NP-MRD: Showing NP-Card for 12-oxo-resibufogenin (NP0028569)

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Record Information

Version

2.0

Created at

2021-06-19 20:25:26 UTC

Updated at

2021-06-29 23:55:26 UTC

NP-MRD ID

NP0028569

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-oxo-resibufogenin

Provided By

JEOL Database JEOL Logo

Description

12-oxo-resibufogenin is found in Mucor polymorphosporus. 12-oxo-resibufogenin was first documented in 2005 (Ye, M., et al.). Based on a literature review very few articles have been published on 12-Oxoresibufogenin.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192122253D          

 59 64  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306192122253D          

 59 64  0  0  0  0            999 V2000
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   -1.7884    4.7088    0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6003    3.2212    0.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548    4.6938    2.4060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5077    3.1740    2.6833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0710    5.0170    3.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0337    6.6224    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1746    3.2267    2.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8967    4.7606    1.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018    4.7341   -0.2578 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0771    3.0021   -1.3256 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9975    3.6076    0.0325 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4472    1.6849    1.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0733    1.1376   -0.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0758   -2.8327   -0.9145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4443   -1.3308   -1.5761 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6759   -2.6009   -1.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9076   -2.7334    2.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0415   -5.9068    0.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5307   -4.9269    1.6148 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7319   -2.6894    3.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4497   -1.5486    3.5802 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1551   -0.1090    2.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  5  1  0  0  0  0
  5  7  1  0  0  0  0
 10 11  1  0  0  0  0
  5  6  1  0  0  0  0
 16 29  1  0  0  0  0
 12 11  1  0  0  0  0
 26 18  1  0  0  0  0
 18 16  1  0  0  0  0
 27 26  1  0  0  0  0
 12 47  1  1  0  0  0
  2  1  1  6  0  0  0
 18 19  1  0  0  0  0
  2 12  1  0  0  0  0
 19 20  1  0  0  0  0
 11 46  1  6  0  0  0
 20 21  2  0  0  0  0
  8  2  1  0  0  0  0
 21 22  1  0  0  0  0
  8  9  1  0  0  0  0
 22 24  1  0  0  0  0
  9 10  1  0  0  0  0
 24 25  1  0  0  0  0
 25 19  2  0  0  0  0
 12 13  1  0  0  0  0
 22 23  2  0  0  0  0
 11 29  1  0  0  0  0
 16 17  1  6  0  0  0
 16 14  1  0  0  0  0
  8 41  1  6  0  0  0
 29 27  1  0  0  0  0
 29 28  1  6  0  0  0
 27 28  1  0  0  0  0
 14 13  1  0  0  0  0
  8  7  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
 14 15  2  0  0  0  0
  9 42  1  0  0  0  0
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  3 33  1  0  0  0  0
  3 34  1  0  0  0  0
  4 35  1  0  0  0  0
  4 36  1  0  0  0  0
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  7 39  1  0  0  0  0
  7 40  1  0  0  0  0
  6 38  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
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 17 50  1  0  0  0  0
 17 51  1  0  0  0  0
 17 52  1  0  0  0  0
 27 59  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0028569

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@]([H])(C([H])([H])C([H])([H])[C@]3([H])[C@]2([H])C([H])([H])C(=O)[C@]2(C([H])([H])[H])[C@@]([H])(C4=C([H])OC(=O)C([H])=C4[H])C([H])([H])[C@@]4([H])O[C@@]324)C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O5/c1-22-8-7-15(25)9-14(22)4-5-16-18(22)10-19(26)23(2)17(11-20-24(16,23)29-20)13-3-6-21(27)28-12-13/h3,6,12,14-18,20,25H,4-5,7-11H2,1-2H3/t14-,15+,16-,17-,18+,20-,22+,23+,24-/m1/s1

> <INCHI_KEY>
XUAKCUKUNPSUIW-NASMJONLSA-N

> <FORMULA>
C24H30O5

> <MOLECULAR_WEIGHT>
398.499

> <EXACT_MASS>
398.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.88804963237375

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,4R,6R,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-6-(2-oxo-2H-pyran-5-yl)-3-oxapentacyclo[8.8.0.0^{2,4}.0^{2,7}.0^{11,16}]octadecan-8-one

> <ALOGPS_LOGP>
2.34

> <JCHEM_LOGP>
2.696278107666666

> <ALOGPS_LOGS>
-4.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.38562731775356

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.29639621531718

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3563815432640403

> <JCHEM_POLAR_SURFACE_AREA>
76.13

> <JCHEM_REFRACTIVITY>
107.03329999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.39e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4R,6R,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.0^{2,4}.0^{2,7}.0^{11,16}]octadecan-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 59 64  0  0  0  0  0  0  0  0999 V2000
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    1.7053   -0.8669    2.0223 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.4443   -1.3308   -1.5761 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4497   -1.5486    3.5802 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1551   -0.1090    2.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
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 27 26  1  0
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  2  1  1  6
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  8  2  1  0
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 25 19  2  0
 12 13  1  0
 22 23  2  0
 11 29  1  0
 16 17  1  6
 16 14  1  0
  8 41  1  6
 29 27  1  0
 29 28  1  6
 27 28  1  0
 14 13  1  0
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  2  3  1  0
  3  4  1  0
 14 15  2  0
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 10 45  1  0
 13 48  1  0
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  3 33  1  0
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  5 37  1  1
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  6 38  1  0
  1 30  1  0
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 18 53  1  1
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 25 56  1  0
 17 50  1  0
 17 51  1  0
 17 52  1  0
 27 59  1  1
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.707   2.963  -1.545  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.461   2.983  -0.013  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.660   3.763   0.606  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.494   4.093   2.088  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.205   4.865   2.349  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.280   6.154   1.745  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.007   4.129   1.784  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.850   3.779   0.285  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.095   3.042  -0.230  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.212   1.628   0.321  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.947   0.786   0.086  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.344   1.517   0.557  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.571   0.642   0.232  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.468  -0.746   0.838  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.440  -1.238   1.414  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.170  -1.531   0.587  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.256  -2.111  -0.830  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.031  -2.613   1.727  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.409  -4.027   1.298  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.745  -4.372   0.873  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.049  -5.622   0.508  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.035  -6.691   0.529  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.328  -7.831   0.187  0.00  0.00           O+0
HETATM   24  O   UNK     0      -0.222  -6.345   0.945  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.493  -5.020   1.319  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.016  -1.976   2.744  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.705  -0.867   2.022  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.300  -1.200   0.762  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.006  -0.581   0.735  0.00  0.00           C+0
HETATM   30  H   UNK     0       0.025   2.356  -2.084  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.657   3.976  -1.962  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.701   2.572  -1.787  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.788   4.709   0.060  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.600   3.221   0.462  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.355   4.694   2.406  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.508   3.174   2.683  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.071   5.017   3.426  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.034   6.622   2.142  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.175   3.227   2.381  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.897   4.761   1.902  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.802   4.734  -0.258  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.077   3.002  -1.326  0.00  0.00           H+0
HETATM   43  H   UNK     0       2.998   3.608   0.033  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.447   1.685   1.388  0.00  0.00           H+0
HETATM   45  H   UNK     0       3.073   1.138  -0.150  0.00  0.00           H+0
HETATM   46  H   UNK     0       0.877   0.616  -0.996  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.285   1.575   1.652  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.711   0.518  -0.846  0.00  0.00           H+0
HETATM   49  H   UNK     0      -2.481   1.097   0.635  0.00  0.00           H+0
HETATM   50  H   UNK     0      -1.076  -2.833  -0.915  0.00  0.00           H+0
HETATM   51  H   UNK     0      -0.444  -1.331  -1.576  0.00  0.00           H+0
HETATM   52  H   UNK     0       0.676  -2.601  -1.129  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.908  -2.733   2.285  0.00  0.00           H+0
HETATM   54  H   UNK     0       2.518  -3.612   0.848  0.00  0.00           H+0
HETATM   55  H   UNK     0       3.042  -5.907   0.184  0.00  0.00           H+0
HETATM   56  H   UNK     0      -1.531  -4.927   1.615  0.00  0.00           H+0
HETATM   57  H   UNK     0       1.732  -2.689   3.163  0.00  0.00           H+0
HETATM   58  H   UNK     0       0.450  -1.549   3.580  0.00  0.00           H+0
HETATM   59  H   UNK     0       2.155  -0.109   2.641  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    1   12    8    3                                             
CONECT    3    2    4   33   34                                             
CONECT    4    5    3   35   36                                             
CONECT    5    4    7    6   37                                             
CONECT    6    5   38                                                       
CONECT    7    5    8   39   40                                             
CONECT    8    2    9   41    7                                             
CONECT    9    8   10   42   43                                             
CONECT   10   11    9   44   45                                             
CONECT   11   10   12   46   29                                             
CONECT   12   11   47    2   13                                             
CONECT   13   12   14   48   49                                             
CONECT   14   16   13   15                                                  
CONECT   15   14                                                            
CONECT   16   29   18   17   14                                             
CONECT   17   16   50   51   52                                             
CONECT   18   26   16   19   53                                             
CONECT   19   18   20   25                                                  
CONECT   20   19   21   54                                                  
CONECT   21   20   22   55                                                  
CONECT   22   21   24   23                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   19   56                                                  
CONECT   26   18   27   57   58                                             
CONECT   27   26   29   28   59                                             
CONECT   28   29   27                                                       
CONECT   29   16   11   27   28                                             
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    3                                                            
CONECT   34    3                                                            
CONECT   35    4                                                            
CONECT   36    4                                                            
CONECT   37    5                                                            
CONECT   38    6                                                            
CONECT   39    7                                                            
CONECT   40    7                                                            
CONECT   41    8                                                            
CONECT   42    9                                                            
CONECT   43    9                                                            
CONECT   44   10                                                            
CONECT   45   10                                                            
CONECT   46   11                                                            
CONECT   47   12                                                            
CONECT   48   13                                                            
CONECT   49   13                                                            
CONECT   50   17                                                            
CONECT   51   17                                                            
CONECT   52   17                                                            
CONECT   53   18                                                            
CONECT   54   20                                                            
CONECT   55   21                                                            
CONECT   56   25                                                            
CONECT   57   26                                                            
CONECT   58   26                                                            
CONECT   59   27                                                            
MASTER        0    0    0    0    0    0    0    0   59    0  128    0
END

RDKit          3D

59 64  0  0  0  0  0  0  0  0999 V2000
   -0.7067    2.9629   -1.5451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4612    2.9830   -0.0125 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6595    3.7630    0.6055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4939    4.0934    2.0880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2050    4.8653    2.3494 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2796    6.1538    1.7448 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0067    4.1294    1.7840 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8495    3.7788    0.2848 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0947    3.0424   -0.2302 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2116    1.6277    0.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9466    0.7863    0.0859 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3435    1.5169    0.5571 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5708    0.6423    0.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4680   -0.7458    0.8383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4401   -1.2378    1.4137 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1696   -1.5307    0.5871 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2559   -2.1109   -0.8301 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -2.6132    1.7267 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4089   -4.0273    1.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7452   -4.3717    0.8732 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0489   -5.6222    0.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0347   -6.6910    0.5290 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3281   -7.8312    0.1870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2215   -6.3447    0.9445 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4933   -5.0202    1.3186 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0157   -1.9761    2.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7053   -0.8669    2.0223 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2996   -1.1999    0.7622 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0060   -0.5811    0.7346 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0252    2.3559   -2.0839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6566    3.9758   -1.9621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7009    2.5722   -1.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7884    4.7088    0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6003    3.2212    0.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3548    4.6938    2.4060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5077    3.1740    2.6833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0710    5.0170    3.4261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0337    6.6224    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1746    3.2267    2.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8967    4.7606    1.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018    4.7341   -0.2578 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0771    3.0021   -1.3256 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9975    3.6076    0.0325 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4472    1.6849    1.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0733    1.1376   -0.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8768    0.6156   -0.9959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2848    1.5754    1.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7107    0.5180   -0.8462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4806    1.0969    0.6354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0758   -2.8327   -0.9145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4443   -1.3308   -1.5761 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6759   -2.6009   -1.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9076   -2.7334    2.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5176   -3.6116    0.8481 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0415   -5.9068    0.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5307   -4.9269    1.6148 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7319   -2.6894    3.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4497   -1.5486    3.5802 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1551   -0.1090    2.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  5  1  0
  5  7  1  0
 10 11  1  0
  5  6  1  0
 16 29  1  0
 12 11  1  0
 26 18  1  0
 18 16  1  0
 27 26  1  0
 12 47  1  1
  2  1  1  6
 18 19  1  0
  2 12  1  0
 19 20  1  0
 11 46  1  6
 20 21  2  0
  8  2  1  0
 21 22  1  0
  8  9  1  0
 22 24  1  0
  9 10  1  0
 24 25  1  0
 25 19  2  0
 12 13  1  0
 22 23  2  0
 11 29  1  0
 16 17  1  6
 16 14  1  0
  8 41  1  6
 29 27  1  0
 29 28  1  6
 27 28  1  0
 14 13  1  0
  8  7  1  0
  2  3  1  0
  3  4  1  0
 14 15  2  0
  9 42  1  0
  9 43  1  0
 10 44  1  0
 10 45  1  0
 13 48  1  0
 13 49  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  7 39  1  0
  7 40  1  0
  6 38  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 18 53  1  1
 26 57  1  0
 26 58  1  0
 20 54  1  0
 21 55  1  0
 25 56  1  0
 17 50  1  0
 17 51  1  0
 17 52  1  0
 27 59  1  1
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₀O₅

Average Mass

398.4990 Da

Monoisotopic Mass

398.20932 Da

IUPAC Name

(1R,2S,4R,6R,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-6-(2-oxo-2H-pyran-5-yl)-3-oxapentacyclo[8.8.0.0^{2,4}.0^{2,7}.0^{11,16}]octadecan-8-one

Traditional Name

(1R,2S,4R,6R,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.0^{2,4}.0^{2,7}.0^{11,16}]octadecan-8-one

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])C([H])([H])C([H])([H])[C@@]2(C([H])([H])[H])[C@]([H])(C([H])([H])C([H])([H])[C@]3([H])[C@]2([H])C([H])([H])C(=O)[C@]2(C([H])([H])[H])[C@@]([H])(C4=C([H])OC(=O)C([H])=C4[H])C([H])([H])[C@@]4([H])O[C@@]324)C1([H])[H]

InChI Identifier

InChI=1S/C24H30O5/c1-22-8-7-15(25)9-14(22)4-5-16-18(22)10-19(26)23(2)17(11-20-24(16,23)29-20)13-3-6-21(27)28-12-13/h3,6,12,14-18,20,25H,4-5,7-11H2,1-2H3/t14-,15+,16-,17-,18+,20-,22+,23+,24-/m1/s1

InChI Key

XUAKCUKUNPSUIW-NASMJONLSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, 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
Mucor polymorphosporus	JEOL database	Ye, M., et al, Tetrahedron 61, 8947 (2005)

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	2.34	ALOGPS
logP	2.7	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	18.3	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	76.13 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	107.03 m³·mol⁻¹	ChemAxon
Polarizability	42.89 Å³	ChemAxon
Number of Rings	6	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

9742249

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11567479

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ye, M., et al. (2005). Ye, M., et al, Tetrahedron 61, 8947 (2005). Tetrahedron.

Showing NP-Card for 12-oxo-resibufogenin (NP0028569)

MOL for NP0028569 (12-oxo-resibufogenin)

3D MOL for NP0028569 (12-oxo-resibufogenin)

3D SDF for NP0028569 (12-oxo-resibufogenin)

3D-SDF for NP0028569 (12-oxo-resibufogenin)

PDB for NP0028569 (12-oxo-resibufogenin)

3D PDB for NP0028569 (12-oxo-resibufogenin)

SMILES for NP0028569 (12-oxo-resibufogenin)

INCHI for NP0028569 (12-oxo-resibufogenin)

Structure for NP0028569 (12-oxo-resibufogenin)

3D Structure for NP0028569 (12-oxo-resibufogenin)