MiMeDB: Showing metabocard for 11-O-methylpseurotin A (MMDBc0013440)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:45:33 UTC

Update Date

2022-08-31 06:36:09 UTC

Metabolite ID

MMDBc0013440

Metabolite Identification

Common Name

11-O-methylpseurotin A

Description

11-O-methylpseurotin A belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. Based on a literature review a small amount of articles have been published on 11-O-methylpseurotin A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152106452D          

 37 39  0  0  1  0            999 V2000
   -3.6821    0.8573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2610    1.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0975    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9285    0.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8422   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3662   -1.5223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8512   -0.8548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458   -1.4360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5156   -0.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2102   -0.6824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0886   -0.6343    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
    3.6951   -0.0149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4211   -0.1494    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6674   -0.4849    0.0000 C   0  0  1  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
    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3596    0.7388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7545    1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7545   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5391    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5391   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5812   -1.3054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8445    1.4062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4995    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4995   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5074    0.6711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7106    1.6320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5097   -0.7837    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0023   -1.4548    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3349   -0.9698    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537    0.3356    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3378    1.6633    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  5  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  2  0  0  0  0
 12  6  2  0  0  0  0
 13  2  1  0  0  0  0
 14 10  2  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 15  1  0  0  0  0
 17 13  2  0  0  0  0
 17 16  1  0  0  0  0
 18 13  1  0  0  0  0
 19 14  1  0  0  0  0
 22 18  1  0  0  0  0
 22 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 19  1  6  0  0  0
 23 20  1  0  0  0  0
 24 21  2  0  0  0  0
 24 23  1  0  0  0  0
 16 25  1  6  0  0  0
 26 18  2  0  0  0  0
 27 19  2  0  0  0  0
 20 28  1  1  0  0  0
 29 21  1  0  0  0  0
 30  3  1  0  0  0  0
 15 30  1  1  0  0  0
 31  4  1  0  0  0  0
 23 31  1  1  0  0  0
 32 17  1  0  0  0  0
 22 32  1  6  0  0  0
 33  6  1  0  0  0  0
 34 12  1  0  0  0  0
 15 35  1  1  0  0  0
 16 36  1  6  0  0  0
 20 37  1  6  0  0  0
M  END


  Mrv1652305152106452D          

 37 39  0  0  1  0            999 V2000
   -3.6821    0.8573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6674    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2610    1.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0975    2.1840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9285    0.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8422   -0.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3662   -1.5223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8512   -0.8548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458   -1.4360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5156   -0.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2102   -0.6824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0886   -0.6343    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
    3.6951   -0.0149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4211   -0.1494    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6674   -0.4849    0.0000 C   0  0  1  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
    0.7846    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3596    0.7388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7545    1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7545   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5391    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5391   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5812   -1.3054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8445    1.4062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4995    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4995   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5074    0.6711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7106    1.6320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5097   -0.7837    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0023   -1.4548    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3349   -0.9698    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537    0.3356    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3378    1.6633    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  5  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  2  0  0  0  0
 12  6  2  0  0  0  0
 13  2  1  0  0  0  0
 14 10  2  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 15  1  0  0  0  0
 17 13  2  0  0  0  0
 17 16  1  0  0  0  0
 18 13  1  0  0  0  0
 19 14  1  0  0  0  0
 22 18  1  0  0  0  0
 22 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 19  1  6  0  0  0
 23 20  1  0  0  0  0
 24 21  2  0  0  0  0
 24 23  1  0  0  0  0
 16 25  1  6  0  0  0
 26 18  2  0  0  0  0
 27 19  2  0  0  0  0
 20 28  1  1  0  0  0
 29 21  1  0  0  0  0
 30  3  1  0  0  0  0
 15 30  1  1  0  0  0
 31  4  1  0  0  0  0
 23 31  1  1  0  0  0
 32 17  1  0  0  0  0
 22 32  1  6  0  0  0
 33  6  1  0  0  0  0
 34 12  1  0  0  0  0
 15 35  1  1  0  0  0
 16 36  1  6  0  0  0
 20 37  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0013440

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(CC)=C(/[H])[C@]([H])(OC)[C@]([H])(O)C1=C(C)C(=O)[C@]2(O1)C(O)=N[C@@](OC)(C(=O)C1=CC=CC=C1)[C@]2([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C23H27NO8/c1-5-6-12-15(30-3)16(25)17-13(2)18(26)22(32-17)20(28)23(31-4,24-21(22)29)19(27)14-10-8-7-9-11-14/h6-12,15-16,20,25,28H,5H2,1-4H3,(H,24,29)/b12-6-/t15-,16-,20+,22+,23+/m0/s1

> <INCHI_KEY>
BSXLPZRKEPWAAT-CHZVKGAWSA-N

> <FORMULA>
C23H27NO8

> <MOLECULAR_WEIGHT>
445.468

> <EXACT_MASS>
445.173666833

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.492980422633195

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R,8S,9R)-8-benzoyl-6,9-dihydroxy-2-[(1S,2S,3Z)-1-hydroxy-2-methoxyhex-3-en-1-yl]-8-methoxy-3-methyl-1-oxa-7-azaspiro[4.4]nona-2,6-dien-4-one

> <ALOGPS_LOGP>
2.01

> <JCHEM_LOGP>
2.6968727513333324

> <ALOGPS_LOGS>
-3.86

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.108503625779672

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.507402801858492

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7504430855649593

> <JCHEM_POLAR_SURFACE_AREA>
134.88000000000002

> <JCHEM_REFRACTIVITY>
115.67279999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.19e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5R,8S,9R)-8-benzoyl-6,9-dihydroxy-2-[(1S,2S,3Z)-1-hydroxy-2-methoxyhex-3-en-1-yl]-8-methoxy-3-methyl-1-oxa-7-azaspiro[4.4]nona-2,6-dien-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      -6.873   1.600   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.246   2.445   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.221   1.879   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.915   4.077   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.466   0.974   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.305  -0.558   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.150  -2.842   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.056  -1.596   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.619  -2.681   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.429  -0.189   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.992  -1.274   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.899  -1.184   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.898  -0.028   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.653  -0.279   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.246  -0.905   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.465   2.016   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.271   1.379   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.275   2.016   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.275  -0.476   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.740   1.540   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       4.740  -0.000   0.000  0.00  0.00           N+0
HETATM   25  O   UNK     0      -1.085  -2.437   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       1.941   3.481   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       7.176   2.625   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.799   3.481   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.799  -1.941   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -2.814   1.253   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.060   3.046   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       1.465  -0.476   0.000  0.00  0.00           O+0
HETATM   33  H   UNK     0      -6.551  -1.463   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.738  -2.716   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.492  -1.810   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.407   0.626   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       4.364   3.105   0.000  0.00  0.00           H+0
CONECT    1    5                                                            
CONECT    2   13                                                            
CONECT    3   30                                                            
CONECT    4   31                                                            
CONECT    5    1    6                                                       
CONECT    6    5   12   33                                                  
CONECT    7    8    9                                                       
CONECT    8    7   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   14                                                       
CONECT   11    9   14                                                       
CONECT   12    6   15   34                                                  
CONECT   13    2   17   18                                                  
CONECT   14   10   11   19                                                  
CONECT   15   12   16   30   35                                             
CONECT   16   15   17   25   36                                             
CONECT   17   13   16   32                                                  
CONECT   18   13   22   26                                                  
CONECT   19   14   23   27                                                  
CONECT   20   22   23   28   37                                             
CONECT   21   22   24   29                                                  
CONECT   22   18   20   21   32                                             
CONECT   23   19   20   24   31                                             
CONECT   24   21   23                                                       
CONECT   25   16                                                            
CONECT   26   18                                                            
CONECT   27   19                                                            
CONECT   28   20                                                            
CONECT   29   21                                                            
CONECT   30    3   15                                                       
CONECT   31    4   23                                                       
CONECT   32   17   22                                                       
CONECT   33    6                                                            
CONECT   34   12                                                            
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   20                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   78    0
END

Synonyms

Not Available

Molecular Formula

C₂₃H₂₇NO₈

Average Mass

445.468

Monoisotopic Mass

445.173666833

IUPAC Name

(5R,8S,9R)-8-benzoyl-6,9-dihydroxy-2-[(1S,2S,3Z)-1-hydroxy-2-methoxyhex-3-en-1-yl]-8-methoxy-3-methyl-1-oxa-7-azaspiro[4.4]nona-2,6-dien-4-one

Traditional Name

(5R,8S,9R)-8-benzoyl-6,9-dihydroxy-2-[(1S,2S,3Z)-1-hydroxy-2-methoxyhex-3-en-1-yl]-8-methoxy-3-methyl-1-oxa-7-azaspiro[4.4]nona-2,6-dien-4-one

CAS Registry Number

Not Available

SMILES

[H]\C(CC)=C(/[H])[C@]([H])(OC)[C@]([H])(O)C1=C(C)C(=O)[C@]2(O1)C(O)=N[C@@](OC)(C(=O)C1=CC=CC=C1)[C@]2([H])O

InChI Identifier

InChI=1S/C23H27NO8/c1-5-6-12-15(30-3)16(25)17-13(2)18(26)22(32-17)20(28)23(31-4,24-21(22)29)19(27)14-10-8-7-9-11-14/h6-12,15-16,20,25,28H,5H2,1-4H3,(H,24,29)/b12-6-/t15-,16-,20+,22+,23+/m0/s1

InChI Key

BSXLPZRKEPWAAT-CHZVKGAWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Benzoyl
Aryl alkyl ketone
Monocyclic benzene moiety
3-furanone
Pyrrolidone
2-pyrrolidone
Benzenoid
Dihydrofuran
Pyrrolidine
Vinylogous ester
Secondary alcohol
Lactam
Carboxamide group
Secondary carboxylic acid amide
Azacycle
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Organonitrogen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.062 g/L	ALOGPS
logP	2.01	ALOGPS
logP	2.7	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	1.51	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	134.88 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	115.67 m³·mol⁻¹	ChemAxon
Polarizability	45.49 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

23310679

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23656807

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for 11-O-methylpseurotin A (MMDBc0013440)

MOL for #<Metabolite:0x00007f46bd540bb8>

3D MOL for #<Metabolite:0x00007f46bd540bb8>

3D SDF for #<Metabolite:0x00007f46bd540bb8>

3D-SDF for #<Metabolite:0x00007f46bd540bb8>

PDB for #<Metabolite:0x00007f46bd540bb8>

3D PDB for #<Metabolite:0x00007f46bd540bb8>

SMILES for #<Metabolite:0x00007f46bd540bb8>

INCHI for #<Metabolite:0x00007f46bd540bb8>

Structure for #<Metabolite:0x00007f46bd540bb8>

3D Structure for #<Metabolite:0x00007f46bd540bb8>