NP-MRD: Showing NP-Card for cladieunicellin G (NP0041167)

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Record Information

Version

2.0

Created at

2021-06-20 23:08:48 UTC

Updated at

2021-06-30 00:15:30 UTC

NP-MRD ID

NP0041167

Secondary Accession Numbers

None

Natural Product Identification

Common Name

cladieunicellin G

Provided By

JEOL Database JEOL Logo

Description

(1R,2S,3R,6R,7R,8R,9R,12S)-9,12-dihydroxy-3,9-dimethyl-13-methylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0²,⁷]Pentadecan-3-yl acetate belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton. cladieunicellin G is found in Cladiella sp. cladieunicellin G was first documented in 2012 (Chen, Y.-H., et al.). Based on a literature review very few articles have been published on (1R,2S,3R,6R,7R,8R,9R,12S)-9,12-dihydroxy-3,9-dimethyl-13-methylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0²,⁷]Pentadecan-3-yl acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212101083D          

 63 65  0  0  0  0            999 V2000
   -0.1785   -2.6909    2.6139 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3764   -2.6574    1.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5263   -1.7163    1.0693 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1932   -0.5928    0.0681 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.3114   -0.5890   -1.7457 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306212101083D          

 63 65  0  0  0  0            999 V2000
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    2.0755    2.2940    0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6475    3.5367   -0.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3111   -3.2263   -2.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9619   -2.1419   -3.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1507   -2.4159   -0.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1325   -3.8762    0.6998 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6073   -3.5118   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636   -4.9421    1.1896 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  0  0  0  0
 17  7  1  0  0  0  0
  2  1  2  3  0  0  0
  7  6  1  0  0  0  0
 26 27  1  0  0  0  0
  6  5  1  0  0  0  0
 21 23  1  6  0  0  0
  5  4  1  0  0  0  0
 17 18  1  0  0  0  0
  4  8  1  0  0  0  0
  9 11  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 21  1  0  0  0  0
  4 32  1  6  0  0  0
  8  7  1  0  0  0  0
  6 33  1  6  0  0  0
 21 24  1  0  0  0  0
 21 22  1  0  0  0  0
  7 34  1  1  0  0  0
 24 25  1  0  0  0  0
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 15 16  1  0  0  0  0
 11 12  1  0  0  0  0
 25 26  1  0  0  0  0
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 15  9  1  0  0  0  0
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 26  2  1  0  0  0  0
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 20 52  1  0  0  0  0
 20 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0041167

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H36O5/c1-12(2)15-7-10-22(6,27-14(4)23)19-17-11-13(3)16(24)8-9-21(5,25)20(26-17)18(15)19/h12,15-20,24-25H,3,7-11H2,1-2,4-6H3/t15-,16+,17-,18-,19-,20-,21-,22-/m1/s1

> <INCHI_KEY>
JFAUVIHJDLKYTJ-CSHDGZMQSA-N

> <FORMULA>
C22H36O5

> <MOLECULAR_WEIGHT>
380.525

> <EXACT_MASS>
380.256274259

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
42.30872502655513

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,3R,6R,7R,8R,9R,12S)-9,12-dihydroxy-3,9-dimethyl-13-methylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-3-yl acetate

> <ALOGPS_LOGP>
1.95

> <JCHEM_LOGP>
2.2986926643333323

> <ALOGPS_LOGS>
-3.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.731584362254168

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.940706094116173

> <JCHEM_PKA_STRONGEST_BASIC>
-2.962981674909856

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
103.0818

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3R,6R,7R,8R,9R,12S)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
   -0.1785   -2.6909    2.6139 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3764   -2.6574    1.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5263   -1.7163    1.0693 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0436    0.3450    0.4447 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3317    1.5748    1.3494 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1077    1.1916    2.6146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0084    2.0349    1.7254 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2107    3.1311    2.5014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6818    3.3447    2.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3482    3.8514    2.9795 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5741    0.4220    3.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6073   -3.5118   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636   -4.9421    1.1896 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0
  4  3  1  0
 17  7  1  0
  2  1  2  3
  7  6  1  0
 26 27  1  0
  6  5  1  0
 21 23  1  6
  5  4  1  0
 17 18  1  0
  4  8  1  0
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 24 25  1  0
  8 35  1  1
 15 16  1  0
 11 12  1  0
 25 26  1  0
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 15  9  1  0
 12 14  2  0
 26  2  1  0
 18 19  1  0
 16 17  1  0
 18 20  1  0
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 16 44  1  0
 16 45  1  0
 17 46  1  6
 24 58  1  0
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 25 60  1  0
 25 61  1  0
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 22 54  1  0
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 20 52  1  0
 20 53  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      -0.179  -2.691   2.614  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.376  -2.657   1.388  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.526  -1.716   1.069  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.193  -0.593   0.068  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.827  -1.236  -1.169  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.311  -0.589  -1.746  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.571   0.694  -0.924  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.044   0.345   0.445  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.332   1.575   1.349  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.108   1.192   2.615  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.008   2.035   1.725  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.211   3.131   2.501  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.682   3.345   2.691  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.348   3.851   2.979  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.085   2.658   0.565  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.307   3.096  -0.669  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.086   1.924  -1.632  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.692   2.356  -2.920  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.062   2.987  -2.651  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.141   3.306  -3.790  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.518  -1.562  -1.929  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.177  -2.618  -2.993  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.587  -0.762  -2.487  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.084  -2.213  -0.643  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.508  -3.545  -0.143  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.039  -3.611   0.285  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.191  -4.946   0.761  0.00  0.00           O+0
HETATM   28  H   UNK     0       0.146  -2.032   3.413  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.971  -3.396   2.851  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.338  -2.327   0.651  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.930  -1.294   1.994  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.106  -0.023  -0.138  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.001  -0.309  -2.758  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.640   0.891  -0.799  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.711  -0.241   0.979  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.115   0.839   2.379  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.574   0.422   3.181  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.230   2.039   3.295  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.122   2.476   3.187  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.158   3.518   1.722  0.00  0.00           H+0
HETATM   41  H   UNK     0      -2.843   4.224   3.321  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.264   3.542   1.185  0.00  0.00           H+0
HETATM   43  H   UNK     0       2.075   2.294   0.266  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.648   3.537  -0.364  0.00  0.00           H+0
HETATM   45  H   UNK     0       0.875   3.891  -1.164  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.087   1.606  -1.962  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.872   1.465  -3.532  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.701   2.333  -2.051  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.975   3.949  -2.137  0.00  0.00           H+0
HETATM   50  H   UNK     0      -2.586   3.171  -3.595  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.281   4.281  -3.314  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.355   3.478  -4.752  0.00  0.00           H+0
HETATM   53  H   UNK     0       1.128   2.880  -4.000  0.00  0.00           H+0
HETATM   54  H   UNK     0      -2.029  -3.285  -3.169  0.00  0.00           H+0
HETATM   55  H   UNK     0      -0.311  -3.226  -2.716  0.00  0.00           H+0
HETATM   56  H   UNK     0      -0.962  -2.142  -3.957  0.00  0.00           H+0
HETATM   57  H   UNK     0      -3.309  -1.362  -2.744  0.00  0.00           H+0
HETATM   58  H   UNK     0      -3.151  -2.416  -0.825  0.00  0.00           H+0
HETATM   59  H   UNK     0      -2.117  -1.488   0.173  0.00  0.00           H+0
HETATM   60  H   UNK     0      -1.679  -4.318  -0.904  0.00  0.00           H+0
HETATM   61  H   UNK     0      -2.132  -3.876   0.700  0.00  0.00           H+0
HETATM   62  H   UNK     0       0.607  -3.512  -0.589  0.00  0.00           H+0
HETATM   63  H   UNK     0       1.064  -4.942   1.190  0.00  0.00           H+0
CONECT    1    2   28   29                                                  
CONECT    2    3    1   26                                                  
CONECT    3    2    4   30   31                                             
CONECT    4    3    5    8   32                                             
CONECT    5    6    4                                                       
CONECT    6    7    5   21   33                                             
CONECT    7   17    6    8   34                                             
CONECT    8    4    9    7   35                                             
CONECT    9   11    8   10   15                                             
CONECT   10    9   36   37   38                                             
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12   39   40   41                                             
CONECT   14   12                                                            
CONECT   15   16    9   42   43                                             
CONECT   16   15   17   44   45                                             
CONECT   17    7   18   16   46                                             
CONECT   18   17   19   20   47                                             
CONECT   19   18   48   49   50                                             
CONECT   20   18   51   52   53                                             
CONECT   21   23    6   24   22                                             
CONECT   22   21   54   55   56                                             
CONECT   23   21   57                                                       
CONECT   24   21   25   58   59                                             
CONECT   25   24   26   60   61                                             
CONECT   26   27   25    2   62                                             
CONECT   27   26   63                                                       
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    3                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    6                                                            
CONECT   34    7                                                            
CONECT   35    8                                                            
CONECT   36   10                                                            
CONECT   37   10                                                            
CONECT   38   10                                                            
CONECT   39   13                                                            
CONECT   40   13                                                            
CONECT   41   13                                                            
CONECT   42   15                                                            
CONECT   43   15                                                            
CONECT   44   16                                                            
CONECT   45   16                                                            
CONECT   46   17                                                            
CONECT   47   18                                                            
CONECT   48   19                                                            
CONECT   49   19                                                            
CONECT   50   19                                                            
CONECT   51   20                                                            
CONECT   52   20                                                            
CONECT   53   20                                                            
CONECT   54   22                                                            
CONECT   55   22                                                            
CONECT   56   22                                                            
CONECT   57   23                                                            
CONECT   58   24                                                            
CONECT   59   24                                                            
CONECT   60   25                                                            
CONECT   61   25                                                            
CONECT   62   26                                                            
CONECT   63   27                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  130    0
END

RDKit          3D

63 65  0  0  0  0  0  0  0  0999 V2000
   -0.1785   -2.6909    2.6139 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3764   -2.6574    1.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5263   -1.7163    1.0693 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1932   -0.5928    0.0681 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8273   -1.2359   -1.1693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3114   -0.5890   -1.7457 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5707    0.6937   -0.9239 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0436    0.3450    0.4447 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3317    1.5748    1.3494 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1077    1.1916    2.6146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0084    2.0349    1.7254 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2107    3.1311    2.5014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6818    3.3447    2.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3482    3.8514    2.9795 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0847    2.6582    0.5646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3072    3.0963   -0.6688 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0864    1.9236   -1.6324 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6919    2.3558   -2.9203 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0621    2.9868   -2.6505 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1413    3.3058   -3.7901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5182   -1.5619   -1.9291 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1765   -2.6182   -2.9925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5871   -0.7618   -2.4866 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0842   -2.2129   -0.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5082   -3.5447   -0.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0388   -3.6114    0.2852 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1911   -4.9458    0.7610 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1459   -2.0322    3.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9711   -3.3959    2.8514 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3383   -2.3270    0.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9299   -1.2943    1.9937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1062   -0.0231   -0.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0012   -0.3093   -2.7580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6398    0.8906   -0.7986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7114   -0.2411    0.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1155    0.8385    2.3790 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5741    0.4220    3.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2295    2.0391    3.2954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1219    2.4761    3.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1581    3.5179    1.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8426    4.2241    3.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2643    3.5424    1.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0755    2.2940    0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6475    3.5367   -0.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8753    3.8912   -1.1643 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0873    1.6060   -1.9618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8717    1.4646   -3.5323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7007    2.3331   -2.0509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9753    3.9492   -2.1369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5860    3.1709   -3.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2811    4.2811   -3.3140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3550    3.4780   -4.7516 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1280    2.8798   -3.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288   -3.2845   -3.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3111   -3.2263   -2.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9619   -2.1419   -3.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3087   -1.3621   -2.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1507   -2.4159   -0.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1168   -1.4877    0.1733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6794   -4.3180   -0.9037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1325   -3.8762    0.6998 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6073   -3.5118   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636   -4.9421    1.1896 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0
  4  3  1  0
 17  7  1  0
  2  1  2  3
  7  6  1  0
 26 27  1  0
  6  5  1  0
 21 23  1  6
  5  4  1  0
 17 18  1  0
  4  8  1  0
  9 11  1  1
  8  9  1  0
  9 10  1  0
  6 21  1  0
  4 32  1  6
  8  7  1  0
  6 33  1  6
 21 24  1  0
 21 22  1  0
  7 34  1  1
 24 25  1  0
  8 35  1  1
 15 16  1  0
 11 12  1  0
 25 26  1  0
 12 13  1  0
 15  9  1  0
 12 14  2  0
 26  2  1  0
 18 19  1  0
 16 17  1  0
 18 20  1  0
 15 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  6
 24 58  1  0
 24 59  1  0
 25 60  1  0
 25 61  1  0
 26 62  1  6
  3 30  1  0
  3 31  1  0
  1 28  1  0
  1 29  1  0
 27 63  1  0
 23 57  1  0
 18 47  1  6
 10 36  1  0
 10 37  1  0
 10 38  1  0
 22 54  1  0
 22 55  1  0
 22 56  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 19 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 20 53  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Value	Source
(1R,2S,3R,6R,7R,8R,9R,12S)-9,12-Dihydroxy-3,9-dimethyl-13-methylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0,]pentadecan-3-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₆O₅

Average Mass

380.5250 Da

Monoisotopic Mass

380.25627 Da

IUPAC Name

(1R,2S,3R,6R,7R,8R,9R,12S)-9,12-dihydroxy-3,9-dimethyl-13-methylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-3-yl acetate

Traditional Name

(1R,2S,3R,6R,7R,8R,9R,12S)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-3-yl acetate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C22H36O5/c1-12(2)15-7-10-22(6,27-14(4)23)19-17-11-13(3)16(24)8-9-21(5,25)20(26-17)18(15)19/h12,15-20,24-25H,3,7-11H2,1-2,4-6H3/t15-,16+,17-,18-,19-,20-,21-,22-/m1/s1

InChI Key

JFAUVIHJDLKYTJ-CSHDGZMQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Cladiella sp.	JEOL database	Chen, Y.-H., et al, Chem. Pharm. Bull. 60, 160 (2012)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Eunicellane and asbestinane diterpenoids

Alternative Parents

Substituents

Eunicellane-type diterpenoid
Cladiellane diterpenoid
Tertiary alcohol
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Carbonyl group
Organic oxide
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxygen 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
logP	1.95	ALOGPS
logP	2.3	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	13.94	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	103.08 m³·mol⁻¹	ChemAxon
Polarizability	42.31 Å³	ChemAxon
Number of Rings	3	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

28289654

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

56925415

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chen, Y.-H., et al. (2012). Chen, Y.-H., et al, Chem. Pharm. Bull. 60, 160 (2012). Chem. Pharm. Bull..

Showing NP-Card for cladieunicellin G (NP0041167)

MOL for NP0041167 (cladieunicellin G)

3D MOL for NP0041167 (cladieunicellin G)

3D SDF for NP0041167 (cladieunicellin G)

3D-SDF for NP0041167 (cladieunicellin G)

PDB for NP0041167 (cladieunicellin G)

3D PDB for NP0041167 (cladieunicellin G)

SMILES for NP0041167 (cladieunicellin G)

INCHI for NP0041167 (cladieunicellin G)

Structure for NP0041167 (cladieunicellin G)

3D Structure for NP0041167 (cladieunicellin G)