NP-MRD: Showing NP-Card for [(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate (NP0293516)

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Record Information

Version

2.0

Created at

2022-09-10 01:33:39 UTC

Updated at

2022-09-10 01:33:39 UTC

NP-MRD ID

NP0293516

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate

Description

Spicatolide A belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. [(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate is found in Pseudelephantopus spicatus. Based on a literature review very few articles have been published on spicatolide A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102203332D          

 28 30  0  0  1  0            999 V2000
   -0.9578    1.4867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2014    1.8161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1084    2.6358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4620    1.3257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3691    0.5060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0325    0.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8281    0.2567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0130    1.0962    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4222    1.6721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6256    2.4716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4197    2.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0348    3.0475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8323    1.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4538    0.7063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8755    1.4153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9526    0.0973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4001   -0.4143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8722   -1.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6730   -1.4739    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2013   -2.1508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2105   -2.0998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4272   -1.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6754   -0.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2712    0.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7977    1.0781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8290   -1.0622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0353   -0.8086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3699   -1.2962    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  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 17 16  1  6  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  1  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  2  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    6.1258    1.5319   -1.5617 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1923    0.9937   -0.5408 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6324    0.4266    0.4936 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8350    1.1336   -0.7598 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9635    0.6130    0.2270 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5245    0.8559   -0.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5988   -0.0315   -0.3853 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6019   -1.5146   -0.3337 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9562   -2.0592    0.9011 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9898   -2.9328    1.1571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3196   -3.4767    2.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6954   -3.2763    0.1480 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6757   -2.1576   -0.9363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7443   -1.2650   -0.4537 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7510   -1.4923    0.9997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4105   -0.1247   -1.1066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6352    0.7829   -0.5090 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3703    1.3211    0.6550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8232    1.6242    0.4712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9617    3.1781    0.3264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5672    1.4675    1.6717 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6080    1.0724   -0.6263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1742   -0.3523   -0.4719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1503   -1.3647   -0.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4580   -2.2486   -1.5601 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1573    1.8693   -1.2346 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0679    2.1742   -0.7178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7179    3.2614   -0.6666 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7299    1.3833   -2.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2779    2.6044   -1.3646 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0890    0.9961   -1.4395 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1682    0.9651    1.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1029   -0.4838    0.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3805   -1.9526   -1.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4230   -3.6962    2.4873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0778   -2.7836    3.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7801   -4.4396    2.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6330   -2.1733   -2.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7840   -3.1520   -0.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9641   -2.6084    1.2281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9216   -1.2902    1.6295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6521   -1.0490    1.4731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8835    2.3385    0.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2222    0.8697    1.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0252    3.4569    0.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6438    3.4716   -0.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3780    3.6088    1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3951    1.9686    1.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5818    1.6633   -0.6673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2078    1.2369   -1.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4285   -0.4395    0.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0427   -0.5048   -1.1062 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  8  1  0
  8 13  1  0
 13 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  1
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 17 26  1  6
 26 27  1  0
 27 28  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 27  6  1  0
 17  7  1  0
 24 14  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  5 32  1  0
  5 33  1  0
  8 34  1  6
 13 38  1  0
 13 39  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 18 43  1  0
 18 44  1  0
 20 45  1  0
 20 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 23 52  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
M  END


  Mrv1652309102203332D          

 28 30  0  0  1  0            999 V2000
   -0.9578    1.4867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2014    1.8161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1084    2.6358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4620    1.3257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3691    0.5060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0325    0.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8281    0.2567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0130    1.0962    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4222    1.6721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6256    2.4716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4197    2.6953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0348    3.0475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8323    1.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4538    0.7063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8755    1.4153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9526    0.0973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4001   -0.4143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8722   -1.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6730   -1.4739    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2013   -2.1508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2105   -2.0998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4272   -1.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6754   -0.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2712    0.4429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7977    1.0781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8290   -1.0622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0353   -0.8086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3699   -1.2962    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  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 17 16  1  6  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  1  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  2  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0293516

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1=C2[C@H](C[C@@]3(C)O[C@]2(C[C@](C)(O)CCC3=O)OC1=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H24O9/c1-10(20)25-8-12-15-13(26-11(2)21)7-18(4)14(22)5-6-17(3,24)9-19(15,28-18)27-16(12)23/h13,24H,5-9H2,1-4H3/t13-,17+,18+,19-/m0/s1

> <INCHI_KEY>
CIQHYIPVUYZISN-CJODITQLSA-N

> <FORMULA>
C19H24O9

> <MOLECULAR_WEIGHT>
396.392

> <EXACT_MASS>
396.142032353

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.89406113726345

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,6S,8R,12R)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0^{1,5}]tetradec-4-en-4-yl]methyl acetate

> <JCHEM_LOGP>
0.5575260706666669

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.861287193589376

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.835019814459013

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8619428235689393

> <JCHEM_POLAR_SURFACE_AREA>
125.43

> <JCHEM_REFRACTIVITY>
92.23629999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,6S,8R,12R)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0^{1,5}]tetradec-4-en-4-yl]methyl acetate

> <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      -1.788   2.775   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.376   3.390   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.202   4.920   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       0.862   2.475   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.689   0.944   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.927   0.029   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.412   0.479   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.758   2.046   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.655   3.121   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.034   4.614   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.517   5.031   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.932   5.689   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.287   2.424   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.447   1.318   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.234   2.642   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.512   0.182   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.480  -0.773   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.361  -2.195   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.856  -2.751   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.976  -4.015   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.860  -3.920   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.264  -2.059   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.727  -0.559   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.973   0.827   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.956   2.012   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       3.414  -1.983   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.933  -1.509   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.691  -2.420   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   27                                                  
CONECT    7    6    8   17                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15   16   24                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    7   18   26                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   14   25                                                  
CONECT   25   24                                                            
CONECT   26   17   27                                                       
CONECT   27   26    6   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₄O₉

Average Mass

396.3920 Da

Monoisotopic Mass

396.14203 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1=C2[C@H](C[C@@]3(C)O[C@]2(C[C@](C)(O)CCC3=O)OC1=O)OC(C)=O

InChI Identifier

InChI=1S/C19H24O9/c1-10(20)25-8-12-15-13(26-11(2)21)7-18(4)14(22)5-6-17(3,24)9-19(15,28-18)27-16(12)23/h13,24H,5-9H2,1-4H3/t13-,17+,18+,19-/m0/s1

InChI Key

CIQHYIPVUYZISN-CJODITQLSA-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
Pseudelephantopus spicatus	LOTUS Database	35616633

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
Germacrane sesquiterpenoid
Sesquiterpenoid
Furopyran
Tricarboxylic acid or derivatives
Ketal
2-furanone
Oxane
Pyran
Dihydrofuran
Furan
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Lactone
Ketone
Carboxylic acid ester
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen 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

C00040341

Chemspider ID

23310930

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44445367

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate (NP0293516)

MOL for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

3D MOL for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

3D SDF for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

3D-SDF for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

PDB for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

3D PDB for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

SMILES for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

INCHI for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

Structure for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)

3D Structure for NP0293516 ([(1r,6s,8r,12r)-6-(acetyloxy)-12-hydroxy-8,12-dimethyl-3,9-dioxo-2,14-dioxatricyclo[6.5.1.0¹,⁵]tetradec-4-en-4-yl]methyl acetate)