NP-MRD: Showing NP-Card for Panglimycin F (NP0007463)

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Record Information

Version

2.0

Created at

2020-12-09 04:20:24 UTC

Updated at

2021-07-15 16:57:39 UTC

NP-MRD ID

NP0007463

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Panglimycin F

Provided By

NPAtlas

Description

Panglimycin F belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane. Panglimycin F is found in Streptomyces. Based on a literature review very few articles have been published on Panglimycin F.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118403D          

 46 50  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306242118403D          

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 22 42  1  0  0  0  0
 24 43  1  6  0  0  0
 25 44  1  0  0  0  0
 26 45  1  0  0  0  0
 26 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0007463

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=C([H])C([H])=C1[H])C(=O)[C@@]13O[C@@]1(C([H])([H])C([H])([H])[C@]1(O[H])C([H])([H])[C@@]([H])(C([H])([H])[H])C([H])([H])C(=O)[C@]31O[H])[C@]2([H])O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H20O7/c1-9-7-12(21)18(25)16(24,8-9)5-6-17-15(23)13-10(3-2-4-11(13)20)14(22)19(17,18)26-17/h2-4,9,15,20,23-25H,5-8H2,1H3/t9-,15+,16-,17-,18+,19+/m0/s1

> <INCHI_KEY>
OREXHBWUTDHYPX-NGQCPRAGSA-N

> <FORMULA>
C19H20O7

> <MOLECULAR_WEIGHT>
360.362

> <EXACT_MASS>
360.120902984

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
34.941797298598246

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,5R,7S,10S,11R)-2,7,11,13-tetrahydroxy-5-methyl-19-oxapentacyclo[8.8.1.0^{1,10}.0^{2,7}.0^{12,17}]nonadeca-12,14,16-triene-3,18-dione

> <ALOGPS_LOGP>
1.13

> <JCHEM_LOGP>
0.33726689100000073

> <ALOGPS_LOGS>
-1.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.789149034320443

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.162397788015967

> <JCHEM_PKA_STRONGEST_BASIC>
-3.510915509499613

> <JCHEM_POLAR_SURFACE_AREA>
127.59

> <JCHEM_REFRACTIVITY>
87.789

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.86e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5R,7S,10S,11R)-2,7,11,13-tetrahydroxy-5-methyl-19-oxapentacyclo[8.8.1.0^{1,10}.0^{2,7}.0^{12,17}]nonadeca-12,14,16-triene-3,18-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 50  0  0  0  0  0  0  0  0999 V2000
    4.8737   -0.0768    0.1249 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4915   -0.7339    0.2463 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8195   -0.3200    1.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6286    0.5364    1.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2046    1.0965    2.3272 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9316    0.7687    0.0519 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4745    2.1073    0.0780 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8944    0.6692   -1.1082 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7558    1.7567   -1.0438 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1155    0.6810   -2.3800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3280    1.0222   -2.2069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9831    0.0421   -1.2330 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2247   -1.1351   -1.0836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2391   -0.1659   -0.0790 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8704   -0.6051    1.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1874   -1.0848    2.1341 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3242   -0.4878    1.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8539   -0.6940    2.5650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2187   -0.6107    2.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9988   -0.3294    1.6100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4382   -0.1308    0.3686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2660    0.1418   -0.6857 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0584   -0.2068    0.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4578    0.0225   -1.1399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8856    1.3287   -1.5303 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6970   -0.5810   -1.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1796    0.1887    1.1659 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8369    0.8162   -0.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6263   -0.7883   -0.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7262   -1.8368    0.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5437    0.3021    2.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5384   -1.1443    2.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2119    2.2086    0.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6081    2.3129   -0.2269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5740    1.3396   -3.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1459   -0.3480   -2.8466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5609    2.0650   -2.0042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8242    0.7932   -3.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1997   -0.9109    3.3916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6749   -0.7640    3.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0686   -0.2708    1.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8965    0.2771   -1.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9459   -0.6896   -1.8519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4659    1.9185   -0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0771   -1.4969   -1.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4401   -0.5601   -1.8586 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
  4  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  6
 14 13  1  6
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 25  1  0
  8 26  1  0
 26  2  1  0
 14  6  1  0
 23 17  1  0
 14 12  1  0
 24 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  1
  3 31  1  0
  3 32  1  0
  7 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
 22 42  1  0
 24 43  1  6
 25 44  1  0
 26 45  1  0
 26 46  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       4.874  -0.077   0.125  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.491  -0.734   0.246  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.820  -0.320   1.497  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.629   0.536   1.310  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.205   1.097   2.327  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.932   0.769   0.052  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.475   2.107   0.078  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.894   0.669  -1.108  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.756   1.757  -1.044  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.115   0.681  -2.380  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.328   1.022  -2.207  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.983   0.042  -1.233  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.225  -1.135  -1.084  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.239  -0.166  -0.079  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.870  -0.605   1.168  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.187  -1.085   2.134  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.324  -0.488   1.298  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.854  -0.694   2.565  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.219  -0.611   2.713  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.999  -0.329   1.610  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.438  -0.131   0.369  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.266   0.142  -0.686  0.00  0.00           O+0
HETATM   23  C   UNK     0      -3.058  -0.207   0.184  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.458   0.023  -1.140  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.886   1.329  -1.530  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.697  -0.581  -1.007  0.00  0.00           C+0
HETATM   27  H   UNK     0       5.180   0.189   1.166  0.00  0.00           H+0
HETATM   28  H   UNK     0       4.837   0.816  -0.508  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.626  -0.788  -0.266  0.00  0.00           H+0
HETATM   30  H   UNK     0       3.726  -1.837   0.343  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.544   0.302   2.104  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.538  -1.144   2.181  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.212   2.209   0.773  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.608   2.313  -0.227  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.574   1.340  -3.159  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.146  -0.348  -2.847  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.561   2.065  -2.004  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.824   0.793  -3.196  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.200  -0.911   3.392  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.675  -0.764   3.682  0.00  0.00           H+0
HETATM   41  H   UNK     0      -6.069  -0.271   1.759  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.896   0.277  -1.605  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.946  -0.690  -1.852  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.466   1.919  -0.827  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.077  -1.497  -1.229  0.00  0.00           H+0
HETATM   46  H   UNK     0       3.440  -0.560  -1.859  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    1    3   26   30                                             
CONECT    3    2    4   31   32                                             
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8   14                                             
CONECT    7    6   33                                                       
CONECT    8    6    9   10   26                                             
CONECT    9    8   34                                                       
CONECT   10    8   11   35   36                                             
CONECT   11   10   12   37   38                                             
CONECT   12   11   13   14   24                                             
CONECT   13   12   14                                                       
CONECT   14   13   15    6   12                                             
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   23                                                  
CONECT   18   17   19   39                                                  
CONECT   19   18   20   40                                                  
CONECT   20   19   21   41                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21   42                                                       
CONECT   23   21   24   17                                                  
CONECT   24   23   25   12   43                                             
CONECT   25   24   44                                                       
CONECT   26    8    2   45   46                                             
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    2                                                            
CONECT   31    3                                                            
CONECT   32    3                                                            
CONECT   33    7                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   10                                                            
CONECT   37   11                                                            
CONECT   38   11                                                            
CONECT   39   18                                                            
CONECT   40   19                                                            
CONECT   41   20                                                            
CONECT   42   22                                                            
CONECT   43   24                                                            
CONECT   44   25                                                            
CONECT   45   26                                                            
CONECT   46   26                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  100    0
END

RDKit          3D

46 50  0  0  0  0  0  0  0  0999 V2000
    4.8737   -0.0768    0.1249 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4915   -0.7339    0.2463 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8195   -0.3200    1.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6286    0.5364    1.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2046    1.0965    2.3272 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9316    0.7687    0.0519 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4745    2.1073    0.0780 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8944    0.6692   -1.1082 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7558    1.7567   -1.0438 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1155    0.6810   -2.3800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3280    1.0222   -2.2069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9831    0.0421   -1.2330 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2247   -1.1351   -1.0836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2391   -0.1659   -0.0790 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8704   -0.6051    1.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1874   -1.0848    2.1341 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3242   -0.4878    1.2984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8539   -0.6940    2.5650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2187   -0.6107    2.7130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9988   -0.3294    1.6100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4382   -0.1308    0.3686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2660    0.1418   -0.6857 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0584   -0.2068    0.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4578    0.0225   -1.1399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8856    1.3287   -1.5303 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6970   -0.5810   -1.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1796    0.1887    1.1659 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8369    0.8162   -0.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6263   -0.7883   -0.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7262   -1.8368    0.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5437    0.3021    2.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5384   -1.1443    2.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2119    2.2086    0.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6081    2.3129   -0.2269 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5740    1.3396   -3.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1459   -0.3480   -2.8466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5609    2.0650   -2.0042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8242    0.7932   -3.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1997   -0.9109    3.3916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6749   -0.7640    3.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0686   -0.2708    1.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8965    0.2771   -1.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9459   -0.6896   -1.8519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4659    1.9185   -0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0771   -1.4969   -1.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4401   -0.5601   -1.8586 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
  4  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  6
 14 13  1  6
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 25  1  0
  8 26  1  0
 26  2  1  0
 14  6  1  0
 23 17  1  0
 14 12  1  0
 24 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  1
  3 31  1  0
  3 32  1  0
  7 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
 22 42  1  0
 24 43  1  6
 25 44  1  0
 26 45  1  0
 26 46  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀O₇

Average Mass

360.3620 Da

Monoisotopic Mass

360.12090 Da

IUPAC Name

(1S,2R,5R,7S,10S,11R)-2,7,11,13-tetrahydroxy-5-methyl-19-oxapentacyclo[8.8.1.0^{1,10}.0^{2,7}.0^{12,17}]nonadeca-12,14,16-triene-3,18-dione

Traditional Name

(1S,2R,5R,7S,10S,11R)-2,7,11,13-tetrahydroxy-5-methyl-19-oxapentacyclo[8.8.1.0^{1,10}.0^{2,7}.0^{12,17}]nonadeca-12,14,16-triene-3,18-dione

CAS Registry Number

Not Available

SMILES

C[C@H]1CC(=O)C2(O)C34OC3(CCC2(O)C1)[C@H](O)C1=C(C=CC=C1O)C4=O

InChI Identifier

InChI=1S/C19H20O7/c1-9-7-12(21)18(25)16(24,8-9)5-6-17-15(23)13-10(3-2-4-11(13)20)14(22)19(17,18)26-17/h2-4,9,15,20,23-25H,5-8H2,1H3/t9-,15+,16?,17?,18?,19?/m0/s1

InChI Key

OREXHBWUTDHYPX-NGQCPRAGSA-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
Streptomyces	NPAtlas	18081255

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Tetralins

Sub Class

Not Available

Direct Parent

Tetralins

Alternative Parents

Substituents

Tetralin
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Oxepane
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.13	ALOGPS
logP	0.34	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	9.16	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	127.59 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	87.79 m³·mol⁻¹	ChemAxon
Polarizability	34.94 Å³	ChemAxon
Number of Rings	5	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

NPAtlas ID

NPA017458

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78445552

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587948

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Panglimycin F (NP0007463)

MOL for NP0007463 (Panglimycin F)

3D MOL for NP0007463 (Panglimycin F)

3D SDF for NP0007463 (Panglimycin F)

3D-SDF for NP0007463 (Panglimycin F)

PDB for NP0007463 (Panglimycin F)

3D PDB for NP0007463 (Panglimycin F)

SMILES for NP0007463 (Panglimycin F)

INCHI for NP0007463 (Panglimycin F)

Structure for NP0007463 (Panglimycin F)

3D Structure for NP0007463 (Panglimycin F)