NP-MRD: Showing NP-Card for Paecilomycin F (NP0009178)

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Record Information

Version

1.0

Created at

2020-12-09 06:36:32 UTC

Updated at

2021-07-15 17:02:31 UTC

NP-MRD ID

NP0009178

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Paecilomycin F

Provided By

NPAtlas

Description

Paecilomycin F is found in Curvularia lunata and Paecilomyces sp. SC0924. It was first documented in 2010 (PMID: 20429578).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106333D          

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   -0.7528    3.3345    0.4274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2507    3.5442   -1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9149    2.3322   -1.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    1.7931   -2.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  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  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
  9  3  1  0  0  0  0
 25  7  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  4 30  1  0  0  0  0
  6 31  1  0  0  0  0
  9 32  1  0  0  0  0
 10 33  1  0  0  0  0
 11 34  1  0  0  0  0
 12 35  1  0  0  0  0
 12 36  1  0  0  0  0
 13 37  1  1  0  0  0
 14 38  1  0  0  0  0
 15 39  1  6  0  0  0
 16 40  1  0  0  0  0
 17 41  1  1  0  0  0
 18 42  1  0  0  0  0
 19 43  1  0  0  0  0
 19 44  1  0  0  0  0
 20 45  1  0  0  0  0
 20 46  1  0  0  0  0
 21 47  1  0  0  0  0
 21 48  1  0  0  0  0
 22 49  1  1  0  0  0
 23 50  1  0  0  0  0
 23 51  1  0  0  0  0
 23 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0009178

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O7/c1-11-5-3-7-14(20)18(23)15(21)8-4-6-12-9-13(25-2)10-16(22)17(12)19(24)26-11/h4,6,9-11,14-15,18,20-23H,3,5,7-8H2,1-2H3/b6-4-/t11-,14+,15-,18+/m0/s1

> <INCHI_KEY>
VBHMOJMVNMGQQV-FAAALFOVSA-N

> <FORMULA>
C19H26O7

> <MOLECULAR_WEIGHT>
366.41

> <EXACT_MASS>
366.167853177

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.9649681926726

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,7R,8R,9S)-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-1H-2-benzoxacyclotetradecin-1-one

> <ALOGPS_LOGP>
0.89

> <JCHEM_LOGP>
2.1627516460000002

> <ALOGPS_LOGS>
-2.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.125163317717163

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.593605815803429

> <JCHEM_PKA_STRONGEST_BASIC>
-3.180650854119591

> <JCHEM_POLAR_SURFACE_AREA>
116.45000000000002

> <JCHEM_REFRACTIVITY>
96.57289999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.23e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,7R,8R,9S)-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-2-benzoxacyclotetradecin-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
    6.3192   -0.6822   -0.9850 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7824   -0.1226    0.1770 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4281    0.0543    0.4059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    0.6167    1.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6863    0.8048    1.8425 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3771    1.3795    3.0676 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7046    0.4373    0.9211 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0673   -0.1228   -0.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4512   -0.2987   -0.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2333   -0.5795   -1.3391 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2365   -1.4661   -1.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1692   -2.1363   -0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5582   -2.0584    0.3807 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8929   -3.2414    1.1361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6795   -1.8354   -0.5500 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3067   -1.0578   -1.6229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8215   -1.0434    0.1197 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0012   -1.7313   -0.1493 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9263    0.3698   -0.4036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1477    1.3809    0.3902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4247    2.4061   -0.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9345    2.3852   -0.1129 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1590    2.5194   -1.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6709    1.2293    0.5690 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3290    0.7523    1.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1142    0.5265    2.5922 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7152   -1.5329   -1.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4701    0.0955   -1.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3155   -1.1290   -0.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7884    0.9111    2.3251 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1033    1.6289    3.6998 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8295   -0.7272   -1.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4435   -0.1602   -2.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2914   -1.7298   -2.2371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5860   -2.0159    0.7443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0055   -3.2583   -0.3246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6277   -1.2723    1.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8345   -3.0804    1.4157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1032   -2.8024   -0.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8612   -0.2646   -1.2647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6799   -1.0578    1.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8459   -2.5482   -0.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0313    0.6522   -0.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7076    0.4122   -1.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8767    1.9901    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4757    0.9410    1.1582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5038    2.0336   -1.5130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8510    3.4242   -0.3834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7528    3.3345    0.4274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2507    3.5442   -1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9149    2.3322   -1.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    1.7931   -2.1872 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  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  2  0
  9  3  1  0
 25  7  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  6 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  1
 14 38  1  0
 15 39  1  6
 16 40  1  0
 17 41  1  1
 18 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  1
 23 50  1  0
 23 51  1  0
 23 52  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       6.319  -0.682  -0.985  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.782  -0.123   0.177  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.428   0.054   0.406  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.036   0.617   1.591  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.686   0.805   1.843  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.377   1.379   3.068  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.705   0.437   0.921  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.067  -0.123  -0.256  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.451  -0.299  -0.481  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.233  -0.580  -1.339  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.237  -1.466  -1.310  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.169  -2.136  -0.100  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.558  -2.058   0.381  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.893  -3.241   1.136  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.680  -1.835  -0.550  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.307  -1.058  -1.623  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.821  -1.043   0.120  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.001  -1.731  -0.149  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.926   0.370  -0.404  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.148   1.381   0.390  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.425   2.406  -0.461  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.935   2.385  -0.113  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.159   2.519  -1.419  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.671   1.229   0.569  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.329   0.752   1.340  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.114   0.527   2.592  0.00  0.00           O+0
HETATM   27  H   UNK     0       5.715  -1.533  -1.365  0.00  0.00           H+0
HETATM   28  H   UNK     0       6.470   0.096  -1.782  0.00  0.00           H+0
HETATM   29  H   UNK     0       7.316  -1.129  -0.698  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.788   0.911   2.325  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.103   1.629   3.700  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.829  -0.727  -1.418  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.444  -0.160  -2.342  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.291  -1.730  -2.237  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.586  -2.016   0.744  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.006  -3.258  -0.325  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.628  -1.272   1.189  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.834  -3.080   1.416  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.103  -2.802  -0.956  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.861  -0.265  -1.265  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.680  -1.058   1.228  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.846  -2.548  -0.693  0.00  0.00           H+0
HETATM   43  H   UNK     0      -5.031   0.652  -0.346  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.708   0.412  -1.479  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.877   1.990   1.007  0.00  0.00           H+0
HETATM   46  H   UNK     0      -2.476   0.941   1.158  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.504   2.034  -1.513  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.851   3.424  -0.383  0.00  0.00           H+0
HETATM   49  H   UNK     0      -0.753   3.334   0.427  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.251   3.544  -1.833  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.915   2.332  -1.280  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.540   1.793  -2.187  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   30                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   31                                                       
CONECT    7    5    8   25                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    3   32                                                  
CONECT   10    8   11   33                                                  
CONECT   11   10   12   34                                                  
CONECT   12   11   13   35   36                                             
CONECT   13   12   14   15   37                                             
CONECT   14   13   38                                                       
CONECT   15   13   16   17   39                                             
CONECT   16   15   40                                                       
CONECT   17   15   18   19   41                                             
CONECT   18   17   42                                                       
CONECT   19   17   20   43   44                                             
CONECT   20   19   21   45   46                                             
CONECT   21   20   22   47   48                                             
CONECT   22   21   23   24   49                                             
CONECT   23   22   50   51   52                                             
CONECT   24   22   25                                                       
CONECT   25   24   26    7                                                  
CONECT   26   25                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    4                                                            
CONECT   31    6                                                            
CONECT   32    9                                                            
CONECT   33   10                                                            
CONECT   34   11                                                            
CONECT   35   12                                                            
CONECT   36   12                                                            
CONECT   37   13                                                            
CONECT   38   14                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   17                                                            
CONECT   42   18                                                            
CONECT   43   19                                                            
CONECT   44   19                                                            
CONECT   45   20                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
CONECT   48   21                                                            
CONECT   49   22                                                            
CONECT   50   23                                                            
CONECT   51   23                                                            
CONECT   52   23                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  106    0
END

RDKit          3D

52 53  0  0  0  0  0  0  0  0999 V2000
    6.3192   -0.6822   -0.9850 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7824   -0.1226    0.1770 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4281    0.0543    0.4059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    0.6167    1.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6863    0.8048    1.8425 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3771    1.3795    3.0676 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7046    0.4373    0.9211 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0673   -0.1228   -0.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4512   -0.2987   -0.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2333   -0.5795   -1.3391 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2365   -1.4661   -1.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1692   -2.1363   -0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5582   -2.0584    0.3807 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8929   -3.2414    1.1361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6795   -1.8354   -0.5500 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3067   -1.0578   -1.6229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8215   -1.0434    0.1197 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0012   -1.7313   -0.1493 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9263    0.3698   -0.4036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1477    1.3809    0.3902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4247    2.4061   -0.4606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9345    2.3852   -0.1129 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1590    2.5194   -1.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6709    1.2293    0.5690 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3290    0.7523    1.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1142    0.5265    2.5922 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7152   -1.5329   -1.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4701    0.0955   -1.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3155   -1.1290   -0.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7884    0.9111    2.3251 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1033    1.6289    3.6998 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8295   -0.7272   -1.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4435   -0.1602   -2.3421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2914   -1.7298   -2.2371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5860   -2.0159    0.7443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0055   -3.2583   -0.3246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6277   -1.2723    1.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8345   -3.0804    1.4157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1032   -2.8024   -0.9558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8612   -0.2646   -1.2647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6799   -1.0578    1.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8459   -2.5482   -0.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0313    0.6522   -0.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7076    0.4122   -1.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8767    1.9901    1.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4757    0.9410    1.1582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5038    2.0336   -1.5130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8510    3.4242   -0.3834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7528    3.3345    0.4274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2507    3.5442   -1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9149    2.3322   -1.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    1.7931   -2.1872 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  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  2  0
  9  3  1  0
 25  7  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  6 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  1
 14 38  1  0
 15 39  1  6
 16 40  1  0
 17 41  1  1
 18 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  1
 23 50  1  0
 23 51  1  0
 23 52  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₇

Average Mass

366.4100 Da

Monoisotopic Mass

366.16785 Da

IUPAC Name

(3S,7R,8R,9S)-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-1H-2-benzoxacyclotetradecin-1-one

Traditional Name

(3S,7R,8R,9S)-7,8,9,16-tetrahydroxy-14-methoxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-2-benzoxacyclotetradecin-1-one

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=C1)\C=C/C[C@H](O)[C@H](O)[C@H](O)CCC[C@H](C)OC2=O

InChI Identifier

InChI=1S/C19H26O7/c1-11-5-3-7-14(20)18(23)15(21)8-4-6-12-9-13(25-2)10-16(22)17(12)19(24)26-11/h4,6,9-11,14-15,18,20-23H,3,5,7-8H2,1-2H3/b6-4-/t11-,14+,15-,18+/m0/s1

InChI Key

VBHMOJMVNMGQQV-FAAALFOVSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

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 lunata	LOTUS Database	35616633
Paecilomyces sp. SC0924	NPAtlas	20429578

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	0.89	ALOGPS
logP	2.16	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	9.59	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	96.57 m³·mol⁻¹	ChemAxon
Polarizability	37.96 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

Xu L, He Z, Xue J, Chen X, Wei X: beta-Resorcylic acid lactones from a Paecilomyces fungus. J Nat Prod. 2010 May 28;73(5):885-9. doi: 10.1021/np900853n. [PubMed:20429578 ]

Showing NP-Card for Paecilomycin F (NP0009178)

MOL for NP0009178 (Paecilomycin F)

3D MOL for NP0009178 (Paecilomycin F)

3D SDF for NP0009178 (Paecilomycin F)

3D-SDF for NP0009178 (Paecilomycin F)

PDB for NP0009178 (Paecilomycin F)

3D PDB for NP0009178 (Paecilomycin F)

SMILES for NP0009178 (Paecilomycin F)

INCHI for NP0009178 (Paecilomycin F)

Structure for NP0009178 (Paecilomycin F)

3D Structure for NP0009178 (Paecilomycin F)