NP-MRD: Showing NP-Card for (1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate (NP0209349)

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Record Information

Version

2.0

Created at

2022-09-05 06:43:13 UTC

Updated at

2022-09-05 06:43:13 UTC

NP-MRD ID

NP0209349

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate

Description

(1S,2R,3R,5S,9S,10R,11R)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]Pentadec-14-en-3-yl (2R)-2-methylbutanoate 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. (1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate is found in Achillea nobilis. Based on a literature review very few articles have been published on (1S,2R,3R,5S,9S,10R,11R)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]Pentadec-14-en-3-yl (2R)-2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052208432D          

 27 30  0  0  1  0            999 V2000
    4.1130    0.8996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3842    0.5130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2685   -0.3039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8614   -0.8776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4559   -0.4463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1660    0.3478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6430    0.8754    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5371    1.6936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8315    2.1209    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9103    2.9421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6610    3.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3327    2.8056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7398    4.1057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0681    4.5846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4905    4.4480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5693    5.2692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0574    1.8357    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9515    2.6538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2361    1.9145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7977    1.0526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2570    0.4295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5263   -0.3504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3363   -0.5071    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6056   -1.2869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8770    0.1160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6077    0.8959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2481    0.3613    0.0000 C   0  0  1  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  6  0  0  0
  6  7  1  0  0  0  0
  7  2  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  6  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 26  1  6  0  0  0
 27 23  1  6  0  0  0
  6 27  1  0  0  0  0
 20 27  1  0  0  0  0
M  END

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
   -1.9355    4.2399    0.0093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4333    3.0246   -0.0562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7759    2.6246   -0.4625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6987    3.4281   -0.8026 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8504    1.2175   -0.4070 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5234    0.7889   -0.6175 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7492    1.7287    0.2706 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3144    1.7986   -0.1576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3104    0.4193   -0.2618 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7138    0.6214   -0.0698 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6634    0.2883   -0.9957 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3057   -0.2255   -2.0834 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1149    0.5081   -0.7729 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9111    0.1157   -1.9753 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6146   -0.2497    0.4381 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4902   -1.7377    0.2592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1497   -0.4384    0.9000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9112   -1.5375    1.0510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0286    0.3515    2.0504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4622   -1.0143    0.7969 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5582   -2.4938    0.6710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7679   -2.7705    0.1965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4698   -1.4595    0.0157 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6175   -1.4413   -0.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5959   -0.9222    1.2922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4087   -0.6619    1.7552 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2580   -0.6330   -0.4669 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9266    4.4434    0.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5612    5.0775   -0.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2747    1.0981   -1.6754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8886    1.5726    1.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2463    2.3722    0.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2438    2.3335   -1.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1000   -0.0353   -1.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2443    1.5995   -0.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3027   -0.9056   -1.9494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2603    0.2033   -2.8755 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7756    0.8210   -2.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6908   -0.0100    0.5570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0978    0.0359    1.3592 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3693   -2.2013    1.2677 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5837   -2.0137   -0.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4160   -2.1878   -0.1623 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0273   -2.1251    0.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6748   -2.1668    1.9461 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8678   -1.0158    1.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4296   -0.1219    2.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7732   -3.1795    0.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2250   -3.7204   -0.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9266   -2.4440   -1.2597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4999   -0.7841   -1.7473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5507   -1.0588   -0.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7946   -1.1567   -1.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 11  1  0
 11 12  2  0
 11 10  1  0
 10  9  1  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
  6 27  1  0
 27 23  1  0
 23 24  1  6
 23 25  1  0
 25 26  1  0
 20 26  1  1
 20 21  1  0
 21 22  2  0
 20 17  1  0
 17 18  1  0
 17 19  1  1
 17  9  1  0
  2  7  1  0
 20 27  1  0
 22 23  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 15 39  1  0
 15 40  1  0
 13 35  1  1
 14 36  1  0
 14 37  1  0
 14 38  1  0
  9 34  1  6
  8 32  1  0
  8 33  1  0
  7 31  1  1
  6 30  1  6
  1 28  1  0
  1 29  1  0
 27 53  1  6
 24 50  1  0
 24 51  1  0
 24 52  1  0
 21 48  1  0
 22 49  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
M  END


  Mrv1652309052208432D          

 27 30  0  0  1  0            999 V2000
    4.1130    0.8996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3842    0.5130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2685   -0.3039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8614   -0.8776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4559   -0.4463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1660    0.3478    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6430    0.8754    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5371    1.6936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8315    2.1209    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9103    2.9421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6610    3.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3327    2.8056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7398    4.1057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0681    4.5846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4905    4.4480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5693    5.2692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0574    1.8357    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9515    2.6538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2361    1.9145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7977    1.0526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2570    0.4295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5263   -0.3504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3363   -0.5071    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6056   -1.2869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8770    0.1160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6077    0.8959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2481    0.3613    0.0000 C   0  0  1  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  6  0  0  0
  6  7  1  0  0  0  0
  7  2  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  6  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 26  1  6  0  0  0
 27 23  1  6  0  0  0
  6 27  1  0  0  0  0
 20 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0209349

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)C(=O)O[C@@H]1C[C@@H]2[C@H](OC(=O)C2=C)[C@@H]2[C@]3(C)OO[C@]2(C=C3)[C@]1(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O7/c1-6-10(2)16(21)24-13-9-12-11(3)17(22)25-14(12)15-18(4)7-8-20(15,27-26-18)19(13,5)23/h7-8,10,12-15,23H,3,6,9H2,1-2,4-5H3/t10-,12+,13-,14+,15-,18-,19-,20+/m1/s1

> <INCHI_KEY>
CUOLHDCSNYOKFZ-RECCWCMFSA-N

> <FORMULA>
C20H26O7

> <MOLECULAR_WEIGHT>
378.421

> <EXACT_MASS>
378.167853177

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
38.83104841221587

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,3R,5S,9S,10R,11R)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0^{1,10}.0^{5,9}]pentadec-14-en-3-yl (2R)-2-methylbutanoate

> <JCHEM_LOGP>
2.6335475280000002

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.750192610383532

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7828657522182434

> <JCHEM_POLAR_SURFACE_AREA>
91.29

> <JCHEM_REFRACTIVITY>
93.54429999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3R,5S,9S,10R,11R)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0^{1,10}.0^{5,9}]pentadec-14-en-3-yl (2R)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       7.678   1.679   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.317   0.958   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.101  -0.567   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.208  -1.638   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       4.584  -0.833   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.043   0.649   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.934   1.634   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.736   3.161   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.419   3.959   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.566   5.492   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.967   6.131   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.221   5.237   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.114   7.664   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.860   8.558   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.516   8.303   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.663   9.836   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.974   3.427   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.776   4.954   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.441   3.574   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.489   1.965   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.480   0.802   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.982  -0.654   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.494  -0.947   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.997  -2.402   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.504   0.217   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       3.001   1.672   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.330   0.675   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   27                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15                                                            
CONECT   17    9   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21   26   27                                             
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   27                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   20                                                       
CONECT   27   23    6   20                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,3R,5S,9S,10R,11R)-2-Hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0,.0,]pentadec-14-en-3-yl (2R)-2-methylbutanoic acid	Generator

Chemical Formula

C₂₀H₂₆O₇

Average Mass

378.4210 Da

Monoisotopic Mass

378.16785 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)C(=O)O[C@@H]1C[C@@H]2[C@H](OC(=O)C2=C)[C@@H]2[C@]3(C)OO[C@]2(C=C3)[C@]1(C)O

InChI Identifier

InChI=1S/C20H26O7/c1-6-10(2)16(21)24-13-9-12-11(3)17(22)25-14(12)15-18(4)7-8-20(15,27-26-18)19(13,5)23/h7-8,10,12-15,23H,3,6,9H2,1-2,4-5H3/t10-,12+,13-,14+,15-,18-,19-,20+/m1/s1

InChI Key

CUOLHDCSNYOKFZ-RECCWCMFSA-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 nobilis	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
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Gamma butyrolactone
Ortho-dioxolane
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Dialkyl peroxide
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen 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

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

162903848

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate (NP0209349)

MOL for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

3D MOL for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

3D SDF for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

3D-SDF for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

PDB for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

3D PDB for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

SMILES for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

INCHI for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

Structure for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)

3D Structure for NP0209349 ((1s,2r,3r,5s,9s,10r,11r)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadec-14-en-3-yl (2r)-2-methylbutanoate)