NP-MRD: Showing NP-Card for Cassiaside B2 (NP0047474)

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Record Information

Version

2.0

Created at

2022-03-17 20:40:48 UTC

Updated at

2022-03-17 20:40:48 UTC

NP-MRD ID

NP0047474

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cassiaside B2

Description

Cassiaside B2 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. Cassiaside B2 is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Cassiaside B2 has been detected, but not quantified in, a few different foods, such as coffee and coffee products, herbs and spices, and pulses. Cassiaside B2 is found in Cassia tora and Senna obtusifolia. This could make cassiaside B2 a potential biomarker for the consumption of these foods.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 05061306442D          

 64 70  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.4315    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.7171   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.4315    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.4315   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.0026    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 11  1  1  0  0  0  0
 11  3  2  0  0  0  0
 12  4  2  0  0  0  0
 12  5  1  0  0  0  0
 13  4  1  0  0  0  0
 13  6  2  0  0  0  0
 14  3  1  0  0  0  0
 15  5  2  0  0  0  0
 16  6  1  0  0  0  0
 17  7  1  0  0  0  0
 18  8  1  0  0  0  0
 19 10  1  0  0  0  0
 20  9  1  0  0  0  0
 21 12  1  0  0  0  0
 21 16  2  0  0  0  0
 22 14  1  0  0  0  0
 22 15  1  0  0  0  0
 23 17  1  0  0  0  0
 24 19  1  0  0  0  0
 25 20  1  0  0  0  0
 26 18  1  0  0  0  0
 27 21  1  0  0  0  0
 27 22  2  0  0  0  0
 28 23  1  0  0  0  0
 29 24  1  0  0  0  0
 30 25  1  0  0  0  0
 31 28  1  0  0  0  0
 32 29  1  0  0  0  0
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 35 34  1  0  0  0  0
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 63 20  1  0  0  0  0
 63 39  1  0  0  0  0
 64 35  1  0  0  0  0
 64 39  1  0  0  0  0
M  END


  Mrv0541 05061306442D          

 64 70  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   11.4315   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 11  3  2  0  0  0  0
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M  END
> <DATABASE_ID>
NP0047474

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC2OC(COC3OC(CO)C(O)C(OC4OC(COC5OC(CO)C(O)C(O)C5O)C(O)C(O)C4O)C3O)C(O)C(O)C2O)=C2C(O)=C3C(=O)C=C(C)OC3=CC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C39H52O25/c1-11-3-14(42)22-15(58-11)5-12-4-13(55-2)6-16(21(12)27(22)47)59-38-32(52)29(49)24(44)19(62-38)10-57-37-34(54)35(26(46)18(8-41)61-37)64-39-33(53)30(50)25(45)20(63-39)9-56-36-31(51)28(48)23(43)17(7-40)60-36/h3-6,17-20,23-26,28-41,43-54H,7-10H2,1-2H3

> <INCHI_KEY>
HFJDWELARBQGBQ-UHFFFAOYSA-N

> <FORMULA>
C39H52O25

> <MOLECULAR_WEIGHT>
920.8152

> <EXACT_MASS>
920.279767214

> <JCHEM_ACCEPTOR_COUNT>
25

> <JCHEM_AVERAGE_POLARIZABILITY>
88.66694599996408

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
14

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-{[6-({[3,5-dihydroxy-6-(hydroxymethyl)-4-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}oxan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-8-methoxy-2-methyl-4H-benzo[g]chromen-4-one

> <ALOGPS_LOGP>
-1.15

> <JCHEM_LOGP>
-4.834346913333331

> <ALOGPS_LOGS>
-1.67

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.69258410242475

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.990019518369645

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6786130721304886

> <JCHEM_POLAR_SURFACE_AREA>
392.5900000000002

> <JCHEM_REFRACTIVITY>
203.36670000000012

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.99e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-{[6-({[3,5-dihydroxy-6-(hydroxymethyl)-4-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}oxan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-8-methoxy-2-methylbenzo[g]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      24.006  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.671   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.005   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      22.673  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.671   3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.005   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.339  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.336   8.470   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      21.339   4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.004   4.620   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      20.005  -2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      21.339   6.160   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      20.005  -0.770   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      20.005   6.930   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.671   6.930   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      16.004   6.160   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      21.339   0.000   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.337   6.160   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      18.672   6.160   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      24.006  -4.620   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      13.337   1.540   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      21.339  -4.620   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      10.669   9.240   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      22.673   3.850   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      17.338   3.850   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      18.672  -3.080   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       8.002  10.780   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      22.673   6.930   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      18.672   0.000   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0       5.335   9.240   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0      20.005   8.470   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      14.671   8.470   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0      21.339   1.540   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      12.003   6.930   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      22.673  -0.770   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      13.337   4.620   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0       8.002   6.160   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      18.672   4.620   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0      17.338   6.930   0.000  0.00  0.00           O+0
CONECT    1   11                                                            
CONECT    2   55                                                            
CONECT    3   11   14                                                       
CONECT    4   12   13                                                       
CONECT    5   12   15                                                       
CONECT    6   13   16                                                       
CONECT    7   17   40                                                       
CONECT    8   18   41                                                       
CONECT    9   20   56                                                       
CONECT   10   19   57                                                       
CONECT   11    1    3   58                                                  
CONECT   12    4    5   21                                                  
CONECT   13    4    6   55                                                  
CONECT   14    3   22   42                                                  
CONECT   15    5   22   58                                                  
CONECT   16    6   21   59                                                  
CONECT   17    7   23   60                                                  
CONECT   18    8   26   61                                                  
CONECT   19   10   24   62                                                  
CONECT   20    9   25   63                                                  
CONECT   21   12   16   27                                                  
CONECT   22   14   15   27                                                  
CONECT   23   17   28   43                                                  
CONECT   24   19   29   44                                                  
CONECT   25   20   30   45                                                  
CONECT   26   18   35   46                                                  
CONECT   27   21   22   47                                                  
CONECT   28   23   31   48                                                  
CONECT   29   24   32   49                                                  
CONECT   30   25   33   50                                                  
CONECT   31   28   36   51                                                  
CONECT   32   29   38   52                                                  
CONECT   33   30   39   53                                                  
CONECT   34   35   37   54                                                  
CONECT   35   26   34   64                                                  
CONECT   36   31   56   60                                                  
CONECT   37   34   57   61                                                  
CONECT   38   32   59   62                                                  
CONECT   39   33   63   64                                                  
CONECT   40    7                                                            
CONECT   41    8                                                            
CONECT   42   14                                                            
CONECT   43   23                                                            
CONECT   44   24                                                            
CONECT   45   25                                                            
CONECT   46   26                                                            
CONECT   47   27                                                            
CONECT   48   28                                                            
CONECT   49   29                                                            
CONECT   50   30                                                            
CONECT   51   31                                                            
CONECT   52   32                                                            
CONECT   53   33                                                            
CONECT   54   34                                                            
CONECT   55    2   13                                                       
CONECT   56    9   36                                                       
CONECT   57   10   37                                                       
CONECT   58   11   15                                                       
CONECT   59   16   38                                                       
CONECT   60   17   36                                                       
CONECT   61   18   37                                                       
CONECT   62   19   38                                                       
CONECT   63   20   39                                                       
CONECT   64   35   39                                                       
MASTER        0    0    0    0    0    0    0    0   64    0  140    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₅₂O₂₅

Average Mass

920.8152 Da

Monoisotopic Mass

920.27977 Da

IUPAC Name

6-{[6-({[3,5-dihydroxy-6-(hydroxymethyl)-4-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}oxan-2-yl]oxy}methyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-5-hydroxy-8-methoxy-2-methyl-4H-benzo[g]chromen-4-one

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(OC2OC(COC3OC(CO)C(O)C(OC4OC(COC5OC(CO)C(O)C(O)C5O)C(O)C(O)C4O)C3O)C(O)C(O)C2O)=C2C(O)=C3C(=O)C=C(C)OC3=CC2=C1

InChI Identifier

InChI=1S/C39H52O25/c1-11-3-14(42)22-15(58-11)5-12-4-13(55-2)6-16(21(12)27(22)47)59-38-32(52)29(49)24(44)19(62-38)10-57-37-34(54)35(26(46)18(8-41)61-37)64-39-33(53)30(50)25(45)20(63-39)9-56-36-31(51)28(48)23(43)17(7-40)60-36/h3-6,17-20,23-26,28-41,43-54H,7-10H2,1-2H3

InChI Key

HFJDWELARBQGBQ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cassia tora	Plant	KNApSAcK
Coffea arabica L.	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Coffea canephora	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Senna obtusifolia	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
Naphthopyranone glycoside
Phenolic glycoside
Naphthopyranone
Naphthopyran
Chromone
Glycosyl compound
1-naphthol
O-glycosyl compound
Benzopyran
Naphthalene
1-benzopyran
Anisole
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Oxane
Vinylogous acid
Heteroaromatic compound
Secondary alcohol
Acetal
Organoheterocyclic compound
Ether
Oxacycle
Polyol
Alcohol
Hydrocarbon derivative
Primary alcohol
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-1.2	ALOGPS
logP	-4.8	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	7.99	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	25	ChemAxon
Hydrogen Donor Count	14	ChemAxon
Polar Surface Area	392.59 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	203.37 m³·mol⁻¹	ChemAxon
Polarizability	88.67 Å³	ChemAxon
Number of Rings	7	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

HMDB0032833

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB010810

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

85185010

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Cassiaside B2 (NP0047474)

MOL for NP0047474 (Cassiaside B2)

3D MOL for NP0047474 (Cassiaside B2)

3D SDF for NP0047474 (Cassiaside B2)

3D-SDF for NP0047474 (Cassiaside B2)

PDB for NP0047474 (Cassiaside B2)

3D PDB for NP0047474 (Cassiaside B2)

SMILES for NP0047474 (Cassiaside B2)

INCHI for NP0047474 (Cassiaside B2)

Structure for NP0047474 (Cassiaside B2)

3D Structure for NP0047474 (Cassiaside B2)