NP-MRD: Showing NP-Card for Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside (NP0053955)

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Record Information

Version

2.0

Created at

2022-04-28 00:27:39 UTC

Updated at

2022-04-28 00:27:39 UTC

NP-MRD ID

NP0053955

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside

Description

(2S,3R,4S,5S,6S)-2-{[(2R,3R,4S,5S,6S)-2-{[(2S,3R,4R,5S,6S)-6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxo-4H-chromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,5-dihydroxy-6-methyloxan-4-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside is found in Rhamnus petiolaris . Based on a literature review very few articles have been published on (2S,3R,4S,5S,6S)-2-{[(2R,3R,4S,5S,6S)-2-{[(2S,3R,4R,5S,6S)-6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxo-4H-chromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,5-dihydroxy-6-methyloxan-4-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282202272D          

 65 71  0  0  1  0            999 V2000
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  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 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
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 17 19  1  6  0  0  0
 19 20  1  0  0  0  0
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 30 29  1  1  0  0  0
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 32 33  1  0  0  0  0
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 43 48  1  0  0  0  0
 46 49  1  0  0  0  0
 31 50  1  6  0  0  0
 22 51  1  6  0  0  0
 16 52  1  1  0  0  0
 15 53  1  6  0  0  0
 14 54  1  1  0  0  0
  8 55  1  0  0  0  0
 55 56  2  0  0  0  0
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 59 60  2  0  0  0  0
 55 60  1  0  0  0  0
 59 61  1  0  0  0  0
 58 62  1  0  0  0  0
  3 63  1  0  0  0  0
  1 64  1  0  0  0  0
 64 65  1  0  0  0  0
M  END

     RDKit          3D

113119  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652304282202272D          

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 64 65  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0053955

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(OC(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@@H](CO[C@@H]4O[C@@H](C)[C@H](O)[C@H](O[C@@H]5O[C@@H](C)[C@H](O)[C@H](OC(=O)\C=C\C6=CC=C(O)C=C6)[C@H]5O)[C@H]4O)[C@H](O)[C@@H](O)[C@@H]3O)C2=O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C43H48O22/c1-16-30(50)39(64-43-36(56)38(29(49)17(2)60-43)63-27(48)11-6-18-4-8-20(44)9-5-18)35(55)41(59-16)58-15-26-31(51)33(53)34(54)42(62-26)65-40-32(52)28-24(47)13-21(57-3)14-25(28)61-37(40)19-7-10-22(45)23(46)12-19/h4-14,16-17,26,29-31,33-36,38-39,41-47,49-51,53-56H,15H2,1-3H3/b11-6+/t16-,17-,26-,29-,30-,31-,33+,34-,35+,36+,38-,39-,41+,42-,43-/m0/s1

> <INCHI_KEY>
XDOLXXPUESIUMX-PZHZMNJOSA-N

> <FORMULA>
C43H48O22

> <MOLECULAR_WEIGHT>
916.835

> <EXACT_MASS>
916.263723186

> <JCHEM_ACCEPTOR_COUNT>
21

> <JCHEM_ATOM_COUNT>
113

> <JCHEM_AVERAGE_POLARIZABILITY>
88.67385720689481

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6S)-2-{[(2R,3R,4S,5S,6S)-2-{[(2S,3R,4R,5S,6S)-6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxo-4H-chromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,5-dihydroxy-6-methyloxan-4-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
2.03

> <JCHEM_LOGP>
1.283532798333334

> <ALOGPS_LOGS>
-3.22

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.51405255802712

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.131290137167144

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6789566937010862

> <JCHEM_POLAR_SURFACE_AREA>
339.74000000000007

> <JCHEM_REFRACTIVITY>
217.0456

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.49e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6S)-2-{[(2R,3R,4S,5S,6S)-2-{[(2S,3R,4R,5S,6S)-6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,5-dihydroxy-6-methyloxan-4-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <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      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.000  -9.240   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -2.667 -12.320   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -0.000 -13.860   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -2.667 -13.860   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -5.335 -16.940   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -2.667 -18.480   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -4.001 -19.250   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -5.335 -18.480   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -4.001 -20.790   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.667 -21.560   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -2.667 -23.100   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -1.334 -23.870   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -1.334 -25.410   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -2.667 -26.180   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -4.001 -25.410   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -4.001 -23.870   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -2.667 -27.720   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      -0.000 -16.940   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       2.667 -12.320   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       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   65  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
CONECT    1    2    6   64                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   63                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   55                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15   54                                                  
CONECT   15   14   16   53                                                  
CONECT   16   15   17   52                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   13                                                       
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23   51                                                  
CONECT   23   22   24   29                                                  
CONECT   24   23   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   21                                                       
CONECT   27   25                                                            
CONECT   28   24                                                            
CONECT   29   23   30                                                       
CONECT   30   29   31   35                                                  
CONECT   31   30   32   50                                                  
CONECT   32   31   33   38                                                  
CONECT   33   32   34   37                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34   30                                                       
CONECT   36   34                                                            
CONECT   37   33                                                            
CONECT   38   32   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   48                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   49                                                  
CONECT   47   46   48                                                       
CONECT   48   47   43                                                       
CONECT   49   46                                                            
CONECT   50   31                                                            
CONECT   51   22                                                            
CONECT   52   16                                                            
CONECT   53   15                                                            
CONECT   54   14                                                            
CONECT   55    8   56   60                                                  
CONECT   56   55   57                                                       
CONECT   57   56   58                                                       
CONECT   58   57   59   62                                                  
CONECT   59   58   60   61                                                  
CONECT   60   59   55                                                       
CONECT   61   59                                                            
CONECT   62   58                                                            
CONECT   63    3                                                            
CONECT   64    1   65                                                       
CONECT   65   64                                                            
MASTER        0    0    0    0    0    0    0    0   65    0  142    0
END

View in JSmol

Synonyms

Value	Source
(2S,3R,4S,5S,6S)-2-{[(2R,3R,4S,5S,6S)-2-{[(2S,3R,4R,5S,6S)-6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxo-4H-chromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,5-dihydroxy-6-methyloxan-4-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₄₃H₄₈O₂₂

Average Mass

916.8350 Da

Monoisotopic Mass

916.26372 Da

IUPAC Name

Traditional Name

(2S,3R,4S,5S,6S)-2-{[(2R,3R,4S,5S,6S)-2-{[(2S,3R,4R,5S,6S)-6-{[2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-3,5-dihydroxy-6-methyloxan-4-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(OC(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@@H](CO[C@@H]4O[C@@H](C)[C@H](O)[C@H](O[C@@H]5O[C@@H](C)[C@H](O)[C@H](OC(=O)\C=C\C6=CC=C(O)C=C6)[C@H]5O)[C@H]4O)[C@H](O)[C@@H](O)[C@@H]3O)C2=O)=C1

InChI Identifier

InChI=1S/C43H48O22/c1-16-30(50)39(64-43-36(56)38(29(49)17(2)60-43)63-27(48)11-6-18-4-8-20(44)9-5-18)35(55)41(59-16)58-15-26-31(51)33(53)34(54)42(62-26)65-40-32(52)28-24(47)13-21(57-3)14-25(28)61-37(40)19-7-10-22(45)23(46)12-19/h4-14,16-17,26,29-31,33-36,38-39,41-47,49-51,53-56H,15H2,1-3H3/b11-6+/t16-,17-,26-,29-,30-,31-,33+,34-,35+,36+,38-,39-,41+,42-,43-/m0/s1

InChI Key

XDOLXXPUESIUMX-PZHZMNJOSA-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
Rhamnus petiolaris	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-3-O-glycosides

Alternative Parents

Substituents

Oligosaccharide
Flavonoid-3-o-glycoside
7-methoxyflavonoid-skeleton
Hydroxyflavonoid
Flavone
5-hydroxyflavonoid
4'-hydroxyflavonoid
3'-hydroxyflavonoid
Coumaric acid ester
Cinnamic acid ester
Hydroxycinnamic acid or derivatives
Coumaric acid or derivatives
Cinnamic acid or derivatives
O-glycosyl compound
Glycosyl compound
Chromone
1-benzopyran
Benzopyran
Styrene
Catechol
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Benzenoid
Pyran
Oxane
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	2.03	ALOGPS
logP	1.28	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	7.13	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	21	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	339.74 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	217.05 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

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

162864107

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside (NP0053955)

MOL for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

3D MOL for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

3D SDF for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

3D-SDF for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

PDB for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

3D PDB for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

SMILES for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

INCHI for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

Structure for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)

3D Structure for NP0053955 (Rhamnetin 3-(3''''-p-coumaryl-rhamnosyl)(1->3)-rhamnosyl-(1->6)-galactoside)