NP-MRD: Showing NP-Card for (3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate (NP0195257)

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Record Information

Version

2.0

Created at

2022-09-04 13:05:05 UTC

Updated at

2022-09-04 13:05:05 UTC

NP-MRD ID

NP0195257

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate

Description

Inuchinenolide C belongs to the class of organic compounds known as sesquiterpene lactones. These are sesquiterpenoids containing a lactone ring. (3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate is found in Inula hupehensis. (3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate was first documented in 2016 (PMID: 26936053). Based on a literature review very few articles have been published on inuchinenolide C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042215052D          

 26 28  0  0  1  0            999 V2000
    1.0366   -2.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1106   -1.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4893   -1.1323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3150   -1.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8136   -0.3737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6352   -0.4476    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1496    0.1974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9746    0.1974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3326    0.9407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4890   -0.4476    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3107   -0.3737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7338    0.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5587    0.3222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9819    1.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605   -0.3983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6349   -1.1323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0136   -1.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0876   -2.4968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8362   -2.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5108   -2.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9101   -3.6652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3054   -1.2519    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2684   -2.0761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5621   -1.6099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5621   -2.4349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8188   -1.2519    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26  2  1  6  0  0  0
  6 26  1  0  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
   -4.0445    0.5898    1.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6025   -0.1544    0.8067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3030   -1.2686    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5127   -1.5905    0.3859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3839   -1.9024   -0.6714 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0608   -1.4862   -0.2805 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0532   -1.7168   -1.3476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2355   -0.5195   -1.7348 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6412   -0.9612   -2.8899 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5251    0.1733   -0.7330 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0037   -0.1019   -0.6112 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3444   -1.4166   -0.3214 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2534   -2.0942   -1.0838 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5986   -3.5126   -0.7433 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8117   -1.5392   -2.0792 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3758    0.7593    0.6054 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0455    1.2133    1.2238 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7934    2.4746    0.6898 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6310    3.6183    1.4579 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3673    4.9084    0.8007 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7157    3.5091    2.6941 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0985    0.1370    0.6953 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4646   -1.1026    1.4516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2931    0.5517    0.9852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4603    1.9285    0.9620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3028   -0.0522    0.0744 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9996    0.4439    2.2746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4478    1.4097    2.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8857   -2.0602    0.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4333   -2.6444   -1.2036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6447   -1.9777   -2.2831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9910    0.1875   -2.2039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4519   -0.2776   -3.1306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9398   -2.0292   -2.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0254   -0.9650   -3.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5170    1.2865   -0.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5373    0.2985   -1.5151 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8703   -3.5002    0.3450 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4222   -3.8894   -1.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6851   -4.1336   -0.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9715    1.6192    0.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9579    0.1908    1.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966    1.1729    2.3251 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0202    4.9359   -0.1201 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6322    5.7808    1.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6777    4.9545    0.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2810   -1.2131    2.2857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4535   -1.0295    1.9896 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4819   -2.0342    0.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5094    0.2388    2.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1189    2.2299    0.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4406    0.5605   -0.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 26  1  0
 26 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  1  1
 22 17  1  0
 17 16  1  0
 16 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 11 10  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 10  8  1  0
 26  6  1  0
 10 22  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
  8 32  1  6
  7 30  1  0
  7 31  1  0
  6 29  1  1
  1 27  1  0
  1 28  1  0
 26 52  1  6
 24 50  1  1
 25 51  1  0
 23 47  1  0
 23 48  1  0
 23 49  1  0
 17 43  1  1
 16 41  1  0
 16 42  1  0
 11 37  1  6
 14 38  1  0
 14 39  1  0
 14 40  1  0
 10 36  1  6
 20 44  1  0
 20 45  1  0
 20 46  1  0
M  END


  Mrv1652309042215052D          

 26 28  0  0  1  0            999 V2000
    1.0366   -2.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1106   -1.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4893   -1.1323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3150   -1.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8136   -0.3737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6352   -0.4476    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1496    0.1974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9746    0.1974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3326    0.9407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4890   -0.4476    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3107   -0.3737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7338    0.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5587    0.3222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9819    1.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605   -0.3983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6349   -1.1323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0136   -1.6751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0876   -2.4968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8362   -2.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5108   -2.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9101   -3.6652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3054   -1.2519    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2684   -2.0761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5621   -1.6099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5621   -2.4349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8188   -1.2519    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26  2  1  6  0  0  0
  6 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195257

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@@H]2OC(=O)C(=C)[C@H]2[C@H](O)[C@]2(C)C(CC(OC(C)=O)[C@@H]12)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O7/c1-8-6-12-15(9(2)18(23)26-12)17(22)19(5)14(25-11(4)21)7-13(16(8)19)24-10(3)20/h8,12-17,22H,2,6-7H2,1,3-5H3/t8-,12-,13?,14?,15+,16+,17-,19+/m0/s1

> <INCHI_KEY>
QFJNAUKGMNMIGV-YRBNLPDFSA-N

> <FORMULA>
C19H26O7

> <MOLECULAR_WEIGHT>
366.41

> <EXACT_MASS>
366.167853177

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.602075357324765

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aS,4S,4aR,7aS,8S,9aS)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-dodecahydroazuleno[6,5-b]furan-7-yl acetate

> <JCHEM_LOGP>
0.7862477436666676

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.227921202516228

> <JCHEM_PKA_STRONGEST_BASIC>
-3.136507266019401

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
89.20400000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3aS,4S,4aR,7aS,8S,9aS)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3aH-azuleno[6,5-b]furan-7-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.935  -4.661   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.073  -3.127   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.913  -2.114   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.588  -2.456   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       1.519  -0.698   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.052  -0.836   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.013   0.368   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.553   0.368   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.221   1.756   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.513  -0.836   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.047  -0.698   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.836   0.625   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.376   0.601   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.166   1.923   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      11.126  -0.744   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.652  -2.114   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.492  -3.127   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.630  -4.661   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.028  -5.308   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.287  -4.422   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.166  -6.842   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.170  -2.337   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.101  -3.875   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.783  -3.005   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.783  -4.545   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.395  -2.337   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   22                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   11   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   10   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₇

Average Mass

366.4100 Da

Monoisotopic Mass

366.16785 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@@H]2OC(=O)C(=C)[C@H]2[C@H](O)[C@]2(C)C(CC(OC(C)=O)[C@@H]12)OC(C)=O

InChI Identifier

InChI=1S/C19H26O7/c1-8-6-12-15(9(2)18(23)26-12)17(22)19(5)14(25-11(4)21)7-13(16(8)19)24-10(3)20/h8,12-17,22H,2,6-7H2,1,3-5H3/t8-,12-,13?,14?,15+,16+,17-,19+/m0/s1

InChI Key

QFJNAUKGMNMIGV-YRBNLPDFSA-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
Inula hupehensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpene lactones. These are sesquiterpenoids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Sesquiterpene lactones

Alternative Parents

Substituents

Helenalin-skeleton
Ambrosanolide
Pseudoguaiane sesquiterpenoid
Sesquiterpenoid
Tricarboxylic acid or derivatives
Gamma butyrolactone
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Lactone
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
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

C00021072

Chemspider ID

23325564

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44457222

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Piao D, Kim T, Zhang HY, Choi HG, Lee CS, Choi HJ, Chang HW, Woo MH, Son JK: DNA Topoisomerase Inhibitory Activity of Constituents from the Flowers of Inula japonica. Chem Pharm Bull (Tokyo). 2016;64(3):276-81. doi: 10.1248/cpb.c15-00780. [PubMed:26936053 ]
LOTUS database [Link]

Showing NP-Card for (3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate (NP0195257)

MOL for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

3D MOL for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

3D SDF for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

3D-SDF for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

PDB for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

3D PDB for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

SMILES for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

INCHI for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

Structure for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)

3D Structure for NP0195257 ((3as,4s,4ar,7as,8s,9as)-5-(acetyloxy)-4-hydroxy-4a,8-dimethyl-3-methylidene-2-oxo-octahydro-3ah-azuleno[6,5-b]furan-7-yl acetate)