NP-MRD: Showing NP-Card for O-demethylated-zeaenol (NP0017938)

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Record Information

Version

2.0

Created at

2021-01-06 02:34:17 UTC

Updated at

2021-07-15 17:26:51 UTC

NP-MRD ID

NP0017938

Secondary Accession Numbers

None

Natural Product Identification

Common Name

O-demethylated-zeaenol

Provided By

NPAtlas

Description

O-demethylated-zeaenol is found in Curvularia. O-demethylated-zeaenol was first documented in 2018 (PMID: 29671780).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242104293D          

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M  END

     RDKit          3D

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 12 41  1  0  0  0  0
 13 42  1  0  0  0  0
 14 43  1  0  0  0  0
 16 44  1  0  0  0  0
 18 45  1  0  0  0  0
 19 46  1  0  0  0  0
 21 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0017938

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(O[H])=C2C(=C1[H])\C([H])=C([H])/C([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])[C@@]([H])(O[H])\C([H])=C([H])/C([H])([H])[C@@]([H])(OC2=O)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H22O7/c1-10-4-2-6-13(20)17(23)14(21)7-3-5-11-8-12(19)9-15(22)16(11)18(24)25-10/h2-3,5-6,8-10,13-14,17,19-23H,4,7H2,1H3/b5-3-,6-2-/t10-,13-,14-,17+/m0/s1

> <INCHI_KEY>
MOILXISIBFKWOB-NHQZHHNRSA-N

> <FORMULA>
C18H22O7

> <MOLECULAR_WEIGHT>
350.367

> <EXACT_MASS>
350.136553048

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
35.55331487225821

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,7S,8S,9S)-7,8,9,14,16-pentahydroxy-3-methyl-3,4,7,8,9,10-hexahydro-1H-2-benzoxacyclotetradecin-1-one

> <ALOGPS_LOGP>
0.84

> <JCHEM_LOGP>
1.810843393333334

> <ALOGPS_LOGS>
-2.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.382174991770695

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.536970993174254

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2111779776287355

> <JCHEM_POLAR_SURFACE_AREA>
127.45

> <JCHEM_REFRACTIVITY>
93.05319999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.32e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,7S,8S,9S)-7,8,9,14,16-pentahydroxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
   -0.3714    3.8255   -0.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0506    2.6108    0.7958 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1643    1.7381    0.9819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4651    2.3170    0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3363    1.6236   -0.0401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9795    0.3103   -0.6126 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0600   -0.0567   -1.4658 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8310   -0.7844    0.3925 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1450   -1.3255    0.5674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9926   -1.9354   -0.0244 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3865   -2.3668   -1.2882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5005   -1.7603    0.0686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1177   -1.4250    1.4269 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1365   -1.0769    1.7225 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2805   -0.9612    0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -1.9140    1.1027 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4479   -2.0120    0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4094   -2.9896    0.6996 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6401   -1.1518   -0.6660 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6690   -0.2251   -0.9274 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8980    0.6470   -2.0136 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4758   -0.1022   -0.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5867    1.0489   -0.5588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3187    1.0120   -1.8237 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1110    1.9998    0.2269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8522    3.4680   -0.9278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0216    4.5003    0.5951 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5600    4.3676   -0.3149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3395    3.0294    1.8108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0131    0.9352    0.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0467    1.2468    1.9627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7655    3.2923    1.1366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3287    2.0777   -0.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1179    0.3647   -1.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8881    0.3614   -1.1283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5999   -0.3776    1.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5036   -1.6032   -0.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2397   -2.7900    0.6738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4060   -3.3753   -1.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1905   -1.0997   -0.7376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0895   -2.7829   -0.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -1.4592    2.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3200   -0.8888    2.7931 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2235   -2.6124    1.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2544   -3.0332    0.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5335   -1.2114   -1.2545 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7506    0.5442   -2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25  2  1  0
 22 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  6 34  1  6
  7 35  1  0
  8 36  1  1
  9 37  1  0
 10 38  1  1
 11 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 14 43  1  0
 16 44  1  0
 18 45  1  0
 19 46  1  0
 21 47  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.371   3.825  -0.002  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.051   2.611   0.796  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.164   1.738   0.982  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.465   2.317   0.729  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.336   1.624  -0.040  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.979   0.310  -0.613  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.060  -0.057  -1.466  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.831  -0.784   0.393  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.145  -1.325   0.567  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.993  -1.935  -0.024  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.386  -2.367  -1.288  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.500  -1.760   0.069  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.118  -1.425   1.427  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.137  -1.077   1.722  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.281  -0.961   0.843  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.300  -1.914   1.103  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.448  -2.012   0.373  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.409  -2.990   0.700  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.640  -1.152  -0.666  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.669  -0.225  -0.927  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.898   0.647  -2.014  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.476  -0.102  -0.186  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.587   1.049  -0.559  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.319   1.012  -1.824  0.00  0.00           O+0
HETATM   25  O   UNK     0       1.111   2.000   0.227  0.00  0.00           O+0
HETATM   26  H   UNK     0      -0.852   3.468  -0.928  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.022   4.500   0.595  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.560   4.368  -0.315  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.340   3.029   1.811  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.013   0.935   0.201  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.047   1.247   1.963  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.765   3.292   1.137  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.329   2.078  -0.224  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.118   0.365  -1.334  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.888   0.361  -1.128  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.600  -0.378   1.380  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.504  -1.603  -0.313  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.240  -2.790   0.674  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.406  -3.375  -1.337  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.191  -1.100  -0.738  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.090  -2.783  -0.243  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.893  -1.459   2.218  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.320  -0.889   2.793  0.00  0.00           H+0
HETATM   44  H   UNK     0       3.224  -2.612   1.940  0.00  0.00           H+0
HETATM   45  H   UNK     0       6.254  -3.033   0.133  0.00  0.00           H+0
HETATM   46  H   UNK     0       5.534  -1.211  -1.254  0.00  0.00           H+0
HETATM   47  H   UNK     0       4.751   0.544  -2.527  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    1    3   25   29                                             
CONECT    3    2    4   30   31                                             
CONECT    4    3    5   32                                                  
CONECT    5    4    6   33                                                  
CONECT    6    5    7    8   34                                             
CONECT    7    6   35                                                       
CONECT    8    6    9   10   36                                             
CONECT    9    8   37                                                       
CONECT   10    8   11   12   38                                             
CONECT   11   10   39                                                       
CONECT   12   10   13   40   41                                             
CONECT   13   12   14   42                                                  
CONECT   14   13   15   43                                                  
CONECT   15   14   16   22                                                  
CONECT   16   15   17   44                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   45                                                       
CONECT   19   17   20   46                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20   47                                                       
CONECT   22   20   23   15                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    2                                                       
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    2                                                            
CONECT   30    3                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    5                                                            
CONECT   34    6                                                            
CONECT   35    7                                                            
CONECT   36    8                                                            
CONECT   37    9                                                            
CONECT   38   10                                                            
CONECT   39   11                                                            
CONECT   40   12                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
CONECT   43   14                                                            
CONECT   44   16                                                            
CONECT   45   18                                                            
CONECT   46   19                                                            
CONECT   47   21                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   96    0
END

RDKit          3D

47 48  0  0  0  0  0  0  0  0999 V2000
   -0.3714    3.8255   -0.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0506    2.6108    0.7958 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1643    1.7381    0.9819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4651    2.3170    0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3363    1.6236   -0.0401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9795    0.3103   -0.6126 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0600   -0.0567   -1.4658 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8310   -0.7844    0.3925 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1450   -1.3255    0.5674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9926   -1.9354   -0.0244 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3865   -2.3668   -1.2882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5005   -1.7603    0.0686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1177   -1.4250    1.4269 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1365   -1.0769    1.7225 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2805   -0.9612    0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -1.9140    1.1027 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4479   -2.0120    0.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4094   -2.9896    0.6996 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6401   -1.1518   -0.6660 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6690   -0.2251   -0.9274 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8980    0.6470   -2.0136 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4758   -0.1022   -0.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5867    1.0489   -0.5588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3187    1.0120   -1.8237 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1110    1.9998    0.2269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8522    3.4680   -0.9278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0216    4.5003    0.5951 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5600    4.3676   -0.3149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3395    3.0294    1.8108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0131    0.9352    0.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0467    1.2468    1.9627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7655    3.2923    1.1366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3287    2.0777   -0.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1179    0.3647   -1.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8881    0.3614   -1.1283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5999   -0.3776    1.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5036   -1.6032   -0.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2397   -2.7900    0.6738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4060   -3.3753   -1.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1905   -1.0997   -0.7376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0895   -2.7829   -0.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -1.4592    2.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3200   -0.8888    2.7931 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2235   -2.6124    1.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2544   -3.0332    0.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5335   -1.2114   -1.2545 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7506    0.5442   -2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25  2  1  0
 22 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  1
  3 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  6 34  1  6
  7 35  1  0
  8 36  1  1
  9 37  1  0
 10 38  1  1
 11 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 14 43  1  0
 16 44  1  0
 18 45  1  0
 19 46  1  0
 21 47  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₈H₂₂O₇

Average Mass

350.3670 Da

Monoisotopic Mass

350.13655 Da

IUPAC Name

(3S,7S,8S,9S)-7,8,9,14,16-pentahydroxy-3-methyl-3,4,7,8,9,10-hexahydro-1H-2-benzoxacyclotetradecin-1-one

Traditional Name

(3S,7S,8S,9S)-7,8,9,14,16-pentahydroxy-3-methyl-3,4,7,8,9,10-hexahydro-2-benzoxacyclotetradecin-1-one

CAS Registry Number

Not Available

SMILES

C[C@H]1C\C=C/[C@H](O)[C@@H](O)[C@@H](O)C\C=C/C2=C(C(O)=CC(O)=C2)C(=O)O1

InChI Identifier

InChI=1S/C18H22O7/c1-10-4-2-6-13(20)17(23)14(21)7-3-5-11-8-12(19)9-15(22)16(11)18(24)25-10/h2-3,5-6,8-10,13-14,17,19-23H,4,7H2,1H3/b5-3-,6-2-/t10-,13-,14-,17+/m0/s1

InChI Key

MOILXISIBFKWOB-NHQZHHNRSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Curvularia	NPAtlas	29671780

Chemical Taxonomy

Classification

Not classified

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	0.84	ALOGPS
logP	1.81	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	8.54	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	127.45 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	93.05 m³·mol⁻¹	ChemAxon
Polarizability	35.55 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Yin C, Jin L, Sun F, Xu X, Shao M, Zhang Y: Phytotoxic and Antifungal Metabolites from Curvularia crepinii QTYC-1 Isolated from the Gut of Pantala flavescens. Molecules. 2018 Apr 19;23(4). pii: molecules23040951. doi: 10.3390/molecules23040951. [PubMed:29671780 ]

Showing NP-Card for O-demethylated-zeaenol (NP0017938)

MOL for NP0017938 (O-demethylated-zeaenol)

3D MOL for NP0017938 (O-demethylated-zeaenol)

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3D-SDF for NP0017938 (O-demethylated-zeaenol)

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3D PDB for NP0017938 (O-demethylated-zeaenol)

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INCHI for NP0017938 (O-demethylated-zeaenol)

Structure for NP0017938 (O-demethylated-zeaenol)

3D Structure for NP0017938 (O-demethylated-zeaenol)