NP-MRD: Showing NP-Card for triacontyl 3-(4-hydroxyphenyl)prop-2-enoate (NP0286152)

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Record Information

Version

2.0

Created at

2022-09-09 14:36:26 UTC

Updated at

2022-09-09 14:36:26 UTC

NP-MRD ID

NP0286152

Secondary Accession Numbers

None

Natural Product Identification

Common Name

triacontyl 3-(4-hydroxyphenyl)prop-2-enoate

Description

143200-86-6 Belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid. triacontyl 3-(4-hydroxyphenyl)prop-2-enoate is found in Dendrobium fimbriatum. 143200-86-6 Is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231518132D          

 42 42  0  0  0  0            999 V2000
   11.4315  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657  -21.4500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801  -20.2125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.2946  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.0091  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.7235  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.4380  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525  -22.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670  -22.6875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   36.4380  -22.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.7235  -22.2750    0.0000 C   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  1  0  0  0  0
  4  5  1  0  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  1  0  0  0  0
  9 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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 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  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 34 32  1  4  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 36 42  1  0  0  0  0
M  END

     RDKit          3D

110110  0  0  0  0  0  0  0  0999 V2000
   15.1169    1.2552    0.2293 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.3165   -1.9635   -2.0541 C   0  0  0  0  0  0  0  0  0  0  0  0
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 21 84  1  0
 21 85  1  0
 22 86  1  0
 22 87  1  0
 23 88  1  0
 23 89  1  0
 24 90  1  0
 24 91  1  0
 25 92  1  0
 25 93  1  0
 26 94  1  0
 26 95  1  0
 27 96  1  0
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 28 98  1  0
 28 99  1  0
 29100  1  0
 29101  1  0
 30102  1  0
 30103  1  0
 34104  1  0
 35105  1  0
 37106  1  0
 38107  1  0
 40108  1  0
 41109  1  0
 42110  1  0
M  END


  Mrv1533004231518132D          

 42 42  0  0  0  0            999 V2000
   11.4315  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657  -21.4500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801  -20.2125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.2946  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.0091  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.7235  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.4380  -21.0375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525  -21.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525  -22.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670  -22.6875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   36.4380  -22.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.7235  -22.2750    0.0000 C   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  1  0  0  0  0
  4  5  1  0  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  1  0  0  0  0
  9 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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 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  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 34 32  1  4  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 36 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0286152

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C39H68O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-36-42-39(41)35-32-37-30-33-38(40)34-31-37/h30-35,40H,2-29,36H2,1H3

> <INCHI_KEY>
DUIIKPOJUKGTSI-UHFFFAOYSA-N

> <FORMULA>
C39H68O3

> <MOLECULAR_WEIGHT>
584.97

> <EXACT_MASS>
584.51684605

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
110

> <JCHEM_AVERAGE_POLARIZABILITY>
79.95309030135924

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
triacontyl 3-(4-hydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
11.02

> <JCHEM_LOGP>
15.094432632333334

> <ALOGPS_LOGS>
-7.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.398661260312757

> <JCHEM_PKA_STRONGEST_BASIC>
-5.9547309780583015

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
183.30949999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
32

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.05e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
triacontyl 3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      21.339 -40.040   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      22.673 -39.270   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      24.006 -40.040   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      25.340 -39.270   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      26.674 -40.040   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      28.007 -39.270   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      29.341 -40.040   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      30.675 -39.270   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      32.008 -40.040   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      33.342 -39.270   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      34.676 -40.040   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      36.009 -39.270   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      37.343 -40.040   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      38.677 -39.270   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      40.010 -40.040   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      41.344 -39.270   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      42.678 -40.040   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      44.011 -39.270   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      45.345 -40.040   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      46.679 -39.270   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      48.012 -40.040   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      49.346 -39.270   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      50.680 -40.040   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      52.013 -39.270   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      53.347 -40.040   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      54.681 -39.270   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      56.015 -40.040   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      57.348 -39.270   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      58.682 -40.040   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      60.016 -39.270   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      61.349 -40.040   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      62.683 -39.270   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      62.683 -37.730   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      64.017 -40.040   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      65.350 -39.270   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      66.684 -40.040   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      68.018 -39.270   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      69.351 -40.040   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      69.351 -41.580   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      70.685 -42.350   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      68.018 -42.350   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      66.684 -41.580   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   42                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   36                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₆₈O₃

Average Mass

584.9700 Da

Monoisotopic Mass

584.51685 Da

IUPAC Name

triacontyl 3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

triacontyl 3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C39H68O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-36-42-39(41)35-32-37-30-33-38(40)34-31-37/h30-35,40H,2-29,36H2,1H3

InChI Key

DUIIKPOJUKGTSI-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

Species Name	Source	Reference
Dendrobium fimbriatum	LOTUS Database	35616633

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
Fatty alcohol ester
Cinnamic acid ester
Styrene
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Phenol
Fatty acyl
Monocyclic benzene moiety
Benzenoid
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxide
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
logP	11.02	ALOGPS
logP	15.09	ChemAxon
logS	-7.7	ALOGPS
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	32	ChemAxon
Refractivity	183.31 m³·mol⁻¹	ChemAxon
Polarizability	79.95 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

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

71344737

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for triacontyl 3-(4-hydroxyphenyl)prop-2-enoate (NP0286152)

MOL for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0286152 (triacontyl 3-(4-hydroxyphenyl)prop-2-enoate)