NP-MRD: Showing NP-Card for cymatherelactone (NP0041095)

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Record Information

Version

2.0

Created at

2021-06-20 23:05:45 UTC

Updated at

2021-06-30 00:15:24 UTC

NP-MRD ID

NP0041095

Secondary Accession Numbers

None

Natural Product Identification

Common Name

cymatherelactone

Provided By

JEOL Database JEOL Logo

Description

cymatherelactone is found in Cymathere triplicata. cymatherelactone was first documented in 2012 (PMID: 22071135). Based on a literature review very few articles have been published on Cymatherelactone.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI

  Mrv1652306212101053D          

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M  END

     RDKit          3D

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  7 29  1  0  0  0  0
 10 34  1  0  0  0  0
 10 35  1  0  0  0  0
  3 27  1  6  0  0  0
  2 25  1  0  0  0  0
  2 26  1  0  0  0  0
  1 22  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
 16 42  1  1  0  0  0
 18 43  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0041095

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O3/c1-2-15-14-9-12(14)13-10-16-18(21-16)11(13)7-5-3-4-6-8-17(19)20-15/h5,7,11-16,18H,2-4,6,8-10H2,1H3/b7-5-/t11-,12-,13+,14+,15+,16-,18+/m0/s1

> <INCHI_KEY>
FIICQHIPIFWHRY-HFOVYDPPSA-N

> <FORMULA>
C18H26O3

> <MOLECULAR_WEIGHT>
290.403

> <EXACT_MASS>
290.188194697

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.64177194598816

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,4R,5R,12Z,14S,15R,17S)-5-ethyl-6,16-dioxatetracyclo[12.4.0.0^{2,4}.0^{15,17}]octadec-12-en-7-one

> <ALOGPS_LOGP>
3.00

> <JCHEM_LOGP>
3.3598898669999997

> <ALOGPS_LOGS>
-4.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.206391902468401

> <JCHEM_POLAR_SURFACE_AREA>
38.83

> <JCHEM_REFRACTIVITY>
81.1324

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.15e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4R,5R,12Z,14S,15R,17S)-5-ethyl-6,16-dioxatetracyclo[12.4.0.0^{2,4}.0^{15,17}]octadec-12-en-7-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
    0.9133    2.7055   -3.3523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0838    1.8080   -2.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4723    0.3953   -2.4039 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6015    0.5173   -1.5132 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6506   -0.3153   -1.7440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7415   -1.1111   -2.6684 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6979   -0.1421   -0.6708 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0402   -1.4679    0.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8555   -2.1695    0.6851 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2767   -1.3909    1.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0957   -2.1134    2.4550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2009   -1.7728    2.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7911   -0.5822    1.6360 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7287   -1.0476    0.4721 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1700   -0.9240    1.0238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0954    0.0534    2.1542 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4309    1.2911    1.8806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6748    0.2568    2.5291 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5308   -0.1873   -0.7587 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9523   -0.6784   -2.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4847   -0.5907   -1.7778 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8300    2.8375   -2.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4764    3.6953   -3.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1816    2.2850   -4.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3193    2.2815   -1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0065    1.7718   -3.2149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7842   -0.0022   -3.3781 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3641    0.5945    0.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5898    0.2798   -1.1479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4593   -2.1533   -0.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297   -1.2938    0.7495 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1979   -3.1515    1.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.3682   -0.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0399   -1.2841    2.6486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0087   -0.3759    1.5679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3407   -3.0169    3.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9242   -2.4242    2.8519 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0008    0.0613    1.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5367   -2.0925    0.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8898   -0.6043    0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4954   -1.8929    1.4196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8803    0.0160    2.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3594    0.4028    3.5488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6898    0.8651   -0.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3909   -1.6674   -2.2067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3870    0.0399   -2.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0145   -1.5474   -1.6391 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
 14 19  1  0
 19 21  1  0
  8  7  1  0
 16 15  1  0
  7  5  1  0
 14 15  1  0
  5  6  2  0
 14 13  1  0
  5  4  1  0
 19 20  1  0
  4  3  1  0
 13 12  1  0
 21  3  1  0
 13 18  1  0
  3  2  1  0
 12 11  2  0
  2  1  1  0
 18 16  1  0
 18 17  1  0
 16 17  1  0
 11 10  1  0
 21 20  1  0
 10  9  1  0
 21 47  1  1
 19 44  1  1
 20 45  1  0
 20 46  1  0
 13 38  1  6
 15 40  1  0
 15 41  1  0
 14 39  1  6
 12 37  1  0
 11 36  1  0
  9 32  1  0
  9 33  1  0
  8 30  1  0
  8 31  1  0
  7 28  1  0
  7 29  1  0
 10 34  1  0
 10 35  1  0
  3 27  1  6
  2 25  1  0
  2 26  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
 16 42  1  1
 18 43  1  1
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       0.913   2.705  -3.352  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.084   1.808  -2.627  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.472   0.395  -2.404  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.601   0.517  -1.513  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.651  -0.315  -1.744  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.741  -1.111  -2.668  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.698  -0.142  -0.671  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.040  -1.468   0.009  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.856  -2.170   0.685  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.277  -1.391   1.868  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.096  -2.113   2.455  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.201  -1.773   2.361  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.791  -0.582   1.636  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.729  -1.048   0.472  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.170  -0.924   1.024  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.095   0.053   2.154  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.431   1.291   1.881  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.675   0.257   2.529  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.531  -0.187  -0.759  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.952  -0.678  -2.124  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.485  -0.591  -1.778  0.00  0.00           C+0
HETATM   22  H   UNK     0       1.830   2.837  -2.769  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.476   3.695  -3.519  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.182   2.285  -4.327  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.319   2.281  -1.667  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.006   1.772  -3.215  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.784  -0.002  -3.378  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.364   0.595   0.067  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.590   0.280  -1.148  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.459  -2.153  -0.739  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.830  -1.294   0.750  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.198  -3.151   1.037  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.070  -2.368  -0.055  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.040  -1.284   2.649  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.009  -0.376   1.568  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.341  -3.017   3.014  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.924  -2.424   2.852  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.001   0.061   1.242  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.537  -2.092   0.195  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.890  -0.604   0.264  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.495  -1.893   1.420  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.880   0.016   2.891  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.359   0.403   3.549  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.690   0.865  -0.553  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.391  -1.667  -2.207  0.00  0.00           H+0
HETATM   46  H   UNK     0      -2.387   0.040  -2.809  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.015  -1.547  -1.639  0.00  0.00           H+0
CONECT    1    2   22   23   24                                             
CONECT    2    3    1   25   26                                             
CONECT    3    4   21    2   27                                             
CONECT    4    5    3                                                       
CONECT    5    7    6    4                                                  
CONECT    6    5                                                            
CONECT    7    8    5   28   29                                             
CONECT    8    9    7   30   31                                             
CONECT    9    8   10   32   33                                             
CONECT   10   11    9   34   35                                             
CONECT   11   12   10   36                                                  
CONECT   12   13   11   37                                                  
CONECT   13   14   12   18   38                                             
CONECT   14   19   15   13   39                                             
CONECT   15   16   14   40   41                                             
CONECT   16   15   18   17   42                                             
CONECT   17   18   16                                                       
CONECT   18   13   16   17   43                                             
CONECT   19   14   21   20   44                                             
CONECT   20   19   21   45   46                                             
CONECT   21   19    3   20   47                                             
CONECT   22    1                                                            
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    2                                                            
CONECT   26    2                                                            
CONECT   27    3                                                            
CONECT   28    7                                                            
CONECT   29    7                                                            
CONECT   30    8                                                            
CONECT   31    8                                                            
CONECT   32    9                                                            
CONECT   33    9                                                            
CONECT   34   10                                                            
CONECT   35   10                                                            
CONECT   36   11                                                            
CONECT   37   12                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   15                                                            
CONECT   41   15                                                            
CONECT   42   16                                                            
CONECT   43   18                                                            
CONECT   44   19                                                            
CONECT   45   20                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  100    0
END

RDKit          3D

47 50  0  0  0  0  0  0  0  0999 V2000
    0.9133    2.7055   -3.3523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0838    1.8080   -2.6270 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4723    0.3953   -2.4039 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6015    0.5173   -1.5132 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6506   -0.3153   -1.7440 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7415   -1.1111   -2.6684 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6979   -0.1421   -0.6708 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0402   -1.4679    0.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8555   -2.1695    0.6851 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2767   -1.3909    1.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0957   -2.1134    2.4550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2009   -1.7728    2.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7911   -0.5822    1.6360 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7287   -1.0476    0.4721 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1700   -0.9240    1.0238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0954    0.0534    2.1542 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4309    1.2911    1.8806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6748    0.2568    2.5291 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5308   -0.1873   -0.7587 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9523   -0.6784   -2.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4847   -0.5907   -1.7778 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8300    2.8375   -2.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4764    3.6953   -3.5190 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1816    2.2850   -4.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3193    2.2815   -1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0065    1.7718   -3.2149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7842   -0.0022   -3.3781 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3641    0.5945    0.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5898    0.2798   -1.1479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4593   -2.1533   -0.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297   -1.2938    0.7495 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1979   -3.1515    1.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.3682   -0.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0399   -1.2841    2.6486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0087   -0.3759    1.5679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3407   -3.0169    3.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9242   -2.4242    2.8519 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0008    0.0613    1.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5367   -2.0925    0.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8898   -0.6043    0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4954   -1.8929    1.4196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8803    0.0160    2.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3594    0.4028    3.5488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6898    0.8651   -0.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3909   -1.6674   -2.2067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3870    0.0399   -2.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0145   -1.5474   -1.6391 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
 14 19  1  0
 19 21  1  0
  8  7  1  0
 16 15  1  0
  7  5  1  0
 14 15  1  0
  5  6  2  0
 14 13  1  0
  5  4  1  0
 19 20  1  0
  4  3  1  0
 13 12  1  0
 21  3  1  0
 13 18  1  0
  3  2  1  0
 12 11  2  0
  2  1  1  0
 18 16  1  0
 18 17  1  0
 16 17  1  0
 11 10  1  0
 21 20  1  0
 10  9  1  0
 21 47  1  1
 19 44  1  1
 20 45  1  0
 20 46  1  0
 13 38  1  6
 15 40  1  0
 15 41  1  0
 14 39  1  6
 12 37  1  0
 11 36  1  0
  9 32  1  0
  9 33  1  0
  8 30  1  0
  8 31  1  0
  7 28  1  0
  7 29  1  0
 10 34  1  0
 10 35  1  0
  3 27  1  6
  2 25  1  0
  2 26  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
 16 42  1  1
 18 43  1  1
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₆O₃

Average Mass

290.4030 Da

Monoisotopic Mass

290.18819 Da

IUPAC Name

(1S,2S,4R,5R,12Z,14S,15R,17S)-5-ethyl-6,16-dioxatetracyclo[12.4.0.0^{2,4}.0^{15,17}]octadec-12-en-7-one

Traditional Name

(1S,2S,4R,5R,12Z,14S,15R,17S)-5-ethyl-6,16-dioxatetracyclo[12.4.0.0^{2,4}.0^{15,17}]octadec-12-en-7-one

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C18H26O3/c1-2-15-14-9-12(14)13-10-16-18(21-16)11(13)7-5-3-4-6-8-17(19)20-15/h5,7,11-16,18H,2-4,6,8-10H2,1H3/b7-5-/t11-,12-,13+,14+,15+,16-,18+/m0/s1

InChI Key

FIICQHIPIFWHRY-HFOVYDPPSA-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
Cymathere triplicata	JEOL database	Choi, H., et al, Phytochem. 73, 134 (2012)

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	ALOGPS
logP	3.36	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	38.83 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	81.13 m³·mol⁻¹	ChemAxon
Polarizability	32.64 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

29214789

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Choi H, Proteau PJ, Byrum T, Pereira AR, Gerwick WH: Cymatherelactone and cymatherols A-C, polycyclic oxylipins from the marine brown alga Cymathere triplicata. Phytochemistry. 2012 Jan;73(1):134-41. doi: 10.1016/j.phytochem.2011.09.014. Epub 2011 Nov 7. [PubMed:22071135 ]
Choi, H., et al. (2012). Choi, H., et al, Phytochem. 73, 134 (2012). Phytochem..

Showing NP-Card for cymatherelactone (NP0041095)

MOL for NP0041095 (cymatherelactone)

3D MOL for NP0041095 (cymatherelactone)

3D SDF for NP0041095 (cymatherelactone)

3D-SDF for NP0041095 (cymatherelactone)

PDB for NP0041095 (cymatherelactone)

3D PDB for NP0041095 (cymatherelactone)

SMILES for NP0041095 (cymatherelactone)

INCHI for NP0041095 (cymatherelactone)

Structure for NP0041095 (cymatherelactone)

3D Structure for NP0041095 (cymatherelactone)