NP-MRD: Showing NP-Card for Flavidulol C (NP0049321)

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Record Information

Version

2.0

Created at

2022-03-17 21:10:36 UTC

Updated at

2022-03-17 21:10:36 UTC

NP-MRD ID

NP0049321

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Flavidulol C

Description

Flavidulol C belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. Flavidulol C is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Flavidulol C has been detected, but not quantified in, mushrooms. Flavidulol C is found in Lactarius flavidulus . This could make flavidulol C a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 05061310532D          

 38 41  0  0  0  0            999 V2000
   -2.5223   -1.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282    3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528    2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587   -0.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168   -1.7213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891    3.6412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5223    0.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5223   -0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282    1.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0374    1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433    0.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528   -0.9937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587    2.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4682   -0.7388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740    2.6586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4682    1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740    0.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4457   -0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602    1.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0374   -0.7388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433    2.6586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528    1.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587    0.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168   -0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891    1.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168    0.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4457    0.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312   -0.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    0.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312    1.9912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746   -0.0713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312   -1.3088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    3.2287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  7  1  0  0  0  0
 12  8  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 21  1  1  0  0  0  0
 21  9  1  0  0  0  0
 21 13  2  0  0  0  0
 22  2  1  0  0  0  0
 22 10  1  0  0  0  0
 22 14  2  0  0  0  0
 23  3  1  0  0  0  0
 23 11  2  0  0  0  0
 23 17  1  0  0  0  0
 24  4  1  0  0  0  0
 24 12  2  0  0  0  0
 24 18  1  0  0  0  0
 25 15  1  0  0  0  0
 26 16  1  0  0  0  0
 27 17  1  0  0  0  0
 27 25  2  0  0  0  0
 28 18  1  0  0  0  0
 28 26  2  0  0  0  0
 29 19  1  0  0  0  0
 30 20  1  0  0  0  0
 30 29  1  0  0  0  0
 31 19  2  0  0  0  0
 31 25  1  0  0  0  0
 32 20  2  0  0  0  0
 32 26  1  0  0  0  0
 33 27  1  0  0  0  0
 33 29  2  0  0  0  0
 34 28  1  0  0  0  0
 34 30  2  0  0  0  0
 35 33  1  0  0  0  0
 36 34  1  0  0  0  0
 37  5  1  0  0  0  0
 37 31  1  0  0  0  0
 38  6  1  0  0  0  0
 38 32  1  0  0  0  0
M  END


  Mrv0541 05061310532D          

 38 41  0  0  0  0            999 V2000
   -2.5223   -1.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282    3.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528    2.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587   -0.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168   -1.7213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891    3.6412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5223    0.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5223   -0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282    1.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0374    1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433    0.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528   -0.9937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587    2.9136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4682   -0.7388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740    2.6586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4682    1.4211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740    0.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4457   -0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602    1.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0374   -0.7388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433    2.6586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528    1.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587    0.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168   -0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891    1.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0168    0.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4457    0.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312   -0.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312    1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    0.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312    1.9912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746   -0.0713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312   -1.3088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    3.2287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  7  1  0  0  0  0
 12  8  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 21  1  1  0  0  0  0
 21  9  1  0  0  0  0
 21 13  2  0  0  0  0
 22  2  1  0  0  0  0
 22 10  1  0  0  0  0
 22 14  2  0  0  0  0
 23  3  1  0  0  0  0
 23 11  2  0  0  0  0
 23 17  1  0  0  0  0
 24  4  1  0  0  0  0
 24 12  2  0  0  0  0
 24 18  1  0  0  0  0
 25 15  1  0  0  0  0
 26 16  1  0  0  0  0
 27 17  1  0  0  0  0
 27 25  2  0  0  0  0
 28 18  1  0  0  0  0
 28 26  2  0  0  0  0
 29 19  1  0  0  0  0
 30 20  1  0  0  0  0
 30 29  1  0  0  0  0
 31 19  2  0  0  0  0
 31 25  1  0  0  0  0
 32 20  2  0  0  0  0
 32 26  1  0  0  0  0
 33 27  1  0  0  0  0
 33 29  2  0  0  0  0
 34 28  1  0  0  0  0
 34 30  2  0  0  0  0
 35 33  1  0  0  0  0
 36 34  1  0  0  0  0
 37  5  1  0  0  0  0
 37 31  1  0  0  0  0
 38  6  1  0  0  0  0
 38 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0049321

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=C(O)C2=C1C\C=C(C)/CC\C=C(C)/C2)C1=C(O)C2=C(C\C=C(C)/CC\C=C(C)/C2)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C34H42O4/c1-21-9-7-11-23(3)17-27-25(15-13-21)31(37-5)19-29(33(27)35)30-20-32(38-6)26-16-14-22(2)10-8-12-24(4)18-28(26)34(30)36/h11-14,19-20,35-36H,7-10,15-18H2,1-6H3/b21-13-,22-14-,23-11-,24-12-

> <INCHI_KEY>
FFUHECWLQYKEQO-SISZSTKXSA-N

> <FORMULA>
C34H42O4

> <MOLECULAR_WEIGHT>
514.6949

> <EXACT_MASS>
514.308309832

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
61.10481156961008

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{1-hydroxy-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-2-yl}-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-1-ol

> <ALOGPS_LOGP>
7.20

> <JCHEM_LOGP>
8.684814195333335

> <ALOGPS_LOGS>
-6.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.701833740886604

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.854574365303469

> <JCHEM_PKA_STRONGEST_BASIC>
-4.524783511537415

> <JCHEM_POLAR_SURFACE_AREA>
58.92

> <JCHEM_REFRACTIVITY>
161.44920000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.32e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{1-hydroxy-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-2-yl}-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

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      -4.708  -2.625   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.439   6.209   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.339   4.669   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.070  -1.085   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.031  -3.213   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.700   6.797   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.708   1.407   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.439   2.177   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.708  -0.133   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.439   3.717   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.803   2.653   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.534   0.931   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.339  -1.855   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.070   5.439   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.874  -1.379   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.605   4.963   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.874   2.653   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.605   0.931   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.699  -0.133   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.032   3.717   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.803  -1.379   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.534   4.963   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.339   3.129   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.070   0.455   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.031  -0.133   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.700   3.717   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.031   1.407   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.700   2.177   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.699   1.407   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.032   2.177   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.365  -0.903   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.366   4.487   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.365   2.177   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.366   1.407   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       1.365   3.717   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       5.366  -0.133   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       1.365  -2.443   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       5.366   6.027   0.000  0.00  0.00           O+0
CONECT    1   21                                                            
CONECT    2   22                                                            
CONECT    3   23                                                            
CONECT    4   24                                                            
CONECT    5   37                                                            
CONECT    6   38                                                            
CONECT    7    9   11                                                       
CONECT    8   10   12                                                       
CONECT    9    7   21                                                       
CONECT   10    8   22                                                       
CONECT   11    7   23                                                       
CONECT   12    8   24                                                       
CONECT   13   15   21                                                       
CONECT   14   16   22                                                       
CONECT   15   13   25                                                       
CONECT   16   14   26                                                       
CONECT   17   23   27                                                       
CONECT   18   24   28                                                       
CONECT   19   29   31                                                       
CONECT   20   30   32                                                       
CONECT   21    1    9   13                                                  
CONECT   22    2   10   14                                                  
CONECT   23    3   11   17                                                  
CONECT   24    4   12   18                                                  
CONECT   25   15   27   31                                                  
CONECT   26   16   28   32                                                  
CONECT   27   17   25   33                                                  
CONECT   28   18   26   34                                                  
CONECT   29   19   30   33                                                  
CONECT   30   20   29   34                                                  
CONECT   31   19   25   37                                                  
CONECT   32   20   26   38                                                  
CONECT   33   27   29   35                                                  
CONECT   34   28   30   36                                                  
CONECT   35   33                                                            
CONECT   36   34                                                            
CONECT   37    5   31                                                       
CONECT   38    6   32                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Value	Source
5,5',8,8',9,9',12,12'-Octahydro-4,4'-dimethoxy-7,7',11,11'-tetramethyl[2,2'-bibenzocyclodecene]-1,1'-diol, 9ci	HMDB

Chemical Formula

C₃₄H₄₂O₄

Average Mass

514.6949 Da

Monoisotopic Mass

514.30831 Da

IUPAC Name

2-{1-hydroxy-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-2-yl}-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-1-ol

Traditional Name

2-{1-hydroxy-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-2-yl}-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-1-ol

CAS Registry Number

117568-34-0

SMILES

COC1=CC(=C(O)C2=C1C\C=C(C)/CC\C=C(C)/C2)C1=C(O)C2=C(C\C=C(C)/CC\C=C(C)/C2)C(OC)=C1

InChI Identifier

InChI=1S/C34H42O4/c1-21-9-7-11-23(3)17-27-25(15-13-21)31(37-5)19-29(33(27)35)30-20-32(38-6)26-16-14-22(2)10-8-12-24(4)18-28(26)34(30)36/h11-14,19-20,35-36H,7-10,15-18H2,1-6H3/b21-13-,22-14-,23-11-,24-12-

InChI Key

FFUHECWLQYKEQO-SISZSTKXSA-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...
Lactarius flavidulus	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 anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Anisole
Alkyl aryl ether
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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	7.2	ALOGPS
logP	8.68	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	8.85	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.92 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	161.45 m³·mol⁻¹	ChemAxon
Polarizability	61.1 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	No	ChemAxon

External Links

HMDB ID

HMDB0039150

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB018670

KNApSAcK ID

Not Available

Chemspider ID

30777331

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752564

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Flavidulol C (NP0049321)

MOL for NP0049321 (Flavidulol C)

3D MOL for NP0049321 (Flavidulol C)

3D SDF for NP0049321 (Flavidulol C)

3D-SDF for NP0049321 (Flavidulol C)

PDB for NP0049321 (Flavidulol C)

3D PDB for NP0049321 (Flavidulol C)

SMILES for NP0049321 (Flavidulol C)

INCHI for NP0049321 (Flavidulol C)

Structure for NP0049321 (Flavidulol C)

3D Structure for NP0049321 (Flavidulol C)