NP-MRD: Showing NP-Card for Certonardoside J (NP0080522)

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Record Information

Version

1.0

Created at

2022-04-29 01:31:46 UTC

Updated at

2022-04-29 01:31:47 UTC

NP-MRD ID

NP0080522

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Certonardoside J

Description

CHEMBL1208172 belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24. Certonardoside J is found in Certonardoa semiregularis. Based on a literature review very few articles have been published on CHEMBL1208172.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203312D          

 49 53  0  0  1  0            999 V2000
   -3.8560    1.2638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  3 48  1  6  0  0  0
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M  END

     RDKit          3D

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 36 37  1  1
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 41 42  1  1
 10 43  1  0
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 45105  1  0
 45106  1  0
 45107  1  0
 46108  1  1
 47109  1  0
 48110  1  6
 49111  1  0
M  END


  Mrv1652304292203312D          

 49 53  0  0  1  0            999 V2000
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   -4.4080    1.8769    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.3461    2.8330    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7941    2.2199    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0490    1.4353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9871    2.3915    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7322    3.1761    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2842    3.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0912    3.6176    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6432    4.2307    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3883    5.0154    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6037    4.7604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1729    5.2703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1333    5.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9252    3.3476    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3732    2.7345    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6281    1.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4351    1.7784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3805    3.0701    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2943    3.8905    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5127    4.0621    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8483    4.8157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9074    4.4426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0950    2.6576    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8094    3.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5239    2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2384    3.0701    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9529    2.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6673    3.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3818    2.6576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0963    3.0701    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0963    3.8951    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3818    4.3076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8107    4.3076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5252    3.8951    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5252    3.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8107    2.6576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2397    4.3076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9542    3.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8107    5.1326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2384    3.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9529    4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5239    4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0950    1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2399    2.1825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2421    1.6068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7051    3.2746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2150    1.7053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
 12 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  6  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  6  0  0  0
 21 24  1  6  0  0  0
 20 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 28 27  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 31  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 32 38  1  0  0  0  0
 36 39  1  6  0  0  0
 39 40  1  0  0  0  0
 35 41  1  1  0  0  0
 28 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 25 45  1  1  0  0  0
 17 46  1  6  0  0  0
  5 47  1  6  0  0  0
  3 48  1  6  0  0  0
  2 49  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0080522

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1CO[C@@H](OCC[C@@H](CC[C@@H](C)[C@H]2[C@@H](O)[C@@H](O)[C@H]3[C@@H]4C[C@H](OS(O)(=O)=O)[C@H]5[C@@H](O)[C@@H](O)CC[C@]5(C)[C@H]4CC[C@]23C)C(C)C)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C35H62O13S/c1-17(2)19(11-14-46-33-32(41)29(38)24(45-6)16-47-33)8-7-18(3)25-30(39)31(40)26-20-15-23(48-49(42,43)44)27-28(37)22(36)10-13-34(27,4)21(20)9-12-35(25,26)5/h17-33,36-41H,7-16H2,1-6H3,(H,42,43,44)/t18-,19-,20-,21+,22+,23+,24-,25+,26-,27+,28+,29+,30-,31+,32-,33-,34-,35-/m1/s1

> <INCHI_KEY>
WTIPFRWIYJVRGS-XCIXNCJBSA-N

> <FORMULA>
C35H62O13S

> <MOLECULAR_WEIGHT>
722.93

> <EXACT_MASS>
722.39111323

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
111

> <JCHEM_AVERAGE_POLARIZABILITY>
79.8558250910627

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1S,2R,5S,6R,7R,8S,10R,11S,12S,13R,14R,15R)-14-[(2R,5R)-5-(2-{[(2R,3R,4R,5R)-3,4-dihydroxy-5-methoxyoxan-2-yl]oxy}ethyl)-6-methylheptan-2-yl]-5,6,12,13-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-8-yl]oxidanesulfonic acid

> <ALOGPS_LOGP>
0.07

> <JCHEM_LOGP>
0.33701587982229325

> <ALOGPS_LOGS>
-3.21

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.246727431220004

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.4139563346380752

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1508990314049647

> <JCHEM_POLAR_SURFACE_AREA>
212.66999999999996

> <JCHEM_REFRACTIVITY>
177.7708000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.42e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2R,5S,6R,7R,8S,10R,11S,12S,13R,14R,15R)-14-[(2R,5R)-5-(2-{[(2R,3R,4R,5R)-3,4-dihydroxy-5-methoxyoxan-2-yl]oxy}ethyl)-6-methylheptan-2-yl]-5,6,12,13-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-8-yl]oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -7.198   2.359   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.228   3.503   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.752   4.968   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.246   5.288   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.216   4.144   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.692   2.679   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.709   4.464   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.233   5.929   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.264   7.073   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.770   6.753   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -6.801   7.897   0.000  0.00  0.00           O+0
HETATM   12  S   UNK     0      -6.325   9.362   0.000  0.00  0.00           S+0
HETATM   13  O   UNK     0      -4.860   8.886   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -7.789   9.838   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      -5.849  10.827   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.727   6.249   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.697   5.104   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.172   3.640   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.679   3.320   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.710   5.731   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.549   7.262   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.957   7.583   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.583   8.989   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       1.694   8.293   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.044   4.961   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.378   5.731   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.711   4.961   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.045   5.731   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.379   4.961   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.712   5.731   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      10.046   4.961   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      11.380   5.731   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.380   7.271   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      10.046   8.041   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      12.713   8.041   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      14.047   7.271   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.047   5.731   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.713   4.961   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      15.381   8.041   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      16.714   7.271   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      12.713   9.581   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       6.045   7.271   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.379   8.041   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.711   8.041   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.044   3.421   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       0.448   4.074   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -4.185   2.999   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -8.783   6.113   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      -9.735   3.183   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   49                                                  
CONECT    3    2    4   48                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   47                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   19                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12                                                            
CONECT   16    8   17   22                                                  
CONECT   17   16   18   20   46                                             
CONECT   18   17   19                                                       
CONECT   19   18    7                                                       
CONECT   20   17   21   25                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   16   23                                                  
CONECT   23   22                                                            
CONECT   24   21                                                            
CONECT   25   20   26   45                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   42                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   38                                                  
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   41                                                  
CONECT   36   35   37   39                                                  
CONECT   37   36   38                                                       
CONECT   38   37   32                                                       
CONECT   39   36   40                                                       
CONECT   40   39                                                            
CONECT   41   35                                                            
CONECT   42   28   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   25                                                            
CONECT   46   17                                                            
CONECT   47    5                                                            
CONECT   48    3                                                            
CONECT   49    2                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₆₂O₁₃S

Average Mass

722.9300 Da

Monoisotopic Mass

722.39111 Da

IUPAC Name

[(1S,2R,5S,6R,7R,8S,10R,11S,12S,13R,14R,15R)-14-[(2R,5R)-5-(2-{[(2R,3R,4R,5R)-3,4-dihydroxy-5-methoxyoxan-2-yl]oxy}ethyl)-6-methylheptan-2-yl]-5,6,12,13-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-8-yl]oxidanesulfonic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CO[C@@H]1CO[C@@H](OCC[C@@H](CC[C@@H](C)[C@H]2[C@@H](O)[C@@H](O)[C@H]3[C@@H]4C[C@H](OS(O)(=O)=O)[C@H]5[C@@H](O)[C@@H](O)CC[C@]5(C)[C@H]4CC[C@]23C)C(C)C)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C35H62O13S/c1-17(2)19(11-14-46-33-32(41)29(38)24(45-6)16-47-33)8-7-18(3)25-30(39)31(40)26-20-15-23(48-49(42,43)44)27-28(37)22(36)10-13-34(27,4)21(20)9-12-35(25,26)5/h17-33,36-41H,7-16H2,1-6H3,(H,42,43,44)/t18-,19-,20-,21+,22+,23+,24-,25+,26-,27+,28+,29+,30-,31+,32-,33-,34-,35-/m1/s1

InChI Key

WTIPFRWIYJVRGS-XCIXNCJBSA-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
Certonardoa semiregularis	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Stigmastanes and derivatives

Direct Parent

Stigmastanes and derivatives

Alternative Parents

Substituents

C24-propyl-sterol-skeleton
Stigmastane-skeleton
Triterpenoid
Sulfated steroid skeleton
3-hydroxysteroid
4-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
3-beta-hydroxysteroid
16-hydroxysteroid
16-beta-hydroxysteroid
Glycosyl compound
O-glycosyl compound
Alkyl sulfate
Sulfuric acid ester
Sulfate-ester
Oxane
Sulfuric acid monoester
Monosaccharide
Organic sulfuric acid or derivatives
Cyclic alcohol
Secondary alcohol
Polyol
Acetal
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen 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	0.07	ALOGPS
logP	0.34	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	-1.4	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	212.67 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	177.77 m³·mol⁻¹	ChemAxon
Polarizability	79.86 Å³	ChemAxon
Number of Rings	5	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

441265

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

505379

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Certonardoside J (NP0080522)

MOL for NP0080522 (Certonardoside J)

3D MOL for NP0080522 (Certonardoside J)

3D SDF for NP0080522 (Certonardoside J)

3D-SDF for NP0080522 (Certonardoside J)

PDB for NP0080522 (Certonardoside J)

3D PDB for NP0080522 (Certonardoside J)

SMILES for NP0080522 (Certonardoside J)

INCHI for NP0080522 (Certonardoside J)

Structure for NP0080522 (Certonardoside J)

3D Structure for NP0080522 (Certonardoside J)