NP-MRD: Showing NP-Card for 1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate (NP0179517)

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Record Information

Version

2.0

Created at

2022-09-03 17:42:53 UTC

Updated at

2022-09-03 17:42:54 UTC

NP-MRD ID

NP0179517

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate

Description

14-[5-({4-[(4,5-Dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-5,6,8,10-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-12-yl acetate belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton. 1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate is found in Echinaster sepositus. 14-[5-({4-[(4,5-Dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-5,6,8,10-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-12-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231521202D          

 55 60  0  0  0  0            999 V2000
   -6.5157   -0.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5425    0.3987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8418    0.8342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8686    1.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5961    2.0478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1679    2.0943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1947    2.9188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4404    1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4136    0.8806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1143    0.4451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0875   -0.3794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3600   -0.7685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6176   -0.4086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4724    0.4035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0459   -1.0035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2287   -0.8906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9249   -2.6189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6955   -3.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784   -3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4052   -4.6989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2812   -1.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0934   -2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3737   -2.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1858   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8100   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4661   -3.8037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2146   -5.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -4.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3100   -4.1439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0332   -2.3061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -2.9574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8505   -2.4190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4350   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2471   -1.5857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8420   -2.1574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6345   -1.9281    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
 22 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 35 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 29 47  1  0  0  0  0
 34 47  1  0  0  0  0
 47 48  1  0  0  0  0
 17 49  1  0  0  0  0
 49 50  1  0  0  0  0
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 15 52  1  0  0  0  0
 52 53  1  0  0  0  0
 12 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END

     RDKit          3D

123128  0  0  0  0  0  0  0  0999 V2000
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M  END


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M  END
> <DATABASE_ID>
NP0179517

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1C(O)C(O)COC1OC1C(CO)OC(OC(CCC(C)C2CC(OC(C)=O)C3C2(C)CCC2C4(C)CCC(O)C(O)C4C(O)CC32O)C(C)C)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H68O15/c1-18(2)25(53-36-32(48)33(27(16-41)54-36)55-37-34(50-7)31(47)24(45)17-51-37)9-8-19(3)21-14-26(52-20(4)42)35-38(21,5)13-11-28-39(6)12-10-22(43)30(46)29(39)23(44)15-40(28,35)49/h18-19,21-37,41,43-49H,8-17H2,1-7H3

> <INCHI_KEY>
OTSSQSGFARMFRO-UHFFFAOYSA-N

> <FORMULA>
C40H68O15

> <MOLECULAR_WEIGHT>
788.969

> <EXACT_MASS>
788.45582149

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
123

> <JCHEM_AVERAGE_POLARIZABILITY>
86.78603376997349

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-5,6,8,10-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-12-yl acetate

> <ALOGPS_LOGP>
0.59

> <JCHEM_LOGP>
0.09358697366666646

> <ALOGPS_LOGS>
-3.31

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.865704192142026

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.209241743067475

> <JCHEM_PKA_STRONGEST_BASIC>
-2.906887638472144

> <JCHEM_POLAR_SURFACE_AREA>
234.28999999999996

> <JCHEM_REFRACTIVITY>
194.07370000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.87e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-5,6,8,10-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-12-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0     -12.163  -0.795   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -12.213   0.744   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0     -10.905   1.557   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.955   3.096   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0     -12.313   3.823   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -9.647   3.909   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -9.697   5.448   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -8.289   3.183   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -8.239   1.644   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -9.547   0.831   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -9.497  -0.708   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -8.139  -1.435   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.753  -0.763   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -6.482   0.753   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -5.686  -1.873   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.160  -1.662   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.215  -2.878   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.690  -2.668   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.744  -3.883   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.362  -2.246   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.623  -8.771   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.981  -9.498   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.289  -8.685   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.031 -11.037   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.594  -3.453   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      10.376  -8.820   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       7.867  -9.726   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       4.312  -7.735   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -3.795  -4.305   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -2.850  -5.521   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -5.321  -4.515   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      -6.412  -3.231   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      -7.928  -2.960   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      -9.038  -4.027   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0     -10.518  -3.599   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    3   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   53                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   52                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   49                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   30                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   30   47                                                  
CONECT   30   29   22   31   32                                             
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   47                                                  
CONECT   35   34   36   37   43                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   35   44                                                  
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   29   34   48                                             
CONECT   48   47                                                            
CONECT   49   17   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
CONECT   52   15   53                                                       
CONECT   53   52   12   54                                                  
CONECT   54   53   55                                                       
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  120    0
END

View in JSmol

Synonyms

Value	Source
14-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-5,6,8,10-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0,.0,]heptadecan-12-yl acetic acid	Generator
14-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-5,6,8,10-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-12-yl acetic acid	Generator

Chemical Formula

C₄₀H₆₈O₁₅

Average Mass

788.9690 Da

Monoisotopic Mass

788.45582 Da

IUPAC Name

14-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-5,6,8,10-tetrahydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-12-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1C(O)C(O)COC1OC1C(CO)OC(OC(CCC(C)C2CC(OC(C)=O)C3C2(C)CCC2C4(C)CCC(O)C(O)C4C(O)CC32O)C(C)C)C1O

InChI Identifier

InChI=1S/C40H68O15/c1-18(2)25(53-36-32(48)33(27(16-41)54-36)55-37-34(50-7)31(47)24(45)17-51-37)9-8-19(3)21-14-26(52-20(4)42)35-38(21,5)13-11-28-39(6)12-10-22(43)30(46)29(39)23(44)15-40(28,35)49/h18-19,21-37,41,43-49H,8-17H2,1-7H3

InChI Key

OTSSQSGFARMFRO-UHFFFAOYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Echinaster sepositus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal glycosides

Alternative Parents

Substituents

Steroidal glycoside
Trihydroxy bile acid, alcohol, or derivatives
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
Steroid ester
3-hydroxysteroid
4-hydroxysteroid
6-hydroxysteroid
Hydroxysteroid
Disaccharide
Glycosyl compound
O-glycosyl compound
Oxane
Cyclic alcohol
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organooxygen compound
Primary alcohol
Alcohol
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	0.59	ALOGPS
logP	0.094	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	234.29 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	194.07 m³·mol⁻¹	ChemAxon
Polarizability	86.79 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate (NP0179517)

MOL for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

3D MOL for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

3D SDF for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

3D-SDF for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

PDB for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

3D PDB for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

SMILES for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

INCHI for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

Structure for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)

3D Structure for NP0179517 (1-[5-({4-[(4,5-dihydroxy-3-methoxyoxan-2-yl)oxy]-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl}oxy)-6-methylheptan-2-yl]-3b,5,6,7-tetrahydroxy-9a,11a-dimethyl-tetradecahydrocyclopenta[a]phenanthren-3-yl acetate)