NP-MRD: Showing NP-Card for [(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0324176)

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Record Information

Version

2.0

Created at

2022-09-12 04:04:57 UTC

Updated at

2022-09-12 04:04:57 UTC

NP-MRD ID

NP0324176

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

Description

CHEMBL504221 belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. [(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate is found in Prunus mume. Based on a literature review very few articles have been published on CHEMBL504221.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122206042D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309122206042D          

 50 52  0  0  1  0            999 V2000
    9.4537   -1.3947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9017   -2.0078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1566   -2.7925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0947   -1.8363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5427   -2.4494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7357   -2.2779    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1837   -2.8910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3767   -2.7194    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8247   -3.3325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0177   -3.1610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -3.7741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9136   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1066   -3.3325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5546   -2.7194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7476   -2.8910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8096   -1.9348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331   -4.2590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781   -5.0437    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3631   -5.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0275   -6.4648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5124   -7.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329   -7.0460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1769   -7.8859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6618   -8.5533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3262   -9.3070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8112   -9.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4756  -10.7281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6551  -10.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3196  -11.5680    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1702  -10.1469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5058   -9.3932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0531   -5.0437    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5682   -5.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7477   -5.6249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4122   -4.8712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2628   -6.2923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982   -4.2590    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0136   -4.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1217   -1.9348    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3148   -1.7633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6738   -1.3217    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4188   -0.5371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119   -0.3656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0598   -0.9787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3569    0.4190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4808   -1.4933    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0328   -0.8802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7778   -0.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9709    0.0760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3299    0.5176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
 18 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 32 37  1  0  0  0  0
 11 37  1  0  0  0  0
 37 38  1  1  0  0  0
  8 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
 41 46  1  0  0  0  0
  6 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0324176

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@H]1O[C@H](CO[C@]2(COC(C)=O)O[C@H](COC(=O)\C=C\C3=CC=C(O)C=C3)[C@H](OC(C)=O)[C@H]2O)[C@H](O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H40O18/c1-16(33)42-12-24-28(46-18(3)35)30(48-20(5)37)27(40)23(49-24)14-45-32(15-44-17(2)34)31(41)29(47-19(4)36)25(50-32)13-43-26(39)11-8-21-6-9-22(38)10-7-21/h6-11,23-25,27-31,38,40-41H,12-15H2,1-5H3/b11-8+/t23-,24-,25-,27+,28-,29+,30-,31-,32-/m1/s1

> <INCHI_KEY>
IWFNDNSEUAIXJM-KVWRXITHSA-N

> <FORMULA>
C32H40O18

> <MOLECULAR_WEIGHT>
712.654

> <EXACT_MASS>
712.221464448

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
69.29060917536799

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3R,4R,5R)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2R,3S,4R,5R,6R)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
0.14100648399999777

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.085885338911577

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.39775114978733

> <JCHEM_PKA_STRONGEST_BASIC>
-3.660003175606798

> <JCHEM_POLAR_SURFACE_AREA>
246.17999999999995

> <JCHEM_REFRACTIVITY>
161.01280000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3R,4R,5R)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2R,3S,4R,5R,6R)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      17.647  -2.604   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.616  -3.748   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      17.092  -5.213   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      15.110  -3.428   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      14.080  -4.572   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.573  -4.252   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.543  -5.396   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.036  -5.076   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.006  -6.221   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.500  -5.901   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.469  -7.045   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.439  -5.901   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.932  -6.221   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.902  -5.076   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.396  -5.396   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.378  -3.612   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       7.715  -7.950   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.239  -9.415   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.144 -10.661   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.518 -12.068   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.423 -13.313   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.955 -13.152   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.797 -14.720   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.702 -15.966   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.076 -17.373   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.981 -18.619   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.354 -20.026   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.823 -20.187   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.197 -21.594   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.918 -18.941   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.544 -17.534   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.699  -9.415   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.794 -10.661   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.262 -10.500   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.636  -9.093   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       2.357 -11.746   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.223  -7.950   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.759  -7.474   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       9.561  -3.612   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       8.054  -3.291   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      10.591  -2.467   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      10.115  -1.003   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       8.609  -0.682   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.578  -1.827   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       8.133   0.782   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      12.097  -2.787   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      13.128  -1.643   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      12.652  -0.178   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      11.146   0.142   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      13.682   0.966   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   46                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   39                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   17   37                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   11   18                                                       
CONECT   18   17   19   32                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   25                                                       
CONECT   32   18   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   32   11   38                                                  
CONECT   38   37                                                            
CONECT   39    8   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   46                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   41    6   47                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₀O₁₈

Average Mass

712.6540 Da

Monoisotopic Mass

712.22146 Da

IUPAC Name

[(2R,3R,4R,5R)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2R,3S,4R,5R,6R)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@H]1O[C@H](CO[C@]2(COC(C)=O)O[C@H](COC(=O)\C=C\C3=CC=C(O)C=C3)[C@H](OC(C)=O)[C@H]2O)[C@H](O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI Identifier

InChI=1S/C32H40O18/c1-16(33)42-12-24-28(46-18(3)35)30(48-20(5)37)27(40)23(49-24)14-45-32(15-44-17(2)34)31(41)29(47-19(4)36)25(50-32)13-43-26(39)11-8-21-6-9-22(38)10-7-21/h6-11,23-25,27-31,38,40-41H,12-15H2,1-5H3/b11-8+/t23-,24-,25-,27+,28-,29+,30-,31-,32-/m1/s1

InChI Key

IWFNDNSEUAIXJM-KVWRXITHSA-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

Species Name	Source	Reference
Prunus mume	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
Coumaric acid ester
Hydroxycinnamic acid or derivatives
Cinnamic acid or derivatives
Cinnamic acid ester
Coumaric acid or derivatives
Glycosyl compound
C-glycosyl compound
Disaccharide
Styrene
Fatty acid ester
Ketal
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acyl
Monocyclic benzene moiety
Oxane
Benzenoid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Ether
Acetal
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic oxygen compound
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	0.14	ChemAxon
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	246.18 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	161.01 m³·mol⁻¹	ChemAxon
Polarizability	69.29 Å³	ChemAxon
Number of Rings	3	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

24711556

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44575960

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0324176)

MOL for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0324176 ([(2r,3r,4r,5r)-3-(acetyloxy)-5-[(acetyloxy)methyl]-5-{[(2r,3s,4r,5r,6r)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-hydroxyoxan-2-yl]methoxy}-4-hydroxyoxolan-2-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)