NP-MRD: Showing NP-Card for Karajinone A (NP0074143)

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Record Information

Version

2.0

Created at

2022-04-28 19:18:43 UTC

Updated at

2022-04-28 19:18:43 UTC

NP-MRD ID

NP0074143

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Karajinone A

Description

(1R,2R,3R,4S,5S,7R,9R,10R,11S,12R,13S,15R)-2,4,7-tris(acetyloxy)-12-[(acetyloxy)methyl]-5,9,12-trimethyl-8-oxo-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]Heptadecan-15-yl benzoate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. Karajinone A is found in Euphorbia decipiens and Euphorbia polycaulis. Based on a literature review very few articles have been published on (1R,2R,3R,4S,5S,7R,9R,10R,11S,12R,13S,15R)-2,4,7-tris(acetyloxy)-12-[(acetyloxy)methyl]-5,9,12-trimethyl-8-oxo-17-oxapentacyclo[7.6.2.0¹,¹⁰.0³,⁷.0¹¹,¹³]Heptadecan-15-yl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282221182D          

 47 52  0  0  1  0            999 V2000
    2.0712    0.8967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2514    0.0916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7461    1.3712    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8878    2.1840    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4133    2.8588    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6005    3.0005    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6602    2.1777    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2585    1.0384    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8166    0.3417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6885    1.6461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9256    2.5260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9774    1.7146    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2350    2.0743    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1753    2.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8581    3.3602    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7984    4.1831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0559    4.5428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9923    3.1535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0520    3.9763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    4.4394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2947    1.2514    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    5.3007    3.7892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7981    0.5479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5371    0.1812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2242    0.6379    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891   -0.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  1  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  1  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  6  0  0  0
  7 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 14  1  0  0  0  0
  6 15  1  0  0  0  0
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 25 31  1  1  0  0  0
  5 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
  4 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
  3 38  1  0  0  0  0
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 36 40  1  1  0  0  0
 40 41  1  0  0  0  0
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 41 43  1  0  0  0  0
  3 44  1  1  0  0  0
 44 45  1  0  0  0  0
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 45 47  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282221182D          

 47 52  0  0  1  0            999 V2000
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    1.6005    3.0005    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6602    2.1777    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2585    1.0384    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8166    0.3417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6885    1.6461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9256    2.5260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9774    1.7146    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2350    2.0743    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1753    2.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8581    3.3602    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7984    4.1831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0559    4.5428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0037    5.3656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6268    4.0797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5671    3.2569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2499    2.7937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9923    3.1535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0520    3.9763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    4.4394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2947    1.2514    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4258    0.8496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1341    1.2727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1218    2.0976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8301    2.5207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4013    2.4994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4258    0.4369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8552    3.5555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4728    4.2865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6485    4.3209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9147    4.9832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7045    2.3004    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0676    1.5596    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4753    0.9853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8804    1.4179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0904    3.0296    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9148    3.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3007    3.7892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3534    2.3612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7981    0.5479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5371    0.1812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2242    0.6379    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891   -0.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  1  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  1  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  6  0  0  0
  7 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 14  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 13 25  1  0  0  0  0
 12 25  1  1  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 25 31  1  1  0  0  0
  5 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
  4 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
  3 38  1  0  0  0  0
 37 39  1  1  0  0  0
 36 40  1  1  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
  3 44  1  1  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0074143

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@@]2(OC(C)=O)[C@H]([C@H]1OC(C)=O)[C@@H](OC(C)=O)[C@@]13CO[C@](C)([C@@H]1[C@@H]1[C@H](C[C@H]3OC(=O)C3=CC=CC=C3)[C@@]1(C)COC(C)=O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H42O12/c1-17-14-35(47-21(5)39)26(27(17)44-19(3)37)29(45-20(4)38)34-16-43-33(7,31(35)41)28(34)25-23(32(25,6)15-42-18(2)36)13-24(34)46-30(40)22-11-9-8-10-12-22/h8-12,17,23-29H,13-16H2,1-7H3/t17-,23-,24+,25-,26+,27-,28-,29+,32+,33+,34+,35+/m0/s1

> <INCHI_KEY>
HBLTZTMUODEVKI-PXJIEZJASA-N

> <FORMULA>
C35H42O12

> <MOLECULAR_WEIGHT>
654.709

> <EXACT_MASS>
654.267626792

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
66.39784595596839

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,4S,5S,7R,9R,10R,11S,12R,13S,15R)-2,4,7-tris(acetyloxy)-12-[(acetyloxy)methyl]-5,9,12-trimethyl-8-oxo-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-15-yl benzoate

> <ALOGPS_LOGP>
3.35

> <JCHEM_LOGP>
2.7894232826666654

> <ALOGPS_LOGS>
-4.73

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.221322245284558

> <JCHEM_POLAR_SURFACE_AREA>
157.8

> <JCHEM_REFRACTIVITY>
160.24540000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.21e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,4S,5S,7R,9R,10R,11S,12R,13S,15R)-2,4,7-tris(acetyloxy)-12-[(acetyloxy)methyl]-5,9,12-trimethyl-8-oxo-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-15-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       3.866   1.674   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.203   0.171   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.126   2.560   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.391   4.077   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.505   5.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.988   5.601   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.099   4.065   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.349   1.938   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.524   0.638   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.285   3.073   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.728   4.715   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.825   3.200   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.439   3.872   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.327   5.408   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.602   6.272   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.490   7.808   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.104   8.480   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.007  10.016   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.170   7.615   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.059   6.079   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.333   5.215   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.719   5.886   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.830   7.422   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.556   8.287   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.550   2.336   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.795   1.586   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.117   2.376   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -2.094   3.915   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.416   4.705   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -0.749   4.666   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.795   0.816   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.330   6.637   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.616   8.002   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.077   8.066   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       5.441   9.302   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.915   4.294   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.593   2.911   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.487   1.839   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.110   2.647   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       7.635   5.655   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       9.174   5.712   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       9.895   7.073   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       9.993   4.408   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       5.223   1.023   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       6.603   0.338   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       7.885   1.191   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       6.700  -1.199   0.000  0.00  0.00           C+0
CONECT    1    2    3    8                                                  
CONECT    2    1                                                            
CONECT    3    1    4   38   44                                             
CONECT    4    3    5   36                                                  
CONECT    5    4    6   32                                                  
CONECT    6    5    7   11   15                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    1    9   10                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    6                                                       
CONECT   12    7   13   25                                                  
CONECT   13   12   14   25                                                  
CONECT   14   13   15                                                       
CONECT   15   14    6   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   13   12   26   31                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   25                                                            
CONECT   32    5   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36    4   37   40                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37    3                                                       
CONECT   39   37                                                            
CONECT   40   36   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44    3   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  104    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,3R,4S,5S,7R,9R,10R,11S,12R,13S,15R)-2,4,7-Tris(acetyloxy)-12-[(acetyloxy)methyl]-5,9,12-trimethyl-8-oxo-17-oxapentacyclo[7.6.2.0,.0,.0,]heptadecan-15-yl benzoic acid	Generator

Chemical Formula

C₃₅H₄₂O₁₂

Average Mass

654.7090 Da

Monoisotopic Mass

654.26763 Da

IUPAC Name

(1R,2R,3R,4S,5S,7R,9R,10R,11S,12R,13S,15R)-2,4,7-tris(acetyloxy)-12-[(acetyloxy)methyl]-5,9,12-trimethyl-8-oxo-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-15-yl benzoate

Traditional Name

(1R,2R,3R,4S,5S,7R,9R,10R,11S,12R,13S,15R)-2,4,7-tris(acetyloxy)-12-[(acetyloxy)methyl]-5,9,12-trimethyl-8-oxo-17-oxapentacyclo[7.6.2.0^{1,10}.0^{3,7}.0^{11,13}]heptadecan-15-yl benzoate

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@@]2(OC(C)=O)[C@H]([C@H]1OC(C)=O)[C@@H](OC(C)=O)[C@@]13CO[C@](C)([C@@H]1[C@@H]1[C@H](C[C@H]3OC(=O)C3=CC=CC=C3)[C@@]1(C)COC(C)=O)C2=O

InChI Identifier

InChI=1S/C35H42O12/c1-17-14-35(47-21(5)39)26(27(17)44-19(3)37)29(45-20(4)38)34-16-43-33(7,31(35)41)28(34)25-23(32(25,6)15-42-18(2)36)13-24(34)46-30(40)22-11-9-8-10-12-22/h8-12,17,23-29H,13-16H2,1-7H3/t17-,23-,24+,25-,26+,27-,28-,29+,32+,33+,34+,35+/m0/s1

InChI Key

HBLTZTMUODEVKI-PXJIEZJASA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Euphorbia decipiens	Plant	KNApSAcK
Euphorbia polycaulis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Aromatic monoterpenoid
Benzoate ester
Carane monoterpenoid
Monoterpenoid
Benzoic acid or derivatives
Benzoyl
Alpha-acyloxy ketone
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Ketone
Carboxylic acid ester
Ether
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.35	ALOGPS
logP	2.79	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	157.8 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	160.25 m³·mol⁻¹	ChemAxon
Polarizability	66.4 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15381527

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Karajinone A (NP0074143)

MOL for NP0074143 (Karajinone A)

3D MOL for NP0074143 (Karajinone A)

3D SDF for NP0074143 (Karajinone A)

3D-SDF for NP0074143 (Karajinone A)

PDB for NP0074143 (Karajinone A)

3D PDB for NP0074143 (Karajinone A)

SMILES for NP0074143 (Karajinone A)

INCHI for NP0074143 (Karajinone A)

Structure for NP0074143 (Karajinone A)

3D Structure for NP0074143 (Karajinone A)