2528   -2.1996    1.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7602   -2.5580    2.0336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6082   -2.9334    3.2098 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9584   -2.3780    1.3572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8331   -1.2126    0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7959   -1.3511   -0.5998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4747   -2.5992   -0.5489 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8989   -0.3313   -0.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6216   -0.4002   -1.8998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4741    1.0791   -0.2401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3119    1.5264   -1.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3260    2.4260   -0.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7787    2.2906    0.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2944    3.6214    1.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1895    1.4150    1.8580 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0160    1.1295    1.3021 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3156    0.1145    0.2698 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7038   -0.1970    0.3467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6429    0.1996   -0.5927 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2375    0.8716   -1.5776 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0488   -0.1218   -0.4894 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0079    0.3193   -1.5279 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5015   -0.8148    0.5340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9666   -1.1551    0.6495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4091   -1.1440    0.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1565   -2.4713    0.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7384   -3.5175    1.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2605   -0.4298    1.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2631   -1.3946   -1.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8665   -3.2889   -0.8915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6143   -0.6495    0.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8925   -0.4786   -2.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2419   -1.3357   -1.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2798    0.4722   -2.0177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4144    1.1813    0.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3916    1.7005   -0.4967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9051    0.6052   -1.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7278    2.0608   -1.9450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7707    3.4739   -0.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4676    2.5149   -1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1673    4.3075    1.5557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1360    3.4337    2.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5221    4.0009    0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8365    1.2834    2.0688 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2867    0.6980   -0.7177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6635    0.0689   -2.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1461    1.4177   -1.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9905   -0.1632   -1.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7981   -1.1263    1.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2100   -1.8438   -0.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1170   -1.6086    1.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5786   -0.2280    0.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3207   -1.5266   -0.8498 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
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  1 27  1  0
  1 28  1  0
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  7 30  1  0
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M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(-)-Blumealactone a	HMDB
10-Hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradecan-2-yl (2E)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₈O₆

Average Molecular Weight

364.4327

Monoisotopic Molecular Weight

364.188588628

IUPAC Name

10-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradecan-2-yl (2E)-2-methylbut-2-enoate

Traditional Name

10-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradecan-2-yl (2E)-2-methylbut-2-enoate

CAS Registry Number

111545-46-1

SMILES

C\C=C(/C)C(=O)OC1C2OC2(C)CCCC(C)C(O)C2OC(=O)C(=C)C12

InChI Identifier

InChI=1S/C20H28O6/c1-6-10(2)18(22)25-16-13-12(4)19(23)24-15(13)14(21)11(3)8-7-9-20(5)17(16)26-20/h6,11,13-17,21H,4,7-9H2,1-3,5H3/b10-6+

InChI Key

ZMXFZZOCUKHAFO-UXBLZVDNSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Germacrane sesquiterpenoid
Sesquiterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Gamma butyrolactone
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Tetrahydrofuran
Enoate ester
Secondary alcohol
Lactone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0036665)
Cell membrane (HMDB: HMDB0036665)

Cellular substructure

Extracellular (HMDB: HMDB0036665)
Membrane (HMDB: HMDB0036665)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036665)

Source

Endogenous

Endogenous (HMDB: HMDB0036665)

Plant

Plant (HMDB: HMDB0036665)

Animal

Animal (HMDB: HMDB0036665)

Exogenous

Food

Food (HMDB: HMDB0036665)

Tea

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0036665)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0036665)

Cellular process

Cell signaling (HMDB: HMDB0036665)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0036665)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0036665)

Nutrient

Nutrient (HMDB: HMDB0036665)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036665)

Emulsifier (HMDB: HMDB0036665)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	205 - 208 °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	0.36 g/L	ALOGPS
logP	2.7	ALOGPS
logP	3.35	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	5.22	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	85.36 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	94.39 m³·mol⁻¹	ChemAxon
Polarizability	39.18 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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]+	185.614	31661259
DarkChem	[M-H]-	181.023	31661259
DeepCCS	[M-2H]-	219.885	30932474
DeepCCS	[M+Na]+	195.167	30932474
AllCCS	[M+H]+	188.2	32859911
AllCCS	[M+H-H2O]+	185.5	32859911
AllCCS	[M+NH4]+	190.6	32859911
AllCCS	[M+Na]+	191.3	32859911
AllCCS	[M-H]-	189.8	32859911
AllCCS	[M+Na-2H]-	190.3	32859911
AllCCS	[M+HCOO]-	190.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Blumealactone A	C\C=C(/C)C(=O)OC1C2OC2(C)CCCC(C)C(O)C2OC(=O)C(=C)C12	3719.0	Standard polar	33892256
Blumealactone A	C\C=C(/C)C(=O)OC1C2OC2(C)CCCC(C)C(O)C2OC(=O)C(=C)C12	2570.0	Standard non polar	33892256
Blumealactone A	C\C=C(/C)C(=O)OC1C2OC2(C)CCCC(C)C(O)C2OC(=O)C(=C)C12	2708.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Blumealactone A,1TMS,isomer #1	C=C1C(=O)OC2C(O[Si](C)(C)C)C(C)CCCC3(C)OC3C(OC(=O)/C(C)=C/C)C12	2683.1	Semi standard non polar	33892256
Blumealactone A,1TBDMS,isomer #1	C=C1C(=O)OC2C(O[Si](C)(C)C(C)(C)C)C(C)CCCC3(C)OC3C(OC(=O)/C(C)=C/C)C12	2919.4	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 - Blumealactone A GC-MS (Non-derivatized) - 70eV, Positive	splash10-053s-9023000000-a266b91793d22f9331a9	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Blumealactone A GC-MS (1 TMS) - 70eV, Positive	splash10-053r-9000000000-c9544b5bdf85c57b6483	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Blumealactone A GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Blumealactone A 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 - Blumealactone A 10V, Positive-QTOF	splash10-014i-3059000000-194da3418bbac711423c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 20V, Positive-QTOF	splash10-00lr-9143000000-7ed9a65ae0d2e9f50e54	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 40V, Positive-QTOF	splash10-0kur-9110000000-108cb2f0509341a377be	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 10V, Negative-QTOF	splash10-03di-2019000000-877ca9181c6daca0fa8c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 20V, Negative-QTOF	splash10-01ot-5049000000-901ec7eadc5b95aa6636	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 40V, Negative-QTOF	splash10-052b-9510000000-c9de32f28afd520bdff9	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 10V, Negative-QTOF	splash10-03di-2009000000-2e93960d023862c37966	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 20V, Negative-QTOF	splash10-03di-0039000000-3a324837b67f4064e245	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 40V, Negative-QTOF	splash10-0zfr-9021000000-8f4ad42888bb4a6b5758	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 10V, Positive-QTOF	splash10-014i-0039000000-1db934106f61b4de2d86	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 20V, Positive-QTOF	splash10-014i-0095000000-7a02e0e650c5baf79a3a	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Blumealactone A 40V, Positive-QTOF	splash10-067j-9085000000-119ef5bf056866354a5a	2021-09-23	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

FDB015593

KNApSAcK ID

C00015496

Chemspider ID

35014187

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

85116077

PDB ID

Not Available

ChEBI ID

175668

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 Blumealactone A (HMDB0036665)

MOL for HMDB0036665 (Blumealactone A)

3D MOL for HMDB0036665 (Blumealactone A)

3D SDF for HMDB0036665 (Blumealactone A)

3D-SDF for HMDB0036665 (Blumealactone A)

PDB for HMDB0036665 (Blumealactone A)

3D PDB for HMDB0036665 (Blumealactone A)

SMILES for HMDB0036665 (Blumealactone A)

INCHI for HMDB0036665 (Blumealactone A)

Structure for HMDB0036665 (Blumealactone A)

3D Structure for HMDB0036665 (Blumealactone A)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra