NP-MRD: Showing NP-Card for {3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate (NP0243522)

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Record Information

Version

1.0

Created at

2022-09-07 04:05:24 UTC

Updated at

2022-09-07 04:05:24 UTC

NP-MRD ID

NP0243522

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate

Description

{3,4,5-Trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid. {3,4,5-Trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171517402D          

 47 50  0  0  0  0            999 V2000
   -0.8140   -0.2747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9268   -1.5915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0983   -2.3985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8829   -2.6534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4960   -2.1014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2807   -2.3563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4522   -3.1633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8937   -1.8043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  3 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004171517402D          

 47 50  0  0  0  0            999 V2000
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    4.9333   -2.8439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4484   -3.5113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7583   -2.8439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2432   -3.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0637   -3.4251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0132   -2.0592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3458   -1.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7508   -0.8556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5758   -0.8469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9408   -0.8556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3608   -0.1454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1857   -0.1541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6057    0.5560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4306    0.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8356   -0.1714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6606   -0.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0805    0.5301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0656   -0.8988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8905   -0.9074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2955   -1.6261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1205   -1.6348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5255   -2.3535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1055   -3.0636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5105   -3.7824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2806   -3.0550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8756   -2.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2007    1.2748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6206    1.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3757    1.2834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9707    2.0022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9558    0.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1308    0.5819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4852   -2.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2994   -2.6956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4709   -1.8886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2556   -1.6337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 27  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 31 37  1  0  0  0  0
 24 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 22 42  1  0  0  0  0
 42 43  1  0  0  0  0
  5 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
  3 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0243522

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C=CC(=O)OC2C(O)C(CO)OC2(CO)OC2OC(COC(=O)C=CC3=CC=C(O)C=C3)C(O)C(O)C2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C31H36O16/c1-42-20-12-17(4-9-19(20)35)6-11-24(37)45-29-26(39)21(13-32)46-31(29,15-33)47-30-28(41)27(40)25(38)22(44-30)14-43-23(36)10-5-16-2-7-18(34)8-3-16/h2-12,21-22,25-30,32-35,38-41H,13-15H2,1H3

> <INCHI_KEY>
AMQSKEKZBYHALN-UHFFFAOYSA-N

> <FORMULA>
C31H36O16

> <MOLECULAR_WEIGHT>
664.613

> <EXACT_MASS>
664.200335079

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
65.82047703864198

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
0.98

> <JCHEM_LOGP>
0.7741445633333335

> <ALOGPS_LOGS>
-3.06

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.992013418513432

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.271054101384072

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9814532563443565

> <JCHEM_POLAR_SURFACE_AREA>
251.35999999999996

> <JCHEM_REFRACTIVITY>
158.33450000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.72e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -1.519  -0.513   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.055  -0.989   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.265  -2.495   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.730  -2.971   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.050  -4.477   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.515  -4.953   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.659  -3.923   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.124  -4.398   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.444  -5.905   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       7.268  -3.368   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.733  -3.844   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.209  -5.309   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.304  -6.554   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.749  -5.309   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.654  -6.554   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.186  -6.393   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      11.225  -3.844   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.979  -2.939   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.735  -1.597   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.275  -1.581   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       9.223  -1.597   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.007  -0.271   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.547  -0.288   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      12.331   1.038   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.871   1.022   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      14.627  -0.320   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      16.166  -0.336   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      16.950   0.990   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      16.922  -1.678   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      18.462  -1.694   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      19.218  -3.035   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      20.758  -3.052   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      21.514  -4.393   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      20.730  -5.719   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      21.486  -7.060   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      19.190  -5.703   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      18.434  -4.361   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.575   2.380   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      12.359   3.705   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      10.035   2.396   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       9.279   3.737   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       9.251   1.070   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       7.711   1.086   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       0.906  -5.508   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -0.559  -5.032   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -0.879  -3.525   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -2.344  -3.050   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   46                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   44                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   11   19   21                                             
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23   42                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   38                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   37                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   31                                                       
CONECT   38   24   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   22   43                                                  
CONECT   43   42                                                            
CONECT   44    5   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45    3   47                                                  
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  100    0
END

View in JSmol

Synonyms

Value	Source
{3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₃₁H₃₆O₁₆

Average Mass

664.6130 Da

Monoisotopic Mass

664.20034 Da

IUPAC Name

{3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

{3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=CC(C=CC(=O)OC2C(O)C(CO)OC2(CO)OC2OC(COC(=O)C=CC3=CC=C(O)C=C3)C(O)C(O)C2O)=CC=C1O

InChI Identifier

InChI=1S/C31H36O16/c1-42-20-12-17(4-9-19(20)35)6-11-24(37)45-29-26(39)21(13-32)46-31(29,15-33)47-30-28(41)27(40)25(38)22(44-30)14-43-23(36)10-5-16-2-7-18(34)8-3-16/h2-12,21-22,25-30,32-35,38-41H,13-15H2,1H3

InChI Key

AMQSKEKZBYHALN-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acid esters

Alternative Parents

Substituents

Coumaric acid ester
Coumaric acid or derivatives
Cinnamic acid ester
C-glycosyl compound
Disaccharide
Glycosyl compound
O-glycosyl compound
Methoxyphenol
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Ketal
Fatty acyl
Benzenoid
Oxane
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Tetrahydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Carboxylic acid ester
Organoheterocyclic compound
Acetal
Polyol
Carboxylic acid derivative
Oxacycle
Ether
Carbonyl group
Alcohol
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	0.98	ALOGPS
logP	0.77	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	9.27	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	251.36 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	158.33 m³·mol⁻¹	ChemAxon
Polarizability	65.82 Å³	ChemAxon
Number of Rings	4	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

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DrugBank ID

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Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

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PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for {3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate (NP0243522)

MOL for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0243522 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(4-hydroxyphenyl)prop-2-enoate)