NP-MRD: Showing NP-Card for n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid (NP0249835)

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Record Information

Version

2.0

Created at

2022-09-07 12:30:37 UTC

Updated at

2022-09-07 12:30:37 UTC

NP-MRD ID

NP0249835

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid

Description

N-[2-(ethoxycarbonyl)phenyl]docosanimidic acid belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated. n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid is found in Gentiana tibetica. N-[2-(ethoxycarbonyl)phenyl]docosanimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251510212D          

 35 35  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004251510212D          

 35 35  0  0  0  0            999 V2000
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   10.0026  -13.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -14.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -16.0875    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  2  0  0  0  0
 22 24  1  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
 29 30  2  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0249835

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCCCC(=O)NC1=CC=CC=C1C(=O)OCC

> <INCHI_IDENTIFIER>
InChI=1S/C31H53NO3/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-27-30(33)32-29-26-24-23-25-28(29)31(34)35-4-2/h23-26H,3-22,27H2,1-2H3,(H,32,33)

> <INCHI_KEY>
ZCKYIMVVSFEAIM-UHFFFAOYSA-N

> <FORMULA>
C31H53NO3

> <MOLECULAR_WEIGHT>
487.769

> <EXACT_MASS>
487.402544571

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
64.02171699744642

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
ethyl 2-docosanamidobenzoate

> <ALOGPS_LOGP>
9.60

> <JCHEM_LOGP>
11.368581584

> <ALOGPS_LOGS>
-7.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.431771038358015

> <JCHEM_PKA_STRONGEST_BASIC>
-3.623400486960237

> <JCHEM_POLAR_SURFACE_AREA>
55.400000000000006

> <JCHEM_REFRACTIVITY>
149.7408

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.14e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ethyl 2-docosanamidobenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0     -14.670 -25.410   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -13.337 -24.640   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.003 -25.410   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.669 -24.640   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.336 -25.410   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002 -24.640   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668 -25.410   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335 -24.640   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.001 -25.410   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667 -24.640   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334 -25.410   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000 -24.640   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334 -25.410   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667 -24.640   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001 -25.410   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335 -24.640   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668 -25.410   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002 -24.640   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336 -25.410   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.669 -24.640   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.003 -25.410   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.337 -24.640   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.337 -23.100   0.000  0.00  0.00           O+0
HETATM   24  N   UNK     0      14.670 -25.410   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      16.004 -24.640   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.004 -23.100   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      17.338 -22.330   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      18.672 -23.100   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      18.672 -24.640   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.338 -25.410   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      17.338 -26.950   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      16.004 -27.720   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      18.672 -27.720   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      18.672 -29.260   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      20.005 -30.030   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   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25   31                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   70    0
END

View in JSmol

Synonyms

Value	Source
N-[2-(Ethoxycarbonyl)phenyl]docosanimidate	Generator

Chemical Formula

C₃₁H₅₃NO₃

Average Mass

487.7690 Da

Monoisotopic Mass

487.40254 Da

IUPAC Name

ethyl 2-docosanamidobenzoate

Traditional Name

ethyl 2-docosanamidobenzoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCCCC(=O)NC1=CC=CC=C1C(=O)OCC

InChI Identifier

InChI=1S/C31H53NO3/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-27-30(33)32-29-26-24-23-25-28(29)31(34)35-4-2/h23-26H,3-22,27H2,1-2H3,(H,32,33)

InChI Key

ZCKYIMVVSFEAIM-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
Gentiana tibetica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Acylaminobenzoic acid and derivatives

Alternative Parents

Substituents

Acylaminobenzoic acid or derivatives
Benzoate ester
Anilide
Benzoyl
N-arylamide
Fatty acyl
Fatty amide
Vinylogous amide
Carboxamide group
Carboxylic acid ester
Secondary carboxylic acid amide
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organonitrogen 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	9.6	ALOGPS
logP	11.37	ChemAxon
logS	-7.4	ALOGPS
pKa (Strongest Acidic)	12.43	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.4 Å²	ChemAxon
Rotatable Bond Count	24	ChemAxon
Refractivity	149.74 m³·mol⁻¹	ChemAxon
Polarizability	64.02 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

5317244

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-(ethoxycarbonyl)phenyl]docosanimidic acid (NP0249835)

MOL for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

3D MOL for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

3D SDF for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

3D-SDF for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

PDB for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

3D PDB for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

SMILES for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

INCHI for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

Structure for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)

3D Structure for NP0249835 (n-[2-(ethoxycarbonyl)phenyl]docosanimidic acid)