NP-MRD: Showing NP-Card for (2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate (NP0325388)

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Record Information

Version

2.0

Created at

2022-09-12 06:06:35 UTC

Updated at

2022-09-12 06:06:35 UTC

NP-MRD ID

NP0325388

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

Description

(2R)-2-(acetyloxy)-3-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages. (2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate is found in Populus lasiocarpa. Based on a literature review very few articles have been published on (2R)-2-(acetyloxy)-3-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122208062D          

 32 33  0  0  1  0            999 V2000
    6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   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
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  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
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 12 13  2  0  0  0  0
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 15 16  1  0  0  0  0
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 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
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 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
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 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
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 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 25 32  1  0  0  0  0
M  END

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
    0.9028   -3.7100    1.5157 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0561   -3.1087    0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8421   -3.5982   -0.6371 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3140   -1.9872   -0.1770 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3769   -1.3462   -1.3959 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7736    0.0860   -1.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0255    0.3575   -0.8940 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3540    0.2120    0.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5017   -0.1781    1.2531 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7266    0.5105    0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6211    0.9204    0.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9794    1.2367    0.4138 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4627    1.1408    1.6996 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7894    1.4588    2.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6138    1.8724    1.0091 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9277    2.1957    1.2712 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1490    1.9753   -0.2864 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8495    1.6641   -0.5936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8638   -1.5816   -2.2770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0505   -1.1487   -1.7567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6661   -1.5982   -0.6263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1529   -2.5058    0.0557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9533   -1.0345   -0.1673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5557   -0.0837   -0.8226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8281    0.4870   -0.3861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4096    1.5071   -1.1483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5904    2.1018   -0.8257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2561    1.6696    0.3287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4522    2.2740    0.6532 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.3507    0.2053    2.2699 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5058    0.0959    0.7270 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3171   -4.7336    1.5590 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3776   -3.0378    2.2585 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1773   -1.9050   -1.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7386    0.3969   -2.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0507    0.7507   -0.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9612    0.3927    1.9339 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8065    0.8129    2.4902 H   0  0  0  0  0  0  0  0  0  0  0  0
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   10.2982    2.1314    2.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8261    2.3076   -1.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4574    1.7372   -1.6101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5944   -1.1029   -3.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8570   -2.6873   -2.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0603    0.2794   -1.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8764    1.8175   -2.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0390    2.9038   -1.4327 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0105    2.0463    1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2143    0.6048    2.5509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1017   -0.6922    1.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
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 30 31  1  0
 30 32  2  0
 18 12  1  0
 32 25  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  6
  6 37  1  0
  6 38  1  0
 10 39  1  0
 11 40  1  0
 13 41  1  0
 14 42  1  0
 16 43  1  0
 17 44  1  0
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 23 48  1  0
 24 49  1  0
 26 50  1  0
 27 51  1  0
 29 52  1  0
 31 53  1  0
 32 54  1  0
M  END


  Mrv1652309122208062D          

 32 33  0  0  1  0            999 V2000
    6.4302   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.7171   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  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  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
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 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
  5 19  1  0  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
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 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 25 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325388

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H](COC(=O)\C=C\C1=CC=C(O)C=C1)COC(=O)\C=C\C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O9/c1-15(24)32-19(13-30-22(28)10-5-16-2-7-18(25)8-3-16)14-31-23(29)11-6-17-4-9-20(26)21(27)12-17/h2-12,19,25-27H,13-14H2,1H3/b10-5+,11-6+/t19-/m1/s1

> <INCHI_KEY>
GLVFLAONFKWEJN-ROFDTJRBSA-N

> <FORMULA>
C23H22O9

> <MOLECULAR_WEIGHT>
442.42

> <EXACT_MASS>
442.126382288

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
45.02564783676838

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-2-(acetyloxy)-3-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
3.759196858666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.614714018508485

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.992300291216798

> <JCHEM_PKA_STRONGEST_BASIC>
-5.954731209211855

> <JCHEM_POLAR_SURFACE_AREA>
139.59

> <JCHEM_REFRACTIVITY>
114.74569999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-(acetyloxy)-3-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2E)-3-(3,4-dihydroxyphenyl)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      12.003 -16.170   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.003 -14.630   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      13.337 -13.860   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      10.669 -13.860   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.002 -12.320   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.000 -16.940   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      13.337 -12.320   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      14.670 -10.010   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      20.005 -11.550   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      21.339 -12.320   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      22.673 -14.630   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      20.005 -16.170   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   19                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   12                                                       
CONECT   19    5   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   32                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   25                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Value	Source
(2R)-2-(Acetyloxy)-3-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₃H₂₂O₉

Average Mass

442.4200 Da

Monoisotopic Mass

442.12638 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H](COC(=O)\C=C\C1=CC=C(O)C=C1)COC(=O)\C=C\C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C23H22O9/c1-15(24)32-19(13-30-22(28)10-5-16-2-7-18(25)8-3-16)14-31-23(29)11-6-17-4-9-20(26)21(27)12-17/h2-12,19,25-27H,13-14H2,1H3/b10-5+,11-6+/t19-/m1/s1

InChI Key

GLVFLAONFKWEJN-ROFDTJRBSA-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
Populus lasiocarpa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Triradylcglycerols

Direct Parent

Triacylglycerols

Alternative Parents

Substituents

Triacyl-sn-glycerol
Coumaric acid ester
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Tricarboxylic acid or derivatives
Catechol
Styrene
Phenol
1-hydroxy-4-unsubstituted benzenoid
Fatty acid ester
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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

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

162851043

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate (NP0325388)

MOL for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D MOL for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D SDF for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D-SDF for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

PDB for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D PDB for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

SMILES for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

INCHI for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

Structure for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)

3D Structure for NP0325388 ((2r)-2-(acetyloxy)-3-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}propyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate)