NP-MRD: Showing NP-Card for {13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid (NP0306811)

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Record Information

Version

2.0

Created at

2022-09-10 23:31:44 UTC

Updated at

2022-09-10 23:31:45 UTC

NP-MRD ID

NP0306811

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid

Description

{13,14-Dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]Hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. {13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid is found in Reaumuria vermiculata. Based on a literature review very few articles have been published on {13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]Hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112201312D          

 27 30  0  0  0  0            999 V2000
    4.3164    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664   -0.1105    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6809   -0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    0.0000 C   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
  6  7  2  0  0  0  0
  6  8  2  0  0  0  0
  6  9  1  0  0  0  0
  4 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
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  2  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 15 27  1  0  0  0  0
 21 27  2  0  0  0  0
M  END

     RDKit          3D

 35 38  0  0  0  0  0  0  0  0999 V2000
    3.2520    2.5147   -0.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6771    1.7221   -1.0243 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8541    0.6333   -0.7747 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4019   -0.6247   -0.6317 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7691   -0.8464   -0.7297 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7073   -0.7475    0.6762 S   0  0  0  0  0  6  0  0  0  0  0  0
    5.9375    0.0802    0.4120 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1292   -2.1303    1.1416 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8393   -0.0429    1.9143 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5871   -1.7334   -0.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2325   -1.5969   -0.2698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6044   -2.6678   -0.0218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0707   -3.7995    0.1030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8864   -2.4625    0.0705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4718   -1.3055   -0.0531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8468   -1.1632    0.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6266   -2.2772    0.3072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4182    0.0807   -0.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7925    0.2419    0.0275 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6199    1.1870   -0.3304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2454    1.0531   -0.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3930    2.1077   -0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9407    3.2530   -0.8153 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0907    1.9634   -0.7936 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4882    0.7897   -0.6667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3062   -0.3209   -0.4166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6700   -0.1921   -0.3044 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3306    2.3053    0.1414 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7257    2.3054    0.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0808    3.5807   -0.3133 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8908   -0.3553    1.8347 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0143   -2.7229   -0.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6235   -2.1481    0.3837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2546    1.1293   -0.0660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0561    2.1898   -0.4445 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
  6  9  1  0
  6  7  2  0
  6  8  2  0
  4 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
 16 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 27  2  0
 27 26  1  0
 26 25  2  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
 25  3  1  0
 26 11  1  0
 27 15  1  0
 22 21  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  9 31  1  0
 10 32  1  0
 17 33  1  0
 19 34  1  0
 20 35  1  0
M  END


  Mrv1652309112201312D          

 27 30  0  0  0  0            999 V2000
    4.3164    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664   -0.1105    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6809   -0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    0.0000 C   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
  6  7  2  0  0  0  0
  6  8  2  0  0  0  0
  6  9  1  0  0  0  0
  4 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
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  2  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 15 27  1  0  0  0  0
 21 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0306811

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OS(O)(=O)=O)C=C2C(=O)OC3=C(O)C(O)=CC4=C3C2=C1OC4=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H8O11S/c1-23-11-7(26-27(20,21)22)3-5-9-8-4(14(18)25-13(9)11)2-6(16)10(17)12(8)24-15(5)19/h2-3,16-17H,1H3,(H,20,21,22)

> <INCHI_KEY>
YSJGIOJYGKGLQE-UHFFFAOYSA-N

> <FORMULA>
C15H8O11S

> <MOLECULAR_WEIGHT>
396.28

> <EXACT_MASS>
395.978732252

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
33.87093474596529

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0^{4,16}.0^{11,15}]hexadeca-1(14),4,6,8(16),11(15),12-hexaen-6-yl}oxidanesulfonic acid

> <JCHEM_LOGP>
1.3365031276666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.813034251880358

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.720844948125471

> <JCHEM_PKA_STRONGEST_BASIC>
-4.7959551731739944

> <JCHEM_POLAR_SURFACE_AREA>
165.89

> <JCHEM_REFRACTIVITY>
85.08169999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
{13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0^{4,16}.0^{11,15}]hexadeca-1(14),4,6,8(16),11(15),12-hexaen-6-yl}oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       8.057   2.461   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.827   1.127   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.057  -0.206   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.827  -1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.367  -1.540   0.000  0.00  0.00           O+0
HETATM    6  S   UNK     0      11.137  -0.206   0.000  0.00  0.00           S+0
HETATM    7  O   UNK     0      11.907   1.127   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       9.804   0.564   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      12.471  -0.976   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.057  -2.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.517  -2.874   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.747  -4.207   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.517  -5.541   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       4.207  -4.207   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.437  -2.874   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.897  -2.874   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.127  -4.207   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.127  -1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.413  -1.540   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.897  -0.206   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.437  -0.206   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.207   1.127   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.437   2.461   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.747   1.127   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.517  -0.206   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.747  -1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.207  -1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6                                                            
CONECT   10    4   11                                                       
CONECT   11   10   12   26                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   27                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24    3   26                                                  
CONECT   26   25   11   27                                                  
CONECT   27   26   15   21                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
{13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0,.0,]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonate	Generator
{13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0,.0,]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulphonate	Generator
{13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0,.0,]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulphonic acid	Generator

Chemical Formula

C₁₅H₈O₁₁S

Average Mass

396.2800 Da

Monoisotopic Mass

395.97873 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=C(OS(O)(=O)=O)C=C2C(=O)OC3=C(O)C(O)=CC4=C3C2=C1OC4=O

InChI Identifier

InChI=1S/C15H8O11S/c1-23-11-7(26-27(20,21)22)3-5-9-8-4(14(18)25-13(9)11)2-6(16)10(17)12(8)24-15(5)19/h2-3,16-17H,1H3,(H,20,21,22)

InChI Key

YSJGIOJYGKGLQE-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

Species Name	Source	Reference
Reaumuria vermiculata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Ellagic_acid
7,8-dihydroxycoumarin
Isocoumarin
Coumarin
Arylsulfate
Benzopyran
1-benzopyran
2-benzopyran
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Sulfuric acid monoester
Pyran
Sulfate-ester
Benzenoid
Sulfuric acid ester
Heteroaromatic compound
Organic sulfuric acid or derivatives
Lactone
Oxacycle
Organoheterocyclic compound
Ether
Organic oxygen compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
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

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163049964

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid (NP0306811)

MOL for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

3D MOL for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

3D SDF for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

3D-SDF for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

PDB for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

3D PDB for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

SMILES for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

INCHI for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

Structure for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)

3D Structure for NP0306811 ({13,14-dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl}oxidanesulfonic acid)