NP-MRD: Showing NP-Card for n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid (NP0203188)

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Record Information

Version

2.0

Created at

2022-09-04 22:35:06 UTC

Updated at

2022-09-04 22:35:06 UTC

NP-MRD ID

NP0203188

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid

Description

N-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid belongs to the class of organic compounds known as 1-hydroxy-2-unsubstituted benzenoids. These are phenols that are unsubstituted at the 2-position. n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid is found in Acnistus arborescens and Croton bonplandianus. N-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161520302D          

 39 39  0  0  0  0            999 V2000
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M  END

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M  END


  Mrv1533004161520302D          

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   11.4315  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -19.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -18.5625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657  -19.8000    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
   32.1512  -20.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -19.8000    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  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 33 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0203188

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCC1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C36H65NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-36(39)37-33-32-34-28-30-35(38)31-29-34/h28-31,38H,2-27,32-33H2,1H3,(H,37,39)

> <INCHI_KEY>
WCHTVXNKYFQVGW-UHFFFAOYSA-N

> <FORMULA>
C36H65NO2

> <MOLECULAR_WEIGHT>
543.921

> <EXACT_MASS>
543.501530337

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
74.99491182171053

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[2-(4-hydroxyphenyl)ethyl]octacosanamide

> <ALOGPS_LOGP>
10.15

> <JCHEM_LOGP>
12.717709210333332

> <ALOGPS_LOGS>
-7.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.295062164085657

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.504587594545225

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2661573740448295

> <JCHEM_POLAR_SURFACE_AREA>
49.33

> <JCHEM_REFRACTIVITY>
170.36299999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
29

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.67e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[2-(4-hydroxyphenyl)ethyl]octacosanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      17.338 -34.650   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.672 -35.420   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.005 -34.650   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.339 -35.420   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.673 -34.650   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      24.006 -35.420   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      25.340 -34.650   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      26.674 -35.420   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      28.007 -34.650   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      29.341 -35.420   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      30.675 -34.650   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      32.008 -35.420   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      33.342 -34.650   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      34.676 -35.420   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      36.009 -34.650   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      37.343 -35.420   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      38.677 -34.650   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      40.010 -35.420   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      41.344 -34.650   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      42.678 -35.420   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      44.011 -34.650   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      45.345 -35.420   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      46.679 -34.650   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      48.012 -35.420   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      49.346 -34.650   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      50.680 -35.420   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      52.013 -34.650   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      53.347 -35.420   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      53.347 -36.960   0.000  0.00  0.00           O+0
HETATM   30  N   UNK     0      54.681 -34.650   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      56.015 -35.420   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      57.348 -34.650   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      58.682 -35.420   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      60.016 -34.650   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      61.349 -35.420   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      61.349 -36.960   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      62.683 -37.730   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      60.016 -37.730   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      58.682 -36.960   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   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   39                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   33                                                       
MASTER        0    0    0    0    0    0    0    0   39    0   78    0
END

View in JSmol

Synonyms

Value	Source
N-[2-(4-Hydroxyphenyl)ethyl]octacosanimidate	Generator

Chemical Formula

C₃₆H₆₅NO₂

Average Mass

543.9210 Da

Monoisotopic Mass

543.50153 Da

IUPAC Name

N-[2-(4-hydroxyphenyl)ethyl]octacosanamide

Traditional Name

N-[2-(4-hydroxyphenyl)ethyl]octacosanamide

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCC1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C36H65NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-36(39)37-33-32-34-28-30-35(38)31-29-34/h28-31,38H,2-27,32-33H2,1H3,(H,37,39)

InChI Key

WCHTVXNKYFQVGW-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
Acnistus arborescens	LOTUS Database	35616633
Croton bonplandianus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-hydroxy-2-unsubstituted benzenoids. These are phenols that are unsubstituted at the 2-position.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenols

Sub Class

1-hydroxy-2-unsubstituted benzenoids

Direct Parent

1-hydroxy-2-unsubstituted benzenoids

Alternative Parents

Substituents

1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Fatty amide
Fatty acyl
N-acyl-amine
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	10.15	ALOGPS
logP	12.72	ChemAxon
logS	-7.5	ALOGPS
pKa (Strongest Acidic)	9.5	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	49.33 Å²	ChemAxon
Rotatable Bond Count	29	ChemAxon
Refractivity	170.36 m³·mol⁻¹	ChemAxon
Polarizability	74.99 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

90873687

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid (NP0203188)

MOL for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

3D MOL for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

3D SDF for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

3D-SDF for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

PDB for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

3D PDB for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

SMILES for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

INCHI for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

Structure for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)

3D Structure for NP0203188 (n-[2-(4-hydroxyphenyl)ethyl]octacosanimidic acid)