NP-MRD: Showing NP-Card for beta-1,15-dihydro-8,10-diepi-chandonanthone (NP0038170)

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Record Information

Version

2.0

Created at

2021-06-20 20:55:50 UTC

Updated at

2021-06-30 00:10:48 UTC

NP-MRD ID

NP0038170

Secondary Accession Numbers

None

Natural Product Identification

Common Name

beta-1,15-dihydro-8,10-diepi-chandonanthone

Provided By

JEOL Database JEOL Logo

Description

beta-1,15-dihydro-8,10-diepi-chandonanthone is found in Chandonanthus hirtellus. beta-1,15-dihydro-8,10-diepi-chandonanthone was first documented in 2009 (Wang, Y., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202122553D          

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     RDKit          3D

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  Mrv1652306202122553D          

 56 59  0  0  0  0            999 V2000
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    1.4706   -2.2532   -0.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2424    1.4337    0.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4461    0.5582    1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0361    1.3276    1.8811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3694   -2.4118    1.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4954   -1.2900    2.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6766    0.1449    3.3832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0182   -1.4742    3.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3495   -1.5947    1.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3732    0.6172   -0.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6585    0.6512    1.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0713    0.4301    2.9986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3632    2.2270    2.6415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7260    2.2414    0.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9644    2.7202    2.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5860   -2.9165   -0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8587   -1.3758   -0.7886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9641   -4.3904   -0.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7473   -3.9949   -1.8893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5081   -3.5116   -0.2038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6720   -0.1990   -1.9435 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 15  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 14  1  0  0  0  0
 18 21  1  0  0  0  0
 14 13  1  0  0  0  0
 21 22  1  0  0  0  0
  4 22  1  0  0  0  0
 24  7  1  0  0  0  0
 22 23  2  0  0  0  0
  7  9  1  0  0  0  0
  4  2  1  0  0  0  0
  9 10  1  0  0  0  0
  2  1  1  0  0  0  0
 11 10  1  1  0  0  0
  2  3  1  0  0  0  0
 13 12  1  0  0  0  0
 21 56  1  1  0  0  0
  7  6  1  0  0  0  0
 13 44  1  1  0  0  0
  7  8  1  1  0  0  0
  6  5  1  0  0  0  0
 18 19  1  6  0  0  0
 11 24  1  0  0  0  0
 18 20  1  0  0  0  0
 21 20  1  0  0  0  0
  5  4  1  0  0  0  0
 15 16  1  0  0  0  0
 11 12  1  0  0  0  0
 15 47  1  1  0  0  0
 14 45  1  0  0  0  0
 14 46  1  0  0  0  0
  9 40  1  0  0  0  0
  9 41  1  0  0  0  0
 10 42  1  0  0  0  0
 10 43  1  0  0  0  0
  6 35  1  0  0  0  0
  6 36  1  0  0  0  0
  5 33  1  0  0  0  0
  5 34  1  0  0  0  0
  4 32  1  1  0  0  0
 17 51  1  0  0  0  0
 17 52  1  0  0  0  0
  2 28  1  1  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  3 31  1  0  0  0  0
  8 37  1  0  0  0  0
  8 38  1  0  0  0  0
  8 39  1  0  0  0  0
 19 53  1  0  0  0  0
 19 54  1  0  0  0  0
 19 55  1  0  0  0  0
 16 48  1  0  0  0  0
 16 49  1  0  0  0  0
 16 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0038170

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])([H])C([H])(C([H])([H])[H])[C@@]1([H])C(=O)[C@@]2([H])O[C@]2(C([H])([H])[H])C([H])([H])[C@@]2([H])O[C@@]3(O[C@@](C([H])([H])[H])(C([H])([H])C3([H])[H])C([H])([H])C1([H])[H])[C@@]([H])(C([H])([H])[H])C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O4/c1-12(2)15-6-7-18(4)8-9-20(24-18)13(3)10-14(22-20)11-19(5)17(23-19)16(15)21/h12-15,17H,6-11H2,1-5H3/t13-,14-,15-,17+,18+,19+,20-/m0/s1

> <INCHI_KEY>
SNAPTEKGOSBDRH-SBPXRTMWSA-N

> <FORMULA>
C20H32O4

> <MOLECULAR_WEIGHT>
336.472

> <EXACT_MASS>
336.23005951

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
37.2256651602855

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,4S,6R,8S,10S,13R)-2,6,13-trimethyl-10-(propan-2-yl)-7,16,17-trioxatetracyclo[11.2.1.1^{1,4}.0^{6,8}]heptadecan-9-one

> <ALOGPS_LOGP>
3.01

> <JCHEM_LOGP>
4.0188991489999975

> <ALOGPS_LOGS>
-4.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.55572844630492

> <JCHEM_PKA_STRONGEST_BASIC>
-3.860898150838287

> <JCHEM_POLAR_SURFACE_AREA>
48.06

> <JCHEM_REFRACTIVITY>
91.44869999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.32e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4S,6R,8S,10S,13R)-10-isopropyl-2,6,13-trimethyl-7,16,17-trioxatetracyclo[11.2.1.1^{1,4}.0^{6,8}]heptadecan-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
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    0.3928   -2.3119   -3.3128 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9530   -0.4317   -4.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2120    0.6653   -5.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8962    1.5292   -3.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5656    1.8710   -3.3865 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1912    2.0269   -4.9758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7127    0.5612   -4.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4954   -1.2900    2.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3495   -1.5947    1.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3732    0.6172   -0.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6585    0.6512    1.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0713    0.4301    2.9986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3632    2.2270    2.6415 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9644    2.7202    2.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6720   -0.1990   -1.9435 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 15  1  0
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 21 22  1  0
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 13 12  1  0
 21 56  1  1
  7  6  1  0
 13 44  1  1
  7  8  1  1
  6  5  1  0
 18 19  1  6
 11 24  1  0
 18 20  1  0
 21 20  1  0
  5  4  1  0
 15 16  1  0
 11 12  1  0
 15 47  1  1
 14 45  1  0
 14 46  1  0
  9 40  1  0
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 10 42  1  0
 10 43  1  0
  6 35  1  0
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  5 33  1  0
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  4 32  1  1
 17 51  1  0
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  2 28  1  1
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  1 27  1  0
  3 29  1  0
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  3 31  1  0
  8 37  1  0
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  8 39  1  0
 19 53  1  0
 19 54  1  0
 19 55  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       1.995  -0.029  -4.750  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.254   0.696  -3.623  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.035   1.320  -4.170  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.978  -0.165  -2.358  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.277  -0.683  -1.709  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.117  -1.379  -0.343  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.578  -0.535   0.828  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.378   0.762   1.008  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.561  -1.351   2.126  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.378  -0.776   2.871  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.588  -0.496   1.736  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.345  -1.682   1.442  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.656  -1.284   1.008  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.670   0.240   0.957  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.629   0.587   2.005  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.139   2.022   1.898  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.087  -1.976  -0.290  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.960  -2.311  -1.241  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.253  -3.616  -0.997  0.00  0.00           C+0
HETATM   20  O   UNK     0      -2.315  -2.124  -2.624  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.334  -1.215  -2.093  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.041  -1.335  -2.657  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.393  -2.312  -3.313  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.207  -0.169   0.585  0.00  0.00           O+0
HETATM   25  H   UNK     0       1.403  -0.849  -5.168  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.953  -0.432  -4.409  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.212   0.665  -5.569  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.896   1.529  -3.306  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.566   1.871  -3.386  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.191   2.027  -4.976  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.713   0.561  -4.575  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.483   0.503  -1.647  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.751  -1.413  -2.378  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.992   0.141  -1.612  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.104  -1.771  -0.062  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.471  -2.253  -0.483  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.242   1.434   0.153  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.446   0.558   1.132  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.036   1.328   1.881  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.369  -2.412   1.918  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.495  -1.290   2.693  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.677   0.145   3.383  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.018  -1.474   3.615  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.349  -1.595   1.800  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.373   0.617  -0.026  0.00  0.00           H+0
HETATM   46  H   UNK     0      -3.659   0.651   1.184  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.071   0.430   2.999  0.00  0.00           H+0
HETATM   48  H   UNK     0      -0.363   2.227   2.642  0.00  0.00           H+0
HETATM   49  H   UNK     0      -0.726   2.241   0.908  0.00  0.00           H+0
HETATM   50  H   UNK     0      -1.964   2.720   2.073  0.00  0.00           H+0
HETATM   51  H   UNK     0      -3.586  -2.917  -0.022  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.859  -1.376  -0.789  0.00  0.00           H+0
HETATM   53  H   UNK     0      -1.964  -4.390  -0.690  0.00  0.00           H+0
HETATM   54  H   UNK     0      -0.747  -3.995  -1.889  0.00  0.00           H+0
HETATM   55  H   UNK     0      -0.508  -3.512  -0.204  0.00  0.00           H+0
HETATM   56  H   UNK     0      -1.672  -0.199  -1.944  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    4    1    3   28                                             
CONECT    3    2   29   30   31                                             
CONECT    4   22    2    5   32                                             
CONECT    5    6    4   33   34                                             
CONECT    6    7    5   35   36                                             
CONECT    7   24    9    6    8                                             
CONECT    8    7   37   38   39                                             
CONECT    9    7   10   40   41                                             
CONECT   10    9   11   42   43                                             
CONECT   11   15   10   24   12                                             
CONECT   12   13   11                                                       
CONECT   13   17   14   12   44                                             
CONECT   14   15   13   45   46                                             
CONECT   15   11   14   16   47                                             
CONECT   16   15   48   49   50                                             
CONECT   17   13   18   51   52                                             
CONECT   18   17   21   19   20                                             
CONECT   19   18   53   54   55                                             
CONECT   20   18   21                                                       
CONECT   21   18   22   56   20                                             
CONECT   22   21    4   23                                                  
CONECT   23   22                                                            
CONECT   24    7   11                                                       
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    2                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    5                                                            
CONECT   34    5                                                            
CONECT   35    6                                                            
CONECT   36    6                                                            
CONECT   37    8                                                            
CONECT   38    8                                                            
CONECT   39    8                                                            
CONECT   40    9                                                            
CONECT   41    9                                                            
CONECT   42   10                                                            
CONECT   43   10                                                            
CONECT   44   13                                                            
CONECT   45   14                                                            
CONECT   46   14                                                            
CONECT   47   15                                                            
CONECT   48   16                                                            
CONECT   49   16                                                            
CONECT   50   16                                                            
CONECT   51   17                                                            
CONECT   52   17                                                            
CONECT   53   19                                                            
CONECT   54   19                                                            
CONECT   55   19                                                            
CONECT   56   21                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  118    0
END

RDKit          3D

56 59  0  0  0  0  0  0  0  0999 V2000
    1.9948   -0.0292   -4.7497 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2537    0.6957   -3.6230 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0352    1.3199   -4.1701 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9775   -0.1648   -2.3585 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2767   -0.6832   -1.7091 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1171   -1.3795   -0.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5778   -0.5348    0.8284 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.3775   -0.7758    2.8714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5878   -0.4957    1.7355 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -1.2530   -3.6160   -0.9967 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3338   -1.2153   -2.0933 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0411   -1.3351   -2.6574 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3928   -2.3119   -3.3128 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2068   -0.1690    0.5848 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4033   -0.8490   -5.1675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9530   -0.4317   -4.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2120    0.6653   -5.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8962    1.5292   -3.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5656    1.8710   -3.3865 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1912    2.0269   -4.9758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7127    0.5612   -4.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4829    0.5033   -1.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7510   -1.4130   -2.3776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9924    0.1414   -1.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1040   -1.7708   -0.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4706   -2.2532   -0.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2424    1.4337    0.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4461    0.5582    1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0361    1.3276    1.8811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3694   -2.4118    1.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4954   -1.2900    2.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6766    0.1449    3.3832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0182   -1.4742    3.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3495   -1.5947    1.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3732    0.6172   -0.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6585    0.6512    1.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0713    0.4301    2.9986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3632    2.2270    2.6415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7260    2.2414    0.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9644    2.7202    2.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5860   -2.9165   -0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8587   -1.3758   -0.7886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9641   -4.3904   -0.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7473   -3.9949   -1.8893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5081   -3.5116   -0.2038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6720   -0.1990   -1.9435 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 15  1  0
 13 17  1  0
 17 18  1  0
 15 14  1  0
 18 21  1  0
 14 13  1  0
 21 22  1  0
  4 22  1  0
 24  7  1  0
 22 23  2  0
  7  9  1  0
  4  2  1  0
  9 10  1  0
  2  1  1  0
 11 10  1  1
  2  3  1  0
 13 12  1  0
 21 56  1  1
  7  6  1  0
 13 44  1  1
  7  8  1  1
  6  5  1  0
 18 19  1  6
 11 24  1  0
 18 20  1  0
 21 20  1  0
  5  4  1  0
 15 16  1  0
 11 12  1  0
 15 47  1  1
 14 45  1  0
 14 46  1  0
  9 40  1  0
  9 41  1  0
 10 42  1  0
 10 43  1  0
  6 35  1  0
  6 36  1  0
  5 33  1  0
  5 34  1  0
  4 32  1  1
 17 51  1  0
 17 52  1  0
  2 28  1  1
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  8 37  1  0
  8 38  1  0
  8 39  1  0
 19 53  1  0
 19 54  1  0
 19 55  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₄

Average Mass

336.4720 Da

Monoisotopic Mass

336.23006 Da

IUPAC Name

(1S,2S,4S,6R,8S,10S,13R)-2,6,13-trimethyl-10-(propan-2-yl)-7,16,17-trioxatetracyclo[11.2.1.1^{1,4}.0^{6,8}]heptadecan-9-one

Traditional Name

(1S,2S,4S,6R,8S,10S,13R)-10-isopropyl-2,6,13-trimethyl-7,16,17-trioxatetracyclo[11.2.1.1^{1,4}.0^{6,8}]heptadecan-9-one

CAS Registry Number

Not Available

SMILES

[H]C([H])([H])C([H])(C([H])([H])[H])[C@@]1([H])C(=O)[C@@]2([H])O[C@]2(C([H])([H])[H])C([H])([H])[C@@]2([H])O[C@@]3(O[C@@](C([H])([H])[H])(C([H])([H])C3([H])[H])C([H])([H])C1([H])[H])[C@@]([H])(C([H])([H])[H])C2([H])[H]

InChI Identifier

InChI=1S/C20H32O4/c1-12(2)15-6-7-18(4)8-9-20(24-18)13(3)10-14(22-20)11-19(5)17(23-19)16(15)21/h12-15,17H,6-11H2,1-5H3/t13-,14-,15-,17+,18+,19+,20-/m0/s1

InChI Key

SNAPTEKGOSBDRH-SBPXRTMWSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, 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
Plicanthus hirtellus	JEOL database	Wang, Y., et al, Tetrahedron 65, 4035 (2009)

Chemical Taxonomy

Classification

Not classified

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	3.01	ALOGPS
logP	4.02	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	19.56	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	48.06 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	91.45 m³·mol⁻¹	ChemAxon
Polarizability	37.23 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

Not Available

References

General References

Wang, Y., et al. (2009). Wang, Y., et al, Tetrahedron 65, 4035 (2009). Tetrahedron.

Showing NP-Card for beta-1,15-dihydro-8,10-diepi-chandonanthone (NP0038170)

MOL for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

3D MOL for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

3D SDF for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

3D-SDF for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

PDB for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

3D PDB for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

SMILES for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

INCHI for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

Structure for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)

3D Structure for NP0038170 (beta-1,15-dihydro-8,10-diepi-chandonanthone)