NP-MRD: Showing NP-Card for Grifolin monomethyl ether (NP0139273)

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Record Information

Version

2.0

Created at

2022-06-29 19:46:58 UTC

Updated at

2022-06-29 19:46:58 UTC

NP-MRD ID

NP0139273

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Grifolin monomethyl ether

Description

64432-04-8 Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Grifolin monomethyl ether is found in Albatrellus ovinus. Based on a literature review very few articles have been published on 64432-04-8.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 59 59  0  0  0  0  0  0  0  0999 V2000
    5.5244    3.0576    1.4539 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9632    1.7926    1.2786 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3490    0.8625    0.3397 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3822    1.1310   -0.5506 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7397    0.1763   -1.4750 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8577    0.4496   -2.4465 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0565   -1.0186   -1.4851 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0222   -1.3069   -0.6055 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3723   -2.5376   -0.6699 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6731   -0.3489    0.3124 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5914   -0.5953    1.2688 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3234    0.1250    0.9231 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648   -0.4941    0.7302 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0585   -1.9505    0.8485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0778    0.2876    0.3818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1274    0.0543    1.4564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3110    0.8328    1.0654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4863    0.2993    0.8604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6688   -1.1616    1.0239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5996    1.2042    0.5112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1511    0.9336   -0.8305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6996   -0.4047   -1.0406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9947   -0.5410   -1.2716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8664    0.6484   -1.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5674   -1.8924   -1.4862 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7987    3.4720    0.4725 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7229    3.7283    1.8638 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3581    3.0757    2.1893 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9042    2.0767   -0.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4390    0.9436   -3.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5895    1.1067   -1.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3790   -0.4913   -2.6847 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3179   -1.7713   -2.1934 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5950   -3.2541   -1.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8946   -0.1843    2.2760 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4025   -1.6724    1.4522 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3128    1.2041    0.8169 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8723   -2.2000    1.9208 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1226   -2.3085    0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8715   -2.5342    0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4447   -0.0629   -0.5976 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1686    1.3605    0.2819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2835   -0.9993    1.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108    0.5501    2.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1890    1.9019    0.9447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1963   -1.7829    0.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7429   -1.3656    1.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1760   -1.4717    2.0055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3736    1.0341    1.3273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3193    2.2785    0.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9232    1.7307   -1.0488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3837    1.1289   -1.6480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0759   -1.2839   -1.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7993    1.2755   -0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5834    1.2875   -2.1731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9513    0.3589   -1.3786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3133   -2.2404   -2.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6770   -1.8744   -1.3981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1342   -2.6197   -0.7587 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  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
 10  3  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 14 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 25 57  1  0
 25 58  1  0
 25 59  1  0
M  END


  Mrv1652306292221462D          

 25 25  0  0  0  0            999 V2000
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  4 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0139273

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C)=CC(O)=C1C\C=C(/C)CC\C=C(/C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O2/c1-17(2)9-7-10-18(3)11-8-12-19(4)13-14-21-22(24)15-20(5)16-23(21)25-6/h9,11,13,15-16,24H,7-8,10,12,14H2,1-6H3/b18-11+,19-13+

> <INCHI_KEY>
OJJOUHFECGXRFJ-NWLVNBMCSA-N

> <FORMULA>
C23H34O2

> <MOLECULAR_WEIGHT>
342.523

> <EXACT_MASS>
342.255880335

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.24361896265361

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-methoxy-5-methyl-2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]phenol

> <ALOGPS_LOGP>
6.88

> <JCHEM_LOGP>
7.073426167333334

> <ALOGPS_LOGS>
-5.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.420075640637004

> <JCHEM_PKA_STRONGEST_BASIC>
-4.846229463376709

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
111.3913

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-methoxy-5-methyl-2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]phenol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   25                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    2                                                       
CONECT    8    6    9                                                       
CONECT    9    8                                                            
CONECT   10    5   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    4                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₄O₂

Average Mass

342.5230 Da

Monoisotopic Mass

342.25588 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(C)=CC(O)=C1C\C=C(/C)CC\C=C(/C)CCC=C(C)C

InChI Identifier

InChI=1S/C23H34O2/c1-17(2)9-7-10-18(3)11-8-12-19(4)13-14-21-22(24)15-20(5)16-23(21)25-6/h9,11,13,15-16,24H,7-8,10,12,14H2,1-6H3/b18-11+,19-13+

InChI Key

OJJOUHFECGXRFJ-NWLVNBMCSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Albatrellus ovinus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Farsesane sesquiterpenoid
Methoxyphenol
Anisole
M-cresol
Phenoxy compound
Phenol ether
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Toluene
Monocyclic benzene moiety
Benzenoid
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4523292

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5373218

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Grifolin monomethyl ether (NP0139273)

MOL for NP0139273 (Grifolin monomethyl ether)

3D MOL for NP0139273 (Grifolin monomethyl ether)

3D SDF for NP0139273 (Grifolin monomethyl ether)

3D-SDF for NP0139273 (Grifolin monomethyl ether)

PDB for NP0139273 (Grifolin monomethyl ether)

3D PDB for NP0139273 (Grifolin monomethyl ether)

SMILES for NP0139273 (Grifolin monomethyl ether)

INCHI for NP0139273 (Grifolin monomethyl ether)

Structure for NP0139273 (Grifolin monomethyl ether)

3D Structure for NP0139273 (Grifolin monomethyl ether)