MiMeDB: Showing metabocard for Ganodermanondiol (MMDBc0016026)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:44:36 UTC

Update Date

2022-12-15 22:51:45 UTC

Metabolite ID

MMDBc0016026

Metabolite Identification

Common Name

Ganodermanondiol

Description

Ganodermanondiol belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review a significant number of articles have been published on Ganodermanondiol.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108442D          

 37 40  0  0  1  0            999 V2000
    3.5139    1.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7787   -2.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7762   -2.0151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0495    2.1087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0955    0.9510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6900    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1741    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0119   -1.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3858    0.2675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9067   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7188   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8794    0.9189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4801   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8779    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3142   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5021   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1629   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0658    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2030    0.3804    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7094   -0.2709    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1582   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6264   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2506   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5945   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0622    0.8060    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0627   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558    1.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9703   -0.6798    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5339   -0.2441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8142   -1.0201    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.4067   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7513    0.0418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2072    1.9637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6967    1.0317    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8992   -0.4264    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5309   -2.2316    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3731    1.5702    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0  0  0  0
 12  9  1  0  0  0  0
 16 15  1  0  0  0  0
 17 13  1  0  0  0  0
 18 14  1  0  0  0  0
 19  1  1  1  0  0  0
 19  9  1  0  0  0  0
 20 13  1  0  0  0  0
 20 19  1  6  0  0  0
 21 14  2  0  0  0  0
 22 10  2  0  0  0  0
 22 21  1  0  0  0  0
 23 11  1  0  0  0  0
 24 15  1  0  0  0  0
 25 12  1  0  0  0  0
 26  2  1  0  0  0  0
 26  3  1  0  0  0  0
 26 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27  4  1  0  0  0  0
 27  5  1  0  0  0  0
 27 25  1  0  0  0  0
 28  6  1  6  0  0  0
 28 16  1  0  0  0  0
 28 21  1  0  0  0  0
 28 23  1  0  0  0  0
 29  7  1  6  0  0  0
 29 18  1  0  0  0  0
 29 20  1  0  0  0  0
 30  8  1  1  0  0  0
 30 17  1  0  0  0  0
 30 22  1  0  0  0  0
 30 29  1  0  0  0  0
 31 24  2  0  0  0  0
 25 32  1  1  0  0  0
 33 27  1  0  0  0  0
 19 34  1  6  0  0  0
 20 35  1  1  0  0  0
 36 23  1  0  0  0  0
 25 37  1  1  0  0  0
M  END


  Mrv1652305152108442D          

 37 40  0  0  1  0            999 V2000
    3.5139    1.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7787   -2.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7762   -2.0151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0495    2.1087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0955    0.9510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6900    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1741    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0119   -1.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3858    0.2675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9067   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7188   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8794    0.9189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4801   -1.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8779    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3142   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5021   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1629   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0658    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2030    0.3804    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7094   -0.2709    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1582   -0.5346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6264   -1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2506   -1.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5945   -0.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0622    0.8060    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0627   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558    1.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9703   -0.6798    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5339   -0.2441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8142   -1.0201    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.4067   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7513    0.0418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2072    1.9637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6967    1.0317    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8992   -0.4264    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5309   -2.2316    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3731    1.5702    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0  0  0  0
 12  9  1  0  0  0  0
 16 15  1  0  0  0  0
 17 13  1  0  0  0  0
 18 14  1  0  0  0  0
 19  1  1  1  0  0  0
 19  9  1  0  0  0  0
 20 13  1  0  0  0  0
 20 19  1  6  0  0  0
 21 14  2  0  0  0  0
 22 10  2  0  0  0  0
 22 21  1  0  0  0  0
 23 11  1  0  0  0  0
 24 15  1  0  0  0  0
 25 12  1  0  0  0  0
 26  2  1  0  0  0  0
 26  3  1  0  0  0  0
 26 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27  4  1  0  0  0  0
 27  5  1  0  0  0  0
 27 25  1  0  0  0  0
 28  6  1  6  0  0  0
 28 16  1  0  0  0  0
 28 21  1  0  0  0  0
 28 23  1  0  0  0  0
 29  7  1  6  0  0  0
 29 18  1  0  0  0  0
 29 20  1  0  0  0  0
 30  8  1  1  0  0  0
 30 17  1  0  0  0  0
 30 22  1  0  0  0  0
 30 29  1  0  0  0  0
 31 24  2  0  0  0  0
 25 32  1  1  0  0  0
 33 27  1  0  0  0  0
 19 34  1  6  0  0  0
 20 35  1  1  0  0  0
 36 23  1  0  0  0  0
 25 37  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0016026

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](C)(CC[C@]([H])(O)C(C)(C)O)[C@@]1([H])CC[C@@]2(C)C3=CCC4([H])C(C)(C)C(=O)CC[C@]4(C)C3=CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O3/c1-19(9-12-25(32)27(4,5)33)20-13-17-30(8)22-10-11-23-26(2,3)24(31)15-16-28(23,6)21(22)14-18-29(20,30)7/h10,14,19-20,23,25,32-33H,9,11-13,15-18H2,1-8H3/t19-,20-,23?,25+,28-,29-,30+/m1/s1

> <INCHI_KEY>
AAJIHHYEPHRIET-JNAHJFNHSA-N

> <FORMULA>
C30H48O3

> <MOLECULAR_WEIGHT>
456.711

> <EXACT_MASS>
456.360345406

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
55.78582618333625

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,11R,14R,15R)-14-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),9-dien-5-one

> <ALOGPS_LOGP>
6.84

> <JCHEM_LOGP>
5.767839759333333

> <ALOGPS_LOGS>
-5.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.325091178549847

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.849642066659626

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0890278698803355

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
137.18659999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,11R,14R,15R)-14-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),9-dien-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       6.559   2.137   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.520  -4.434   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.382  -3.762   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.092   3.936   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.178   1.775   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.488   0.179   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.792   0.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.356  -3.399   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.453   0.499   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.026  -3.624   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.542  -3.895   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.508   1.715   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.496  -1.985   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.972   0.451   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.520  -0.363   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.004  -0.092   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.771  -2.849   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.456   0.722   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.979   0.710   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.924  -0.506   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.495  -0.998   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.503  -2.175   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.534  -2.717   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.043  -1.811   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.983   1.505   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.050  -2.988   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.038   2.720   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.011  -1.269   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.463  -0.456   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.987  -1.904   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      17.559  -2.082   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       1.402   0.078   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       2.253   3.666   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0       5.034   1.926   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       5.412  -0.796   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      14.058  -4.166   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.563   2.931   0.000  0.00  0.00           H+0
CONECT    1   19                                                            
CONECT    2   26                                                            
CONECT    3   26                                                            
CONECT    4   27                                                            
CONECT    5   27                                                            
CONECT    6   28                                                            
CONECT    7   29                                                            
CONECT    8   30                                                            
CONECT    9   12   19                                                       
CONECT   10   11   22                                                       
CONECT   11   10   23                                                       
CONECT   12    9   25                                                       
CONECT   13   17   20                                                       
CONECT   14   18   21                                                       
CONECT   15   16   24                                                       
CONECT   16   15   28                                                       
CONECT   17   13   30                                                       
CONECT   18   14   29                                                       
CONECT   19    1    9   20   34                                             
CONECT   20   13   19   29   35                                             
CONECT   21   14   22   28                                                  
CONECT   22   10   21   30                                                  
CONECT   23   11   26   28   36                                             
CONECT   24   15   26   31                                                  
CONECT   25   12   27   32   37                                             
CONECT   26    2    3   23   24                                             
CONECT   27    4    5   25   33                                             
CONECT   28    6   16   21   23                                             
CONECT   29    7   18   20   30                                             
CONECT   30    8   17   22   29                                             
CONECT   31   24                                                            
CONECT   32   25                                                            
CONECT   33   27                                                            
CONECT   34   19                                                            
CONECT   35   20                                                            
CONECT   36   23                                                            
CONECT   37   25                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

Synonyms

Not Available

Molecular Formula

C₃₀H₄₈O₃

Average Mass

456.711

Monoisotopic Mass

456.360345406

IUPAC Name

(2S,11R,14R,15R)-14-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),9-dien-5-one

Traditional Name

(2S,11R,14R,15R)-14-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),9-dien-5-one

CAS Registry Number

Not Available

SMILES

[H][C@@](C)(CC[C@]([H])(O)C(C)(C)O)[C@@]1([H])CC[C@@]2(C)C3=CCC4([H])C(C)(C)C(=O)CC[C@]4(C)C3=CC[C@]12C

InChI Identifier

InChI=1S/C30H48O3/c1-19(9-12-25(32)27(4,5)33)20-13-17-30(8)22-10-11-23-26(2,3)24(31)15-16-28(23,6)21(22)14-18-29(20,30)7/h10,14,19-20,23,25,32-33H,9,11-13,15-18H2,1-8H3/t19-,20-,23?,25+,28-,29-,30+/m1/s1

InChI Key

AAJIHHYEPHRIET-JNAHJFNHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
25-hydroxysteroid
24-hydroxysteroid
Dihydroxy bile acid, alcohol, or derivatives
Cholane-skeleton
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
14-alpha-methylsteroid
Oxosteroid
3-oxosteroid
3-oxo-delta-7-steroid
Steroid
Delta-7-steroid
Tertiary alcohol
Cyclic ketone
Secondary alcohol
Ketone
1,2-diol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0018 g/L	ALOGPS
logP	6.84	ALOGPS
logP	5.77	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	13.85	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	137.19 m³·mol⁻¹	ChemAxon
Polarizability	55.79 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Basidiomycota	3	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

C00023866

Chemspider ID

8429051

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10253565

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Ganodermanondiol (MMDBc0016026)

MOL for #<Metabolite:0x00007f46cc908228>

3D MOL for #<Metabolite:0x00007f46cc908228>

3D SDF for #<Metabolite:0x00007f46cc908228>

3D-SDF for #<Metabolite:0x00007f46cc908228>

PDB for #<Metabolite:0x00007f46cc908228>

3D PDB for #<Metabolite:0x00007f46cc908228>

SMILES for #<Metabolite:0x00007f46cc908228>

INCHI for #<Metabolite:0x00007f46cc908228>

Structure for #<Metabolite:0x00007f46cc908228>

3D Structure for #<Metabolite:0x00007f46cc908228>