NP-MRD: Showing NP-Card for 5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid (NP0322935)

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Record Information

Version

2.0

Created at

2022-09-12 02:01:42 UTC

Updated at

2022-09-12 02:01:42 UTC

NP-MRD ID

NP0322935

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid

Description

5-({4,5-Dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,13,14,14a,14b-icosahydropicen-3-yl)oxy]oxane-2-carboxylic acid belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton. 5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid is found in Ononis spinosa. 5-({4,5-Dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,13,14,14a,14b-icosahydropicen-3-yl)oxy]oxane-2-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251514122D          

 64 71  0  0  0  0            999 V2000
   12.2645    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4395    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2645    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.9645    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.2020    3.9849    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
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  6 13  1  0  0  0  0
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  2 63  1  0  0  0  0
 63 64  1  0  0  0  0
M  END

     RDKit          3D

138145  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004251514122D          

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M  END
> <DATABASE_ID>
NP0322935

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(O)C(O)COC2OC2C(O)C(O)C(OC2OC2CCC3(C)C(CCC4(C)C3C(=O)CC3=C5CC(C)(C)CC(O)C5(C)CCC43C)C2(C)C)C(O)=O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C47H74O17/c1-20-28(51)30(53)33(56)39(60-20)63-35-29(52)24(49)19-59-40(35)64-36-32(55)31(54)34(38(57)58)62-41(36)61-27-11-12-45(7)25(43(27,4)5)10-13-47(9)37(45)23(48)16-21-22-17-42(2,3)18-26(50)44(22,6)14-15-46(21,47)8/h20,24-37,39-41,49-56H,10-19H2,1-9H3,(H,57,58)

> <INCHI_KEY>
KHQMXKRETWUVJU-UHFFFAOYSA-N

> <FORMULA>
C47H74O17

> <MOLECULAR_WEIGHT>
911.092

> <EXACT_MASS>
910.492600923

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
138

> <JCHEM_AVERAGE_POLARIZABILITY>
97.13139564502941

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,13,14,14a,14b-icosahydropicen-3-yl)oxy]oxane-2-carboxylic acid

> <ALOGPS_LOGP>
2.21

> <JCHEM_LOGP>
1.8904339090000053

> <ALOGPS_LOGS>
-3.60

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.05800285638441

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.4135826527997724

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6121826294395296

> <JCHEM_POLAR_SURFACE_AREA>
271.59

> <JCHEM_REFRACTIVITY>
223.42460000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.29e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1H-picen-3-yl)oxy]oxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      22.894   6.105   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.354   6.105   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      20.584   4.771   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      19.044   4.771   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      18.274   3.437   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      19.044   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.584   2.104   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      21.354   3.437   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      21.354   0.770   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      22.894   0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      20.584  -0.564   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      19.044  -0.564   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      18.274   0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      16.734   0.770   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      15.964  -0.564   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.734  -1.897   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      18.274  -1.897   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      15.964  -3.231   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      16.734  -4.565   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      14.424  -3.231   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      13.654  -1.897   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      14.424  -0.564   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.654   0.770   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.264  -0.564   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.034   3.437   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.494   3.437   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       7.494  -1.897   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       1.334   3.437   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       5.023   3.635   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      11.397   3.643   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      12.650   2.920   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      13.654  -4.565   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      12.114  -4.565   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0      14.424  -5.898   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0      18.274   6.105   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      16.734   6.105   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      19.044   7.438   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      18.274   8.772   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0      20.584   7.438   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0      21.354   8.772   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   63                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   59                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    6   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   56                                                  
CONECT   21   20   22                                                       
CONECT   22   21   15   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   53                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   34                                             
CONECT   28   27                                                            
CONECT   29   27   30   53                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   51                                             
CONECT   33   32                                                            
CONECT   34   32   27   35                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   51                                                  
CONECT   39   38   40   47                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43   44                                             
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   41   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   39   48   49                                             
CONECT   48   47                                                            
CONECT   49   47   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   32   38   52                                             
CONECT   52   51                                                            
CONECT   53   29   24   54   55                                             
CONECT   54   53                                                            
CONECT   55   53                                                            
CONECT   56   20   57   58                                                  
CONECT   57   56                                                            
CONECT   58   56                                                            
CONECT   59    4   60   61                                                  
CONECT   60   59                                                            
CONECT   61   59   62   63                                                  
CONECT   62   61                                                            
CONECT   63   61    2   64                                                  
CONECT   64   63                                                            
MASTER        0    0    0    0    0    0    0    0   64    0  142    0
END

View in JSmol

Synonyms

Value	Source
5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,13,14,14a,14b-icosahydropicen-3-yl)oxy]oxane-2-carboxylate	Generator

Chemical Formula

C₄₇H₇₄O₁₇

Average Mass

911.0920 Da

Monoisotopic Mass

910.49260 Da

IUPAC Name

5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,13,14,14a,14b-icosahydropicen-3-yl)oxy]oxane-2-carboxylic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(O)C(O)COC2OC2C(O)C(O)C(OC2OC2CCC3(C)C(CCC4(C)C3C(=O)CC3=C5CC(C)(C)CC(O)C5(C)CCC43C)C2(C)C)C(O)=O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C47H74O17/c1-20-28(51)30(53)33(56)39(60-20)63-35-29(52)24(49)19-59-40(35)64-36-32(55)31(54)34(38(57)58)62-41(36)61-27-11-12-45(7)25(43(27,4)5)10-13-47(9)37(45)23(48)16-21-22-17-42(2,3)18-26(50)44(22,6)14-15-46(21,47)8/h20,24-37,39-41,49-56H,10-19H2,1-9H3,(H,57,58)

InChI Key

KHQMXKRETWUVJU-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
Ononis spinosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Triterpene saponins

Alternative Parents

Substituents

Triterpene saponin
Triterpenoid
Oligosaccharide
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Glycosyl compound
O-glycosyl compound
Beta-hydroxy acid
Hydroxy acid
Pyran
Oxane
Cyclic alcohol
Secondary alcohol
Ketone
Polyol
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Oxacycle
Acetal
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Alcohol
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	2.21	ALOGPS
logP	1.89	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	3.41	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	271.59 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	223.42 m³·mol⁻¹	ChemAxon
Polarizability	97.13 Å³	ChemAxon
Number of Rings	8	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

76401289

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid (NP0322935)

MOL for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

3D MOL for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

3D SDF for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

3D-SDF for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

PDB for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

3D PDB for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

SMILES for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

INCHI for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

Structure for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)

3D Structure for NP0322935 (5-({4,5-dihydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,13,14a-dodecahydro-1h-picen-3-yl)oxy]oxane-2-carboxylic acid)