NP-MRD: Showing NP-Card for {8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate (NP0202951)

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Record Information

Version

2.0

Created at

2022-09-04 22:16:59 UTC

Updated at

2022-09-04 22:16:59 UTC

NP-MRD ID

NP0202951

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate

Description

{8,10,11-Trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]Tetradeca-2,6-dien-6-yl}methyl acetate belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. {8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate is found in Piptocarpha poeppigiana, Pseudelephantopus spicatus and Vernonanthura squamulosa. Based on a literature review very few articles have been published on {8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]Tetradeca-2,6-dien-6-yl}methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052200172D          

 25 27  0  0  0  0            999 V2000
    7.6573   -1.6305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8323   -1.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4182   -2.3422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4214   -0.9133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5964   -0.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1855   -0.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3652   -0.1080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1955    0.6994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5836    1.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7633    1.3409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5936    2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0480    0.9300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7107    0.1771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8804   -0.6303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1650   -1.0412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5683    0.2449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4923   -1.1837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7769   -1.5946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6620   -1.9911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3126   -1.2718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0280   -0.8609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6398   -1.4143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9109    1.1103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5227    0.5569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3301    0.7266    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
  2  4  1  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
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  4  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 10 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  0  0  0  0
  6 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    6.3665    1.8719    0.3853 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4441    1.0278   -0.4709 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8929   -0.0511   -0.9036 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2083    1.3882   -0.7678 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1041    0.9847   -1.4319 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3207   -0.1756   -0.9913 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0156   -0.1551   -0.6055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5683   -1.4944   -0.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6155   -1.8876    0.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9045   -1.7905   -0.5618 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9752   -2.6092   -1.8266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0363   -2.2865    0.3570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0902   -1.0815    1.3080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8523    0.0302    0.3135 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1276    0.5441   -0.0128 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3536   -0.5357   -0.8456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0407    1.1562    0.8389 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4560    1.3768    2.2999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4077    2.3528    0.1806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5678    0.9673    0.8363 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0854    0.9995   -0.5285 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6429    2.2343   -0.7474 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6740   -2.3220   -0.4705 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7603   -1.5520   -0.9136 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8994   -2.0487   -1.1826 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2801    1.5683    1.4488 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4092    1.6613    0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1829    2.9466    0.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4080    0.6917   -2.5422 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5011    1.8957   -1.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828   -2.3640    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4032   -2.1090   -2.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4711   -3.5903   -1.6172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0409   -2.7623   -2.0692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7390   -3.1578    0.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9607   -2.3928   -0.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2337   -1.2225    2.0052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0565   -0.9951    1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6902    0.4734    0.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0284    2.3552    2.5837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0402    0.6077    2.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5687    1.3574    2.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3793    2.3818    0.0375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1433    1.8547    1.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2976    0.1044    1.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6615    0.8950   -1.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0609    2.8567   -1.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7 21  1  0
 21 22  1  0
 21 20  1  0
 20 17  1  0
 17 18  1  0
 17 19  1  6
 17 14  1  0
 14 15  1  6
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  6
 10 16  1  0
 10  9  1  0
  9  8  2  0
  8 23  1  0
 23 24  1  0
 24 25  2  0
 24  6  1  0
  8  7  1  0
 16 14  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  5 29  1  0
  5 30  1  0
 21 46  1  6
 22 47  1  0
 20 44  1  0
 20 45  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
 19 43  1  0
 15 39  1  0
 13 37  1  0
 13 38  1  0
 12 35  1  0
 12 36  1  0
 11 32  1  0
 11 33  1  0
 11 34  1  0
  9 31  1  0
M  END


  Mrv1652309052200172D          

 25 27  0  0  0  0            999 V2000
    7.6573   -1.6305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8323   -1.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4182   -2.3422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4214   -0.9133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5964   -0.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1855   -0.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3652   -0.1080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1955    0.6994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5836    1.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7633    1.3409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5936    2.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0480    0.9300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7107    0.1771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8804   -0.6303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1650   -1.0412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5683    0.2449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4923   -1.1837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7769   -1.5946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6620   -1.9911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3126   -1.2718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0280   -0.8609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6398   -1.4143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9109    1.1103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5227    0.5569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3301    0.7266    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
  2  4  1  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
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  4  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 10 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  0  0  0  0
  6 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0202951

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1=C2C(O)CC(C)(O)C3(O)CCC(C)(O3)C=C2OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H22O8/c1-9(18)23-8-10-13-11(19)6-16(3,21)17(22)5-4-15(2,25-17)7-12(13)24-14(10)20/h7,11,19,21-22H,4-6,8H2,1-3H3

> <INCHI_KEY>
VXLRPFBAXXIUFB-UHFFFAOYSA-N

> <FORMULA>
C17H22O8

> <MOLECULAR_WEIGHT>
354.355

> <EXACT_MASS>
354.131467668

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.79587921181005

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0^{3,7}]tetradeca-2,6-dien-6-yl}methyl acetate

> <JCHEM_LOGP>
-0.9897270303333322

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.722488268566252

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.972606575974927

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1087318458879007

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000001

> <JCHEM_REFRACTIVITY>
85.81409999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
{8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0^{3,7}]tetradeca-2,6-dien-6-yl}methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      14.294  -3.044   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.754  -3.040   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.981  -4.372   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      11.987  -1.705   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.447  -1.701   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.680  -0.366   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.148  -0.202   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.832   1.306   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.689   2.339   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.158   2.503   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.841   4.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.823   1.736   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.193   0.330   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.510  -1.177   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.175  -1.944   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       4.794   0.457   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.652  -2.210   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.317  -2.977   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.969  -3.717   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.183  -2.374   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.519  -1.607   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.661  -2.640   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       9.167   2.073   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.309   1.039   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.816   1.356   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   24                                                  
CONECT    7    6    8   21                                                  
CONECT    8    7    9   23                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   16                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14   10                                                       
CONECT   17   14   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21                                                       
CONECT   21   20    7   22                                                  
CONECT   22   21                                                            
CONECT   23    8   24                                                       
CONECT   24   23    6   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Value	Source
{8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0,]tetradeca-2,6-dien-6-yl}methyl acetic acid	Generator

Chemical Formula

C₁₇H₂₂O₈

Average Mass

354.3550 Da

Monoisotopic Mass

354.13147 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1=C2C(O)CC(C)(O)C3(O)CCC(C)(O3)C=C2OC1=O

InChI Identifier

InChI=1S/C17H22O8/c1-9(18)23-8-10-13-11(19)6-16(3,21)17(22)5-4-15(2,25-17)7-12(13)24-14(10)20/h7,11,19,21-22H,4-6,8H2,1-3H3

InChI Key

VXLRPFBAXXIUFB-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
Piptocarpha poeppigiana	LOTUS Database	35616633
Pseudelephantopus spicatus	LOTUS Database	35616633
Vernonanthura squamulosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

2-furanone
Dicarboxylic acid or derivatives
Enol ester
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Hemiacetal
Lactone
Secondary alcohol
Carboxylic acid derivative
Polyol
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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

290702

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

328229

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate (NP0202951)

MOL for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

3D MOL for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

3D SDF for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

3D-SDF for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

PDB for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

3D PDB for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

SMILES for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

INCHI for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

Structure for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)

3D Structure for NP0202951 ({8,10,11-trihydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.0³,⁷]tetradeca-2,6-dien-6-yl}methyl acetate)