NP-MRD: Showing NP-Card for Ganoderic acid X (NP0048215)

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Record Information

Version

2.0

Created at

2022-03-17 20:52:57 UTC

Updated at

2022-03-17 20:52:57 UTC

NP-MRD ID

NP0048215

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ganoderic acid X

Description

Ganoderic acid X, also known as ganoderate X, belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Ganoderic acid X is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, ganoderic acid X has been detected, but not quantified in, mushrooms. Ganoderic acid X is found in Ganoderma lucidum . This could make ganoderic acid X a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241209522D          

 37 40  0  0  0  0            999 V2000
   -2.5595   -1.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8445   -1.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1295   -1.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1295   -0.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8445   -0.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8445    0.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1295    1.2176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4159    0.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3293    1.6260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3293   -0.8393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4159   -0.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3692   -0.2743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    0.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3692    1.0608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5595    0.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5595   -0.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2732   -0.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9882   -0.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9882   -1.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7019   -1.6700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0722    2.4579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6236    1.8446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4308    2.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9835    1.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7906    1.5751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3421    0.9619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1492    1.1338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6236   -1.0593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7424   -2.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2732   -1.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8040   -2.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0877    0.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7019    0.5205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4037    1.9188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0722   -1.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3252   -2.4579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7363   -1.5008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 16  1  0  0  0  0
  1 30  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4 11  1  0  0  0  0
  5  6  2  0  0  0  0
  5 16  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 11  1  0  0  0  0
  8 14  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 28  1  0  0  0  0
 13 14  1  0  0  0  0
 14 22  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 30  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 32  1  0  0  0  0
 27 33  1  0  0  0  0
 27 34  2  0  0  0  0
 28 35  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END


  Mrv0541 02241209522D          

 37 40  0  0  0  0            999 V2000
   -2.5595   -1.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8445   -1.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1295   -1.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1295   -0.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8445   -0.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8445    0.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1295    1.2176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4159    0.8050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3293    1.6260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3293   -0.8393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4159   -0.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3692   -0.2743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    0.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3692    1.0608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5595    0.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5595   -0.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2732   -0.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9882   -0.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9882   -1.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7019   -1.6700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0722    2.4579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6236    1.8446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4308    2.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9835    1.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7906    1.5751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3421    0.9619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1492    1.1338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6236   -1.0593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7424   -2.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2732   -1.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8040   -2.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0877    0.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7019    0.5205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4037    1.9188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0722   -1.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3252   -2.4579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7363   -1.5008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 16  1  0  0  0  0
  1 30  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4 11  1  0  0  0  0
  5  6  2  0  0  0  0
  5 16  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 11  1  0  0  0  0
  8 14  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 28  1  0  0  0  0
 13 14  1  0  0  0  0
 14 22  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 30  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 32  1  0  0  0  0
 27 33  1  0  0  0  0
 27 34  2  0  0  0  0
 28 35  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0048215

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CC\C=C(/C)C(O)=O)C1CC(OC(C)=O)C2(C)C3=CCC4C(C)(C)C(O)CCC4(C)C3=CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C32H48O5/c1-19(10-9-11-20(2)28(35)36)24-18-27(37-21(3)33)32(8)23-12-13-25-29(4,5)26(34)15-16-30(25,6)22(23)14-17-31(24,32)7/h11-12,14,19,24-27,34H,9-10,13,15-18H2,1-8H3,(H,35,36)/b20-11+

> <INCHI_KEY>
YCWGPALSXRBKTM-RGVLZGJSSA-N

> <FORMULA>
C32H48O5

> <MOLECULAR_WEIGHT>
512.7205

> <EXACT_MASS>
512.350174646

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
59.845587288584596

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-6-[12-(acetyloxy)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl]-2-methylhept-2-enoic acid

> <ALOGPS_LOGP>
6.93

> <JCHEM_LOGP>
5.7467578066666665

> <ALOGPS_LOGS>
-5.53

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
19.618794118226784

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.656692958327697

> <JCHEM_PKA_STRONGEST_BASIC>
-0.778540788845142

> <JCHEM_POLAR_SURFACE_AREA>
83.82999999999998

> <JCHEM_REFRACTIVITY>
148.04550000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.50e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-6-[12-(acetyloxy)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl]-2-methylhept-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -4.778  -2.347   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.443  -3.117   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.108  -2.347   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.108  -0.807   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.443  -0.037   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.443   1.503   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.108   2.273   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.776   1.503   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.615   3.035   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.615  -1.567   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.776  -0.037   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.689  -0.512   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.595   0.733   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.689   1.980   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.778   0.733   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.778  -0.807   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.110  -0.037   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -7.445  -0.807   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -7.445  -2.347   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -8.777  -3.117   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.135   4.588   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.164   3.443   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.671   3.764   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.703   2.619   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.209   2.940   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.239   1.796   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.745   2.116   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.164  -1.977   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -5.119  -4.295   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.110  -3.117   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.101  -4.295   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.764   0.332   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       8.777   0.972   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       8.220   3.582   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       0.135  -3.117   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       0.607  -4.588   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -1.374  -2.801   0.000  0.00  0.00           C+0
CONECT    1    2   16   30                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   11   14                                             
CONECT    9    8                                                            
CONECT   10   11                                                            
CONECT   11    4    8   10   12                                             
CONECT   12   11   13   28                                                  
CONECT   13   12   14                                                       
CONECT   14    8   13   22                                                  
CONECT   15   16                                                            
CONECT   16    1    5   15   17                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   30                                                  
CONECT   20   19                                                            
CONECT   21   22                                                            
CONECT   22   14   21   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   32                                                  
CONECT   27   26   33   34                                                  
CONECT   28   12   35                                                       
CONECT   29   30                                                            
CONECT   30    1   19   29   31                                             
CONECT   31   30                                                            
CONECT   32   26                                                            
CONECT   33   27                                                            
CONECT   34   27                                                            
CONECT   35   28   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Value	Source
Ganoderate X	Generator
(2E)-6-[12-(Acetyloxy)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl]-2-methylhept-2-enoate	Generator
3alpha-Hydroxy-15alpha-acetoxy-lanosta-7,9(11),24-trien-26-Oic acid	MeSH
Ganoderic acid X	MeSH

Chemical Formula

C₃₂H₄₈O₅

Average Mass

512.7205 Da

Monoisotopic Mass

512.35017 Da

IUPAC Name

(2E)-6-[12-(acetyloxy)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl]-2-methylhept-2-enoic acid

Traditional Name

(2E)-6-[12-(acetyloxy)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-1(17),9-dien-14-yl]-2-methylhept-2-enoic acid

CAS Registry Number

86377-53-9

SMILES

CC(CC\C=C(/C)C(O)=O)C1CC(OC(C)=O)C2(C)C3=CCC4C(C)(C)C(O)CCC4(C)C3=CCC12C

InChI Identifier

InChI=1S/C32H48O5/c1-19(10-9-11-20(2)28(35)36)24-18-27(37-21(3)33)32(8)23-12-13-25-29(4,5)26(34)15-16-30(25,6)22(23)14-17-31(24,32)7/h11-12,14,19,24-27,34H,9-10,13,15-18H2,1-8H3,(H,35,36)/b20-11+

InChI Key

YCWGPALSXRBKTM-RGVLZGJSSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Agaricus bisporus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Ganoderma lucidum	Fungi	KNApSAcK
Pleurotus ostreatus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...

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

Not Available

Substituents

Not Available

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	6.93	ALOGPS
logP	5.75	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	4.66	ChemAxon
pKa (Strongest Basic)	-0.78	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	148.05 m³·mol⁻¹	ChemAxon
Polarizability	59.85 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0035332

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB017048

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14137626

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Ganoderic acid X (NP0048215)

MOL for NP0048215 (Ganoderic acid X)

3D MOL for NP0048215 (Ganoderic acid X)

3D SDF for NP0048215 (Ganoderic acid X)

3D-SDF for NP0048215 (Ganoderic acid X)

PDB for NP0048215 (Ganoderic acid X)

3D PDB for NP0048215 (Ganoderic acid X)

SMILES for NP0048215 (Ganoderic acid X)

INCHI for NP0048215 (Ganoderic acid X)

Structure for NP0048215 (Ganoderic acid X)

3D Structure for NP0048215 (Ganoderic acid X)