NP-MRD: Showing NP-Card for hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0214308)

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Record Information

Version

2.0

Created at

2022-09-05 13:34:22 UTC

Updated at

2022-09-05 13:34:22 UTC

NP-MRD ID

NP0214308

Secondary Accession Numbers

None

Natural Product Identification

Common Name

hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Description

Hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate is found in Euchresta horsfieldii and Rubia tinctorum. Hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231523382D          

 30 30  0  0  0  0            999 V2000
    6.4302  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -14.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -13.6125    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  2  0  0  0  0
 20 18  1  4  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  2  0  0  0  0
 22 30  1  0  0  0  0
M  END

     RDKit          3D

 72 72  0  0  0  0  0  0  0  0999 V2000
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  -10.1736   -1.9306   -0.1150 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0551    2.4139    0.9366 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8924    3.6834    0.9656 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2549    1.9067    0.3132 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6319    0.6617    0.2262 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8845    0.2964   -0.4244 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8228    1.1800   -0.8867 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0091    0.7437   -1.5025 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2647   -0.5930   -1.6645 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4192   -1.0731   -2.2667 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3320   -1.5073   -1.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5937   -2.8524   -1.3709 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6585   -3.8016   -0.9180 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1776   -1.0429   -0.6023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5912   -2.8198    1.7234 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.2111    0.7622   -0.9898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3143   -1.2770   -1.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.8659    0.5064   -0.8833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8956   -2.3217   -0.3170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8678   -1.6256   -1.9620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6916   -1.3303   -1.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4463    0.2727   -1.0827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2250   -1.3833    1.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1224    0.2187    1.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9000    0.4195    2.2207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1231    1.3428    0.7195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8483   -0.7307   -0.4522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6845   -1.3711    1.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2996   -0.3061    0.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4163    0.5335    1.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0092    1.4306   -1.0027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5051    2.2159    0.5633 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3336    2.0658   -0.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2114    3.4392   -0.6560 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3136    3.6323    1.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3233    1.4293    2.5397 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004231523382D          

 30 30  0  0  0  0            999 V2000
    6.4302  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2881  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   15.0039  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -14.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 22 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214308

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(O)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H42O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-30-26(28)20-18-23-17-19-24(27)25(22-23)29-2/h17-20,22,27H,3-16,21H2,1-2H3

> <INCHI_KEY>
ZISDTRGMDDVTKY-UHFFFAOYSA-N

> <FORMULA>
C26H42O4

> <MOLECULAR_WEIGHT>
418.618

> <EXACT_MASS>
418.308309832

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
52.87519140597502

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
8.55

> <JCHEM_LOGP>
8.712800056666666

> <ALOGPS_LOGS>
-6.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.86780689476177

> <JCHEM_PKA_STRONGEST_BASIC>
-4.888712062953741

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
125.35869999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.65e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
hexadecyl 3-(4-hydroxy-3-methoxyphenyl)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      12.003 -23.870   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.337 -23.100   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.670 -23.870   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.004 -23.100   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.338 -23.870   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.672 -23.100   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.005 -23.870   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.339 -23.100   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.673 -23.870   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.006 -23.100   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      25.340 -23.870   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      26.674 -23.100   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      28.007 -23.870   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      29.341 -23.100   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      30.675 -23.870   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      32.008 -23.100   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      33.342 -23.870   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      34.676 -23.100   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      34.676 -21.560   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      36.009 -23.870   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      37.343 -23.100   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      38.677 -23.870   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      40.010 -23.100   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      41.344 -23.870   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      41.344 -25.410   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      42.678 -26.180   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      40.010 -26.180   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      40.010 -27.720   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      38.677 -28.490   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      38.677 -25.410   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   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   30                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   22                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   60    0
END

View in JSmol

Synonyms

Value	Source
Hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₆H₄₂O₄

Average Mass

418.6180 Da

Monoisotopic Mass

418.30831 Da

IUPAC Name

hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Traditional Name

hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(O)C(OC)=C1

InChI Identifier

InChI=1S/C26H42O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-30-26(28)20-18-23-17-19-24(27)25(22-23)29-2/h17-20,22,27H,3-16,21H2,1-2H3

InChI Key

ZISDTRGMDDVTKY-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
Euchresta horsfieldii	LOTUS Database	35616633
Rubia tinctorum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids and derivatives

Alternative Parents

Substituents

Coumaric acid or derivatives
Fatty alcohol ester
Cinnamic acid ester
Methoxyphenol
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
Phenol
Alkyl aryl ether
Fatty acid ester
1-hydroxy-2-unsubstituted benzenoid
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Ether
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organooxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	8.55	ALOGPS
logP	8.71	ChemAxon
logS	-6.8	ALOGPS
pKa (Strongest Acidic)	9.87	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	125.36 m³·mol⁻¹	ChemAxon
Polarizability	52.88 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

149043

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0214308)

MOL for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D MOL for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D SDF for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D-SDF for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

PDB for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D PDB for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

SMILES for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

INCHI for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

Structure for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D Structure for NP0214308 (hexadecyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)