NP-MRD: Showing NP-Card for (-)-Sublanceoside D2 (NP0072382)

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Record Information

Version

2.0

Created at

2022-04-28 17:44:04 UTC

Updated at

2022-04-28 17:44:04 UTC

NP-MRD ID

NP0072382

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Sublanceoside D2

Description

(4S,5R,7R,8R,13R,16S,19R,22R)-7-hydroxy-8-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4R,5S,6S)-4-methoxy-6-methyl-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]Docosa-1(21),10-dien-14-one belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. (-)-Sublanceoside D2 is found in Cynanchum sublanceolatum and Vincetoxicum sublanceolatum. Based on a literature review very few articles have been published on (4S,5R,7R,8R,13R,16S,19R,22R)-7-hydroxy-8-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4R,5S,6S)-4-methoxy-6-methyl-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0⁴,¹³.0⁵,¹⁰.0¹⁹,²²]Docosa-1(21),10-dien-14-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219442D          

 66 74  0  0  1  0            999 V2000
    5.4394    1.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.6280   -1.1910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1386   -0.5268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4691    0.2291    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2890    0.3208    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6195    1.0767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7996    0.9850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2364    1.0206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5494    1.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7295    1.3856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  9 11  1  6  0  0  0
  8 12  1  6  0  0  0
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 14 15  2  0  0  0  0
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 18 19  1  0  0  0  0
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  7 21  1  0  0  0  0
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 17 24  1  0  0  0  0
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  2 26  1  6  0  0  0
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 45 63  1  1  0  0  0
 37 64  1  6  0  0  0
 29 65  1  6  0  0  0
  1 66  1  1  0  0  0
M  END

     RDKit          3D

136144  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652304282219442D          

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M  END
> <DATABASE_ID>
NP0072382

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1C[C@H](O[C@H]2[C@@H](O)C[C@H](O[C@H]3[C@@H](O)C[C@H](O[C@@H]4CC5=CC[C@@H]6[C@H](CCC7=CO[C@@]8(C)OC[C@@H](OC6=O)[C@@H]78)[C@@]5(C)C[C@H]4O)O[C@@H]3C)O[C@@H]2C)O[C@@H](C)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C46H70O20/c1-19-40(64-34-13-27(49)41(20(2)59-34)65-35-14-30(55-6)42(21(3)60-35)66-44-39(53)38(52)37(51)31(16-47)63-44)26(48)12-33(58-19)61-29-11-23-8-9-24-25(45(23,4)15-28(29)50)10-7-22-17-56-46(5)36(22)32(18-57-46)62-43(24)54/h8,17,19-21,24-42,44,47-53H,7,9-16,18H2,1-6H3/t19-,20-,21+,24-,25+,26+,27+,28-,29-,30-,31-,32-,33+,34+,35+,36-,37+,38+,39-,40-,41-,42+,44+,45+,46+/m1/s1

> <INCHI_KEY>
QWYNWYFFARMRAP-IWDYJTCPSA-N

> <FORMULA>
C46H70O20

> <MOLECULAR_WEIGHT>
943.046

> <EXACT_MASS>
942.446044654

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
136

> <JCHEM_AVERAGE_POLARIZABILITY>
98.20937270707125

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,5R,7R,8R,13R,16S,19R,22R)-7-hydroxy-8-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4R,5S,6S)-4-methoxy-6-methyl-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0^{4,13}.0^{5,10}.0^{19,22}]docosa-1(21),10-dien-14-one

> <ALOGPS_LOGP>
0.19

> <JCHEM_LOGP>
0.4885612166666664

> <ALOGPS_LOGS>
-3.30

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.051212803216234

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.189949803458164

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083565219918

> <JCHEM_POLAR_SURFACE_AREA>
269.43999999999994

> <JCHEM_REFRACTIVITY>
222.72180000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.72e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S,5R,7R,8R,13R,16S,19R,22R)-7-hydroxy-8-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4R,5S,6S)-4-methoxy-6-methyl-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.0^{4,13}.0^{5,10}.0^{19,22}]docosa-1(21),10-dien-14-one

> <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      10.154   2.181   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.067   0.941   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.450  -0.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.920  -0.641   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.303  -2.052   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.772  -2.223   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.859  -0.983   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.476   0.428   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.006   0.599   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.623   2.010   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.093   1.839   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.041   1.905   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.759   2.758   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.228   2.586   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.323   3.958   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.832   3.576   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.734   2.039   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.166   1.472   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.069  -0.065   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.982  -1.305   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.479  -1.668   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.650  -3.198   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.577  -0.448   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.248   0.853   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.697   2.606   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.598   1.112   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      13.511  -0.127   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      15.041   0.044   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      15.955  -1.196   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.338  -2.607   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      13.808  -2.778   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.894  -1.538   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      13.191  -4.189   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      16.251  -3.847   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      15.635  -5.258   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      16.548  -6.498   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      15.931  -7.909   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      14.401  -8.080   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.487  -6.840   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      14.104  -5.429   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      11.957  -7.011   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      13.784  -9.491   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      14.697 -10.731   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      16.228 -10.560   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      17.141 -11.799   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      16.524 -13.210   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      14.994 -13.382   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      14.080 -12.142   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      14.377 -14.793   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      12.846 -14.964   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      17.438 -14.450   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      18.968 -14.279   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      19.882 -15.519   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      21.412 -15.348   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      22.029 -13.937   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      21.115 -12.697   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      19.585 -12.868   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      21.732 -11.286   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      23.263 -11.115   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      23.559 -13.765   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      22.325 -16.587   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0      19.265 -16.930   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0      18.671 -11.628   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0      16.845  -9.149   0.000  0.00  0.00           O+0
HETATM   65  C   UNK     0      17.485  -1.025   0.000  0.00  0.00           C+0
HETATM   66  O   UNK     0      10.771   3.592   0.000  0.00  0.00           O+0
CONECT    1    2   10   66                                                  
CONECT    2    1    3   26                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   21                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8    4   10   11                                             
CONECT   10    9    1                                                       
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   24   25                                             
CONECT   18   17   14   19                                                  
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20    7   22                                                  
CONECT   22   21                                                            
CONECT   23   19   24                                                       
CONECT   24   23   17                                                       
CONECT   25   17                                                            
CONECT   26    2   27                                                       
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   65                                                  
CONECT   30   29   31   34                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31   27                                                       
CONECT   33   31                                                            
CONECT   34   30   35                                                       
CONECT   35   34   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   64                                                  
CONECT   38   37   39   42                                                  
CONECT   39   38   40   41                                                  
CONECT   40   39   35                                                       
CONECT   41   39                                                            
CONECT   42   38   43                                                       
CONECT   43   42   44   48                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46   63                                                  
CONECT   46   45   47   51                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47   43                                                       
CONECT   49   47   50                                                       
CONECT   50   49                                                            
CONECT   51   46   52                                                       
CONECT   52   51   53   57                                                  
CONECT   53   52   54   62                                                  
CONECT   54   53   55   61                                                  
CONECT   55   54   56   60                                                  
CONECT   56   55   57   58                                                  
CONECT   57   56   52                                                       
CONECT   58   56   59                                                       
CONECT   59   58                                                            
CONECT   60   55                                                            
CONECT   61   54                                                            
CONECT   62   53                                                            
CONECT   63   45                                                            
CONECT   64   37                                                            
CONECT   65   29                                                            
CONECT   66    1                                                            
MASTER        0    0    0    0    0    0    0    0   66    0  148    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₆H₇₀O₂₀

Average Mass

943.0460 Da

Monoisotopic Mass

942.44604 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CO[C@@H]1C[C@H](O[C@H]2[C@@H](O)C[C@H](O[C@H]3[C@@H](O)C[C@H](O[C@@H]4CC5=CC[C@@H]6[C@H](CCC7=CO[C@@]8(C)OC[C@@H](OC6=O)[C@@H]78)[C@@]5(C)C[C@H]4O)O[C@@H]3C)O[C@@H]2C)O[C@@H](C)[C@@H]1O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C46H70O20/c1-19-40(64-34-13-27(49)41(20(2)59-34)65-35-14-30(55-6)42(21(3)60-35)66-44-39(53)38(52)37(51)31(16-47)63-44)26(48)12-33(58-19)61-29-11-23-8-9-24-25(45(23,4)15-28(29)50)10-7-22-17-56-46(5)36(22)32(18-57-46)62-43(24)54/h8,17,19-21,24-42,44,47-53H,7,9-16,18H2,1-6H3/t19-,20-,21+,24-,25+,26+,27+,28-,29-,30-,31-,32-,33+,34+,35+,36-,37+,38+,39-,40-,41-,42+,44+,45+,46+/m1/s1

InChI Key

QWYNWYFFARMRAP-IWDYJTCPSA-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
Cynanchum sublanceolatum	Plant	KNApSAcK
Vincetoxicum sublanceolatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
O-glycosyl compound
Glycosyl compound
Furofuran
Ketal
Oxane
Tetrahydrofuran
Dihydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxide
Hydrocarbon derivative
Primary alcohol
Carbonyl group
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	0.19	ALOGPS
logP	0.49	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	269.44 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	222.72 m³·mol⁻¹	ChemAxon
Polarizability	98.21 Å³	ChemAxon
Number of Rings	9	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

162872255

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Sublanceoside D2 (NP0072382)

MOL for NP0072382 ((-)-Sublanceoside D2)

3D MOL for NP0072382 ((-)-Sublanceoside D2)

3D SDF for NP0072382 ((-)-Sublanceoside D2)

3D-SDF for NP0072382 ((-)-Sublanceoside D2)

PDB for NP0072382 ((-)-Sublanceoside D2)

3D PDB for NP0072382 ((-)-Sublanceoside D2)

SMILES for NP0072382 ((-)-Sublanceoside D2)

INCHI for NP0072382 ((-)-Sublanceoside D2)

Structure for NP0072382 ((-)-Sublanceoside D2)

3D Structure for NP0072382 ((-)-Sublanceoside D2)