NP-MRD: Showing NP-Card for 3-deacetyl-11-oxoleukamenin E (NP0043016)

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Record Information

Version

2.0

Created at

2021-06-21 00:32:10 UTC

Updated at

2021-06-30 00:18:27 UTC

NP-MRD ID

NP0043016

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-deacetyl-11-oxoleukamenin E

Provided By

JEOL Database JEOL Logo

Description

CHEMBL3092685 belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. 3-deacetyl-11-oxoleukamenin E is found in Salvia cavaleriei. 3-deacetyl-11-oxoleukamenin E was first documented in 2013 (Zheng, H., et al.). Based on a literature review very few articles have been published on CHEMBL3092685.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212102323D          

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     RDKit          3D

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  Mrv1652306212102323D          

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    4.7120   -0.2347    4.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6771    1.7783    3.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1289   -2.7115    1.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7564   -2.2201    2.9451 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1034   -2.7582    2.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2723   -0.5540    0.7617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5547    1.0072    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4752    0.0951    2.3832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902    0.5282    0.7639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7127   -2.2393   -0.4461 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7400   -0.8721   -0.7276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9914    0.4587   -1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0151   -0.8238   -3.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
  5 11  1  0  0  0  0
 11 10  1  0  0  0  0
 10  9  1  0  0  0  0
  9  7  1  0  0  0  0
 17 19  1  0  0  0  0
 17 18  1  0  0  0  0
 13  6  1  0  0  0  0
 22 49  1  6  0  0  0
 22 23  1  0  0  0  0
  6 28  1  6  0  0  0
 23 24  1  0  0  0  0
 10  2  1  0  0  0  0
 24  5  1  0  0  0  0
  5  3  1  6  0  0  0
  6  5  1  0  0  0  0
 11 12  1  0  0  0  0
  2  3  1  0  0  0  0
 19 22  1  0  0  0  0
  2  1  2  3  0  0  0
 13 15  1  0  0  0  0
  7  8  2  0  0  0  0
 13 22  1  0  0  0  0
 13 14  1  1  0  0  0
 24 25  1  0  0  0  0
 16 17  1  0  0  0  0
 19 20  1  1  0  0  0
 16 15  1  0  0  0  0
 19 21  1  0  0  0  0
  6  7  1  0  0  0  0
  3  4  2  0  0  0  0
 16 39  1  0  0  0  0
 16 40  1  0  0  0  0
 17 41  1  1  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
 23 50  1  0  0  0  0
 23 51  1  0  0  0  0
 24 52  1  6  0  0  0
 11 32  1  1  0  0  0
 10 31  1  6  0  0  0
  9 29  1  0  0  0  0
  9 30  1  0  0  0  0
 18 42  1  0  0  0  0
 12 33  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
 14 34  1  0  0  0  0
 14 35  1  0  0  0  0
 14 36  1  0  0  0  0
 25 53  1  0  0  0  0
 20 43  1  0  0  0  0
 20 44  1  0  0  0  0
 20 45  1  0  0  0  0
 21 46  1  0  0  0  0
 21 47  1  0  0  0  0
 21 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0043016

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])[C@]2([H])C(=C([H])[H])C(=O)[C@]11[C@]([H])(O[H])C([H])([H])[C@]3([H])C(C([H])([H])[H])(C([H])([H])[H])[C@@]([H])(O[H])C([H])([H])C([H])([H])[C@@]3(C([H])([H])[H])[C@]1([H])C(=O)C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O5/c1-9-10-7-11(21)15-19(4)6-5-13(22)18(2,3)12(19)8-14(23)20(15,16(9)24)17(10)25/h10,12-15,17,22-23,25H,1,5-8H2,2-4H3/t10-,12+,13-,14+,15-,17+,19+,20+/m0/s1

> <INCHI_KEY>
PXZCGMKCJOVSST-ZZHJHLMKSA-N

> <FORMULA>
C20H28O5

> <MOLECULAR_WEIGHT>
348.439

> <EXACT_MASS>
348.193674002

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.00785375749635

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,4S,6S,9R,10S,13S,16R)-2,6,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane-11,15-dione

> <ALOGPS_LOGP>
1.27

> <JCHEM_LOGP>
0.9230591536666672

> <ALOGPS_LOGS>
-2.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.674584413662945

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.858313757888098

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351436521977574

> <JCHEM_POLAR_SURFACE_AREA>
94.83000000000001

> <JCHEM_REFRACTIVITY>
91.52819999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.63e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4S,6S,9R,10S,13S,16R)-2,6,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane-11,15-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
   -1.7727   -0.0772   -3.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8382   -0.5859   -2.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4657    0.0785   -2.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7535    1.2124   -2.4995 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3009   -0.8330   -1.2521 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9127   -0.4403    0.2126 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5840   -0.6990    0.5042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1583   -0.1147    1.4253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3418   -1.7428   -0.3027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8116   -1.9000   -1.7227 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6927   -2.1954   -1.6662 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1016   -2.6883   -2.9387 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8861   -0.9826    1.3398 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7070   -2.5071    1.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5460   -0.3009    2.6982 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6032   -0.5005    3.7883 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9889   -0.0425    3.3415 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9466    1.3759    3.1549 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4648   -0.7215    2.0246 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8710   -2.1830    2.2981 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7612   -0.0005    1.5564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3469   -0.5611    0.9270 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7168   -1.1445   -0.4472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7929   -0.6138   -1.5438 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1823   -1.2476   -2.7664 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6929   -0.6122   -3.4726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6319    0.8891   -3.7423 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9876    0.6596    0.2521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2777   -2.6957    0.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3972   -1.4459   -0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3591   -2.6735   -2.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9118   -2.9915   -0.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0160   -2.3660   -3.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6494   -2.7847    1.5524 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820   -3.0935    0.7365 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1102   -2.8708    2.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4072    0.7771    2.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5947   -0.6813    3.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6324   -1.5453    4.1116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2927    0.0815    4.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7120   -0.2347    4.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6771    1.7783    3.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1289   -2.7115    1.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7564   -2.2201    2.9451 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1034   -2.7582    2.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2723   -0.5540    0.7617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5547    1.0072    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4752    0.0951    2.3832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902    0.5282    0.7639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7127   -2.2393   -0.4461 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7400   -0.8721   -0.7276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9914    0.4587   -1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0151   -0.8238   -3.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
  5 11  1  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
 17 19  1  0
 17 18  1  0
 13  6  1  0
 22 49  1  6
 22 23  1  0
  6 28  1  6
 23 24  1  0
 10  2  1  0
 24  5  1  0
  5  3  1  6
  6  5  1  0
 11 12  1  0
  2  3  1  0
 19 22  1  0
  2  1  2  3
 13 15  1  0
  7  8  2  0
 13 22  1  0
 13 14  1  1
 24 25  1  0
 16 17  1  0
 19 20  1  1
 16 15  1  0
 19 21  1  0
  6  7  1  0
  3  4  2  0
 16 39  1  0
 16 40  1  0
 17 41  1  1
 15 37  1  0
 15 38  1  0
 23 50  1  0
 23 51  1  0
 24 52  1  6
 11 32  1  1
 10 31  1  6
  9 29  1  0
  9 30  1  0
 18 42  1  0
 12 33  1  0
  1 26  1  0
  1 27  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 25 53  1  0
 20 43  1  0
 20 44  1  0
 20 45  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.773  -0.077  -3.265  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.838  -0.586  -2.458  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.466   0.079  -2.152  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.754   1.212  -2.499  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.301  -0.833  -1.252  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.913  -0.440   0.213  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.584  -0.699   0.504  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.158  -0.115   1.425  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.342  -1.743  -0.303  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.812  -1.900  -1.723  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.693  -2.195  -1.666  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.102  -2.688  -2.939  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.886  -0.983   1.340  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.707  -2.507   1.524  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.546  -0.301   2.698  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.603  -0.500   3.788  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.989  -0.043   3.341  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.947   1.376   3.155  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.465  -0.722   2.025  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.871  -2.183   2.298  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.761  -0.001   1.556  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.347  -0.561   0.927  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.717  -1.145  -0.447  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.793  -0.614  -1.544  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.182  -1.248  -2.766  0.00  0.00           O+0
HETATM   26  H   UNK     0      -2.693  -0.612  -3.473  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.632   0.889  -3.742  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.988   0.660   0.252  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.278  -2.696   0.233  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.397  -1.446  -0.332  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.359  -2.674  -2.272  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.912  -2.991  -0.955  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.016  -2.366  -3.106  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.649  -2.785   1.552  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.182  -3.094   0.737  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.110  -2.871   2.469  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.407   0.777   2.543  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.595  -0.681   3.088  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.632  -1.545   4.112  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.293   0.082   4.665  0.00  0.00           H+0
HETATM   41  H   UNK     0       4.712  -0.235   4.144  0.00  0.00           H+0
HETATM   42  H   UNK     0       3.677   1.778   3.999  0.00  0.00           H+0
HETATM   43  H   UNK     0       5.129  -2.712   1.375  0.00  0.00           H+0
HETATM   44  H   UNK     0       5.756  -2.220   2.945  0.00  0.00           H+0
HETATM   45  H   UNK     0       4.103  -2.758   2.813  0.00  0.00           H+0
HETATM   46  H   UNK     0       6.272  -0.554   0.762  0.00  0.00           H+0
HETATM   47  H   UNK     0       5.555   1.007   1.180  0.00  0.00           H+0
HETATM   48  H   UNK     0       6.475   0.095   2.383  0.00  0.00           H+0
HETATM   49  H   UNK     0       3.290   0.528   0.764  0.00  0.00           H+0
HETATM   50  H   UNK     0       3.713  -2.239  -0.446  0.00  0.00           H+0
HETATM   51  H   UNK     0       4.740  -0.872  -0.728  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.991   0.459  -1.667  0.00  0.00           H+0
HETATM   53  H   UNK     0       4.015  -0.824  -3.052  0.00  0.00           H+0
CONECT    1    2   26   27                                                  
CONECT    2   10    3    1                                                  
CONECT    3    5    2    4                                                  
CONECT    4    3                                                            
CONECT    5   11   24    3    6                                             
CONECT    6   13   28    5    7                                             
CONECT    7    9    8    6                                                  
CONECT    8    7                                                            
CONECT    9   10    7   29   30                                             
CONECT   10   11    9    2   31                                             
CONECT   11    5   10   12   32                                             
CONECT   12   11   33                                                       
CONECT   13    6   15   22   14                                             
CONECT   14   13   34   35   36                                             
CONECT   15   13   16   37   38                                             
CONECT   16   17   15   39   40                                             
CONECT   17   19   18   16   41                                             
CONECT   18   17   42                                                       
CONECT   19   17   22   20   21                                             
CONECT   20   19   43   44   45                                             
CONECT   21   19   46   47   48                                             
CONECT   22   49   23   19   13                                             
CONECT   23   22   24   50   51                                             
CONECT   24   23    5   25   52                                             
CONECT   25   24   53                                                       
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    6                                                            
CONECT   29    9                                                            
CONECT   30    9                                                            
CONECT   31   10                                                            
CONECT   32   11                                                            
CONECT   33   12                                                            
CONECT   34   14                                                            
CONECT   35   14                                                            
CONECT   36   14                                                            
CONECT   37   15                                                            
CONECT   38   15                                                            
CONECT   39   16                                                            
CONECT   40   16                                                            
CONECT   41   17                                                            
CONECT   42   18                                                            
CONECT   43   20                                                            
CONECT   44   20                                                            
CONECT   45   20                                                            
CONECT   46   21                                                            
CONECT   47   21                                                            
CONECT   48   21                                                            
CONECT   49   22                                                            
CONECT   50   23                                                            
CONECT   51   23                                                            
CONECT   52   24                                                            
CONECT   53   25                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  112    0
END

RDKit          3D

53 56  0  0  0  0  0  0  0  0999 V2000
   -1.7727   -0.0772   -3.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8382   -0.5859   -2.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4657    0.0785   -2.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7535    1.2124   -2.4995 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3009   -0.8330   -1.2521 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.5840   -0.6990    0.5042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1583   -0.1147    1.4253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3418   -1.7428   -0.3027 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6927   -2.1954   -1.6662 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1016   -2.6883   -2.9387 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8861   -0.9826    1.3398 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7070   -2.5071    1.5237 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5460   -0.3009    2.6982 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6032   -0.5005    3.7883 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9889   -0.0425    3.3415 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9466    1.3759    3.1549 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4648   -0.7215    2.0246 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8710   -2.1830    2.2981 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7612   -0.0005    1.5564 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3469   -0.5611    0.9270 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7168   -1.1445   -0.4472 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7929   -0.6138   -1.5438 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1823   -1.2476   -2.7664 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6929   -0.6122   -3.4726 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9876    0.6596    0.2521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2777   -2.6957    0.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3972   -1.4459   -0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3591   -2.6735   -2.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9118   -2.9915   -0.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0160   -2.3660   -3.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6494   -2.7847    1.5524 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820   -3.0935    0.7365 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1102   -2.8708    2.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4072    0.7771    2.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5947   -0.6813    3.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6324   -1.5453    4.1116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2927    0.0815    4.6654 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7120   -0.2347    4.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6771    1.7783    3.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1289   -2.7115    1.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7564   -2.2201    2.9451 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1034   -2.7582    2.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2723   -0.5540    0.7617 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5547    1.0072    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4752    0.0951    2.3832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902    0.5282    0.7639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7127   -2.2393   -0.4461 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7400   -0.8721   -0.7276 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9914    0.4587   -1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0151   -0.8238   -3.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
  5 11  1  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
 17 19  1  0
 17 18  1  0
 13  6  1  0
 22 49  1  6
 22 23  1  0
  6 28  1  6
 23 24  1  0
 10  2  1  0
 24  5  1  0
  5  3  1  6
  6  5  1  0
 11 12  1  0
  2  3  1  0
 19 22  1  0
  2  1  2  3
 13 15  1  0
  7  8  2  0
 13 22  1  0
 13 14  1  1
 24 25  1  0
 16 17  1  0
 19 20  1  1
 16 15  1  0
 19 21  1  0
  6  7  1  0
  3  4  2  0
 16 39  1  0
 16 40  1  0
 17 41  1  1
 15 37  1  0
 15 38  1  0
 23 50  1  0
 23 51  1  0
 24 52  1  6
 11 32  1  1
 10 31  1  6
  9 29  1  0
  9 30  1  0
 18 42  1  0
 12 33  1  0
  1 26  1  0
  1 27  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 25 53  1  0
 20 43  1  0
 20 44  1  0
 20 45  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₅

Average Mass

348.4390 Da

Monoisotopic Mass

348.19367 Da

IUPAC Name

(1R,2R,4S,6S,9R,10S,13S,16R)-2,6,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane-11,15-dione

Traditional Name

(1R,2R,4S,6S,9R,10S,13S,16R)-2,6,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane-11,15-dione

CAS Registry Number

Not Available

SMILES

[H]O[C@]1([H])[C@]2([H])C(=C([H])[H])C(=O)[C@]11[C@]([H])(O[H])C([H])([H])[C@]3([H])C(C([H])([H])[H])(C([H])([H])[H])[C@@]([H])(O[H])C([H])([H])C([H])([H])[C@@]3(C([H])([H])[H])[C@]1([H])C(=O)C2([H])[H]

InChI Identifier

InChI=1S/C20H28O5/c1-9-10-7-11(21)15-19(4)6-5-13(22)18(2,3)12(19)8-14(23)20(15,16(9)24)17(10)25/h10,12-15,17,22-23,25H,1,5-8H2,2-4H3/t10-,12+,13-,14+,15-,17+,19+,20+/m0/s1

InChI Key

PXZCGMKCJOVSST-ZZHJHLMKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Salvia cavaleriei	JEOL database	Zheng, H., et al, J. Nat. Prod. 76, 2253 (2013)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Cyclic alcohol
Secondary alcohol
Ketone
Polyol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	1.27	ALOGPS
logP	0.92	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	13.86	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	91.53 m³·mol⁻¹	ChemAxon
Polarizability	37.01 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

31129895

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

76335391

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zheng, H., et al. (2013). Zheng, H., et al, J. Nat. Prod. 76, 2253 (2013). J. Nat. Prod..

Showing NP-Card for 3-deacetyl-11-oxoleukamenin E (NP0043016)

MOL for NP0043016 (3-deacetyl-11-oxoleukamenin E)

3D MOL for NP0043016 (3-deacetyl-11-oxoleukamenin E)

3D SDF for NP0043016 (3-deacetyl-11-oxoleukamenin E)

3D-SDF for NP0043016 (3-deacetyl-11-oxoleukamenin E)

PDB for NP0043016 (3-deacetyl-11-oxoleukamenin E)

3D PDB for NP0043016 (3-deacetyl-11-oxoleukamenin E)

SMILES for NP0043016 (3-deacetyl-11-oxoleukamenin E)

INCHI for NP0043016 (3-deacetyl-11-oxoleukamenin E)

Structure for NP0043016 (3-deacetyl-11-oxoleukamenin E)

3D Structure for NP0043016 (3-deacetyl-11-oxoleukamenin E)