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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 18:03:19 UTC

Update Date

2022-03-07 02:53:40 UTC

HMDB ID

HMDB0033339

Secondary Accession Numbers

HMDB33339

Metabolite Identification

Common Name

Mollicellin A

Description

Mollicellin A, also known as X 14889C, belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. Based on a literature review very few articles have been published on Mollicellin A.

Structure

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

  Mrv0541 05061307042D          

 28 31  0  0  0  0            999 V2000
    1.7913   -0.4843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758    2.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2899    1.0610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9059    0.0724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4684    0.9077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4534    0.0608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3829    1.6108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7527    2.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0317    0.3049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2017    1.6915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5124    1.8834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7087    1.6969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6139    1.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0966    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6844    0.3595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8353    0.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9707    1.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5585    1.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0757    1.2806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3025   -0.1886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5088    0.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1894    3.2753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1454    2.2997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4880    2.7248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8925   -0.9045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1254   -0.2473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8426    1.5847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8656    0.2788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  1  1  0  0  0  0
  9  5  2  0  0  0  0
 10  2  1  0  0  0  0
 11  8  1  0  0  0  0
 12  5  1  0  0  0  0
 12 11  2  0  0  0  0
 13  7  1  0  0  0  0
 14  6  2  0  0  0  0
 15  6  1  0  0  0  0
 16  9  1  0  0  0  0
 17 10  2  0  0  0  0
 17 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 10  1  0  0  0  0
 18 15  2  0  0  0  0
 19 11  1  0  0  0  0
 19 16  2  0  0  0  0
 20 16  1  0  0  0  0
 21  3  1  0  0  0  0
 21  4  1  0  0  0  0
 21  7  1  0  0  0  0
 22  8  2  0  0  0  0
 23 12  1  0  0  0  0
 24 13  2  0  0  0  0
 25 20  2  0  0  0  0
 26 15  1  0  0  0  0
 26 20  1  0  0  0  0
 27 18  1  0  0  0  0
 27 19  1  0  0  0  0
 28 14  1  0  0  0  0
 28 21  1  0  0  0  0
M  END

HMDB0033339
     RDKit          3D
Mollicellin A
 46 49  0  0  0  0  0  0  0  0999 V2000
   -4.6624   -3.0618   -0.2864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3940   -1.6152   -0.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4179   -0.6767   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1974    0.6685   -0.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3069    1.4935   -0.0516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9001    1.1590   -0.0578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7113    2.5934   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5722    3.0794   -0.0009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578    0.2915   -0.0955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1164   -1.0811   -0.1701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1724   -2.1810   -0.2577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5508   -3.2325    0.2624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9218   -2.0695   -0.8843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0496   -0.9785   -0.6322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2669   -1.3504   -0.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3240   -0.4896   -0.6148 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0382    0.8154   -0.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337    1.2037   -0.0679 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5032    2.5896    0.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3277    0.3198   -0.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5907    0.9108   -0.0482 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1843    1.6887   -0.0972 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0523    2.9079   -0.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5183    1.2048    0.3370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052   -0.2638    0.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6082   -0.9975    1.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0156   -0.5821   -0.5929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6568   -0.8051   -0.7676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7648   -3.1045   -0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2521   -3.5864   -1.1694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7446   -3.6135    0.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4403   -1.0298   -0.1826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3192    2.4676   -0.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5506    3.2696   -0.0024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4860   -2.3800   -1.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3353    2.5304    1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1462    3.2864   -0.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3836    3.0365    0.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5849    1.4270    1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3429    1.7652   -0.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4517   -2.0983    1.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6407   -0.6622    1.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4467   -0.7964    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7405   -0.9223    0.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8880   -1.4150   -1.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4383    0.2847   -1.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  6  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 17 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 10  2  1  0
 20 14  1  0
 21  9  1  0
 28 16  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  5 33  1  0
  7 34  1  0
 15 35  1  0
 19 36  1  0
 19 37  1  0
 19 38  1  0
 24 39  1  0
 24 40  1  0
 26 41  1  0
 26 42  1  0
 26 43  1  0
 27 44  1  0
 27 45  1  0
 27 46  1  0
M  END

  Mrv0541 05061307042D          

 28 31  0  0  0  0            999 V2000
    1.7913   -0.4843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0758    2.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2899    1.0610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9059    0.0724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4684    0.9077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4534    0.0608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3829    1.6108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7527    2.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0317    0.3049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2017    1.6915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5124    1.8834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7087    1.6969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6139    1.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0966    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6844    0.3595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8353    0.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9707    1.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5585    1.1748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0757    1.2806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3025   -0.1886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5088    0.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1894    3.2753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1454    2.2997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4880    2.7248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8925   -0.9045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1254   -0.2473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8426    1.5847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8656    0.2788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  1  1  0  0  0  0
  9  5  2  0  0  0  0
 10  2  1  0  0  0  0
 11  8  1  0  0  0  0
 12  5  1  0  0  0  0
 12 11  2  0  0  0  0
 13  7  1  0  0  0  0
 14  6  2  0  0  0  0
 15  6  1  0  0  0  0
 16  9  1  0  0  0  0
 17 10  2  0  0  0  0
 17 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 10  1  0  0  0  0
 18 15  2  0  0  0  0
 19 11  1  0  0  0  0
 19 16  2  0  0  0  0
 20 16  1  0  0  0  0
 21  3  1  0  0  0  0
 21  4  1  0  0  0  0
 21  7  1  0  0  0  0
 22  8  2  0  0  0  0
 23 12  1  0  0  0  0
 24 13  2  0  0  0  0
 25 20  2  0  0  0  0
 26 15  1  0  0  0  0
 26 20  1  0  0  0  0
 27 18  1  0  0  0  0
 27 19  1  0  0  0  0
 28 14  1  0  0  0  0
 28 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0033339

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=CC(O)=C(C=O)C2=C1C(=O)OC1=C(O2)C(C)=C2C(=O)CC(C)(C)OC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H18O7/c1-9-5-12(23)11(8-22)19-16(9)20(25)26-15-6-14-17(10(2)18(15)27-19)13(24)7-21(3,4)28-14/h5-6,8,23H,7H2,1-4H3

> <INCHI_KEY>
UGFXPOLXTFFCRX-UHFFFAOYSA-N

> <FORMULA>
C21H18O7

> <MOLECULAR_WEIGHT>
382.3634

> <EXACT_MASS>
382.10525293

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
39.06879781518286

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-7,15,15,19-tetramethyl-9,17-dioxo-2,10,14-trioxatetracyclo[9.8.0.0³,⁸.0¹³,¹⁸]nonadeca-1(11),3(8),4,6,12,18-hexaene-4-carbaldehyde

> <ALOGPS_LOGP>
3.21

> <JCHEM_LOGP>
4.0829721023333345

> <ALOGPS_LOGS>
-4.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.019394879673655

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.262693285016888

> <JCHEM_PKA_STRONGEST_BASIC>
-4.916487845633247

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
100.75429999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.06e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-7,15,15,19-tetramethyl-9,17-dioxo-2,10,14-trioxatetracyclo[9.8.0.0³,⁸.0¹³,¹⁸]nonadeca-1(11),3(8),4,6,12,18-hexaene-4-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0033339
     RDKit          3D
Mollicellin A
 46 49  0  0  0  0  0  0  0  0999 V2000
   -4.6624   -3.0618   -0.2864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3940   -1.6152   -0.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4179   -0.6767   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1974    0.6685   -0.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3069    1.4935   -0.0516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9001    1.1590   -0.0578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7113    2.5934   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5722    3.0794   -0.0009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578    0.2915   -0.0955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1164   -1.0811   -0.1701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1724   -2.1810   -0.2577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5508   -3.2325    0.2624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9218   -2.0695   -0.8843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0496   -0.9785   -0.6322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2669   -1.3504   -0.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3240   -0.4896   -0.6148 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0382    0.8154   -0.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337    1.2037   -0.0679 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5032    2.5896    0.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3277    0.3198   -0.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5907    0.9108   -0.0482 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1843    1.6887   -0.0972 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0523    2.9079   -0.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5183    1.2048    0.3370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052   -0.2638    0.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6082   -0.9975    1.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0156   -0.5821   -0.5929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6568   -0.8051   -0.7676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7648   -3.1045   -0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2521   -3.5864   -1.1694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7446   -3.6135    0.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4403   -1.0298   -0.1826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3192    2.4676   -0.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5506    3.2696   -0.0024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4860   -2.3800   -1.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3353    2.5304    1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1462    3.2864   -0.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3836    3.0365    0.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5849    1.4270    1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3429    1.7652   -0.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4517   -2.0983    1.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6407   -0.6622    1.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4467   -0.7964    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7405   -0.9223    0.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8880   -1.4150   -1.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4383    0.2847   -1.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  6  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 17 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 10  2  1  0
 20 14  1  0
 21  9  1  0
 28 16  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  5 33  1  0
  7 34  1  0
 15 35  1  0
 19 36  1  0
 19 37  1  0
 19 38  1  0
 24 39  1  0
 24 40  1  0
 26 41  1  0
 26 42  1  0
 26 43  1  0
 27 44  1  0
 27 45  1  0
 27 46  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       3.344  -0.904   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.475   4.679   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.474   1.981   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.758   0.135   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.741   1.694   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.180   0.113   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.781   3.007   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.138   4.989   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.793   0.569   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.710   3.157   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.690   3.516   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.190   3.168   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.346   3.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.380   1.078   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.744   0.671   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.293   0.917   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.145   2.600   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.509   2.193   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.741   2.390   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.165  -0.352   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.016   1.485   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.087   6.114   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.138   4.293   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      12.111   5.086   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       5.399  -1.688   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.701  -0.462   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       7.173   2.958   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      12.816   0.520   0.000  0.00  0.00           O+0
CONECT    1    9                                                            
CONECT    2   10                                                            
CONECT    3   21                                                            
CONECT    4   21                                                            
CONECT    5    9   12                                                       
CONECT    6   14   15                                                       
CONECT    7   13   21                                                       
CONECT    8   11   22                                                       
CONECT    9    1    5   16                                                  
CONECT   10    2   17   18                                                  
CONECT   11    8   12   19                                                  
CONECT   12    5   11   23                                                  
CONECT   13    7   17   24                                                  
CONECT   14    6   17   28                                                  
CONECT   15    6   18   26                                                  
CONECT   16    9   19   20                                                  
CONECT   17   10   13   14                                                  
CONECT   18   10   15   27                                                  
CONECT   19   11   16   27                                                  
CONECT   20   16   25   26                                                  
CONECT   21    3    4    7   28                                             
CONECT   22    8                                                            
CONECT   23   12                                                            
CONECT   24   13                                                            
CONECT   25   20                                                            
CONECT   26   15   20                                                       
CONECT   27   18   19                                                       
CONECT   28   14   21                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

COMPND    HMDB0033339
HETATM    1  C1  UNL     1      -4.662  -3.062  -0.286  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.394  -1.615  -0.205  1.00  0.00           C  
HETATM    3  C3  UNL     1      -5.418  -0.677  -0.160  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.197   0.669  -0.089  1.00  0.00           C  
HETATM    5  O1  UNL     1      -6.307   1.494  -0.052  1.00  0.00           O  
HETATM    6  C5  UNL     1      -3.900   1.159  -0.058  1.00  0.00           C  
HETATM    7  C6  UNL     1      -3.711   2.593  -0.018  1.00  0.00           C  
HETATM    8  O2  UNL     1      -2.572   3.079  -0.001  1.00  0.00           O  
HETATM    9  C7  UNL     1      -2.858   0.292  -0.095  1.00  0.00           C  
HETATM   10  C8  UNL     1      -3.116  -1.081  -0.170  1.00  0.00           C  
HETATM   11  C9  UNL     1      -2.172  -2.181  -0.258  1.00  0.00           C  
HETATM   12  O3  UNL     1      -2.551  -3.232   0.262  1.00  0.00           O  
HETATM   13  O4  UNL     1      -0.922  -2.070  -0.884  1.00  0.00           O  
HETATM   14  C10 UNL     1      -0.050  -0.978  -0.632  1.00  0.00           C  
HETATM   15  C11 UNL     1       1.267  -1.350  -0.799  1.00  0.00           C  
HETATM   16  C12 UNL     1       2.324  -0.490  -0.615  1.00  0.00           C  
HETATM   17  C13 UNL     1       2.038   0.815  -0.241  1.00  0.00           C  
HETATM   18  C14 UNL     1       0.734   1.204  -0.068  1.00  0.00           C  
HETATM   19  C15 UNL     1       0.503   2.590   0.415  1.00  0.00           C  
HETATM   20  C16 UNL     1      -0.328   0.320  -0.263  1.00  0.00           C  
HETATM   21  O5  UNL     1      -1.591   0.911  -0.048  1.00  0.00           O  
HETATM   22  C17 UNL     1       3.184   1.689  -0.097  1.00  0.00           C  
HETATM   23  O6  UNL     1       3.052   2.908  -0.350  1.00  0.00           O  
HETATM   24  C18 UNL     1       4.518   1.205   0.337  1.00  0.00           C  
HETATM   25  C19 UNL     1       4.705  -0.264   0.050  1.00  0.00           C  
HETATM   26  C20 UNL     1       4.608  -0.997   1.376  1.00  0.00           C  
HETATM   27  C21 UNL     1       6.016  -0.582  -0.593  1.00  0.00           C  
HETATM   28  O7  UNL     1       3.657  -0.805  -0.768  1.00  0.00           O  
HETATM   29  H1  UNL     1      -5.765  -3.105  -0.599  1.00  0.00           H  
HETATM   30  H2  UNL     1      -4.252  -3.586  -1.169  1.00  0.00           H  
HETATM   31  H3  UNL     1      -4.745  -3.613   0.647  1.00  0.00           H  
HETATM   32  H4  UNL     1      -6.440  -1.030  -0.183  1.00  0.00           H  
HETATM   33  H5  UNL     1      -6.319   2.468  -0.000  1.00  0.00           H  
HETATM   34  H6  UNL     1      -4.551   3.270  -0.002  1.00  0.00           H  
HETATM   35  H7  UNL     1       1.486  -2.380  -1.092  1.00  0.00           H  
HETATM   36  H8  UNL     1      -0.335   2.530   1.194  1.00  0.00           H  
HETATM   37  H9  UNL     1       0.146   3.286  -0.352  1.00  0.00           H  
HETATM   38  H10 UNL     1       1.384   3.036   0.928  1.00  0.00           H  
HETATM   39  H11 UNL     1       4.585   1.427   1.435  1.00  0.00           H  
HETATM   40  H12 UNL     1       5.343   1.765  -0.136  1.00  0.00           H  
HETATM   41  H13 UNL     1       4.452  -2.098   1.185  1.00  0.00           H  
HETATM   42  H14 UNL     1       3.641  -0.662   1.851  1.00  0.00           H  
HETATM   43  H15 UNL     1       5.447  -0.796   2.045  1.00  0.00           H  
HETATM   44  H16 UNL     1       6.741  -0.922   0.194  1.00  0.00           H  
HETATM   45  H17 UNL     1       5.888  -1.415  -1.310  1.00  0.00           H  
HETATM   46  H18 UNL     1       6.438   0.285  -1.126  1.00  0.00           H  
CONECT    1    2   29   30   31
CONECT    2    3    3   10
CONECT    3    4   32
CONECT    4    5    6    6
CONECT    5   33
CONECT    6    7    9
CONECT    7    8    8   34
CONECT    9   10   10   21
CONECT   10   11
CONECT   11   12   12   13
CONECT   13   14
CONECT   14   15   15   20
CONECT   15   16   35
CONECT   16   17   17   28
CONECT   17   18   22
CONECT   18   19   20   20
CONECT   19   36   37   38
CONECT   20   21
CONECT   22   23   23   24
CONECT   24   25   39   40
CONECT   25   26   27   28
CONECT   26   41   42   43
CONECT   27   44   45   46
END

HMDB0033339
     RDKit          3D
Mollicellin A
 46 49  0  0  0  0  0  0  0  0999 V2000
   -4.6624   -3.0618   -0.2864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3940   -1.6152   -0.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4179   -0.6767   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1974    0.6685   -0.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3069    1.4935   -0.0516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9001    1.1590   -0.0578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7113    2.5934   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5722    3.0794   -0.0009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578    0.2915   -0.0955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1164   -1.0811   -0.1701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1724   -2.1810   -0.2577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5508   -3.2325    0.2624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9218   -2.0695   -0.8843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0496   -0.9785   -0.6322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2669   -1.3504   -0.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3240   -0.4896   -0.6148 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0382    0.8154   -0.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337    1.2037   -0.0679 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5032    2.5896    0.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3277    0.3198   -0.2626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5907    0.9108   -0.0482 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1843    1.6887   -0.0972 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0523    2.9079   -0.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5183    1.2048    0.3370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052   -0.2638    0.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6082   -0.9975    1.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0156   -0.5821   -0.5929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6568   -0.8051   -0.7676 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7648   -3.1045   -0.5986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2521   -3.5864   -1.1694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7446   -3.6135    0.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4403   -1.0298   -0.1826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3192    2.4676   -0.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5506    3.2696   -0.0024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4860   -2.3800   -1.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3353    2.5304    1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1462    3.2864   -0.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3836    3.0365    0.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5849    1.4270    1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3429    1.7652   -0.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4517   -2.0983    1.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6407   -0.6622    1.8508 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4467   -0.7964    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7405   -0.9223    0.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8880   -1.4150   -1.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4383    0.2847   -1.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  6  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 17 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 10  2  1  0
 20 14  1  0
 21  9  1  0
 28 16  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  5 33  1  0
  7 34  1  0
 15 35  1  0
 19 36  1  0
 19 37  1  0
 19 38  1  0
 24 39  1  0
 24 40  1  0
 26 41  1  0
 26 42  1  0
 26 43  1  0
 27 44  1  0
 27 45  1  0
 27 46  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
20-De(1-hydroxypropyl)-20-(1-hydroxyethyl)-lysocellin	HMDB
20-De(1-hydroxypropyl)-20-(1-hydroxyethyl)lysocellin	HMDB
X 14889C	HMDB

Chemical Formula

C₂₁H₁₈O₇

Average Molecular Weight

382.3634

Monoisotopic Molecular Weight

382.10525293

IUPAC Name

5-hydroxy-7,15,15,19-tetramethyl-9,17-dioxo-2,10,14-trioxatetracyclo[9.8.0.0³,⁸.0¹³,¹⁸]nonadeca-1(11),3(8),4,6,12,18-hexaene-4-carbaldehyde

Traditional Name

5-hydroxy-7,15,15,19-tetramethyl-9,17-dioxo-2,10,14-trioxatetracyclo[9.8.0.0³,⁸.0¹³,¹⁸]nonadeca-1(11),3(8),4,6,12,18-hexaene-4-carbaldehyde

CAS Registry Number

68455-06-1

SMILES

CC1=CC(O)=C(C=O)C2=C1C(=O)OC1=C(O2)C(C)=C2C(=O)CC(C)(C)OC2=C1

InChI Identifier

InChI=1S/C21H18O7/c1-9-5-12(23)11(8-22)19-16(9)20(25)26-15-6-14-17(10(2)18(15)27-19)13(24)7-21(3,4)28-14/h5-6,8,23H,7H2,1-4H3

InChI Key

UGFXPOLXTFFCRX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
Chromone
Diaryl ether
Aryl ketone
Aryl alkyl ketone
Alkyl aryl ether
1,4-dioxepine
1-hydroxy-2-unsubstituted benzenoid
Aryl-aldehyde
Dioxepine
Benzenoid
Vinylogous acid
Carboxylic acid ester
Ketone
Lactone
Ether
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aldehyde
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0033339)
Cell membrane (HMDB: HMDB0033339)

Source

Exogenous

Exogenous (HMDB: HMDB0033339)

Food

Food (HMDB: HMDB0033339)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0033339)

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
Water Solubility	0.021 g/L	ALOGPS
logP	3.21	ALOGPS
logP	4.08	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	7.26	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	100.75 m³·mol⁻¹	ChemAxon
Polarizability	39.07 Å³	ChemAxon
Number of Rings	4	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]+	187.732	31661259
DarkChem	[M-H]-	185.585	31661259
DeepCCS	[M+H]+	190.214	30932474
DeepCCS	[M-H]-	187.818	30932474
DeepCCS	[M-2H]-	221.368	30932474
DeepCCS	[M+Na]+	196.302	30932474
AllCCS	[M+H]+	187.5	32859911
AllCCS	[M+H-H2O]+	184.7	32859911
AllCCS	[M+NH4]+	190.0	32859911
AllCCS	[M+Na]+	190.8	32859911
AllCCS	[M-H]-	192.1	32859911
AllCCS	[M+Na-2H]-	191.4	32859911
AllCCS	[M+HCOO]-	190.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Mollicellin A	CC1=CC(O)=C(C=O)C2=C1C(=O)OC1=C(O2)C(C)=C2C(=O)CC(C)(C)OC2=C1	4332.9	Standard polar	33892256
Mollicellin A	CC1=CC(O)=C(C=O)C2=C1C(=O)OC1=C(O2)C(C)=C2C(=O)CC(C)(C)OC2=C1	3076.9	Standard non polar	33892256
Mollicellin A	CC1=CC(O)=C(C=O)C2=C1C(=O)OC1=C(O2)C(C)=C2C(=O)CC(C)(C)OC2=C1	3173.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Mollicellin A,1TMS,isomer #1	CC1=CC(O[Si](C)(C)C)=C(C=O)C2=C1C(=O)OC1=CC3=C(C(=O)CC(C)(C)O3)C(C)=C1O2	3097.9	Semi standard non polar	33892256
Mollicellin A,1TBDMS,isomer #1	CC1=CC(O[Si](C)(C)C(C)(C)C)=C(C=O)C2=C1C(=O)OC1=CC3=C(C(=O)CC(C)(C)O3)C(C)=C1O2	3319.2	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 - Mollicellin A GC-MS (Non-derivatized) - 70eV, Positive	splash10-0udi-0359000000-5774c63c6e22a6ba2005	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mollicellin A GC-MS (1 TMS) - 70eV, Positive	splash10-00di-2173900000-ef8e2ca9e2ead13306c0	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mollicellin A GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Mollicellin 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 - Mollicellin A 10V, Positive-QTOF	splash10-001i-0119000000-4f0570b5d9b33b43afbf	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 20V, Positive-QTOF	splash10-003r-1229000000-98e5caae9133059254e7	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 40V, Positive-QTOF	splash10-0a4i-7931000000-803e605223d5cd1e3515	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 10V, Negative-QTOF	splash10-001i-0109000000-586581acd50b66749b5e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 20V, Negative-QTOF	splash10-001i-1309000000-6809816a84d83dd698e8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 40V, Negative-QTOF	splash10-053r-9621000000-55bc6e16584e667226d0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 10V, Negative-QTOF	splash10-0f89-0009000000-d73806d25fc1090494cc	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 20V, Negative-QTOF	splash10-0w31-0019000000-d241b3644205396dbf90	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 40V, Negative-QTOF	splash10-0002-1096000000-3749521a88d0224368f8	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 10V, Positive-QTOF	splash10-001i-0009000000-f0e15c6065c857f994a4	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 20V, Positive-QTOF	splash10-000x-0009000000-3c7ea38bb2df62b65ec9	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Mollicellin A 40V, Positive-QTOF	splash10-0a4i-2079000000-200637f386fa5f05b494	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

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

FDB011367

KNApSAcK ID

C00016787

Chemspider ID

134710

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13491357

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

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for Mollicellin A (HMDB0033339)

MOL for HMDB0033339 (Mollicellin A)

3D MOL for HMDB0033339 (Mollicellin A)

3D SDF for HMDB0033339 (Mollicellin A)

3D-SDF for HMDB0033339 (Mollicellin A)

PDB for HMDB0033339 (Mollicellin A)

3D PDB for HMDB0033339 (Mollicellin A)

SMILES for HMDB0033339 (Mollicellin A)

INCHI for HMDB0033339 (Mollicellin A)

Structure for HMDB0033339 (Mollicellin A)

3D Structure for HMDB0033339 (Mollicellin A)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra