NP-MRD: Showing NP-Card for 24-Acetyl- 25-cinnamoylvulgaroside (NP0335422)

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Record Information

Version

2.0

Created at

2024-09-11 01:32:26 UTC

Updated at

2024-09-11 01:32:26 UTC

NP-MRD ID

NP0335422

Secondary Accession Numbers

None

Natural Product Identification

Common Name

24-Acetyl- 25-cinnamoylvulgaroside

Description

Based on a literature review very few articles have been published on 24-Acetyl- 25-cinnamoylvulgaroside.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05262304042D          

 44 48  0  0  0  0            999 V2000
   -2.0065    2.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3772   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4587   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4807    1.8614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7356    1.0768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6737    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1836    0.4637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1217    1.4199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8246    0.0221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0795   -0.7625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0125   -2.4846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2312    2.2856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3766    0.6352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5275   -1.3756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6256   -3.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1685   -1.8171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3480   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7825   -2.1602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5393   -3.8571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.1178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5993    1.7553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7205   -1.2041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3400   -2.6241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
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 41 36  1  0  0  0  0
 42 22  1  0  0  0  0
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 43 30  1  0  0  0  0
 43 32  1  0  0  0  0
 44 31  1  0  0  0  0
 44 32  1  0  0  0  0
M  END


  Mrv2104 05262304042D          

 44 48  0  0  0  0            999 V2000
   -2.0065    2.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3772   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4587   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4807    1.8614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7356    1.0768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6737    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1836    0.4637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1217    1.4199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8246    0.0221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0795   -0.7625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0125   -2.4846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2312    2.2856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3766    0.6352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5275   -1.3756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6256   -3.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1685   -1.8171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0880    3.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7825   -2.1602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5393   -3.8571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.1178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5993    1.7553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7205   -1.2041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3400   -2.6241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
 10  7  1  0  0  0  0
 11  8  2  0  0  0  0
 13 12  2  0  0  0  0
 16  9  1  0  0  0  0
 17  9  1  0  0  0  0
 18 14  1  0  0  0  0
 19 15  1  0  0  0  0
 23  1  1  0  0  0  0
 24 10  2  0  0  0  0
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 25 20  2  0  0  0  0
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 28 15  1  0  0  0  0
 29 21  1  0  0  0  0
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 33  2  1  0  0  0  0
 33  3  1  0  0  0  0
 33 16  1  0  0  0  0
 33 27  1  0  0  0  0
 34  4  1  0  0  0  0
 34 17  1  0  0  0  0
 34 27  1  0  0  0  0
 34 28  1  0  0  0  0
 35  5  1  0  0  0  0
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 35 29  1  0  0  0  0
 36 19  1  0  0  0  0
 36 22  1  0  0  0  0
 36 29  1  0  0  0  0
 37 23  2  0  0  0  0
 38 26  1  0  0  0  0
 39 30  2  0  0  0  0
 40 31  2  0  0  0  0
 41 36  1  0  0  0  0
 42 22  1  0  0  0  0
 42 23  1  0  0  0  0
 43 30  1  0  0  0  0
 43 32  1  0  0  0  0
 44 31  1  0  0  0  0
 44 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0335422

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1(O)CCC2C(C)(CCC3C(C)(C)CCCC23C)C1CC(O)C1=CC(=O)OC1OC(=O)\C=C\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1/C36H48O8/c1-23(37)42-22-36(41)19-15-28-34(4)17-9-16-33(2,3)27(34)14-18-35(28,5)29(36)21-26(38)25-20-31(40)44-32(25)43-30(39)13-12-24-10-7-6-8-11-24/h6-8,10-13,20,26-29,32,38,41H,9,14-19,21-22H2,1-5H3/b13-12+

> <INCHI_KEY>
IMXZIJOCFAKDPZ-OUKQBFOZNA-N

> <FORMULA>
C36H48O8

> <MOLECULAR_WEIGHT>
608.772

> <EXACT_MASS>
608.334918506

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
67.25602500955695

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-(2-{2-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-tetradecahydrophenanthren-1-yl}-1-hydroxyethyl)-5-oxo-2,5-dihydrofuran-2-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_LOGP>
6.261624764666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.720095157809867

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.592926217741408

> <JCHEM_PKA_STRONGEST_BASIC>
-3.064099348190271

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000001

> <JCHEM_REFRACTIVITY>
165.88870000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-(2-{2-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-1-yl}-1-hydroxyethyl)-5-oxo-2H-furan-2-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0      -3.745   3.740   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.171  -1.090   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.456  -2.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -1.897   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -10.231   3.475   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.706   2.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.724   3.795   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -9.676   0.866   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -7.694   2.650   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -7.139   0.041   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -7.615  -1.423   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.890  -4.638   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.206  -1.897   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.386   1.760   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.298   4.266   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.170   1.186   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.516  -3.231   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.746  -1.897   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.585  -2.568   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.034  -5.668   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.048  -3.392   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -2.031   5.783   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -2.516  -0.564   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -7.061  -4.032   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -2.873  -7.200   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      -1.386  -0.220   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      -1.119   3.277   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      -5.078  -2.248   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      -4.368  -4.898   0.000  0.00  0.00           O+0
CONECT    1   23                                                            
CONECT    2   33                                                            
CONECT    3   33                                                            
CONECT    4   34                                                            
CONECT    5   35                                                            
CONECT    6    7    8                                                       
CONECT    7    6   10                                                       
CONECT    8    6   11                                                       
CONECT    9   16   17                                                       
CONECT   10    7   24                                                       
CONECT   11    8   24                                                       
CONECT   12   13   24                                                       
CONECT   13   12   30                                                       
CONECT   14   18   27                                                       
CONECT   15   19   28                                                       
CONECT   16    9   33                                                       
CONECT   17    9   34                                                       
CONECT   18   14   35                                                       
CONECT   19   15   36                                                       
CONECT   20   25   31                                                       
CONECT   21   26   29                                                       
CONECT   22   36   42                                                       
CONECT   23    1   37   42                                                  
CONECT   24   10   11   12                                                  
CONECT   25   20   26   32                                                  
CONECT   26   21   25   38                                                  
CONECT   27   14   33   34                                                  
CONECT   28   15   34   35                                                  
CONECT   29   21   35   36                                                  
CONECT   30   13   39   43                                                  
CONECT   31   20   40   44                                                  
CONECT   32   25   43   44                                                  
CONECT   33    2    3   16   27                                             
CONECT   34    4   17   27   28                                             
CONECT   35    5   18   28   29                                             
CONECT   36   19   22   29   41                                             
CONECT   37   23                                                            
CONECT   38   26                                                            
CONECT   39   30                                                            
CONECT   40   31                                                            
CONECT   41   36                                                            
CONECT   42   22   23                                                       
CONECT   43   30   32                                                       
CONECT   44   31   32                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₄₈O₈

Average Mass

608.7720 Da

Monoisotopic Mass

608.33492 Da

IUPAC Name

3-(2-{2-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-tetradecahydrophenanthren-1-yl}-1-hydroxyethyl)-5-oxo-2,5-dihydrofuran-2-yl (2E)-3-phenylprop-2-enoate

Traditional Name

3-(2-{2-[(acetyloxy)methyl]-2-hydroxy-4b,8,8,10a-tetramethyl-decahydrophenanthren-1-yl}-1-hydroxyethyl)-5-oxo-2H-furan-2-yl (2E)-3-phenylprop-2-enoate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1(O)CCC2C(C)(CCC3C(C)(C)CCCC23C)C1CC(O)C1=CC(=O)OC1OC(=O)\C=C\C1=CC=CC=C1

InChI Identifier

InChI=1/C36H48O8/c1-23(37)42-22-36(41)19-15-28-34(4)17-9-16-33(2,3)27(34)14-18-35(28,5)29(36)21-26(38)25-20-31(40)44-32(25)43-30(39)13-12-24-10-7-6-8-11-24/h6-8,10-13,20,26-29,32,38,41H,9,14-19,21-22H2,1-5H3/b13-12+

InChI Key

IMXZIJOCFAKDPZ-OUKQBFOZNA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Classification

Not classified

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	6.26	ChemAxon
pKa (Strongest Acidic)	4.59	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	165.89 m³·mol⁻¹	ChemAxon
Polarizability	67.26 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

Not Available

Showing NP-Card for 24-Acetyl- 25-cinnamoylvulgaroside (NP0335422)

MOL for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

3D MOL for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

3D SDF for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

3D-SDF for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

PDB for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

3D PDB for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

SMILES for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

INCHI for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

Structure for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)

3D Structure for NP0335422 (24-Acetyl- 25-cinnamoylvulgaroside)