NP-MRD: Showing NP-Card for [8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate (NP0196926)

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Record Information

Version

2.0

Created at

2022-09-04 15:06:06 UTC

Updated at

2022-09-04 15:06:06 UTC

NP-MRD ID

NP0196926

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate

Description

Glaucolide B belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. [8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate is found in Chrysolaena platensis, Lepidaploa chalybaea, Lepidaploa tortuosa, Pseudelephantopus spicatus, Quechualia fulta and Stramentopappus pooleae. Glaucolide B is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251507542D          

 31 33  0  0  0  0            999 V2000
   -0.4302    0.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3732    0.8309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6126    1.6204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9372    0.2288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7407    0.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3047   -0.1858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1233   -0.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5950    0.5935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2446    1.3404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7162    2.0173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9677    2.3643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9279    2.8147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3432    3.3967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468    3.1813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5548    4.1941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5382    1.9473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0099    2.6242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8886    1.2004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4170    0.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7674   -0.2233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5143    0.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1178   -0.9702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2958   -0.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737   -0.8302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8717   -1.3943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1492   -0.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023   -1.3464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7729    0.6635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4225    1.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6005    1.4804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942    2.0873    0.0000 C   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  0  0  0  0
  9 10  1  0  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  2  0  0  0  0
 13 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  2  0  0  0  0
  8 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
    5.5509   -0.5643    1.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4287   -0.6781    0.9046 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2500   -0.6685    1.3705 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6358   -0.7920   -0.4644 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4777   -0.8964   -1.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6360    0.3504   -1.1193 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4062    0.4783   -0.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3941   -0.5442   -0.2837 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8629   -1.8434   -0.2206 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3330   -2.9256   -0.8837 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9253   -4.2727   -0.7352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6643   -2.7539   -1.6198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1770   -0.1953    1.0774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6877   -0.1617    1.0878 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0818    0.0998    2.5481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1273   -1.4896    0.8000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4353   -1.8864    0.8390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8951   -3.2650    0.5405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3084   -1.0421    1.1446 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2792    0.8278    0.1814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5365    0.5189   -0.9684 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5688    2.1963    0.6438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5859    3.2356    0.1960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1981    3.0167   -1.2278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3887    3.1070   -2.1849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1060    3.7412   -1.7450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1273    2.2504   -1.5817 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9964    1.9068   -0.6748 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1396    2.5787   -1.1526 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1484    1.6887   -1.4195 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3256    1.9367   -1.8492 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3501   -1.2712    1.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0014    0.4490    1.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2240   -0.8597    2.8689 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9728   -1.8050   -0.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7936   -0.9945   -2.3554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4794   -0.5381   -0.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7137   -4.4782   -1.5036 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4403   -4.4073    0.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1750   -5.0853   -0.8294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1078   -0.9751    1.8427 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1980    0.7458    1.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8810   -0.8632    3.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1436    0.3887    2.6341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3992    0.8410    3.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0822   -3.4048   -0.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1564   -4.0303    0.8509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8413   -3.5165    1.0599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564    2.1639    1.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5948    2.5380    0.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7457    3.3710    0.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1293    4.2288    0.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3592    3.0463   -1.6479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2539    2.3676   -2.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4086    4.1015   -2.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0546    1.7590   -2.5870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8658    2.2745    0.3640 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 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  2  0
 28 27  1  0
 27 26  1  0
 26 24  1  0
 24 25  1  6
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  2  0
 20 14  1  0
 14 15  1  0
 14 13  1  0
 13  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 14 16  1  6
 16 17  1  0
 17 18  1  0
 17 19  2  0
 30  6  1  0
 24 27  1  0
  8  7  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  5 35  1  0
  5 36  1  0
 28 57  1  1
 27 56  1  6
 25 53  1  0
 25 54  1  0
 25 55  1  0
 23 51  1  0
 23 52  1  0
 22 49  1  0
 22 50  1  0
 15 43  1  0
 15 44  1  0
 15 45  1  0
 13 41  1  0
 13 42  1  0
  8 37  1  6
 11 38  1  0
 11 39  1  0
 11 40  1  0
 18 46  1  0
 18 47  1  0
 18 48  1  0
M  END


  Mrv1533004251507542D          

 31 33  0  0  0  0            999 V2000
   -0.4302    0.6434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3732    0.8309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6126    1.6204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9372    0.2288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7407    0.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3047   -0.1858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1233   -0.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5950    0.5935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2446    1.3404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7162    2.0173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9677    2.3643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9279    2.8147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3432    3.3967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468    3.1813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5548    4.1941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5382    1.9473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0099    2.6242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8886    1.2004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4170    0.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7674   -0.2233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5143    0.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1178   -0.9702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2958   -0.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737   -0.8302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8717   -1.3943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1492   -0.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023   -1.3464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7729    0.6635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4225    1.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6005    1.4804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942    2.0873    0.0000 C   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  0  0  0  0
  9 10  1  0  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  2  0  0  0  0
 13 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  2  0  0  0  0
  8 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196926

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1=C2C(OC1=O)C1OC1(C)CCC(=O)C(C)(CC2OC(C)=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O10/c1-10(22)27-9-13-16-14(28-11(2)23)8-21(5,30-12(3)24)15(25)6-7-20(4)18(31-20)17(16)29-19(13)26/h14,17-18H,6-9H2,1-5H3

> <INCHI_KEY>
JNLNEIIZZQABDP-UHFFFAOYSA-N

> <FORMULA>
C21H26O10

> <MOLECULAR_WEIGHT>
438.429

> <EXACT_MASS>
438.152597037

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
42.568687057962094

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate

> <ALOGPS_LOGP>
0.81

> <JCHEM_LOGP>
0.28769745966666493

> <ALOGPS_LOGS>
-2.97

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.048893481777277

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.130866862952288

> <JCHEM_PKA_STRONGEST_BASIC>
-4.243107695722894

> <JCHEM_POLAR_SURFACE_AREA>
134.8

> <JCHEM_REFRACTIVITY>
101.43119999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.67e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -0.803   1.201   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.697   1.551   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.143   3.025   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.750   0.427   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.249   0.777   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.302  -0.347   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.830  -0.156   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.711   1.108   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.057   2.502   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.937   3.766   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.540   4.413   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.332   5.254   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.241   6.341   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.754   5.939   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.636   7.829   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.471   3.635   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.352   4.899   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.125   2.241   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.245   0.977   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.899  -0.417   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.293   0.237   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.553  -1.811   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.019  -1.680   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.484  -1.550   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.360  -2.603   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.012  -1.859   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.618  -2.513   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.176   1.239   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.522   2.633   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.988   2.763   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.402   3.896   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8   24                                                  
CONECT    8    7    9   28                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   16                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   10   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   20   24                                                  
CONECT   24   23    7   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25    6   27                                                  
CONECT   27   26                                                            
CONECT   28    8   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₆O₁₀

Average Mass

438.4290 Da

Monoisotopic Mass

438.15260 Da

IUPAC Name

[8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate

Traditional Name

[8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1=C2C(OC1=O)C1OC1(C)CCC(=O)C(C)(CC2OC(C)=O)OC(C)=O

InChI Identifier

InChI=1S/C21H26O10/c1-10(22)27-9-13-16-14(28-11(2)23)8-21(5,30-12(3)24)15(25)6-7-20(4)18(31-20)17(16)29-19(13)26/h14,17-18H,6-9H2,1-5H3

InChI Key

JNLNEIIZZQABDP-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
Chrysolaena platensis	LOTUS Database	35616633
Lepidaploa chalybaea	LOTUS Database	35616633
Lepidaploa tortuosa	LOTUS Database	35616633
Pseudelephantopus spicatus	LOTUS Database	35616633
Quechualia fulta	LOTUS Database	35616633
Stramentopappus pooleae	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
Tetracarboxylic acid or derivatives
Alpha-acyloxy ketone
2-furanone
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Ketone
Carboxylic acid ester
Cyclic ketone
Organoheterocyclic compound
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Hydrocarbon derivative
Organooxygen compound
Organic oxide
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
logP	0.81	ALOGPS
logP	0.29	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	10.13	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	134.8 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	101.43 m³·mol⁻¹	ChemAxon
Polarizability	42.57 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3084088

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-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate (NP0196926)

MOL for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

3D MOL for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

3D SDF for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

3D-SDF for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

PDB for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

3D PDB for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

SMILES for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

INCHI for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

Structure for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)

3D Structure for NP0196926 ([8,10-bis(acetyloxy)-4,8-dimethyl-7,13-dioxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-11-en-12-yl]methyl acetate)