NP-MRD: Showing NP-Card for (1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione (NP0234040)

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Record Information

Version

2.0

Created at

2022-09-06 15:52:05 UTC

Updated at

2022-09-06 15:52:05 UTC

NP-MRD ID

NP0234040

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione

Description

Atranone P belongs to the class of organic compounds known as dihydropyranones. Dihydropyranones are compounds containing a hydrogenated pyran ring which bears a ketone, and contains one double bond. Based on a literature review a small amount of articles have been published on Atranone P.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062217522D          

 29 31  0  0  1  0            999 V2000
   -2.3931    0.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6482    0.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687    0.5241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    0.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1582   -0.6528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5868   -1.0072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8376   -1.1207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4557    0.6376    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2581    0.4458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8020   -0.2748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6244   -0.2093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0923   -0.8887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9788    0.5357    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7812    0.3439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2116    1.0478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0340    1.1133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6752    1.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9133    1.3581    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5109    1.2152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0622    0.5228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3974    2.6396    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9325    3.2674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750    2.5740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1521    1.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3902    1.4600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4110    2.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3548    1.8144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0342    1.3464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7792    1.7009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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
  8  4  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 18 17  1  1  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  8 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 61 63  0  0  0  0  0  0  0  0999 V2000
    5.6924   -1.3521    0.5657 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8602   -0.5958   -0.2726 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5305   -0.8466   -0.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6428    0.1287   -0.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0600    1.5143   -0.1239 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5346    1.7362    0.0814 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6509    2.4436   -1.2780 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2343   -0.1950   -0.5277 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2404    0.8388   -0.1150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4997    1.4447   -1.2558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7863    1.6967   -1.0913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4868    2.3128   -2.2801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5867    1.4299    0.1013 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4218    2.5962    0.2885 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6892    2.2365    0.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7276    2.9461    0.7946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5923    0.7524    0.9700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6804    0.4105   -0.1598 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2782   -0.9344   -0.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1933   -1.2715   -1.6126 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9358   -2.0282    0.4991 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6272   -1.9605    1.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4656   -2.2076    0.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5579   -1.9171   -0.3647 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8498   -1.5871   -0.0071 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2009   -1.7566    1.4287 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7066   -2.4530   -0.7374 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0880   -2.2436   -0.6176 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9101   -3.1872   -0.6885 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7235   -0.8879    0.4570 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4217   -1.1311    1.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7547   -2.4159    0.3637 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5428    1.9567    0.7849 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9382    1.3360    1.0079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1339    1.5669   -0.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6182    2.8754    0.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4989    3.1540   -1.5176 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8163    3.1035   -0.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3808    1.8543   -2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0980   -0.3005   -1.6566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6236    1.6331    0.5497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5066    0.2901    0.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0212    1.6667   -2.1986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0902    3.1946   -1.9261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7951    2.6894   -3.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1570    1.5573   -2.7469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0879    1.3370    1.0551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5906    0.2826    0.8904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1546    0.7332    1.9646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2085    0.8580   -1.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2850   -3.0268    0.0868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0502   -1.3055    2.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6894   -1.7479    1.7954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5265   -2.9799    2.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2779   -3.2861    1.0706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2423   -1.6443    1.7058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9785   -1.0688   -0.9340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6154   -2.7966   -1.0591 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2823   -1.5556    1.5598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0537   -2.8031    1.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6752   -1.0898    2.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  4  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  1
 25 27  1  0
 27 28  1  0
 28 29  2  0
 28  3  1  0
 25  8  1  0
 18 13  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  0
  6 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  7 39  1  0
  8 40  1  6
  9 41  1  0
  9 42  1  0
 10 43  1  0
 12 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  1
 17 48  1  0
 17 49  1  0
 18 50  1  6
 21 51  1  6
 22 52  1  0
 22 53  1  0
 22 54  1  0
 23 55  1  0
 23 56  1  0
 24 57  1  0
 24 58  1  0
 26 59  1  0
 26 60  1  0
 26 61  1  0
M  END


  Mrv1652309062217522D          

 29 31  0  0  1  0            999 V2000
   -2.3931    0.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6482    0.0561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9687    0.5241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    0.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1582   -0.6528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5868   -1.0072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8376   -1.1207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4557    0.6376    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2581    0.4458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8020   -0.2748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6244   -0.2093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0923   -0.8887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9788    0.5357    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7812    0.3439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2116    1.0478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0340    1.1133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6752    1.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9133    1.3581    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5109    1.2152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0622    0.5228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3974    2.6396    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9325    3.2674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5750    2.5740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1521    1.7764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3902    1.4600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4110    2.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3548    1.8144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0342    1.3464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7792    1.7009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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
  8  4  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 18 17  1  1  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  8 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
  3 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0234040

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C(C)C)[C@@H]2C\C=C(C)/[C@H]3OC(=O)C[C@@H]3C(=O)[C@H](C)CC[C@@]2(C)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O6/c1-12(2)18-16-8-7-14(4)20-15(11-17(24)28-20)19(25)13(3)9-10-23(16,5)29-22(26)21(18)27-6/h7,12-13,15-16,20H,8-11H2,1-6H3/b14-7-/t13-,15-,16+,20-,23-/m1/s1

> <INCHI_KEY>
LDNGIXCVOPOZFN-LWEBIHICSA-N

> <FORMULA>
C23H32O6

> <MOLECULAR_WEIGHT>
404.503

> <EXACT_MASS>
404.21988875

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
43.11557317977583

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3Z,5S,9S,11R,14R)-17-methoxy-4,11,14-trimethyl-18-(propan-2-yl)-6,15-dioxatricyclo[12.4.0.0^{5,9}]octadeca-3,17-diene-7,10,16-trione

> <JCHEM_LOGP>
3.6848174003333307

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.09556466470939

> <JCHEM_PKA_STRONGEST_BASIC>
-4.980685184842804

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
109.33369999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3Z,5S,9S,11R,14R)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0^{5,9}]octadeca-3,17-diene-7,10,16-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.467   0.766   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.077   0.105   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.808   0.978   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.418   0.317   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.295  -1.219   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.095  -1.880   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.564  -2.092   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.851   1.190   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.348   0.832   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.364  -0.513   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.899  -0.391   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.772  -1.659   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.560   1.000   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.058   0.642   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.862   1.956   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.397   2.078   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.860   3.126   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.438   2.535   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.687   2.268   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.849   0.976   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.475   4.927   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.474   6.099   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.940   4.805   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.151   3.316   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.728   2.725   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.767   4.265   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.662   3.387   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.931   2.513   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.321   3.175   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    4    9   25                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   13   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    8   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27    3   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₆

Average Mass

404.5030 Da

Monoisotopic Mass

404.21989 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=C(C(C)C)[C@@H]2C\C=C(C)/[C@H]3OC(=O)C[C@@H]3C(=O)[C@H](C)CC[C@@]2(C)OC1=O

InChI Identifier

InChI=1S/C23H32O6/c1-12(2)18-16-8-7-14(4)20-15(11-17(24)28-20)19(25)13(3)9-10-23(16,5)29-22(26)21(18)27-6/h7,12-13,15-16,20H,8-11H2,1-6H3/b14-7-/t13-,15-,16+,20-,23-/m1/s1

InChI Key

LDNGIXCVOPOZFN-LWEBIHICSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydropyranones. Dihydropyranones are compounds containing a hydrogenated pyran ring which bears a ketone, and contains one double bond.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Pyranones and derivatives

Direct Parent

Dihydropyranones

Alternative Parents

Substituents

Dihydropyranone
Gamma butyrolactone
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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

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

63002490

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139590225

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione (NP0234040)

MOL for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

3D MOL for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

3D SDF for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

3D-SDF for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

PDB for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

3D PDB for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

SMILES for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

INCHI for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

Structure for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)

3D Structure for NP0234040 ((1s,3z,5s,9s,11r,14r)-18-isopropyl-17-methoxy-4,11,14-trimethyl-6,15-dioxatricyclo[12.4.0.0⁵,⁹]octadeca-3,17-diene-7,10,16-trione)