NP-MRD: Showing NP-Card for (2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal (NP0293087)

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Record Information

Version

2.0

Created at

2022-09-10 00:55:06 UTC

Updated at

2022-09-10 00:55:06 UTC

NP-MRD ID

NP0293087

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal

Description

(-)-Ganotheaecolumol H belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. Based on a literature review very few articles have been published on (-)-ganotheaecolumol H.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102202552D          

 28 29  0  0  1  0            999 V2000
    1.6039   -0.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7969   -0.4441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2449   -1.0572    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3071   -0.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1141   -0.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6662   -0.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4731   -0.1741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4112    0.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6042    0.9536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0522    0.3405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7548    0.5120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9123   -1.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6574   -2.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1423   -2.9942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8067   -3.7479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2917   -4.4153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9561   -5.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1356   -5.2553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4410   -5.8365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1055   -6.5901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5904   -7.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2548   -8.0112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4344   -8.0975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7398   -8.6787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5602   -8.5924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1676   -2.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6525   -2.9942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4226   -1.5422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  6  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
  3 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 13 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  3 28  1  0  0  0  0
M  END

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
   -4.3292   -0.1958    3.2847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8064    0.3752    2.2524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5373    0.0404    1.0087 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7102   -0.4319    0.1686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1657    0.4306   -0.8300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3071    0.1173   -1.5339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7918    0.9674   -2.5469 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0160   -1.0167   -1.2890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5745   -1.8650   -0.3165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4114   -1.5761    0.4193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0258   -2.4931    1.3633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8400    1.0951    0.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6751    0.6514   -0.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7673    1.4514   -1.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5250    1.8215   -0.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4441    0.7966    0.0330 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6368    0.5669   -0.5467 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9964    1.4185   -1.7060 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5722   -0.4858   -0.0686 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8560    0.1854    0.3314 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8684   -0.7799    0.8278 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0517   -0.9069    0.2183 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2692   -0.0312   -0.9621 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0491   -1.8467    0.6941 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1424   -1.9237    0.0829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5118   -0.7092    0.2757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5172   -1.4908    0.0623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6175   -1.0769    0.9941 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3957   -0.5358    3.1301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8206   -1.0907    3.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3612    0.5083    4.2005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6163    1.3355   -1.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2619    1.8051   -2.7227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9251   -1.2409   -1.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1064   -2.7845   -0.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2226   -2.4847    1.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2772    2.0842    0.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3276    2.3888   -1.3258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6614    0.8879   -1.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0267    2.5593   -1.1311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2751    2.5099    0.4541 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2554    0.1675    0.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1368    1.3487   -2.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1356    2.4754   -1.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9133    1.0383   -2.2118 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1420   -1.1269    0.6990 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7705   -1.1436   -0.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6213    0.8585    1.1892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2144    0.7958   -0.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6534   -1.3912    1.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3064   -0.2581   -1.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2269    1.0379   -0.7291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5822   -0.3438   -1.7802 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9090   -2.4889    1.5472 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3 28  1  0
 28 26  1  0
 26 27  2  0
 26 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 13 12  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 12  3  1  0
 10  4  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 18 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  0
 20 49  1  0
 21 50  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  0
 12 37  1  0
  5 32  1  0
  7 33  1  0
  8 34  1  0
  9 35  1  0
 11 36  1  0
M  END


  Mrv1652309102202552D          

 28 29  0  0  1  0            999 V2000
    1.6039   -0.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7969   -0.4441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2449   -1.0572    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3071   -0.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1141   -0.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6662   -0.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4731   -0.1741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4112    0.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6042    0.9536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0522    0.3405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7548    0.5120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9123   -1.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6574   -2.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1423   -2.9942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8067   -3.7479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2917   -4.4153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9561   -5.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1356   -5.2553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4410   -5.8365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1055   -6.5901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5904   -7.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2548   -8.0112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4344   -8.0975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7398   -8.6787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5602   -8.5924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1676   -2.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6525   -2.9942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4226   -1.5422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  6  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
  3 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 13 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  3 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0293087

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@]1(OC(=O)C(CC\C=C(/C)CC\C=C(/C)C=O)=C1)C1=CC(O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O6/c1-15(6-4-8-16(2)14-23)7-5-9-17-13-22(27-3,28-21(17)26)19-12-18(24)10-11-20(19)25/h7-8,10-14,24-25H,4-6,9H2,1-3H3/b15-7+,16-8+/t22-/m0/s1

> <INCHI_KEY>
MOFNDUJXTNIVEF-URUUZNIQSA-N

> <FORMULA>
C22H26O6

> <MOLECULAR_WEIGHT>
386.444

> <EXACT_MASS>
386.172938557

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
41.83693847172947

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,6E)-9-[(5S)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxo-2,5-dihydrofuran-3-yl]-2,6-dimethylnona-2,6-dienal

> <JCHEM_LOGP>
4.915222980666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.087140540776538

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.072877051908952

> <JCHEM_PKA_STRONGEST_BASIC>
-3.957139673488921

> <JCHEM_POLAR_SURFACE_AREA>
93.06

> <JCHEM_REFRACTIVITY>
108.46459999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E,6E)-9-[(5S)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal

> <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       2.994  -1.149   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.488  -0.829   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.457  -1.974   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.573  -0.829   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.080  -1.149   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.110  -0.005   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.617  -0.325   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.634   1.460   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.128   1.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.097   0.636   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.409   0.956   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.703  -2.879   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.227  -4.343   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.132  -5.589   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.506  -6.996   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.411  -8.242   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.785  -9.649   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.253  -9.810   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.690 -10.895   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.064 -12.302   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.969 -13.547   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.342 -14.954   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.811 -15.115   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.248 -16.200   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.779 -16.039   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.313  -4.343   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.218  -5.589   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -0.789  -2.879   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   12   28                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    3   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   13   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26    3                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆O₆

Average Mass

386.4440 Da

Monoisotopic Mass

386.17294 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@@]1(OC(=O)C(CC\C=C(/C)CC\C=C(/C)C=O)=C1)C1=CC(O)=CC=C1O

InChI Identifier

InChI=1S/C22H26O6/c1-15(6-4-8-16(2)14-23)7-5-9-17-13-22(27-3,28-21(17)26)19-12-18(24)10-11-20(19)25/h7-8,10-14,24-25H,4-6,9H2,1-3H3/b15-7+,16-8+/t22-/m0/s1

InChI Key

MOFNDUJXTNIVEF-URUUZNIQSA-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 terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Monoterpenoid
Monocyclic monoterpenoid
Aromatic monoterpenoid
Benzylether
Hydroquinone
1-hydroxy-2-unsubstituted benzenoid
Ketal
Phenol
Benzenoid
2-furanone
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Enal
Dihydrofuran
Alpha,beta-unsaturated aldehyde
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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

78441721

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139590272

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal (NP0293087)

MOL for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

3D MOL for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

3D SDF for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

3D-SDF for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

PDB for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

3D PDB for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

SMILES for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

INCHI for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

Structure for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)

3D Structure for NP0293087 ((2e,6e)-9-[(5s)-5-(2,5-dihydroxyphenyl)-5-methoxy-2-oxofuran-3-yl]-2,6-dimethylnona-2,6-dienal)