NP-MRD: Showing NP-Card for (4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione (NP0305126)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 20:41:18 UTC

Updated at

2022-09-10 20:41:18 UTC

NP-MRD ID

NP0305126

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione

Description

5'-Hydroxymonocillin III belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups. (4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione is found in Neophaeosphaeria quadriseptata. (4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione was first documented in 2007 (PMID: 18052326). Based on a literature review very few articles have been published on 5'-hydroxymonocillin III.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102222412D          

 25 27  0  0  1  0            999 V2000
    6.3845    0.5635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2201   -0.2450    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9717   -0.5851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5013   -1.2177    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2952   -1.4421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7040   -2.0174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5396   -2.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0407   -3.4830    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4163   -4.2175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2159   -3.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4814   -3.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7298   -3.5380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2309   -4.1951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2002   -2.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9975   -2.1057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2152   -2.3675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5972   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149   -2.0828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7616   -1.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5440   -0.7506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7083    0.0578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1619   -1.2972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6608   -0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1312   -0.0076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3954   -0.2646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  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  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
M  END

     RDKit          3D

 45 47  0  0  0  0  0  0  0  0999 V2000
   -0.5428    3.3652    0.5488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2894    2.3086   -0.2861 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0786    1.5261    0.7384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3241    0.1535    0.2262 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4841   -0.7283    1.4090 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4519   -0.5874    0.4504 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5844   -1.8012   -0.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2683   -2.4844   -0.7447 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6712   -3.6225   -1.5247 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6177   -3.0384    0.4563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5155   -2.6970    1.0549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4695   -1.6812    0.7940 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8435   -0.8988    1.7696 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1521   -1.3811   -0.4811 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1892   -0.2964   -0.3329 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3735   -0.6957    0.2769 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4305    0.1630    0.4540 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6070   -0.2208    1.0564 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2962    1.4503    0.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1215    1.8571   -0.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0843    3.1756   -1.0168 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0229    0.9919   -0.7892 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8190    1.5191   -1.4346 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0913    2.0953   -2.5588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4625    1.4679   -1.0031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0419    2.7932    1.3576 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1640    3.9279   -0.0667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3172    3.9845    1.0276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0075    2.9087   -0.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0735    1.9866    0.9346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5620    1.5475    1.7233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5548   -0.1816   -0.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4254   -0.2235    0.8201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2325   -2.5561    0.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0559   -1.5121   -1.3832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6349   -1.9362   -1.4285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8317   -4.0542   -1.8045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2394   -3.8845    0.8658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2576   -3.2982    1.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683   -1.1126   -1.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7480   -2.2981   -0.7773 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5035   -1.7060    0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6839   -0.1099    2.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1225    2.1325    0.1433 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3344    3.6513   -1.4629 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  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25  2  1  0
  6  4  1  0
 22 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  6
  3 30  1  0
  3 31  1  0
  4 32  1  6
  6 33  1  1
  7 34  1  0
  7 35  1  0
  8 36  1  6
  9 37  1  0
 10 38  1  0
 11 39  1  0
 14 40  1  0
 14 41  1  0
 16 42  1  0
 18 43  1  0
 19 44  1  0
 21 45  1  0
M  END


  Mrv1652309102222412D          

 25 27  0  0  1  0            999 V2000
    6.3845    0.5635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2201   -0.2450    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9717   -0.5851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5013   -1.2177    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2952   -1.4421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7040   -2.0174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5396   -2.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0407   -3.4830    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4163   -4.2175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2159   -3.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4814   -3.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7298   -3.5380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2309   -4.1951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2002   -2.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9975   -2.1057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2152   -2.3675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5972   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8149   -2.0828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7616   -1.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5440   -0.7506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7083    0.0578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1619   -1.2972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6608   -0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1312   -0.0076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3954   -0.2646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  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  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0305126

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H]2O[C@@H]2C[C@H](O)\C=C\C(=O)CC2=CC(O)=CC(O)=C2C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C18H20O7/c1-9-4-15-16(25-15)8-12(20)3-2-11(19)5-10-6-13(21)7-14(22)17(10)18(23)24-9/h2-3,6-7,9,12,15-16,20-22H,4-5,8H2,1H3/b3-2+/t9-,12-,15-,16-/m1/s1

> <INCHI_KEY>
PDABOOGSLAXXJV-QLTJIAJJSA-N

> <FORMULA>
C18H20O7

> <MOLECULAR_WEIGHT>
348.351

> <EXACT_MASS>
348.120902984

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
34.12479791552461

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,6R,8R,10S,11E)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0^{6,8}]nonadeca-1(19),11,15,17-tetraene-2,13-dione

> <JCHEM_LOGP>
1.974893111333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.344312575572523

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.4965190271243

> <JCHEM_PKA_STRONGEST_BASIC>
-2.90183896173719

> <JCHEM_POLAR_SURFACE_AREA>
116.59000000000002

> <JCHEM_REFRACTIVITY>
89.26539999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4R,6R,8R,10S,11E)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0^{6,8}]nonadeca-1(19),11,15,17-tetraene-2,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      11.918   1.052   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.611  -0.457   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.014  -1.092   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.002  -2.273   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      15.484  -2.692   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      14.381  -3.766   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.074  -5.275   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.143  -6.502   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      13.844  -7.873   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.603  -6.538   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.232  -7.239   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.829  -6.604   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.898  -7.831   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.840  -5.423   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.462  -3.931   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.002  -4.419   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.848  -3.399   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.388  -3.888   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.155  -1.890   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.615  -1.401   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.922   0.108   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.769  -2.421   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.700  -1.195   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.712  -0.014   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      10.071  -0.494   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4    6                                                       
CONECT    6    5    4    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   15   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    2                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₀O₇

Average Mass

348.3510 Da

Monoisotopic Mass

348.12090 Da

IUPAC Name

(4R,6R,8R,10S,11E)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0^{6,8}]nonadeca-1(19),11,15,17-tetraene-2,13-dione

Traditional Name

(4R,6R,8R,10S,11E)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0^{6,8}]nonadeca-1(19),11,15,17-tetraene-2,13-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H]2O[C@@H]2C[C@H](O)\C=C\C(=O)CC2=CC(O)=CC(O)=C2C(=O)O1

InChI Identifier

InChI=1S/C18H20O7/c1-9-4-15-16(25-15)8-12(20)3-2-11(19)5-10-6-13(21)7-14(22)17(10)18(23)24-9/h2-3,6-7,9,12,15-16,20-22H,4-5,8H2,1H3/b3-2+/t9-,12-,15-,16-/m1/s1

InChI Key

PDABOOGSLAXXJV-QLTJIAJJSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Neophaeosphaeria quadriseptata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Hydroxybenzoic acid derivatives

Alternative Parents

Substituents

Dihydroxybenzoic acid
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Vinylogous acid
Carboxylic acid ester
Ketone
Lactone
Cyclic ketone
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Polyol
Alcohol
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Carbonyl group
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	1.97	ChemAxon
pKa (Strongest Acidic)	8.5	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	116.59 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	89.27 m³·mol⁻¹	ChemAxon
Polarizability	34.12 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	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00038292

Chemspider ID

23311666

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24180662

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Paranagama PA, Wijeratne EM, Gunatilaka AA: Uncovering biosynthetic potential of plant-associated fungi: effect of culture conditions on metabolite production by Paraphaeosphaeria quadriseptata and Chaetomium chiversii. J Nat Prod. 2007 Dec;70(12):1939-45. doi: 10.1021/np070504b. Epub 2007 Dec 6. [PubMed:18052326 ]
LOTUS database [Link]

Showing NP-Card for (4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione (NP0305126)

MOL for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

3D MOL for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

3D SDF for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

3D-SDF for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

PDB for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

3D PDB for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

SMILES for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

INCHI for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

Structure for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)

3D Structure for NP0305126 ((4r,6r,8r,10s,11e)-10,17,19-trihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),11,15,17-tetraene-2,13-dione)