NP-MRD: Showing NP-Card for n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid (NP0246533)

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Record Information

Version

2.0

Created at

2022-09-07 08:02:41 UTC

Updated at

2022-09-07 08:02:42 UTC

NP-MRD ID

NP0246533

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid

Description

Tembamide acetate belongs to the class of organic compounds known as benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group. n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid is found in Piper guayranum. Tembamide acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
   -6.0287    2.9117   -1.5278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4345    2.3924   -0.3705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2787    1.6486   -0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5684    1.3260   -1.4799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4016    0.5629   -1.3287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9593    0.1405   -0.1000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7508   -0.6681   -0.0044 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3923    0.1417   -0.6454 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6490   -0.4011   -0.4994 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8778   -0.9319   -0.3567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2639   -2.0698   -0.7401 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9741   -0.1498    0.3216 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4697    0.9585   -0.3059 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4921    1.7096    0.2894 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0011    1.3331    1.5143 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4923    0.2164    2.1365 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4668   -0.5319    1.5294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8264   -1.9428   -0.6066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4800   -3.0617    0.1411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5705   -4.4079   -0.5157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101   -2.8904    1.3220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7069    0.4931    1.0064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8523    1.2330    0.9474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7461    2.3349   -2.4295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1486    2.7514   -1.4509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8483    4.0084   -1.6544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8790    1.6456   -2.4596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8692    0.3238   -2.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4309   -0.7989    1.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1090    0.4516   -1.6955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3528    1.1286   -0.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2295   -1.5021   -1.1837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1004    1.2909   -1.2587 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8777    2.5754   -0.1971 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8063    1.9122    1.9990 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8891   -0.0824    3.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0860   -1.4036    2.0375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7634   -5.2044    0.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4286   -4.4191   -1.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3571   -4.6934   -1.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3520    0.1521    1.9682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4526    1.5169    1.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 22  1  0
 22 23  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  7 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 23  3  1  0
 17 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
 22 41  1  0
 23 42  1  0
  7 29  1  1
  8 30  1  0
  8 31  1  0
  9 32  1  0
 13 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
 17 37  1  0
 20 38  1  0
 20 39  1  0
 20 40  1  0
M  END


  Mrv0541 04121521142D          

 23 24  0  0  0  0            999 V2000
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  6  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  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
  9 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
M  END
> <DATABASE_ID>
NP0246533

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C(CNC(=O)C1=CC=CC=C1)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H19NO4/c1-13(20)23-17(14-8-10-16(22-2)11-9-14)12-19-18(21)15-6-4-3-5-7-15/h3-11,17H,12H2,1-2H3,(H,19,21)

> <INCHI_KEY>
UARXESBXWOAPAK-UHFFFAOYSA-N

> <FORMULA>
C18H19NO4

> <MOLECULAR_WEIGHT>
313.353

> <EXACT_MASS>
313.131408096

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
33.86619437311406

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(4-methoxyphenyl)-2-(phenylformamido)ethyl acetate

> <ALOGPS_LOGP>
2.61

> <JCHEM_LOGP>
2.425154496

> <ALOGPS_LOGS>
-4.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.96800981575057

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9420806526340021

> <JCHEM_POLAR_SURFACE_AREA>
64.63

> <JCHEM_REFRACTIVITY>
86.22290000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.32e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(4-methoxyphenyl)-2-(phenylformamido)ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334 -11.550   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       0.000  -3.080   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    6   10   20                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20    9   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
Tembamide acetic acid	Generator

Chemical Formula

C₁₈H₁₉NO₄

Average Mass

313.3530 Da

Monoisotopic Mass

313.13141 Da

IUPAC Name

1-(4-methoxyphenyl)-2-(phenylformamido)ethyl acetate

Traditional Name

1-(4-methoxyphenyl)-2-(phenylformamido)ethyl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C(CNC(=O)C1=CC=CC=C1)OC(C)=O

InChI Identifier

InChI=1S/C18H19NO4/c1-13(20)23-17(14-8-10-16(22-2)11-9-14)12-19-18(21)15-6-4-3-5-7-15/h3-11,17H,12H2,1-2H3,(H,19,21)

InChI Key

UARXESBXWOAPAK-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
Piper guayranum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzyloxycarbonyls

Direct Parent

Benzyloxycarbonyls

Alternative Parents

Substituents

Benzyloxycarbonyl
Benzamide
Benzoic acid or derivatives
Phenoxy compound
Anisole
Benzoyl
Methoxybenzene
Phenol ether
Alkyl aryl ether
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid ester
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Organonitrogen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic nitrogen 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
logP	2.61	ALOGPS
logP	2.43	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	14.97	ChemAxon
pKa (Strongest Basic)	-0.94	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.63 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	86.22 m³·mol⁻¹	ChemAxon
Polarizability	33.87 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

177584

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-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid (NP0246533)

MOL for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

3D MOL for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

3D SDF for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

3D-SDF for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

PDB for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

3D PDB for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

SMILES for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

INCHI for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

Structure for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)

3D Structure for NP0246533 (n-[2-(acetyloxy)-2-(4-methoxyphenyl)ethyl]benzenecarboximidic acid)