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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:15:58 UTC

Update Date

2022-03-07 02:55:59 UTC

HMDB ID

HMDB0038918

Secondary Accession Numbers

HMDB38918

Metabolite Identification

Common Name

Armillaritin

Description

Armillaritin belongs to the class of organic compounds known as melleolides and analogues. Melleolides and analogues are compounds with a structure characterized by the presence of a 2-hydroxy-4-methoxy-6-methylbenzoic acid derivative linked to a 3,6,6,7b-tetramethyl-cyclobuta[e]indene moiety. Based on a literature review a small amount of articles have been published on Armillaritin.

Structure

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


  Mrv0541 05061310442D          

 29 32  0  0  0  0            999 V2000
    5.2180    3.0232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8310    2.6256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3471    1.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3495    2.4413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2653    2.0511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9470    0.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    0.1942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2912    2.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1936    2.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0844   -0.4737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4304    1.0343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4610    2.2348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6456    0.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5083    1.2627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1428    0.8418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7299    1.3930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7681    1.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8998    1.6302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313    0.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0955    1.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5470    1.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5925    1.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3824    0.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089   -0.4430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3126    1.0789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815    0.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8525    2.6023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0773    0.2079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5342    1.2093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 12  1  1  0  0  0  0
 12  5  2  0  0  0  0
 13  7  2  0  0  0  0
 13 10  1  0  0  0  0
 14  5  1  0  0  0  0
 14  6  2  0  0  0  0
 15  6  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 18 12  1  0  0  0  0
 18 15  2  0  0  0  0
 19 13  1  0  0  0  0
 19 16  1  0  0  0  0
 20 18  1  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 21  9  1  0  0  0  0
 21 11  1  0  0  0  0
 22  4  1  0  0  0  0
 22  8  1  0  0  0  0
 22 17  1  0  0  0  0
 22 19  1  0  0  0  0
 23  7  1  0  0  0  0
 23 11  1  0  0  0  0
 23 17  1  0  0  0  0
 24 10  2  0  0  0  0
 25 14  1  0  0  0  0
 26 15  1  0  0  0  0
 27 20  2  0  0  0  0
 28 23  1  0  0  0  0
 29 16  1  0  0  0  0
 29 20  1  0  0  0  0
M  END

HMDB0038918
     RDKit          3D
Armillaritin
 57 60  0  0  0  0  0  0  0  0999 V2000
    5.1077    0.0467   -2.5052 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3655    0.1437   -1.0235 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6717    0.2149   -0.5715 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9405    0.3032    0.7632 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2744    0.3732    1.1774 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9432    0.3230    1.6676 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6156    0.2523    1.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6235    0.2755    2.1968 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3182    0.1626   -0.1052 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9624    0.0858   -0.6287 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7555    0.0040   -1.8897 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901    0.0894    0.0981 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5011    0.0122   -0.4697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3895    1.0862    0.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1297    0.0038    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6827    0.0451    2.3803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4044   -1.0255    0.1489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1999   -1.8370   -0.7623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5485   -2.5946   -1.8098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1775   -3.3106   -2.6240 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5362   -1.9325   -0.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2761   -1.1913    0.3450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5277   -2.0457    1.4092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5879   -0.7368   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5762    0.7660   -0.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1705    1.3254   -1.5242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2285    1.3840    0.9436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0722    1.0744   -0.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5881    0.0779    0.7583 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6243   -0.9174   -2.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1315   -0.0104   -2.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5792    0.9389   -2.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4938    0.2015   -1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4949    0.4396    2.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1246    0.3934    2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6739    0.2321    2.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4545   -0.0536   -1.5598 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1567    1.8166    0.7897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9750    1.6294   -0.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6112    1.0675    2.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3099   -0.4673    2.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4150   -0.5851    2.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2282   -1.6991    0.7991 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5206   -2.5460   -1.8993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1132   -2.5378   -1.3762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214   -1.5805    2.2826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4526   -1.0912    0.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7234   -1.0910   -1.2799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3840    2.4090   -1.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4467    1.2831   -2.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1059    0.8091   -1.8230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1848    1.8254    0.6551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3532    0.6213    1.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5571    2.1719    1.3215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9452    2.1223    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7287    0.8532   -1.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0486    0.3894    1.7323 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  1  0
  7  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 18 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
  9  2  1  0
 17 13  1  0
 29 22  1  0
 29 15  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  5 34  1  0
  6 35  1  0
  8 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 19 44  1  0
 21 45  1  0
 23 46  1  0
 24 47  1  0
 24 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
 27 52  1  0
 27 53  1  0
 27 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
M  END


  Mrv0541 05061310442D          

 29 32  0  0  0  0            999 V2000
    5.2180    3.0232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8310    2.6256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3471    1.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3495    2.4413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2653    2.0511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9470    0.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    0.1942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2912    2.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1936    2.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0844   -0.4737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4304    1.0343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4610    2.2348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6456    0.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5083    1.2627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1428    0.8418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7299    1.3930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7681    1.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8998    1.6302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0313    0.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0955    1.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5470    1.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5925    1.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3824    0.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9089   -0.4430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3126    1.0789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815    0.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8525    2.6023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0773    0.2079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5342    1.2093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 12  1  1  0  0  0  0
 12  5  2  0  0  0  0
 13  7  2  0  0  0  0
 13 10  1  0  0  0  0
 14  5  1  0  0  0  0
 14  6  2  0  0  0  0
 15  6  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 18 12  1  0  0  0  0
 18 15  2  0  0  0  0
 19 13  1  0  0  0  0
 19 16  1  0  0  0  0
 20 18  1  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 21  9  1  0  0  0  0
 21 11  1  0  0  0  0
 22  4  1  0  0  0  0
 22  8  1  0  0  0  0
 22 17  1  0  0  0  0
 22 19  1  0  0  0  0
 23  7  1  0  0  0  0
 23 11  1  0  0  0  0
 23 17  1  0  0  0  0
 24 10  2  0  0  0  0
 25 14  1  0  0  0  0
 26 15  1  0  0  0  0
 27 20  2  0  0  0  0
 28 23  1  0  0  0  0
 29 16  1  0  0  0  0
 29 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038918

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=CC(O)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC21

> <INCHI_IDENTIFIER>
InChI=1S/C23H28O6/c1-12-5-14(25)6-15(26)18(12)20(27)29-16-8-22(4)17-9-21(2,3)11-23(17,28)7-13(10-24)19(16)22/h5-7,10,16-17,19,25-26,28H,8-9,11H2,1-4H3

> <INCHI_KEY>
CYANGADGENNSLV-UHFFFAOYSA-N

> <FORMULA>
C23H28O6

> <MOLECULAR_WEIGHT>
400.4648

> <EXACT_MASS>
400.188588628

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
42.96058205406119

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-formyl-4a-hydroxy-6,6,7b-trimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 2,4-dihydroxy-6-methylbenzoate

> <ALOGPS_LOGP>
3.00

> <JCHEM_LOGP>
3.795714295666666

> <ALOGPS_LOGS>
-4.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.558023528444801

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.699802643729567

> <JCHEM_PKA_STRONGEST_BASIC>
-3.200716551591449

> <JCHEM_POLAR_SURFACE_AREA>
104.06

> <JCHEM_REFRACTIVITY>
108.3548

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-formyl-4a-hydroxy-6,6,7b-trimethyl-1H,2H,2aH,5H,7H,7aH-cyclobuta[e]inden-2-yl 2,4-dihydroxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038918
     RDKit          3D
Armillaritin
 57 60  0  0  0  0  0  0  0  0999 V2000
    5.1077    0.0467   -2.5052 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3655    0.1437   -1.0235 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6717    0.2149   -0.5715 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9405    0.3032    0.7632 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2744    0.3732    1.1774 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9432    0.3230    1.6676 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6156    0.2523    1.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6235    0.2755    2.1968 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3182    0.1626   -0.1052 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9624    0.0858   -0.6287 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7555    0.0040   -1.8897 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901    0.0894    0.0981 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5011    0.0122   -0.4697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3895    1.0862    0.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1297    0.0038    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6827    0.0451    2.3803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4044   -1.0255    0.1489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1999   -1.8370   -0.7623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5485   -2.5946   -1.8098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1775   -3.3106   -2.6240 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5362   -1.9325   -0.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2761   -1.1913    0.3450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5277   -2.0457    1.4092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5879   -0.7368   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5762    0.7660   -0.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1705    1.3254   -1.5242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2285    1.3840    0.9436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0722    1.0744   -0.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5881    0.0779    0.7583 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6243   -0.9174   -2.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1315   -0.0104   -2.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5792    0.9389   -2.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4938    0.2015   -1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4949    0.4396    2.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1246    0.3934    2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6739    0.2321    2.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4545   -0.0536   -1.5598 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1567    1.8166    0.7897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9750    1.6294   -0.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6112    1.0675    2.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3099   -0.4673    2.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4150   -0.5851    2.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2282   -1.6991    0.7991 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5206   -2.5460   -1.8993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1132   -2.5378   -1.3762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214   -1.5805    2.2826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4526   -1.0912    0.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7234   -1.0910   -1.2799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3840    2.4090   -1.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4467    1.2831   -2.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1059    0.8091   -1.8230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1848    1.8254    0.6551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3532    0.6213    1.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5571    2.1719    1.3215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9452    2.1223    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7287    0.8532   -1.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0486    0.3894    1.7323 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  1  0
  7  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 18 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
  9  2  1  0
 17 13  1  0
 29 22  1  0
 29 15  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  5 34  1  0
  6 35  1  0
  8 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 19 44  1  0
 21 45  1  0
 23 46  1  0
 24 47  1  0
 24 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
 27 52  1  0
 27 53  1  0
 27 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  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       9.740   5.643   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.551   4.901   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.515   3.079   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.519   4.557   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.695   3.829   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.101   1.228   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.533   0.363   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.277   3.905   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.361   4.133   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.891  -0.884   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.803   1.931   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.194   4.172   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.072   0.420   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.149   2.357   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.600   1.571   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.096   2.600   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.434   3.028   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.146   3.043   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.792   1.781   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.645   3.386   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.021   3.455   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.973   3.085   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.714   1.667   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.430  -0.827   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      13.650   2.014   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.552   0.443   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       7.191   4.858   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -0.144   0.388   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       6.597   2.257   0.000  0.00  0.00           O+0
CONECT    1   12                                                            
CONECT    2   21                                                            
CONECT    3   21                                                            
CONECT    4   22                                                            
CONECT    5   12   14                                                       
CONECT    6   14   15                                                       
CONECT    7   13   23                                                       
CONECT    8   16   22                                                       
CONECT    9   17   21                                                       
CONECT   10   13   24                                                       
CONECT   11   21   23                                                       
CONECT   12    1    5   18                                                  
CONECT   13    7   10   19                                                  
CONECT   14    5    6   25                                                  
CONECT   15    6   18   26                                                  
CONECT   16    8   19   29                                                  
CONECT   17    9   22   23                                                  
CONECT   18   12   15   20                                                  
CONECT   19   13   16   22                                                  
CONECT   20   18   27   29                                                  
CONECT   21    2    3    9   11                                             
CONECT   22    4    8   17   19                                             
CONECT   23    7   11   17   28                                             
CONECT   24   10                                                            
CONECT   25   14                                                            
CONECT   26   15                                                            
CONECT   27   20                                                            
CONECT   28   23                                                            
CONECT   29   16   20                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

COMPND    HMDB0038918
HETATM    1  C1  UNL     1       5.108   0.047  -2.505  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.366   0.144  -1.024  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.672   0.215  -0.571  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.941   0.303   0.763  1.00  0.00           C  
HETATM    5  O1  UNL     1       8.274   0.373   1.177  1.00  0.00           O  
HETATM    6  C5  UNL     1       5.943   0.323   1.668  1.00  0.00           C  
HETATM    7  C6  UNL     1       4.616   0.252   1.236  1.00  0.00           C  
HETATM    8  O2  UNL     1       3.623   0.275   2.197  1.00  0.00           O  
HETATM    9  C7  UNL     1       4.318   0.163  -0.105  1.00  0.00           C  
HETATM   10  C8  UNL     1       2.962   0.086  -0.629  1.00  0.00           C  
HETATM   11  O3  UNL     1       2.755   0.004  -1.890  1.00  0.00           O  
HETATM   12  O4  UNL     1       1.790   0.089   0.098  1.00  0.00           O  
HETATM   13  C9  UNL     1       0.501   0.012  -0.470  1.00  0.00           C  
HETATM   14  C10 UNL     1      -0.390   1.086   0.157  1.00  0.00           C  
HETATM   15  C11 UNL     1      -1.130   0.004   0.916  1.00  0.00           C  
HETATM   16  C12 UNL     1      -0.683   0.045   2.380  1.00  0.00           C  
HETATM   17  C13 UNL     1      -0.404  -1.025   0.149  1.00  0.00           C  
HETATM   18  C14 UNL     1      -1.200  -1.837  -0.762  1.00  0.00           C  
HETATM   19  C15 UNL     1      -0.548  -2.595  -1.810  1.00  0.00           C  
HETATM   20  O5  UNL     1      -1.177  -3.311  -2.624  1.00  0.00           O  
HETATM   21  C16 UNL     1      -2.536  -1.933  -0.694  1.00  0.00           C  
HETATM   22  C17 UNL     1      -3.276  -1.191   0.345  1.00  0.00           C  
HETATM   23  O6  UNL     1      -3.528  -2.046   1.409  1.00  0.00           O  
HETATM   24  C18 UNL     1      -4.588  -0.737  -0.221  1.00  0.00           C  
HETATM   25  C19 UNL     1      -4.576   0.766  -0.266  1.00  0.00           C  
HETATM   26  C20 UNL     1      -5.171   1.325  -1.524  1.00  0.00           C  
HETATM   27  C21 UNL     1      -5.229   1.384   0.944  1.00  0.00           C  
HETATM   28  C22 UNL     1      -3.072   1.074  -0.269  1.00  0.00           C  
HETATM   29  C23 UNL     1      -2.588   0.078   0.758  1.00  0.00           C  
HETATM   30  H1  UNL     1       4.624  -0.917  -2.753  1.00  0.00           H  
HETATM   31  H2  UNL     1       6.131  -0.010  -2.994  1.00  0.00           H  
HETATM   32  H3  UNL     1       4.579   0.939  -2.837  1.00  0.00           H  
HETATM   33  H4  UNL     1       7.494   0.202  -1.269  1.00  0.00           H  
HETATM   34  H5  UNL     1       8.495   0.440   2.172  1.00  0.00           H  
HETATM   35  H6  UNL     1       6.125   0.393   2.751  1.00  0.00           H  
HETATM   36  H7  UNL     1       2.674   0.232   2.011  1.00  0.00           H  
HETATM   37  H8  UNL     1       0.454  -0.054  -1.560  1.00  0.00           H  
HETATM   38  H9  UNL     1       0.157   1.817   0.790  1.00  0.00           H  
HETATM   39  H10 UNL     1      -0.975   1.629  -0.596  1.00  0.00           H  
HETATM   40  H11 UNL     1      -0.611   1.068   2.755  1.00  0.00           H  
HETATM   41  H12 UNL     1       0.310  -0.467   2.474  1.00  0.00           H  
HETATM   42  H13 UNL     1      -1.415  -0.585   2.942  1.00  0.00           H  
HETATM   43  H14 UNL     1       0.228  -1.699   0.799  1.00  0.00           H  
HETATM   44  H15 UNL     1       0.521  -2.546  -1.899  1.00  0.00           H  
HETATM   45  H16 UNL     1      -3.113  -2.538  -1.376  1.00  0.00           H  
HETATM   46  H17 UNL     1      -3.521  -1.580   2.283  1.00  0.00           H  
HETATM   47  H18 UNL     1      -5.453  -1.091   0.386  1.00  0.00           H  
HETATM   48  H19 UNL     1      -4.723  -1.091  -1.280  1.00  0.00           H  
HETATM   49  H20 UNL     1      -5.384   2.409  -1.332  1.00  0.00           H  
HETATM   50  H21 UNL     1      -4.447   1.283  -2.342  1.00  0.00           H  
HETATM   51  H22 UNL     1      -6.106   0.809  -1.823  1.00  0.00           H  
HETATM   52  H23 UNL     1      -6.185   1.825   0.655  1.00  0.00           H  
HETATM   53  H24 UNL     1      -5.353   0.621   1.741  1.00  0.00           H  
HETATM   54  H25 UNL     1      -4.557   2.172   1.322  1.00  0.00           H  
HETATM   55  H26 UNL     1      -2.945   2.122   0.041  1.00  0.00           H  
HETATM   56  H27 UNL     1      -2.729   0.853  -1.290  1.00  0.00           H  
HETATM   57  H28 UNL     1      -3.049   0.389   1.732  1.00  0.00           H  
CONECT    1    2   30   31   32
CONECT    2    3    3    9
CONECT    3    4   33
CONECT    4    5    6    6
CONECT    5   34
CONECT    6    7   35
CONECT    7    8    9    9
CONECT    8   36
CONECT    9   10
CONECT   10   11   11   12
CONECT   12   13
CONECT   13   14   17   37
CONECT   14   15   38   39
CONECT   15   16   17   29
CONECT   16   40   41   42
CONECT   17   18   43
CONECT   18   19   21   21
CONECT   19   20   20   44
CONECT   21   22   45
CONECT   22   23   24   29
CONECT   23   46
CONECT   24   25   47   48
CONECT   25   26   27   28
CONECT   26   49   50   51
CONECT   27   52   53   54
CONECT   28   29   55   56
CONECT   29   57
END

HMDB0038918
     RDKit          3D
Armillaritin
 57 60  0  0  0  0  0  0  0  0999 V2000
    5.1077    0.0467   -2.5052 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3655    0.1437   -1.0235 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6717    0.2149   -0.5715 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9405    0.3032    0.7632 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2744    0.3732    1.1774 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9432    0.3230    1.6676 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6156    0.2523    1.2361 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6235    0.2755    2.1968 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3182    0.1626   -0.1052 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9624    0.0858   -0.6287 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7555    0.0040   -1.8897 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901    0.0894    0.0981 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5011    0.0122   -0.4697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3895    1.0862    0.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1297    0.0038    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6827    0.0451    2.3803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4044   -1.0255    0.1489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1999   -1.8370   -0.7623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5485   -2.5946   -1.8098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1775   -3.3106   -2.6240 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5362   -1.9325   -0.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2761   -1.1913    0.3450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5277   -2.0457    1.4092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5879   -0.7368   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5762    0.7660   -0.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1705    1.3254   -1.5242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2285    1.3840    0.9436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0722    1.0744   -0.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5881    0.0779    0.7583 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6243   -0.9174   -2.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1315   -0.0104   -2.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5792    0.9389   -2.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4938    0.2015   -1.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4949    0.4396    2.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1246    0.3934    2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6739    0.2321    2.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4545   -0.0536   -1.5598 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1567    1.8166    0.7897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9750    1.6294   -0.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6112    1.0675    2.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3099   -0.4673    2.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4150   -0.5851    2.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2282   -1.6991    0.7991 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5206   -2.5460   -1.8993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1132   -2.5378   -1.3762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214   -1.5805    2.2826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4526   -1.0912    0.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7234   -1.0910   -1.2799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3840    2.4090   -1.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4467    1.2831   -2.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1059    0.8091   -1.8230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1848    1.8254    0.6551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3532    0.6213    1.7415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5571    2.1719    1.3215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9452    2.1223    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7287    0.8532   -1.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0486    0.3894    1.7323 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  1  0
  7  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 18 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
  9  2  1  0
 17 13  1  0
 29 22  1  0
 29 15  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  5 34  1  0
  6 35  1  0
  8 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 19 44  1  0
 21 45  1  0
 23 46  1  0
 24 47  1  0
 24 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
 27 52  1  0
 27 53  1  0
 27 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3-Formyl-4a-hydroxy-6,6,7b-trimethyl-1H,2H,2ah,4ah,5H,6H,7H,7ah,7BH-cyclobuta[e]inden-2-yl 2,4-dihydroxy-6-methylbenzoic acid	HMDB

Chemical Formula

C₂₃H₂₈O₆

Average Molecular Weight

400.4648

Monoisotopic Molecular Weight

400.188588628

IUPAC Name

3-formyl-4a-hydroxy-6,6,7b-trimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 2,4-dihydroxy-6-methylbenzoate

Traditional Name

3-formyl-4a-hydroxy-6,6,7b-trimethyl-1H,2H,2aH,5H,7H,7aH-cyclobuta[e]inden-2-yl 2,4-dihydroxy-6-methylbenzoate

CAS Registry Number

135247-96-0

SMILES

CC1=CC(O)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC21

InChI Identifier

InChI=1S/C23H28O6/c1-12-5-14(25)6-15(26)18(12)20(27)29-16-8-22(4)17-9-21(2,3)11-23(17,28)7-13(10-24)19(16)22/h5-7,10,16-17,19,25-26,28H,8-9,11H2,1-4H3

InChI Key

CYANGADGENNSLV-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as melleolides and analogues. Melleolides and analogues are compounds with a structure characterized by the presence of a 2-hydroxy-4-methoxy-6-methylbenzoic acid derivative linked to a 3,6,6,7b-tetramethyl-cyclobuta[e]indene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Melleolides and analogues

Alternative Parents

Substituents

Melleolide-skeleton
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Salicylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
M-cresol
Benzoyl
Resorcinol
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Toluene
Monocyclic benzene moiety
Benzenoid
Tertiary alcohol
Cyclic alcohol
Vinylogous acid
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Alcohol
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aldehyde
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0038918)
Cell membrane (HMDB: HMDB0038918)

Cellular substructure

Extracellular (HMDB: HMDB0038918)
Membrane (HMDB: HMDB0038918)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038918)

Source

Endogenous

Endogenous (HMDB: HMDB0038918)

Plant

Plant (HMDB: HMDB0038918)

Animal

Animal (HMDB: HMDB0038918)

Exogenous

Food

Food (HMDB: HMDB0038918)

Vegetable

Mushroom

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0038918)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0038918)

Cellular process

Cell signaling (HMDB: HMDB0038918)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0038918)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0038918)

Nutrient

Nutrient (HMDB: HMDB0038918)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038918)

Emulsifier (HMDB: HMDB0038918)

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	21.65 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.023 g/L	ALOGPS
logP	3	ALOGPS
logP	3.8	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	8.7	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	108.35 m³·mol⁻¹	ChemAxon
Polarizability	42.96 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]+	190.628	31661259
DarkChem	[M-H]-	184.492	31661259
DeepCCS	[M-2H]-	228.765	30932474
DeepCCS	[M+Na]+	203.994	30932474
AllCCS	[M+H]+	196.7	32859911
AllCCS	[M+H-H2O]+	194.4	32859911
AllCCS	[M+NH4]+	198.8	32859911
AllCCS	[M+Na]+	199.5	32859911
AllCCS	[M-H]-	198.1	32859911
AllCCS	[M+Na-2H]-	198.4	32859911
AllCCS	[M+HCOO]-	198.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Armillaritin	CC1=CC(O)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC21	4462.3	Standard polar	33892256
Armillaritin	CC1=CC(O)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC21	2835.0	Standard non polar	33892256
Armillaritin	CC1=CC(O)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC21	3243.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Armillaritin,1TMS,isomer #1	CC1=CC(O[Si](C)(C)C)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC12	3371.7	Semi standard non polar	33892256
Armillaritin,1TMS,isomer #2	CC1=CC(O)=CC(O[Si](C)(C)C)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC12	3324.8	Semi standard non polar	33892256
Armillaritin,1TMS,isomer #3	CC1=CC(O)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O[Si](C)(C)C)CC(C)(C)CC12	3283.4	Semi standard non polar	33892256
Armillaritin,2TMS,isomer #1	CC1=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC12	3345.9	Semi standard non polar	33892256
Armillaritin,2TMS,isomer #2	CC1=CC(O[Si](C)(C)C)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O[Si](C)(C)C)CC(C)(C)CC12	3296.9	Semi standard non polar	33892256
Armillaritin,2TMS,isomer #3	CC1=CC(O)=CC(O[Si](C)(C)C)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O[Si](C)(C)C)CC(C)(C)CC12	3265.0	Semi standard non polar	33892256
Armillaritin,3TMS,isomer #1	CC1=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O[Si](C)(C)C)CC(C)(C)CC12	3309.9	Semi standard non polar	33892256
Armillaritin,1TBDMS,isomer #1	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC12	3595.2	Semi standard non polar	33892256
Armillaritin,1TBDMS,isomer #2	CC1=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC12	3538.4	Semi standard non polar	33892256
Armillaritin,1TBDMS,isomer #3	CC1=CC(O)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O[Si](C)(C)C(C)(C)C)CC(C)(C)CC12	3521.8	Semi standard non polar	33892256
Armillaritin,2TBDMS,isomer #1	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O)CC(C)(C)CC12	3741.7	Semi standard non polar	33892256
Armillaritin,2TBDMS,isomer #2	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O[Si](C)(C)C(C)(C)C)CC(C)(C)CC12	3728.3	Semi standard non polar	33892256
Armillaritin,2TBDMS,isomer #3	CC1=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O[Si](C)(C)C(C)(C)C)CC(C)(C)CC12	3687.9	Semi standard non polar	33892256
Armillaritin,3TBDMS,isomer #1	CC1=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C(=O)OC1CC2(C)C1C(C=O)=CC1(O[Si](C)(C)C(C)(C)C)CC(C)(C)CC12	3885.9	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 - Armillaritin GC-MS (Non-derivatized) - 70eV, Positive	splash10-0f79-3965000000-156670c6bec086410927	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Armillaritin GC-MS (3 TMS) - 70eV, Positive	splash10-0zi0-3094013000-8ea1c6bc7d0ca01dcf28	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Armillaritin GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Armillaritin 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 - Armillaritin 10V, Positive-QTOF	splash10-0ue9-0449600000-ea2d024c54948eb21768	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 20V, Positive-QTOF	splash10-0uyi-0794100000-fc4e5844c732c2606909	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 40V, Positive-QTOF	splash10-0ue9-2920000000-7cc65187f7764a27721c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 10V, Negative-QTOF	splash10-0002-0219000000-3f26e1e96dfa36760d01	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 20V, Negative-QTOF	splash10-007k-0938000000-82210c5b8297d179f921	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 40V, Negative-QTOF	splash10-00di-2920000000-cc0dacc37fc6293c17b6	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 10V, Negative-QTOF	splash10-00r2-0905000000-afad1cb60011c5cc19c0	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 20V, Negative-QTOF	splash10-00di-2921000000-456b807edba2e4640346	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 40V, Negative-QTOF	splash10-00ym-9753000000-c140bc70ccc7558c0bb8	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 10V, Positive-QTOF	splash10-0ue9-0774900000-78ed996c775067dfe6a3	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 20V, Positive-QTOF	splash10-0f89-4973200000-6cc391c257cda6abafb7	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Armillaritin 40V, Positive-QTOF	splash10-0zgs-5920000000-92ca70f4c07253bf8b17	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB018382

KNApSAcK ID

C00055511

Chemspider ID

35014692

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752492

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1872681

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 Armillaritin (HMDB0038918)

MOL for HMDB0038918 (Armillaritin)

3D MOL for HMDB0038918 (Armillaritin)

3D SDF for HMDB0038918 (Armillaritin)

3D-SDF for HMDB0038918 (Armillaritin)

PDB for HMDB0038918 (Armillaritin)

3D PDB for HMDB0038918 (Armillaritin)

SMILES for HMDB0038918 (Armillaritin)

INCHI for HMDB0038918 (Armillaritin)

Structure for HMDB0038918 (Armillaritin)

3D Structure for HMDB0038918 (Armillaritin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra