Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:08:16 UTC

Update Date

2022-03-07 02:55:55 UTC

HMDB ID

HMDB0038793

Secondary Accession Numbers

HMDB38793

Metabolite Identification

Common Name

Melleolide G

Description

Melleolide G 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 Melleolide G.

Structure

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

  Mrv0541 05061310392D          

 31 34  0  0  0  0            999 V2000
   -1.4606    1.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702    2.4911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0897    2.3068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7982   -1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5079    0.5236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6180    0.0598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1896   -0.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695    0.8998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2455    2.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1480    1.9572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3548   -0.6082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863    1.5151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7036    0.7073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0567    0.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7935    0.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -0.2648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6711    1.4877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3853   -0.6857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7092    1.2586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1423    0.1027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3380    0.2864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862    1.7165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8467    1.5184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079    0.8198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7404   -1.3375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3607    2.1073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8241   -1.2904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2232   -0.3182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032    0.2585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5551   -0.4486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0950    1.0748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 13  1  1  0  0  0  0
 13  5  2  0  0  0  0
 14  6  1  0  0  0  0
 14  8  1  0  0  0  0
 15  6  2  0  0  0  0
 15 11  1  0  0  0  0
 16  5  1  0  0  0  0
 16  7  2  0  0  0  0
 17  9  1  0  0  0  0
 17 14  1  0  0  0  0
 18  7  1  0  0  0  0
 19 10  1  0  0  0  0
 20 13  1  0  0  0  0
 20 18  2  0  0  0  0
 21 20  1  0  0  0  0
 22  2  1  0  0  0  0
 22  8  1  0  0  0  0
 22  9  1  0  0  0  0
 22 12  1  0  0  0  0
 23  3  1  0  0  0  0
 23 10  1  0  0  0  0
 23 17  1  0  0  0  0
 24 15  1  0  0  0  0
 24 19  1  0  0  0  0
 24 23  1  0  0  0  0
 25 11  1  0  0  0  0
 26 12  1  0  0  0  0
 27 18  1  0  0  0  0
 28 21  2  0  0  0  0
 29 24  1  0  0  0  0
 30  4  1  0  0  0  0
 30 16  1  0  0  0  0
 31 19  1  0  0  0  0
 31 21  1  0  0  0  0
M  END

HMDB0038793
     RDKit          3D
Melleolide G
 63 66  0  0  0  0  0  0  0  0999 V2000
   -8.8336    0.5564   -0.3423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7474    0.8297    0.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4648    0.5700    0.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4169    0.8392    0.8731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1304    0.5996    0.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9882    0.8956    1.3352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8955    0.0966   -0.8535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5304   -0.1253   -1.2718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1503   -0.5600   -2.3867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4885    0.1529   -0.3922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1343   -0.0383   -0.7545 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7820    1.0983   -0.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3529    0.2804    0.7026 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9132    0.7776    2.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8266    0.0413    0.6953 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6827    1.2529    0.7609 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0074    0.7707    0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5645    1.6934   -0.8445 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9890    0.6270    1.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1774    1.8488    1.9897 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7534   -0.5773   -0.4306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2650   -0.5300   -0.6483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6234   -1.8287   -0.8132 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3756   -1.9763   -0.3875 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6722   -3.3077   -0.5394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4979   -4.2306   -1.1414 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5746   -0.9022    0.2534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1905   -1.4331    1.2765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9576   -0.1779   -1.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7901   -0.6712   -2.9841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2399    0.0764   -1.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7289    1.2156   -1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7443   -0.4995   -0.6815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8070    0.6581    0.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5567    1.2279    1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4478   -0.0018    1.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4205    1.3218    2.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3502    1.7251    0.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0339   -0.4144   -1.8138 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2222    2.0011   -0.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4650    1.4376   -1.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1899    0.6060    2.2189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4315    0.2343    2.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0696    1.8824    2.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0778   -0.6289    1.5242 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    2.0763    0.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7856    1.6804    1.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4369    1.1580   -1.2997 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8455    1.8708   -1.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9789    2.6350   -0.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5475   -0.0832    2.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9701    0.2646    1.0135 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6016    1.9278    2.8056 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2299   -0.6746   -1.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0839   -1.3582    0.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0534    0.1956   -1.4419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0909   -2.7027   -1.2643 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3018   -3.6654    0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1857   -3.1135   -1.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9763   -4.7586   -0.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0406   -1.8488    0.9402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9730   -0.8861   -3.4292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0858   -0.1313   -1.8953 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 17 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
  7 29  1  0
 29 30  1  0
 29 31  2  0
 31  3  1  0
 27 11  1  0
 27 13  1  0
 22 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  6 36  1  0
  6 37  1  0
  6 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 14 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  0
 23 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
 28 61  1  0
 30 62  1  0
 31 63  1  0
M  END

  Mrv0541 05061310392D          

 31 34  0  0  0  0            999 V2000
   -1.4606    1.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702    2.4911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0897    2.3068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7982   -1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5079    0.5236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6180    0.0598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1896   -0.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695    0.8998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2455    2.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1480    1.9572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3548   -0.6082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863    1.5151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7036    0.7073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0567    0.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7935    0.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -0.2648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6711    1.4877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3853   -0.6857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7092    1.2586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1423    0.1027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3380    0.2864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862    1.7165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8467    1.5184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079    0.8198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7404   -1.3375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3607    2.1073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8241   -1.2904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2232   -0.3182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032    0.2585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5551   -0.4486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0950    1.0748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 13  1  1  0  0  0  0
 13  5  2  0  0  0  0
 14  6  1  0  0  0  0
 14  8  1  0  0  0  0
 15  6  2  0  0  0  0
 15 11  1  0  0  0  0
 16  5  1  0  0  0  0
 16  7  2  0  0  0  0
 17  9  1  0  0  0  0
 17 14  1  0  0  0  0
 18  7  1  0  0  0  0
 19 10  1  0  0  0  0
 20 13  1  0  0  0  0
 20 18  2  0  0  0  0
 21 20  1  0  0  0  0
 22  2  1  0  0  0  0
 22  8  1  0  0  0  0
 22  9  1  0  0  0  0
 22 12  1  0  0  0  0
 23  3  1  0  0  0  0
 23 10  1  0  0  0  0
 23 17  1  0  0  0  0
 24 15  1  0  0  0  0
 24 19  1  0  0  0  0
 24 23  1  0  0  0  0
 25 11  1  0  0  0  0
 26 12  1  0  0  0  0
 27 18  1  0  0  0  0
 28 21  2  0  0  0  0
 29 24  1  0  0  0  0
 30  4  1  0  0  0  0
 30 16  1  0  0  0  0
 31 19  1  0  0  0  0
 31 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0038793

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=CC(O)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O)C(C)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O7/c1-13-5-16(30-4)7-18(27)20(13)21(28)31-19-10-23(3)17-9-22(2,12-26)8-14(17)6-15(11-25)24(19,23)29/h5-7,14,17,19,25-27,29H,8-12H2,1-4H3

> <INCHI_KEY>
GGQLLLSSCCXUBL-UHFFFAOYSA-N

> <FORMULA>
C24H32O7

> <MOLECULAR_WEIGHT>
432.5067

> <EXACT_MASS>
432.214803378

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
47.11001363168777

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2a-hydroxy-3,6-bis(hydroxymethyl)-6,7b-dimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

> <ALOGPS_LOGP>
1.93

> <JCHEM_LOGP>
2.6588046116666666

> <ALOGPS_LOGS>
-4.01

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.935169597000563

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.762893782623156

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3867390890546716

> <JCHEM_POLAR_SURFACE_AREA>
116.45

> <JCHEM_REFRACTIVITY>
115.28669999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2a-hydroxy-3,6-bis(hydroxymethyl)-6,7b-dimethyl-1H,2H,4aH,5H,7H,7aH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038793
     RDKit          3D
Melleolide G
 63 66  0  0  0  0  0  0  0  0999 V2000
   -8.8336    0.5564   -0.3423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7474    0.8297    0.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4648    0.5700    0.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4169    0.8392    0.8731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1304    0.5996    0.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9882    0.8956    1.3352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8955    0.0966   -0.8535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5304   -0.1253   -1.2718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1503   -0.5600   -2.3867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4885    0.1529   -0.3922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1343   -0.0383   -0.7545 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7820    1.0983   -0.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3529    0.2804    0.7026 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9132    0.7776    2.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8266    0.0413    0.6953 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6827    1.2529    0.7609 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0074    0.7707    0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5645    1.6934   -0.8445 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9890    0.6270    1.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1774    1.8488    1.9897 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7534   -0.5773   -0.4306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2650   -0.5300   -0.6483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6234   -1.8287   -0.8132 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3756   -1.9763   -0.3875 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6722   -3.3077   -0.5394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4979   -4.2306   -1.1414 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5746   -0.9022    0.2534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1905   -1.4331    1.2765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9576   -0.1779   -1.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7901   -0.6712   -2.9841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2399    0.0764   -1.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7289    1.2156   -1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7443   -0.4995   -0.6815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8070    0.6581    0.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5567    1.2279    1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4478   -0.0018    1.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4205    1.3218    2.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3502    1.7251    0.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0339   -0.4144   -1.8138 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2222    2.0011   -0.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4650    1.4376   -1.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1899    0.6060    2.2189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4315    0.2343    2.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0696    1.8824    2.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0778   -0.6289    1.5242 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    2.0763    0.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7856    1.6804    1.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4369    1.1580   -1.2997 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8455    1.8708   -1.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9789    2.6350   -0.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5475   -0.0832    2.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9701    0.2646    1.0135 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6016    1.9278    2.8056 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2299   -0.6746   -1.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0839   -1.3582    0.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0534    0.1956   -1.4419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0909   -2.7027   -1.2643 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3018   -3.6654    0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1857   -3.1135   -1.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9763   -4.7586   -0.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0406   -1.8488    0.9402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9730   -0.8861   -3.4292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0858   -0.1313   -1.8953 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 17 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
  7 29  1  0
 29 30  1  0
 29 31  2  0
 31  3  1  0
 27 11  1  0
 27 13  1  0
 22 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  6 36  1  0
  6 37  1  0
  6 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 14 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  0
 23 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
 28 61  1  0
 30 62  1  0
 31 63  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      -2.726   2.792   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.971   4.650   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.901   4.306   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.090  -2.309   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.681   0.977   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.887   0.112   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.087  -1.623   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.223   1.680   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.058   3.882   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.143   3.653   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.529  -1.135   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.934   2.828   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.180   1.320   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.706   1.416   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.348   0.169   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.135  -0.494   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.986   2.777   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.586  -1.280   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.324   2.349   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.132   0.192   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.631   0.535   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.441   3.204   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.447   2.834   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.628   1.530   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.249  -2.497   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      10.007   3.934   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -1.538  -2.409   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       0.417  -0.594   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       1.499   0.483   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -6.636  -0.837   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -0.177   2.006   0.000  0.00  0.00           O+0
CONECT    1   13                                                            
CONECT    2   22                                                            
CONECT    3   23                                                            
CONECT    4   30                                                            
CONECT    5   13   16                                                       
CONECT    6   14   15                                                       
CONECT    7   16   18                                                       
CONECT    8   14   22                                                       
CONECT    9   17   22                                                       
CONECT   10   19   23                                                       
CONECT   11   15   25                                                       
CONECT   12   22   26                                                       
CONECT   13    1    5   20                                                  
CONECT   14    6    8   17                                                  
CONECT   15    6   11   24                                                  
CONECT   16    5    7   30                                                  
CONECT   17    9   14   23                                                  
CONECT   18    7   20   27                                                  
CONECT   19   10   24   31                                                  
CONECT   20   13   18   21                                                  
CONECT   21   20   28   31                                                  
CONECT   22    2    8    9   12                                             
CONECT   23    3   10   17   24                                             
CONECT   24   15   19   23   29                                             
CONECT   25   11                                                            
CONECT   26   12                                                            
CONECT   27   18                                                            
CONECT   28   21                                                            
CONECT   29   24                                                            
CONECT   30    4   16                                                       
CONECT   31   19   21                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0038793
HETATM    1  C1  UNL     1      -8.834   0.556  -0.342  1.00  0.00           C  
HETATM    2  O1  UNL     1      -7.747   0.830   0.523  1.00  0.00           O  
HETATM    3  C2  UNL     1      -6.465   0.570   0.024  1.00  0.00           C  
HETATM    4  C3  UNL     1      -5.417   0.839   0.873  1.00  0.00           C  
HETATM    5  C4  UNL     1      -4.130   0.600   0.427  1.00  0.00           C  
HETATM    6  C5  UNL     1      -2.988   0.896   1.335  1.00  0.00           C  
HETATM    7  C6  UNL     1      -3.895   0.097  -0.854  1.00  0.00           C  
HETATM    8  C7  UNL     1      -2.530  -0.125  -1.272  1.00  0.00           C  
HETATM    9  O2  UNL     1      -2.150  -0.560  -2.387  1.00  0.00           O  
HETATM   10  O3  UNL     1      -1.489   0.153  -0.392  1.00  0.00           O  
HETATM   11  C8  UNL     1      -0.134  -0.038  -0.755  1.00  0.00           C  
HETATM   12  C9  UNL     1       0.782   1.098  -0.396  1.00  0.00           C  
HETATM   13  C10 UNL     1       1.353   0.280   0.703  1.00  0.00           C  
HETATM   14  C11 UNL     1       0.913   0.778   2.065  1.00  0.00           C  
HETATM   15  C12 UNL     1       2.827   0.041   0.695  1.00  0.00           C  
HETATM   16  C13 UNL     1       3.683   1.253   0.761  1.00  0.00           C  
HETATM   17  C14 UNL     1       5.007   0.771   0.207  1.00  0.00           C  
HETATM   18  C15 UNL     1       5.565   1.693  -0.844  1.00  0.00           C  
HETATM   19  C16 UNL     1       5.989   0.627   1.348  1.00  0.00           C  
HETATM   20  O4  UNL     1       6.177   1.849   1.990  1.00  0.00           O  
HETATM   21  C17 UNL     1       4.753  -0.577  -0.431  1.00  0.00           C  
HETATM   22  C18 UNL     1       3.265  -0.530  -0.648  1.00  0.00           C  
HETATM   23  C19 UNL     1       2.623  -1.829  -0.813  1.00  0.00           C  
HETATM   24  C20 UNL     1       1.376  -1.976  -0.388  1.00  0.00           C  
HETATM   25  C21 UNL     1       0.672  -3.308  -0.539  1.00  0.00           C  
HETATM   26  O5  UNL     1       1.498  -4.231  -1.141  1.00  0.00           O  
HETATM   27  C22 UNL     1       0.575  -0.902   0.253  1.00  0.00           C  
HETATM   28  O6  UNL     1      -0.191  -1.433   1.277  1.00  0.00           O  
HETATM   29  C23 UNL     1      -4.958  -0.178  -1.719  1.00  0.00           C  
HETATM   30  O7  UNL     1      -4.790  -0.671  -2.984  1.00  0.00           O  
HETATM   31  C24 UNL     1      -6.240   0.076  -1.234  1.00  0.00           C  
HETATM   32  H1  UNL     1      -8.729   1.216  -1.232  1.00  0.00           H  
HETATM   33  H2  UNL     1      -8.744  -0.500  -0.682  1.00  0.00           H  
HETATM   34  H3  UNL     1      -9.807   0.658   0.153  1.00  0.00           H  
HETATM   35  H4  UNL     1      -5.557   1.228   1.869  1.00  0.00           H  
HETATM   36  H5  UNL     1      -2.448  -0.002   1.673  1.00  0.00           H  
HETATM   37  H6  UNL     1      -3.421   1.322   2.303  1.00  0.00           H  
HETATM   38  H7  UNL     1      -2.350   1.725   0.972  1.00  0.00           H  
HETATM   39  H8  UNL     1      -0.034  -0.414  -1.814  1.00  0.00           H  
HETATM   40  H9  UNL     1       0.222   2.001  -0.027  1.00  0.00           H  
HETATM   41  H10 UNL     1       1.465   1.438  -1.205  1.00  0.00           H  
HETATM   42  H11 UNL     1      -0.190   0.606   2.219  1.00  0.00           H  
HETATM   43  H12 UNL     1       1.432   0.234   2.894  1.00  0.00           H  
HETATM   44  H13 UNL     1       1.070   1.882   2.142  1.00  0.00           H  
HETATM   45  H14 UNL     1       3.078  -0.629   1.524  1.00  0.00           H  
HETATM   46  H15 UNL     1       3.297   2.076   0.112  1.00  0.00           H  
HETATM   47  H16 UNL     1       3.786   1.680   1.777  1.00  0.00           H  
HETATM   48  H17 UNL     1       6.437   1.158  -1.300  1.00  0.00           H  
HETATM   49  H18 UNL     1       4.845   1.871  -1.650  1.00  0.00           H  
HETATM   50  H19 UNL     1       5.979   2.635  -0.427  1.00  0.00           H  
HETATM   51  H20 UNL     1       5.547  -0.083   2.078  1.00  0.00           H  
HETATM   52  H21 UNL     1       6.970   0.265   1.014  1.00  0.00           H  
HETATM   53  H22 UNL     1       5.602   1.928   2.806  1.00  0.00           H  
HETATM   54  H23 UNL     1       5.230  -0.675  -1.418  1.00  0.00           H  
HETATM   55  H24 UNL     1       5.084  -1.358   0.251  1.00  0.00           H  
HETATM   56  H25 UNL     1       3.053   0.196  -1.442  1.00  0.00           H  
HETATM   57  H26 UNL     1       3.091  -2.703  -1.264  1.00  0.00           H  
HETATM   58  H27 UNL     1       0.302  -3.665   0.440  1.00  0.00           H  
HETATM   59  H28 UNL     1      -0.186  -3.114  -1.217  1.00  0.00           H  
HETATM   60  H29 UNL     1       1.976  -4.759  -0.430  1.00  0.00           H  
HETATM   61  H30 UNL     1      -1.041  -1.849   0.940  1.00  0.00           H  
HETATM   62  H31 UNL     1      -3.973  -0.886  -3.429  1.00  0.00           H  
HETATM   63  H32 UNL     1      -7.086  -0.131  -1.895  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3
CONECT    3    4    4   31
CONECT    4    5   35
CONECT    5    6    7    7
CONECT    6   36   37   38
CONECT    7    8   29
CONECT    8    9    9   10
CONECT   10   11
CONECT   11   12   27   39
CONECT   12   13   40   41
CONECT   13   14   15   27
CONECT   14   42   43   44
CONECT   15   16   22   45
CONECT   16   17   46   47
CONECT   17   18   19   21
CONECT   18   48   49   50
CONECT   19   20   51   52
CONECT   20   53
CONECT   21   22   54   55
CONECT   22   23   56
CONECT   23   24   24   57
CONECT   24   25   27
CONECT   25   26   58   59
CONECT   26   60
CONECT   27   28
CONECT   28   61
CONECT   29   30   31   31
CONECT   30   62
CONECT   31   63
END

HMDB0038793
     RDKit          3D
Melleolide G
 63 66  0  0  0  0  0  0  0  0999 V2000
   -8.8336    0.5564   -0.3423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7474    0.8297    0.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4648    0.5700    0.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4169    0.8392    0.8731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1304    0.5996    0.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9882    0.8956    1.3352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8955    0.0966   -0.8535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5304   -0.1253   -1.2718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1503   -0.5600   -2.3867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4885    0.1529   -0.3922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1343   -0.0383   -0.7545 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7820    1.0983   -0.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3529    0.2804    0.7026 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9132    0.7776    2.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8266    0.0413    0.6953 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6827    1.2529    0.7609 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0074    0.7707    0.2074 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5645    1.6934   -0.8445 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9890    0.6270    1.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1774    1.8488    1.9897 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7534   -0.5773   -0.4306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2650   -0.5300   -0.6483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6234   -1.8287   -0.8132 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3756   -1.9763   -0.3875 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6722   -3.3077   -0.5394 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4979   -4.2306   -1.1414 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5746   -0.9022    0.2534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1905   -1.4331    1.2765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9576   -0.1779   -1.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7901   -0.6712   -2.9841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2399    0.0764   -1.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7289    1.2156   -1.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7443   -0.4995   -0.6815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8070    0.6581    0.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5567    1.2279    1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4478   -0.0018    1.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4205    1.3218    2.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3502    1.7251    0.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0339   -0.4144   -1.8138 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2222    2.0011   -0.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4650    1.4376   -1.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1899    0.6060    2.2189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4315    0.2343    2.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0696    1.8824    2.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0778   -0.6289    1.5242 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    2.0763    0.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7856    1.6804    1.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4369    1.1580   -1.2997 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8455    1.8708   -1.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9789    2.6350   -0.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5475   -0.0832    2.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9701    0.2646    1.0135 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6016    1.9278    2.8056 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2299   -0.6746   -1.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0839   -1.3582    0.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0534    0.1956   -1.4419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0909   -2.7027   -1.2643 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3018   -3.6654    0.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1857   -3.1135   -1.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9763   -4.7586   -0.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0406   -1.8488    0.9402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9730   -0.8861   -3.4292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0858   -0.1313   -1.8953 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 17 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
  7 29  1  0
 29 30  1  0
 29 31  2  0
 31  3  1  0
 27 11  1  0
 27 13  1  0
 22 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  4 35  1  0
  6 36  1  0
  6 37  1  0
  6 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 14 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  0
 23 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
 28 61  1  0
 30 62  1  0
 31 63  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2a-Hydroxy-3,6-bis(hydroxymethyl)-6,7b-dimethyl-1H,2H,2ah,4ah,5H,6H,7H,7ah,7BH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoic acid	HMDB

Chemical Formula

C₂₄H₃₂O₇

Average Molecular Weight

432.5067

Monoisotopic Molecular Weight

432.214803378

IUPAC Name

2a-hydroxy-3,6-bis(hydroxymethyl)-6,7b-dimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

Traditional Name

2a-hydroxy-3,6-bis(hydroxymethyl)-6,7b-dimethyl-1H,2H,4aH,5H,7H,7aH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

CAS Registry Number

117258-75-0

SMILES

COC1=CC(O)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O)C(C)=C1

InChI Identifier

InChI=1S/C24H32O7/c1-13-5-16(30-4)7-18(27)20(13)21(28)31-19-10-23(3)17-9-22(2,12-26)8-14(17)6-15(11-25)24(19,23)29/h5-7,14,17,19,25-27,29H,8-12H2,1-4H3

InChI Key

GGQLLLSSCCXUBL-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
O-hydroxybenzoic acid ester
P-methoxybenzoic acid or derivatives
Methoxyphenol
Benzoate ester
Salicylic acid or derivatives
Benzoic acid or derivatives
Phenoxy compound
M-cresol
Anisole
Methoxybenzene
Phenol ether
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Toluene
Phenol
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Tertiary alcohol
Cyclobutanol
Carboxylic acid ester
Ether
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Primary alcohol
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0038793)

Source

Endogenous

Endogenous (HMDB: HMDB0038793)

Plant

Plant (HMDB: HMDB0038793)

Animal

Animal (HMDB: HMDB0038793)

Exogenous

Food

Food (HMDB: HMDB0038793)

Vegetable

Mushroom

Exogenous (HMDB: HMDB0038793)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0038793)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0038793)

Lipid metabolism pathway (HMDB: HMDB0038793)

Cellular process

Cell signaling (HMDB: HMDB0038793)

Biochemical process

Lipid transport (HMDB: HMDB0038793)

Role

Biological role

Energy source (HMDB: HMDB0038793)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0038793)

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	0.043 g/L	ALOGPS
logP	1.93	ALOGPS
logP	2.66	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	9.76	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	115.29 m³·mol⁻¹	ChemAxon
Polarizability	47.11 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	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	201.492	31661259
DarkChem	[M-H]-	199.671	31661259
DeepCCS	[M-2H]-	239.676	30932474
DeepCCS	[M+Na]+	215.111	30932474
AllCCS	[M+H]+	203.0	32859911
AllCCS	[M+H-H2O]+	200.9	32859911
AllCCS	[M+NH4]+	204.9	32859911
AllCCS	[M+Na]+	205.4	32859911
AllCCS	[M-H]-	201.3	32859911
AllCCS	[M+Na-2H]-	202.2	32859911
AllCCS	[M+HCOO]-	203.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Melleolide G	COC1=CC(O)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O)C(C)=C1	3840.6	Standard polar	33892256
Melleolide G	COC1=CC(O)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O)C(C)=C1	3273.1	Standard non polar	33892256
Melleolide G	COC1=CC(O)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O)C(C)=C1	3404.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Melleolide G,1TMS,isomer #1	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O)C(O[Si](C)(C)C)=C1	3542.9	Semi standard non polar	33892256
Melleolide G,1TMS,isomer #2	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C)CC4C=C(CO)C23O)C(O)=C1	3508.2	Semi standard non polar	33892256
Melleolide G,1TMS,isomer #3	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO[Si](C)(C)C)C23O)C(O)=C1	3471.6	Semi standard non polar	33892256
Melleolide G,1TMS,isomer #4	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O[Si](C)(C)C)C(O)=C1	3507.6	Semi standard non polar	33892256
Melleolide G,2TMS,isomer #1	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C)CC4C=C(CO)C23O)C(O[Si](C)(C)C)=C1	3461.6	Semi standard non polar	33892256
Melleolide G,2TMS,isomer #2	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO[Si](C)(C)C)C23O)C(O[Si](C)(C)C)=C1	3433.0	Semi standard non polar	33892256
Melleolide G,2TMS,isomer #3	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	3446.0	Semi standard non polar	33892256
Melleolide G,2TMS,isomer #4	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C)CC4C=C(CO[Si](C)(C)C)C23O)C(O)=C1	3378.9	Semi standard non polar	33892256
Melleolide G,2TMS,isomer #5	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C)CC4C=C(CO)C23O[Si](C)(C)C)C(O)=C1	3400.5	Semi standard non polar	33892256
Melleolide G,2TMS,isomer #6	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO[Si](C)(C)C)C23O[Si](C)(C)C)C(O)=C1	3436.2	Semi standard non polar	33892256
Melleolide G,3TMS,isomer #1	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C)CC4C=C(CO[Si](C)(C)C)C23O)C(O[Si](C)(C)C)=C1	3366.0	Semi standard non polar	33892256
Melleolide G,3TMS,isomer #2	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C)CC4C=C(CO)C23O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	3381.8	Semi standard non polar	33892256
Melleolide G,3TMS,isomer #3	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO[Si](C)(C)C)C23O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	3406.9	Semi standard non polar	33892256
Melleolide G,3TMS,isomer #4	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C)CC4C=C(CO[Si](C)(C)C)C23O[Si](C)(C)C)C(O)=C1	3340.0	Semi standard non polar	33892256
Melleolide G,4TMS,isomer #1	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C)CC4C=C(CO[Si](C)(C)C)C23O[Si](C)(C)C)C(O[Si](C)(C)C)=C1	3326.9	Semi standard non polar	33892256
Melleolide G,1TBDMS,isomer #1	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O)C(O[Si](C)(C)C(C)(C)C)=C1	3745.3	Semi standard non polar	33892256
Melleolide G,1TBDMS,isomer #2	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C(C)(C)C)CC4C=C(CO)C23O)C(O)=C1	3731.9	Semi standard non polar	33892256
Melleolide G,1TBDMS,isomer #3	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO[Si](C)(C)C(C)(C)C)C23O)C(O)=C1	3698.7	Semi standard non polar	33892256
Melleolide G,1TBDMS,isomer #4	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O[Si](C)(C)C(C)(C)C)C(O)=C1	3719.1	Semi standard non polar	33892256
Melleolide G,2TBDMS,isomer #1	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C(C)(C)C)CC4C=C(CO)C23O)C(O[Si](C)(C)C(C)(C)C)=C1	3888.3	Semi standard non polar	33892256
Melleolide G,2TBDMS,isomer #2	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO[Si](C)(C)C(C)(C)C)C23O)C(O[Si](C)(C)C(C)(C)C)=C1	3867.8	Semi standard non polar	33892256
Melleolide G,2TBDMS,isomer #3	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO)C23O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	3877.9	Semi standard non polar	33892256
Melleolide G,2TBDMS,isomer #4	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C(C)(C)C)CC4C=C(CO[Si](C)(C)C(C)(C)C)C23O)C(O)=C1	3846.5	Semi standard non polar	33892256
Melleolide G,2TBDMS,isomer #5	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C(C)(C)C)CC4C=C(CO)C23O[Si](C)(C)C(C)(C)C)C(O)=C1	3862.0	Semi standard non polar	33892256
Melleolide G,2TBDMS,isomer #6	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO[Si](C)(C)C(C)(C)C)C23O[Si](C)(C)C(C)(C)C)C(O)=C1	3882.9	Semi standard non polar	33892256
Melleolide G,3TBDMS,isomer #1	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C(C)(C)C)CC4C=C(CO[Si](C)(C)C(C)(C)C)C23O)C(O[Si](C)(C)C(C)(C)C)=C1	4007.1	Semi standard non polar	33892256
Melleolide G,3TBDMS,isomer #2	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C(C)(C)C)CC4C=C(CO)C23O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	4031.2	Semi standard non polar	33892256
Melleolide G,3TBDMS,isomer #3	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO)CC4C=C(CO[Si](C)(C)C(C)(C)C)C23O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	4038.1	Semi standard non polar	33892256
Melleolide G,3TBDMS,isomer #4	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C(C)(C)C)CC4C=C(CO[Si](C)(C)C(C)(C)C)C23O[Si](C)(C)C(C)(C)C)C(O)=C1	4026.3	Semi standard non polar	33892256
Melleolide G,4TBDMS,isomer #1	COC1=CC(C)=C(C(=O)OC2CC3(C)C4CC(C)(CO[Si](C)(C)C(C)(C)C)CC4C=C(CO[Si](C)(C)C(C)(C)C)C23O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1	4180.1	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 - Melleolide G GC-MS (Non-derivatized) - 70eV, Positive	splash10-00xr-3980100000-3943583fce43e07f172e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Melleolide G GC-MS (3 TMS) - 70eV, Positive	splash10-014i-0009000000-637ee50050055750fbc9	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Melleolide G GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Melleolide G 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 - Melleolide G 10V, Positive-QTOF	splash10-0159-0232900000-cbfcae546d46e275258a	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 20V, Positive-QTOF	splash10-014j-0945500000-d79f81ed50f5e1fb19ad	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 40V, Positive-QTOF	splash10-014i-1930000000-fcdc38d74597f3b5e73c	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 10V, Negative-QTOF	splash10-001i-0311900000-562a73e1c71f1cebf30d	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 20V, Negative-QTOF	splash10-0f8i-0846900000-335dcf46ffbaa5c501ac	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 40V, Negative-QTOF	splash10-000i-1930000000-a09f9d56a3b93dcd9e98	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 10V, Positive-QTOF	splash10-00lr-0373900000-819855aaa98337bd6afa	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 20V, Positive-QTOF	splash10-02ar-1945500000-14d88bfd557dc1004b2d	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 40V, Positive-QTOF	splash10-02aa-2900000000-aa54552586ee2dc13f0f	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 10V, Negative-QTOF	splash10-001i-0205900000-dbd66c196fcb6109731b	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 20V, Negative-QTOF	splash10-001r-0952400000-06381fa3b7cc4c61baf4	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Melleolide G 40V, Negative-QTOF	splash10-002u-6956100000-e25d06b8df0848d4706c	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
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

FDB018218

KNApSAcK ID

C00056549

Chemspider ID

35014664

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14166120

PDB ID

Not Available

ChEBI ID

175494

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 Melleolide G (HMDB0038793)

MOL for HMDB0038793 (Melleolide G)

3D MOL for HMDB0038793 (Melleolide G)

3D SDF for HMDB0038793 (Melleolide G)

3D-SDF for HMDB0038793 (Melleolide G)

PDB for HMDB0038793 (Melleolide G)

3D PDB for HMDB0038793 (Melleolide G)

SMILES for HMDB0038793 (Melleolide G)

INCHI for HMDB0038793 (Melleolide G)

Structure for HMDB0038793 (Melleolide G)

3D Structure for HMDB0038793 (Melleolide G)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra