Np mrd loader

Showing NP-Card for Ganoderic acid Ma (NP0336403)

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Record Information
Version2.0
Created at2024-09-11 06:06:43 UTC
Updated at2024-09-11 06:06:43 UTC
NP-MRD IDNP0336403
Secondary Accession NumbersNone
Natural Product Identification
Common NameGanoderic acid Ma
DescriptionGanoderic acid Ma is also known as ganoderate ma. Ganoderic acid Ma was first documented in 2021 (PMID: 34591394). Based on a literature review very few articles have been published on Ganoderic acid Ma.
Structure
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MOLSDFPDBSMILESInChI

MOL for NP0336403 (Ganoderic acid Ma)


  Mrv2104 05262308382D          

 41 44  0  0  0  0            999 V2000
    2.1583   -2.6675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6170   -2.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1117    1.9701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1435    0.5136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4231    0.8525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4206    0.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3344   -1.6191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8185   -2.0212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6563    0.2981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5238   -2.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0302   -1.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2934   -2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5223   -1.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9587   -1.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1465   -1.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7102   -1.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1245   -0.4595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3632    0.5635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8474   -1.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7998   -2.9803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2996    1.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3314    0.3684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8026   -0.9884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3538   -1.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5511    0.4183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8950   -0.0672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8073    0.0035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2390   -0.5527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2708   -0.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4889   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7071    0.0780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6147   -0.8432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1784   -1.2788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4587   -0.5029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7677    2.4556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7996    0.9991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8341    0.8280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3284   -3.8573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9952   -4.3958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0193    1.0490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0511   -0.4075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0  0  0  0
 12 10  1  0  0  0  0
 15 14  1  0  0  0  0
 16 13  1  0  0  0  0
 19  1  1  0  0  0  0
 19 11  1  0  0  0  0
 20  2  1  0  0  0  0
 20 12  2  0  0  0  0
 21  3  1  0  0  0  0
 22  4  1  0  0  0  0
 23 13  1  0  0  0  0
 24 17  1  0  0  0  0
 24 19  1  0  0  0  0
 25 18  1  0  0  0  0
 26 18  1  0  0  0  0
 27 17  1  0  0  0  0
 28 14  1  0  0  0  0
 29 23  2  0  0  0  0
 29 25  1  0  0  0  0
 30 20  1  0  0  0  0
 31  5  1  0  0  0  0
 31  6  1  0  0  0  0
 31 26  1  0  0  0  0
 31 28  1  0  0  0  0
 32  7  1  0  0  0  0
 32 15  1  0  0  0  0
 32 23  1  0  0  0  0
 32 26  1  0  0  0  0
 33  8  1  0  0  0  0
 33 16  1  0  0  0  0
 33 24  1  0  0  0  0
 34  9  1  0  0  0  0
 34 27  1  0  0  0  0
 34 29  1  0  0  0  0
 34 33  1  0  0  0  0
 35 21  2  0  0  0  0
 36 22  2  0  0  0  0
 37 27  1  0  0  0  0
 38 30  2  0  0  0  0
 39 30  1  0  0  0  0
 40 21  1  0  0  0  0
 40 25  1  0  0  0  0
 41 22  1  0  0  0  0
 41 28  1  0  0  0  0
M  END
Download

3D MOL for NP0336403 (Ganoderic acid Ma)

Download
3D SDF for NP0336403 (Ganoderic acid Ma)

  Mrv2104 05262308382D          

 41 44  0  0  0  0            999 V2000
    2.1583   -2.6675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6170   -2.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1117    1.9701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1435    0.5136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4231    0.8525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4206    0.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3344   -1.6191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8185   -2.0212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6563    0.2981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5238   -2.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0302   -1.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2934   -2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5223   -1.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9587   -1.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1465   -1.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7102   -1.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1245   -0.4595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3632    0.5635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8474   -1.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7998   -2.9803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2996    1.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3314    0.3684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8026   -0.9884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3538   -1.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5511    0.4183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8950   -0.0672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8073    0.0035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2390   -0.5527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2708   -0.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4889   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7071    0.0780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6147   -0.8432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1784   -1.2788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4587   -0.5029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7677    2.4556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7996    0.9991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8341    0.8280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3284   -3.8573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9952   -4.3958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0193    1.0490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0511   -0.4075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0  0  0  0
 12 10  1  0  0  0  0
 15 14  1  0  0  0  0
 16 13  1  0  0  0  0
 19  1  1  0  0  0  0
 19 11  1  0  0  0  0
 20  2  1  0  0  0  0
 20 12  2  0  0  0  0
 21  3  1  0  0  0  0
 22  4  1  0  0  0  0
 23 13  1  0  0  0  0
 24 17  1  0  0  0  0
 24 19  1  0  0  0  0
 25 18  1  0  0  0  0
 26 18  1  0  0  0  0
 27 17  1  0  0  0  0
 28 14  1  0  0  0  0
 29 23  2  0  0  0  0
 29 25  1  0  0  0  0
 30 20  1  0  0  0  0
 31  5  1  0  0  0  0
 31  6  1  0  0  0  0
 31 26  1  0  0  0  0
 31 28  1  0  0  0  0
 32  7  1  0  0  0  0
 32 15  1  0  0  0  0
 32 23  1  0  0  0  0
 32 26  1  0  0  0  0
 33  8  1  0  0  0  0
 33 16  1  0  0  0  0
 33 24  1  0  0  0  0
 34  9  1  0  0  0  0
 34 27  1  0  0  0  0
 34 29  1  0  0  0  0
 34 33  1  0  0  0  0
 35 21  2  0  0  0  0
 36 22  2  0  0  0  0
 37 27  1  0  0  0  0
 38 30  2  0  0  0  0
 39 30  1  0  0  0  0
 40 21  1  0  0  0  0
 40 25  1  0  0  0  0
 41 22  1  0  0  0  0
 41 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0336403

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CC\C=C(\C)C(O)=O)C1CC(O)C2(C)C3=C(CCC12C)C1(C)CCC(OC(C)=O)C(C)(C)C1CC3OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1/C34H52O7/c1-19(11-10-12-20(2)30(38)39)24-17-27(37)34(9)29-23(13-16-33(24,34)8)32(7)15-14-28(41-22(4)36)31(5,6)26(32)18-25(29)40-21(3)35/h12,19,24-28,37H,10-11,13-18H2,1-9H3,(H,38,39)/b20-12-

> <INCHI_KEY>
JBMVFHJFFZPAJI-NDENLUEZNA-N

> <FORMULA>
C34H52O7

> <MOLECULAR_WEIGHT>
572.783

> <EXACT_MASS>
572.371304014

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
65.61575165397619

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z)-6-[4,7-bis(acetyloxy)-3-hydroxy-3a,6,6,9a,11a-pentamethyl-1H,2H,3H,3aH,4H,5H,5aH,6H,7H,8H,9H,9aH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]-2-methylhept-2-enoic acid

> <JCHEM_LOGP>
5.318993806666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.61709948095719

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.427019256890048

> <JCHEM_PKA_STRONGEST_BASIC>
-2.966280687047404

> <JCHEM_POLAR_SURFACE_AREA>
110.13000000000001

> <JCHEM_REFRACTIVITY>
157.5959

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-6-[4,7-bis(acetyloxy)-3-hydroxy-3a,6,6,9a,11a-pentamethyl-1H,2H,3H,4H,5H,5aH,7H,8H,9H,10H,11H-cyclopenta[a]phenanthren-1-yl]-2-methylhept-2-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0336403 (Ganoderic acid Ma)
Download
PDB for NP0336403 (Ganoderic acid Ma)
HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0       4.029  -4.979   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.018  -5.352   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.542   3.678   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.068   0.959   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.990   1.591   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.852   0.919   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.958  -3.022   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.261  -3.773   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.825   0.556   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.978  -4.558   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.923  -3.342   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.548  -4.347   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.442  -3.293   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.990  -2.480   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.473  -2.751   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.926  -3.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.966  -0.858   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.011   1.052   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.448  -3.553   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.493  -5.563   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.026   3.406   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.552   0.688   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.965  -1.845   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.394  -2.337   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.495   0.781   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.004  -0.125   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.240   0.007   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.513  -1.032   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.972  -0.668   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.913  -6.990   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.520   0.146   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.481  -1.574   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.933  -2.387   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.456  -0.939   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       7.033   4.584   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      14.559   1.865   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       5.290   1.546   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       0.613  -7.200   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -1.858  -8.205   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       7.503   1.958   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      15.029  -0.761   0.000  0.00  0.00           O+0
CONECT    1   19                                                            
CONECT    2   20                                                            
CONECT    3   21                                                            
CONECT    4   22                                                            
CONECT    5   31                                                            
CONECT    6   31                                                            
CONECT    7   32                                                            
CONECT    8   33                                                            
CONECT    9   34                                                            
CONECT   10   11   12                                                       
CONECT   11   10   19                                                       
CONECT   12   10   20                                                       
CONECT   13   16   23                                                       
CONECT   14   15   28                                                       
CONECT   15   14   32                                                       
CONECT   16   13   33                                                       
CONECT   17   24   27                                                       
CONECT   18   25   26                                                       
CONECT   19    1   11   24                                                  
CONECT   20    2   12   30                                                  
CONECT   21    3   35   40                                                  
CONECT   22    4   36   41                                                  
CONECT   23   13   29   32                                                  
CONECT   24   17   19   33                                                  
CONECT   25   18   29   40                                                  
CONECT   26   18   31   32                                                  
CONECT   27   17   34   37                                                  
CONECT   28   14   31   41                                                  
CONECT   29   23   25   34                                                  
CONECT   30   20   38   39                                                  
CONECT   31    5    6   26   28                                             
CONECT   32    7   15   23   26                                             
CONECT   33    8   16   24   34                                             
CONECT   34    9   27   29   33                                             
CONECT   35   21                                                            
CONECT   36   22                                                            
CONECT   37   27                                                            
CONECT   38   30                                                            
CONECT   39   30                                                            
CONECT   40   21   25                                                       
CONECT   41   22   28                                                       
MASTER        0    0    0    0    0    0    0    0   41    0   88    0
END

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3D PDB for NP0336403 (Ganoderic acid Ma)
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SMILES for NP0336403 (Ganoderic acid Ma)
CC(CC\C=C(\C)C(O)=O)C1CC(O)C2(C)C3=C(CCC12C)C1(C)CCC(OC(C)=O)C(C)(C)C1CC3OC(C)=O
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INCHI for NP0336403 (Ganoderic acid Ma)
InChI=1/C34H52O7/c1-19(11-10-12-20(2)30(38)39)24-17-27(37)34(9)29-23(13-16-33(24,34)8)32(7)15-14-28(41-22(4)36)31(5,6)26(32)18-25(29)40-21(3)35/h12,19,24-28,37H,10-11,13-18H2,1-9H3,(H,38,39)/b20-12-
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Synonyms
ValueSource
Ganoderate maGenerator
Chemical FormulaC34H52O7
Average Mass572.7830 Da
Monoisotopic Mass572.37130 Da
IUPAC Name(2Z)-6-[4,7-bis(acetyloxy)-3-hydroxy-3a,6,6,9a,11a-pentamethyl-1H,2H,3H,3aH,4H,5H,5aH,6H,7H,8H,9H,9aH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]-2-methylhept-2-enoic acid
Traditional Name(2Z)-6-[4,7-bis(acetyloxy)-3-hydroxy-3a,6,6,9a,11a-pentamethyl-1H,2H,3H,4H,5H,5aH,7H,8H,9H,10H,11H-cyclopenta[a]phenanthren-1-yl]-2-methylhept-2-enoic acid
CAS Registry NumberNot Available
SMILES
CC(CC\C=C(\C)C(O)=O)C1CC(O)C2(C)C3=C(CCC12C)C1(C)CCC(OC(C)=O)C(C)(C)C1CC3OC(C)=O
InChI Identifier
InChI=1/C34H52O7/c1-19(11-10-12-20(2)30(38)39)24-17-27(37)34(9)29-23(13-16-33(24,34)8)32(7)15-14-28(41-22(4)36)31(5,6)26(32)18-25(29)40-21(3)35/h12,19,24-28,37H,10-11,13-18H2,1-9H3,(H,38,39)/b20-12-
InChI KeyJBMVFHJFFZPAJI-NDENLUEZNA-N
Experimental Spectra
Not Available
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of OriginNot Available
Chemical Taxonomy
ClassificationNot classified
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP5.32ChemAxon
pKa (Strongest Acidic)4.43ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area110.13 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity157.6 m³·mol⁻¹ChemAxon
Polarizability65.62 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References
  1. Lagunes-Castro MS, Aguila S, Herrera-Covarrubias D, Hernandez-Aguilar ME, Trigos A, Vidal-Limon A, Suarez-Medellin J: Structure-Based Virtual Screening of Sterols and Triterpenoids Isolated from Ganoderma (Agaricomycetes) Medicinal Mushrooms Shows Differences in Their Affinity for Human Glucocorticoid and Mineralocorticoid Receptors. Int J Med Mushrooms. 2021;23(9):1-13. doi: 10.1615/IntJMedMushrooms.2021039290. [PubMed:34591394  ]