NP-MRD: Showing NP-Card for 5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid (NP0165688)

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Record Information

Version

2.0

Created at

2022-09-03 00:53:51 UTC

Updated at

2022-09-03 00:53:51 UTC

NP-MRD ID

NP0165688

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid

Description

Parmosidone B belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone). Based on a literature review very few articles have been published on Parmosidone B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032202532D          

 26 28  0  0  0  0            999 V2000
    5.7025   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5189    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1237    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9401    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5448    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1517    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9682    2.7028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7305    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162   -0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5741   -0.8553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912   -0.1120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0884    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9049   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4837    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6953    0.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5117   -0.1965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0906    1.1689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0625    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6392    2.7028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4275    2.9460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0604    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 16 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
  8 26  1  0  0  0  0
M  END

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -3.9065   -2.5198   -0.8383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5823   -1.1829   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5493   -0.2429   -0.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2722    1.0013    0.4212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2879    1.9198    0.7742 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9287    1.4237    0.5325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6763    2.6847    0.9593 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9273    0.5284    0.1964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2789   -0.7573   -0.2448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3146   -1.7856   -0.6035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7798   -2.9471   -0.5806 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0236   -1.7134   -0.9625 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9106   -0.7125   -0.4848 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2227   -1.1139   -0.6733 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5183   -2.4311   -1.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2771   -0.2924   -0.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6249   -0.7774   -0.4992 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8543   -1.9079   -1.0370 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7080   -0.0228   -0.1273 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0013    0.9020    0.2865 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9639    1.7781    0.7048 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6543    1.3090    0.4763 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4120    2.6535    1.0571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1465    2.8173    2.2405 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6208    0.5044    0.0921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6514    1.0700    0.3574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6037   -2.7828   -1.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9451   -3.3373   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0433   -2.4654   -1.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5725   -0.6137   -0.1025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0462    2.8398    1.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8620    3.1950    1.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262   -3.1399   -0.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9823   -2.3144   -2.3054 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5186   -2.9119   -1.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2496   -0.2142    0.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9231    1.8071    0.7278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3097    2.6498    1.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5895    3.4526    0.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6910    3.6502    2.1154 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 19  1  0
 17 18  2  0
 16 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  2  0
 25 26  1  0
  9  2  1  0
 25 13  1  0
 26  8  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  5 31  1  0
  7 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 19 36  1  0
 21 37  1  0
 23 38  1  0
 23 39  1  0
 24 40  1  0
M  END


  Mrv1652309032202532D          

 26 28  0  0  0  0            999 V2000
    5.7025   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5189    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1237    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9401    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5448    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1517    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9682    2.7028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5470    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7305    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2162   -0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5741   -0.8553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3912   -0.1120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    0.5330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0884    0.2898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9049   -0.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4837    0.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6953    0.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5117   -0.1965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0906    1.1689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6673    1.6553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0625    2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556    1.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6392    2.7028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4275    2.9460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0604    1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8037    1.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 16 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
  8 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0165688

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(O)=C(O)C2=C1C(=O)OC1=C(C)C(C(O)=O)=C(O)C(CO)=C1O2

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O9/c1-5-3-8(19)12(21)15-9(5)17(24)26-13-6(2)10(16(22)23)11(20)7(4-18)14(13)25-15/h3,18-21H,4H2,1-2H3,(H,22,23)

> <INCHI_KEY>
WVKCHHJTEWWJNY-UHFFFAOYSA-N

> <FORMULA>
C17H14O9

> <MOLECULAR_WEIGHT>
362.29

> <EXACT_MASS>
362.063782031

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
33.90961929131884

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaene-6-carboxylic acid

> <ALOGPS_LOGP>
1.79

> <JCHEM_LOGP>
2.6181025499999997

> <ALOGPS_LOGS>
-3.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.150342384696625

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.598062622315256

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2134834360954683

> <JCHEM_POLAR_SURFACE_AREA>
153.75

> <JCHEM_REFRACTIVITY>
88.1409

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.53e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaene-6-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      10.645  -0.960   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.302   0.541   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.431   1.588   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.088   3.090   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      12.217   4.137   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.617   3.544   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.274   5.045   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.488   2.496   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.830   0.995   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.870  -0.209   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.538  -1.597   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       6.330  -0.209   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.370   0.995   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.898   0.541   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.556  -0.960   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.770   1.588   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.298   1.135   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.955  -0.367   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.169   2.182   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.112   3.090   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.983   4.137   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.584   3.544   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.926   5.045   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.398   5.499   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.713   2.496   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.100   3.165   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   26                                                  
CONECT    9    8    2   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   25                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   20                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   16   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   13   26                                                  
CONECT   26   25    8                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₉

Average Mass

362.2900 Da

Monoisotopic Mass

362.06378 Da

IUPAC Name

5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaene-6-carboxylic acid

Traditional Name

5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaene-6-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=C(O)C2=C1C(=O)OC1=C(C)C(C(O)=O)=C(O)C(CO)=C1O2

InChI Identifier

InChI=1S/C17H14O9/c1-5-3-8(19)12(21)15-9(5)17(24)26-13-6(2)10(16(22)23)11(20)7(4-18)14(13)25-15/h3,18-21H,4H2,1-2H3,(H,22,23)

InChI Key

WVKCHHJTEWWJNY-UHFFFAOYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Depsides and depsidones

Sub Class

Not Available

Direct Parent

Depsides and depsidones

Alternative Parents

Substituents

Depsidone
Dihydroxybenzoic acid
Diaryl ether
Salicylic acid or derivatives
Hydroxybenzoic acid
1-hydroxy-2-unsubstituted benzenoid
Dioxepine
1,4-dioxepine
Benzenoid
Dicarboxylic acid or derivatives
Vinylogous acid
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Primary alcohol
Organooxygen compound
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	1.79	ALOGPS
logP	2.62	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	2.6	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	153.75 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	88.14 m³·mol⁻¹	ChemAxon
Polarizability	33.91 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

Not Available

Chemspider ID

78435998

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

132553221

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid (NP0165688)

MOL for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

3D MOL for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

3D SDF for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

3D-SDF for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

PDB for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

3D PDB for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

SMILES for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

INCHI for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

Structure for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)

3D Structure for NP0165688 (5,14,15-trihydroxy-4-(hydroxymethyl)-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-6-carboxylic acid)