NP-MRD: Showing NP-Card for Maximiscin (NP0012290)

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Record Information

Version

2.0

Created at

2021-01-05 21:43:02 UTC

Updated at

2021-07-15 17:11:22 UTC

NP-MRD ID

NP0012290

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Maximiscin

Provided By

NPAtlas

Description

Maximiscin is found in Tolypocladium sp. Maximiscin was first documented in 2014 (PMID: 24285637). Based on a literature review very few articles have been published on Maximiscin.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117073D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306242117073D          

 63 65  0  0  0  0            999 V2000
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    4.4387    4.2894   -1.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  3  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
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  8 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
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 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 16 31  1  0  0  0  0
 31 32  2  0  0  0  0
 10  3  1  0  0  0  0
 31 11  1  0  0  0  0
 29 18  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  2 35  1  0  0  0  0
  3 36  1  1  0  0  0
  4 37  1  0  0  0  0
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 29 62  1  1  0  0  0
 30 63  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0012290

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C(=O)N(O[C@]2([H])C(=C([H])[C@]([H])(O[H])[C@]([H])(O[H])[C@]2([H])O[H])C(=O)OC([H])([H])[H])C([H])=C1[H])[C@@]1([H])[C@]([H])(C([H])=C([H])[H])C([H])([H])[C@]([H])(C([H])([H])[H])C([H])([H])[C@]1([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H31NO8/c1-5-13-9-11(2)8-12(3)17(13)18-15(25)6-7-24(22(18)29)32-21-14(23(30)31-4)10-16(26)19(27)20(21)28/h5-7,10-13,16-17,19-21,25-28H,1,8-9H2,2-4H3/t11-,12+,13-,16+,17-,19+,20+,21-/m1/s1

> <INCHI_KEY>
BHUFOFQGYXAGAC-XMGLCDBZSA-N

> <FORMULA>
C23H31NO8

> <MOLECULAR_WEIGHT>
449.5

> <EXACT_MASS>
449.204966962

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.253218797255585

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (3S,4S,5S,6R)-6-({3-[(1R,2S,4R,6S)-2-ethenyl-4,6-dimethylcyclohexyl]-4-hydroxy-2-oxo-1,2-dihydropyridin-1-yl}oxy)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylate

> <ALOGPS_LOGP>
1.06

> <JCHEM_LOGP>
1.3301178756666676

> <ALOGPS_LOGS>
-3.06

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.674088431632782

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.701278589316152

> <JCHEM_PKA_STRONGEST_BASIC>
-3.385835086574282

> <JCHEM_POLAR_SURFACE_AREA>
136.76000000000002

> <JCHEM_REFRACTIVITY>
116.65849999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.94e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (3S,4S,5S,6R)-6-({3-[(1R,2S,4R,6S)-2-ethenyl-4,6-dimethylcyclohexyl]-4-hydroxy-2-oxopyridin-1-yl}oxy)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
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   -1.4368   -0.1984   -1.2071 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8694    1.4546   -0.7427 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.8387    0.4230    1.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9961   -1.4313    2.1022 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0480   -0.0400    1.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9034    3.3766   -2.3635 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.6455    1.1405    1.1156 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4929   -1.1186    1.3295 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8948   -0.6711    2.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6976   -3.2660    2.8477 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3824   -2.4445    1.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9407   -3.0932   -0.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
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 22 23  1  0
 19 24  2  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 16 31  1  0
 31 32  2  0
 10  3  1  0
 31 11  1  0
 29 18  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  1
  4 37  1  0
  4 38  1  0
  5 39  1  1
  6 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  1
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 10 49  1  6
 13 50  1  0
 14 51  1  0
 15 52  1  0
 18 53  1  1
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 25 58  1  1
 26 59  1  0
 27 60  1  1
 28 61  1  0
 29 62  1  1
 30 63  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      -2.817  -3.264  -0.506  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.453  -2.101  -0.694  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.294  -0.964   0.239  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.641  -0.524   0.727  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.866   0.936   0.830  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.566   1.521  -0.384  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.670   1.743   1.192  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.368   1.205   0.603  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.547   2.341   0.035  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.666   0.213  -0.508  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.437  -0.198  -1.207  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.550  -0.627  -2.542  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.763  -0.598  -3.212  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.435  -1.081  -3.206  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.783  -1.123  -2.595  0.00  0.00           C+0
HETATM   16  N   UNK     0       0.931  -0.709  -1.286  0.00  0.00           N+0
HETATM   17  O   UNK     0       2.120  -0.750  -0.704  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.728  -0.493   0.475  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.868   0.471   0.360  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.869   1.455  -0.743  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.923   1.483  -1.569  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.892   2.373  -0.916  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.863   3.316  -2.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.839   0.423   1.234  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.962  -0.504   2.376  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.996  -1.431   2.102  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.693  -1.323   2.562  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.875  -2.431   3.351  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.256  -1.750   1.171  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.292  -2.305   0.449  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.191  -0.270  -0.666  0.00  0.00           C+0
HETATM   32  O   UNK     0      -0.026   0.097   0.534  0.00  0.00           O+0
HETATM   33  H   UNK     0      -2.988  -4.044  -1.235  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.160  -3.438   0.325  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.133  -1.978  -1.527  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.619  -1.282   1.072  0.00  0.00           H+0
HETATM   37  H   UNK     0      -5.408  -0.919  -0.002  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.835  -1.089   1.679  0.00  0.00           H+0
HETATM   39  H   UNK     0      -5.595   1.073   1.690  0.00  0.00           H+0
HETATM   40  H   UNK     0      -6.540   1.992  -0.098  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.985   2.380  -0.820  0.00  0.00           H+0
HETATM   42  H   UNK     0      -5.792   0.786  -1.157  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.593   1.890   2.295  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.797   2.767   0.764  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.841   0.769   1.450  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.104   2.085  -0.953  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.726   2.685   0.687  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.216   3.233  -0.069  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.406   0.611  -1.186  0.00  0.00           H+0
HETATM   50  H   UNK     0      -2.856  -0.898  -4.153  0.00  0.00           H+0
HETATM   51  H   UNK     0      -0.546  -1.412  -4.245  0.00  0.00           H+0
HETATM   52  H   UNK     0       1.684  -1.472  -3.081  0.00  0.00           H+0
HETATM   53  H   UNK     0       2.048  -0.040   1.223  0.00  0.00           H+0
HETATM   54  H   UNK     0       5.903   3.377  -2.364  0.00  0.00           H+0
HETATM   55  H   UNK     0       4.439   4.289  -1.680  0.00  0.00           H+0
HETATM   56  H   UNK     0       4.256   2.879  -2.821  0.00  0.00           H+0
HETATM   57  H   UNK     0       5.646   1.141   1.116  0.00  0.00           H+0
HETATM   58  H   UNK     0       5.151   0.079   3.289  0.00  0.00           H+0
HETATM   59  H   UNK     0       6.493  -1.119   1.329  0.00  0.00           H+0
HETATM   60  H   UNK     0       2.895  -0.671   2.987  0.00  0.00           H+0
HETATM   61  H   UNK     0       3.698  -3.266   2.848  0.00  0.00           H+0
HETATM   62  H   UNK     0       2.382  -2.445   1.293  0.00  0.00           H+0
HETATM   63  H   UNK     0       3.941  -3.093  -0.047  0.00  0.00           H+0
CONECT    1    2   33   34                                                  
CONECT    2    1    3   35                                                  
CONECT    3    2    4   10   36                                             
CONECT    4    3    5   37   38                                             
CONECT    5    4    6    7   39                                             
CONECT    6    5   40   41   42                                             
CONECT    7    5    8   43   44                                             
CONECT    8    7    9   10   45                                             
CONECT    9    8   46   47   48                                             
CONECT   10    8   11    3   49                                             
CONECT   11   10   12   31                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   50                                                       
CONECT   14   12   15   51                                                  
CONECT   15   14   16   52                                                  
CONECT   16   15   17   31                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   29   53                                             
CONECT   19   18   20   24                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   54   55   56                                             
CONECT   24   19   25   57                                                  
CONECT   25   24   26   27   58                                             
CONECT   26   25   59                                                       
CONECT   27   25   28   29   60                                             
CONECT   28   27   61                                                       
CONECT   29   27   30   18   62                                             
CONECT   30   29   63                                                       
CONECT   31   16   32   11                                                  
CONECT   32   31                                                            
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    2                                                            
CONECT   36    3                                                            
CONECT   37    4                                                            
CONECT   38    4                                                            
CONECT   39    5                                                            
CONECT   40    6                                                            
CONECT   41    6                                                            
CONECT   42    6                                                            
CONECT   43    7                                                            
CONECT   44    7                                                            
CONECT   45    8                                                            
CONECT   46    9                                                            
CONECT   47    9                                                            
CONECT   48    9                                                            
CONECT   49   10                                                            
CONECT   50   13                                                            
CONECT   51   14                                                            
CONECT   52   15                                                            
CONECT   53   18                                                            
CONECT   54   23                                                            
CONECT   55   23                                                            
CONECT   56   23                                                            
CONECT   57   24                                                            
CONECT   58   25                                                            
CONECT   59   26                                                            
CONECT   60   27                                                            
CONECT   61   28                                                            
CONECT   62   29                                                            
CONECT   63   30                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  130    0
END

RDKit          3D

63 65  0  0  0  0  0  0  0  0999 V2000
   -2.8171   -3.2635   -0.5065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4529   -2.1008   -0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2937   -0.9644    0.2391 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6409   -0.5242    0.7268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8660    0.9357    0.8297 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5658    1.5211   -0.3835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6696    1.7430    1.1916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3675    1.2048    0.6025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5468    2.3412    0.0349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6658    0.2128   -0.5085 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4368   -0.1984   -1.2071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5503   -0.6268   -2.5422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7634   -0.5979   -3.2120 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4346   -1.0814   -3.2064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7832   -1.1229   -2.5952 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9313   -0.7088   -1.2859 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1203   -0.7504   -0.7039 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7279   -0.4927    0.4747 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8681    0.4711    0.3601 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8694    1.4546   -0.7427 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9228    1.4833   -1.5689 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8919    2.3727   -0.9158 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8626    3.3157   -1.9999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8387    0.4230    1.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9624   -0.5041    2.3762 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9961   -1.4313    2.1022 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6934   -1.3233    2.5621 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8747   -2.4313    3.3512 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2563   -1.7497    1.1709 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2915   -2.3050    0.4486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1911   -0.2701   -0.6664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0261    0.0971    0.5337 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9877   -4.0440   -1.2351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1596   -3.4376    0.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1328   -1.9780   -1.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6190   -1.2819    1.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4079   -0.9186   -0.0019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8348   -1.0890    1.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5945    1.0730    1.6899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5404    1.9921   -0.0975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9850    2.3800   -0.8195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7923    0.7862   -1.1572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5927    1.8897    2.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7966    2.7665    0.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8407    0.7685    1.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1038    2.0849   -0.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7256    2.6850    0.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2165    3.2335   -0.0688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4061    0.6113   -1.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8563   -0.8984   -4.1528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5458   -1.4118   -4.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842   -1.4721   -3.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0480   -0.0400    1.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9034    3.3766   -2.3635 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4387    4.2894   -1.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2565    2.8789   -2.8207 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6455    1.1405    1.1156 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1512    0.0794    3.2887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4929   -1.1186    1.3295 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8948   -0.6711    2.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6976   -3.2660    2.8477 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3824   -2.4445    1.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9407   -3.0932   -0.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 19 24  2  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 16 31  1  0
 31 32  2  0
 10  3  1  0
 31 11  1  0
 29 18  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  3 36  1  1
  4 37  1  0
  4 38  1  0
  5 39  1  1
  6 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  1
  9 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  6
 13 50  1  0
 14 51  1  0
 15 52  1  0
 18 53  1  1
 23 54  1  0
 23 55  1  0
 23 56  1  0
 24 57  1  0
 25 58  1  1
 26 59  1  0
 27 60  1  1
 28 61  1  0
 29 62  1  1
 30 63  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Methyl (3S,4S,5S,6R)-6-({3-[(1R,2S,4R,6S)-2-ethenyl-4,6-dimethylcyclohexyl]-4-hydroxy-2-oxo-1,2-dihydropyridin-1-yl}oxy)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid	Generator

Chemical Formula

C₂₃H₃₁NO₈

Average Mass

449.5000 Da

Monoisotopic Mass

449.20497 Da

IUPAC Name

methyl (3S,4S,5S,6R)-6-({3-[(1R,2S,4R,6S)-2-ethenyl-4,6-dimethylcyclohexyl]-4-hydroxy-2-oxo-1,2-dihydropyridin-1-yl}oxy)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylate

Traditional Name

methyl (3S,4S,5S,6R)-6-({3-[(1R,2S,4R,6S)-2-ethenyl-4,6-dimethylcyclohexyl]-4-hydroxy-2-oxopyridin-1-yl}oxy)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C[C@H](O)[C@H](O)[C@H](O)[C@@H]1ON1C=CC(O)=C([C@@H]2[C@@H](C)C[C@@H](C)C[C@H]2C=C)C1=O

InChI Identifier

InChI=1S/C23H31NO8/c1-5-13-9-11(2)8-12(3)17(13)18-15(25)6-7-24(22(18)29)32-21-14(23(30)31-4)10-16(26)19(27)20(21)28/h5-7,10-13,16-17,19-21,25-28H,1,8-9H2,2-4H3/t11-,12+,13-,16+,17-,19+,20+,21-/m1/s1

InChI Key

BHUFOFQGYXAGAC-XMGLCDBZSA-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
Tolypocladium sp.	NPAtlas	24285637

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	1.06	ALOGPS
logP	1.33	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	9.7	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	136.76 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	116.66 m³·mol⁻¹	ChemAxon
Polarizability	46.25 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

External Links

NPAtlas ID

NPA019316

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

34485502

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Maximiscin

METLIN ID

Not Available

PubChem Compound

139031017

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Du L, Robles AJ, King JB, Powell DR, Miller AN, Mooberry SL, Cichewicz RH: Crowdsourcing natural products discovery to access uncharted dimensions of fungal metabolite diversity. Angew Chem Int Ed Engl. 2014 Jan 13;53(3):804-9. doi: 10.1002/anie.201306549. Epub 2013 Nov 27. [PubMed:24285637 ]

Showing NP-Card for Maximiscin (NP0012290)

MOL for NP0012290 (Maximiscin)

3D MOL for NP0012290 (Maximiscin)

3D SDF for NP0012290 (Maximiscin)

3D-SDF for NP0012290 (Maximiscin)

PDB for NP0012290 (Maximiscin)

3D PDB for NP0012290 (Maximiscin)

SMILES for NP0012290 (Maximiscin)

INCHI for NP0012290 (Maximiscin)

Structure for NP0012290 (Maximiscin)

3D Structure for NP0012290 (Maximiscin)