NP-MRD: Showing NP-Card for trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside (NP0045708)

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Record Information

Version

2.0

Created at

2022-03-17 19:36:09 UTC

Updated at

2022-03-17 19:36:09 UTC

NP-MRD ID

NP0045708

Secondary Accession Numbers

None

Natural Product Identification

Common Name

trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside

Description

Not Available

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02241212272D          

 30 31  0  0  0  0            999 V2000
   -3.2614    1.1049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758    1.5174    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6903    1.1049    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6903    0.2799    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9759   -0.1326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2614    0.2799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9759   -0.9576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758    2.3424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4048    1.5174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4048   -0.1326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0719   -0.1326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4844   -0.8470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3094   -0.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7219   -0.1326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3094    0.5819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4844    0.5819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5469   -0.1326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7532   -0.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657   -0.8470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9906   -0.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4031   -1.5615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7219   -1.5615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5469   -1.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1653    4.1838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3403    4.1838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9278    3.4694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1028    3.4694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6903    2.7549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3403    2.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6903    4.1838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  2  8  1  1  0  0  0
  4  3  1  0  0  0  0
  3  9  1  6  0  0  0
  4  5  1  0  0  0  0
  4 10  1  1  0  0  0
  5  6  1  0  0  0  0
  5  7  1  6  0  0  0
  8 28  1  0  0  0  0
 11 12  1  0  0  0  0
 11 16  2  0  0  0  0
 11 18  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 17  1  0  0  0  0
 15 16  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 17  1  1  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  1  0  0  0  0
 26 29  1  0  0  0  0
 27 30  2  0  0  0  0
M  END


  Mrv0541 02241212272D          

 30 31  0  0  0  0            999 V2000
   -3.2614    1.1049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758    1.5174    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6903    1.1049    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6903    0.2799    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9759   -0.1326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2614    0.2799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9759   -0.9576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758    2.3424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4048    1.5174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4048   -0.1326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0719   -0.1326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4844   -0.8470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3094   -0.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7219   -0.1326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3094    0.5819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4844    0.5819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5469   -0.1326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7532   -0.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657   -0.8470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9906   -0.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4031   -1.5615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7219   -1.5615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5469   -1.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1653    4.1838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3403    4.1838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9278    3.4694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1028    3.4694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6903    2.7549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3403    2.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6903    4.1838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  2  8  1  1  0  0  0
  4  3  1  0  0  0  0
  3  9  1  6  0  0  0
  4  5  1  0  0  0  0
  4 10  1  1  0  0  0
  5  6  1  0  0  0  0
  5  7  1  6  0  0  0
  8 28  1  0  0  0  0
 11 12  1  0  0  0  0
 11 16  2  0  0  0  0
 11 18  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 17  1  0  0  0  0
 15 16  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 17  1  1  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  1  0  0  0  0
 26 29  1  0  0  0  0
 27 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0045708

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\CO)=CC=C1O[C@@H]1O[C@H](COC(=O)C(C)CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O10/c1-11(9-22)19(26)28-10-15-16(23)17(24)18(25)20(30-15)29-13-6-5-12(4-3-7-21)8-14(13)27-2/h3-6,8,11,15-18,20-25H,7,9-10H2,1-2H3/b4-3+/t11?,15-,16-,17+,18-,20-/m1/s1

> <INCHI_KEY>
NUZPXHFCBKVLFX-QCIYUQLOSA-N

> <FORMULA>
C20H28O10

> <MOLECULAR_WEIGHT>
428.4303

> <EXACT_MASS>
428.168247116

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_AVERAGE_POLARIZABILITY>
43.2144151335092

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{4-[(1E)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenoxy}oxan-2-yl]methyl 3-hydroxy-2-methylpropanoate

> <ALOGPS_LOGP>
0.05

> <JCHEM_LOGP>
-0.5096165796666664

> <ALOGPS_LOGS>
-2.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.20552470608255

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.20102170797362

> <JCHEM_PKA_STRONGEST_BASIC>
-2.52636129505328

> <JCHEM_POLAR_SURFACE_AREA>
155.14

> <JCHEM_REFRACTIVITY>
103.90859999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.42e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{4-[(1E)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenoxy}oxan-2-yl]methyl 3-hydroxy-2-methylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0      -6.088   2.062   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -7.421   2.832   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.755   2.062   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.755   0.522   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.422  -0.248   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.088   0.522   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -7.422  -1.788   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -7.421   4.372   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0     -10.089   2.832   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0     -10.089  -0.248   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.134  -0.248   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.904  -1.581   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.444  -1.581   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.214  -0.248   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.444   1.086   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.904   1.086   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.754  -0.248   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.406  -0.247   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.176  -1.581   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.716  -1.581   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.486  -2.915   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -3.214  -2.915   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.754  -2.915   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0     -13.375   7.810   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0     -11.835   7.810   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -11.065   6.476   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -9.525   6.476   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -8.755   5.142   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -11.835   5.142   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -8.755   7.810   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3    8                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    1    5   17                                                  
CONECT    7    5                                                            
CONECT    8    2   28                                                       
CONECT    9    3                                                            
CONECT   10    4                                                            
CONECT   11   12   16   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   11   15                                                       
CONECT   17   14    6                                                       
CONECT   18   11   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   13   23                                                       
CONECT   23   22                                                            
CONECT   24   25                                                            
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28   30                                                  
CONECT   28    8   27                                                       
CONECT   29   26                                                            
CONECT   30   27                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₁₀

Average Mass

428.4303 Da

Monoisotopic Mass

428.16825 Da

IUPAC Name

[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{4-[(1E)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenoxy}oxan-2-yl]methyl 3-hydroxy-2-methylpropanoate

Traditional Name

[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{4-[(1E)-3-hydroxyprop-1-en-1-yl]-2-methoxyphenoxy}oxan-2-yl]methyl 3-hydroxy-2-methylpropanoate

CAS Registry Number

613232-82-9

SMILES

COC1=CC(\C=C\CO)=CC=C1O[C@@H]1O[C@H](COC(=O)C(C)CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C20H28O10/c1-11(9-22)19(26)28-10-15-16(23)17(24)18(25)20(30-15)29-13-6-5-12(4-3-7-21)8-14(13)27-2/h3-6,8,11,15-18,20-25H,7,9-10H2,1-2H3/b4-3+/t11?,15-,16-,17+,18-,20-/m1/s1

InChI Key

NUZPXHFCBKVLFX-QCIYUQLOSA-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
Capsicum annuum	FooDB	KNAPSACK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
O-glycosyl compound
Cinnamyl alcohol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Styrene
Alkyl aryl ether
Beta-hydroxy acid
Sugar acid
Benzenoid
Monocyclic benzene moiety
Oxane
Monosaccharide
Hydroxy acid
Secondary alcohol
Carboxylic acid ester
Acetal
Polyol
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxide
Hydrocarbon derivative
Primary alcohol
Alcohol
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	0.05	ALOGPS
logP	-0.51	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	155.14 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	103.91 m³·mol⁻¹	ChemAxon
Polarizability	43.21 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB001667

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

101260573

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside (NP0045708)

MOL for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

3D MOL for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

3D SDF for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

3D-SDF for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

PDB for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

3D PDB for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

SMILES for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

INCHI for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

Structure for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)

3D Structure for NP0045708 (trans-p-Ferulyl alcohol 4-O-[6-(2-methyl-3-hydroxypropionyl)] glucopyranoside)