NP-MRD: Showing NP-Card for 3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate (NP0215780)

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Record Information

Version

2.0

Created at

2022-09-05 15:30:30 UTC

Updated at

2022-09-05 15:30:30 UTC

NP-MRD ID

NP0215780

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate

Description

3-Hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]Pentadec-14-en-2-yl acetate belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative. 3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate is found in Achillea ligustica and Achillea millefolium. 3-Hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]Pentadec-14-en-2-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261501072D          

 24 27  0  0  0  0            999 V2000
   -0.7166    2.8728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0642    3.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754    4.1953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6994    3.0654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8105    2.2479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0112    2.3214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828    2.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6563    3.3599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2912    2.1155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4024    1.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9288    0.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2239   -0.0249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0356    0.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6322   -0.4470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1459    0.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8722    1.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0109    0.7749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0907   -0.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3651   -0.8498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6274    0.5549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3530    1.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5560    1.4632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0054    0.8577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2797    0.0797    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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 18 24  1  0  0  0  0
M  END

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
   -3.1479   -1.9515    0.8255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6759   -0.7603    1.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3213    0.4806    0.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4166    0.6136   -0.0252 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5234    1.5397    1.0327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1867    1.0022    1.0154 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7867    0.9367   -0.4070 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4205    2.3990   -0.7656 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5089    3.3433   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1073    2.1718   -2.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8523    1.0503   -2.0287 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6339    0.4887   -0.6565 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2790    1.4075    0.2062 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6723    2.5534    0.0590 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9554   -0.9020   -0.4544 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2107   -1.7033   -1.7256 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0421   -0.9991    0.4488 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3010   -0.5719    0.0820 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4380   -0.6765    1.0337 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4125   -0.1077   -1.0660 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1678   -1.7215    0.2119 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2937   -3.0449    0.2181 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3129   -1.2778    1.6287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4285   -0.3047    1.6978 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0848   -2.1022    0.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6270   -2.8467    1.1580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5608    1.6531    1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5195    0.5347   -1.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4420    3.8705    0.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3708    4.1823   -1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5201    2.9581   -0.8231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0811    2.7758   -3.0068 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4627    0.7067   -2.8398 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4544   -2.7345   -1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8902   -1.2398   -2.4230 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049   -1.7624   -2.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1819   -1.4639    1.7648 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675    0.2894    1.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3947   -0.8887    0.5138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0498   -1.6018   -0.4153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4347   -3.3898    1.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4431   -2.0994    2.3299 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6201   -0.7351    1.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7128   -0.0716    2.7494 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 20  2  0
 18 17  1  0
 15 17  1  1
 15 16  1  0
 15 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  6  7  1  0
  7  8  1  0
  8  9  1  6
  8 14  1  0
 14 13  1  0
 12 13  1  1
 12 11  1  0
 11 10  2  0
 12 15  1  0
  2 24  1  0
 12  7  1  0
 10  8  1  0
 19 37  1  0
 19 38  1  0
 19 39  1  0
 16 34  1  0
 16 35  1  0
 16 36  1  0
 21 40  1  6
 22 41  1  0
 23 42  1  0
 23 43  1  0
 24 44  1  1
  6 27  1  1
  1 25  1  0
  1 26  1  0
  7 28  1  6
  9 29  1  0
  9 30  1  0
  9 31  1  0
 11 33  1  0
 10 32  1  0
M  END


  Mrv1533004261501072D          

 24 27  0  0  0  0            999 V2000
   -0.7166    2.8728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0642    3.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1754    4.1953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6994    3.0654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8105    2.2479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0112    2.3214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828    2.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6563    3.3599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2912    2.1155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4024    1.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9288    0.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2239   -0.0249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0356    0.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6322   -0.4470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1459    0.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8722    1.3318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0109    0.7749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0907   -0.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3651   -0.8498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6274    0.5549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3530    1.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5560    1.4632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0054    0.8577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2797    0.0797    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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 18 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0215780

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1(C)C(O)CC2C(OC(=O)C2=C)C2C3(C)OOC12C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C17H20O7/c1-8-10-7-11(19)16(4,22-9(2)18)17-6-5-15(3,23-24-17)13(17)12(10)21-14(8)20/h5-6,10-13,19H,1,7H2,2-4H3

> <INCHI_KEY>
GWCCKOPANXZXHK-UHFFFAOYSA-N

> <FORMULA>
C17H20O7

> <MOLECULAR_WEIGHT>
336.34

> <EXACT_MASS>
336.120902984

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
33.22002446103474

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate

> <ALOGPS_LOGP>
1.31

> <JCHEM_LOGP>
0.945456737666668

> <ALOGPS_LOGS>
-2.03

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.847440649141397

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3029294600655517

> <JCHEM_POLAR_SURFACE_AREA>
91.29000000000002

> <JCHEM_REFRACTIVITY>
79.7419

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.17e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      -1.338   5.363   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.120   6.305   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.327   7.831   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.305   5.722   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.513   4.196   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.021   4.333   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.955   4.738   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.092   6.272   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.277   3.949   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.484   2.423   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.601   1.432   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.151  -0.046   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.666   0.229   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.780  -0.834   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.872   1.755   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.228   2.486   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.887   1.446   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.036  -0.134   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.548  -1.586   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.038   1.036   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.526   2.488   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.038   2.731   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.010   1.601   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.522   0.149   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    7   22                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   10   16                                                  
CONECT   16   15                                                            
CONECT   17   11   18   22                                                  
CONECT   18   17   19   20   24                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    5   17   23                                             
CONECT   23   22   24                                                       
CONECT   24   23   18                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Value	Source
3-Hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0,.0,]pentadec-14-en-2-yl acetic acid	Generator

Chemical Formula

C₁₇H₂₀O₇

Average Mass

336.3400 Da

Monoisotopic Mass

336.12090 Da

IUPAC Name

3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate

Traditional Name

3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1(C)C(O)CC2C(OC(=O)C2=C)C2C3(C)OOC12C=C3

InChI Identifier

InChI=1S/C17H20O7/c1-8-10-7-11(19)16(4,22-9(2)18)17-6-5-15(3,23-24-17)13(17)12(10)21-14(8)20/h5-6,10-13,19H,1,7H2,2-4H3

InChI Key

GWCCKOPANXZXHK-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
Achillea ligustica	LOTUS Database	35616633
Achillea millefolium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Guaianolides and derivatives

Alternative Parents

Substituents

Guaianolide-skeleton
Sesquiterpenoid
Dicarboxylic acid or derivatives
Gamma butyrolactone
Ortho-dioxolane
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Dialkyl peroxide
Lactone
Secondary alcohol
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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
logP	1.31	ALOGPS
logP	0.95	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	13.85	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	91.29 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	79.74 m³·mol⁻¹	ChemAxon
Polarizability	33.22 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

101656880

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate (NP0215780)

MOL for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

3D MOL for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

3D SDF for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

3D-SDF for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

PDB for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

3D PDB for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

SMILES for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

INCHI for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

Structure for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)

3D Structure for NP0215780 (3-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-2-yl acetate)