NP-MRD: Showing NP-Card for aurantiamide acetate (NP0332835)

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Record Information

Version

2.0

Created at

2024-04-23 00:05:29 UTC

Updated at

2024-09-16 20:03:36 UTC

NP-MRD ID

NP0332835

Natural Product DOI

https://doi.org/10.57994/2110

Secondary Accession Numbers

None

Natural Product Identification

Common Name

aurantiamide acetate

Description

Aurantiamide acetate belongs to the class of organic compounds known as phenylalanine and derivatives. Phenylalanine and derivatives are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. aurantiamide acetate was first documented in 2024 (PMID: 38780134). Based on a literature review a small amount of articles have been published on aurantiamide acetate (PMID: 38906388) (PMID: 38892715) (PMID: 38430771) (PMID: 37405859).

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01052302422D          

 34 35  0  0  1  0            999 V2000
   -0.4114   -1.1125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3031   -0.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3031    0.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4114    0.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1258    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8403    0.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5548    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5548   -0.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2692    0.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4114    1.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258    1.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8403    1.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5548    1.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5548    2.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8403    3.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258    2.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0176   -1.1125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7321   -0.7000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7321    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4465    0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4465    1.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1610    1.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8755    1.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8755    0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1610    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0176    0.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0176   -1.9375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3031   -2.3500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3031   -3.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4114   -3.5875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258   -3.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258   -2.3500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4114   -1.9375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2326    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  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
  7  9  2  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 17  2  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  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
 20 25  1  0  0  0  0
 19 26  2  0  0  0  0
 17 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
M  END


  Mrv2104 01052302422D          

 34 35  0  0  1  0            999 V2000
   -0.4114   -1.1125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3031   -0.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3031    0.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4114    0.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1258    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8403    0.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5548    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5548   -0.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2692    0.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4114    1.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258    1.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8403    1.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5548    1.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5548    2.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8403    3.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258    2.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0176   -1.1125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7321   -0.7000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7321    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4465    0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4465    1.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1610    1.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8755    1.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8755    0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1610    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0176    0.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0176   -1.9375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3031   -2.3500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3031   -3.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4114   -3.5875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258   -3.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258   -2.3500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4114   -1.9375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2326    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  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
  7  9  2  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 17  2  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  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
 20 25  1  0  0  0  0
 19 26  2  0  0  0  0
 17 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0332835

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C.CC(=O)OC[C@H](CC1=CC=CC=C1)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H28N2O4.CH4/c1-20(30)33-19-24(17-21-11-5-2-6-12-21)28-27(32)25(18-22-13-7-3-8-14-22)29-26(31)23-15-9-4-10-16-23;/h2-16,24-25H,17-19H2,1H3,(H,28,32)(H,29,31);1H4/t24-,25-;/m0./s1

> <INCHI_KEY>
DMEQPARTZXHZCA-DKIIUIKKSA-N

> <FORMULA>
C28H32N2O4

> <MOLECULAR_WEIGHT>
460.574

> <EXACT_MASS>
460.236207518

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
48.047739911449824

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-3-phenyl-2-[(2S)-3-phenyl-2-(phenylformamido)propanamido]propyl acetate; methane

> <JCHEM_LOGP>
3.9912943369999994

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.169641981013303

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.820533081744859

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2995821608649532

> <JCHEM_POLAR_SURFACE_AREA>
84.5

> <JCHEM_REFRACTIVITY>
126.43110000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-3-phenyl-2-[(2S)-3-phenyl-2-(phenylformamido)propanamido]propyl acetate; methane

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-JAN-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-JAN-23         0                                  
HETATM    1  O   UNK     0      -0.768  -2.077   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       0.566  -1.307   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       0.566   0.233   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -0.768   1.003   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.102   0.233   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.435   1.003   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -4.769   0.233   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.769  -1.307   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -6.103   1.003   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.768   2.543   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.102   3.313   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.435   2.543   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.769   3.313   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.769   4.853   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.435   5.623   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.102   4.853   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.899  -2.077   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       3.233  -1.307   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       3.233   0.233   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.567   1.003   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.567   2.543   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.901   3.313   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.234   2.543   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.234   1.003   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.901   0.233   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.899   1.003   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.899  -3.617   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.566  -4.387   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.566  -5.927   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.768  -6.697   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.102  -5.927   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.102  -4.387   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.768  -3.617   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.634   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    4   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    2   18   27                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   26                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   19                                                            
CONECT   27   17   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   28                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   70    0
END

View in JSmol

Synonyms

Value	Source
Aurantiamide acetic acid	Generator

Chemical Formula

C₂₈H₃₂N₂O₄

Average Mass

460.5740 Da

Monoisotopic Mass

460.23621 Da

IUPAC Name

(2S)-3-phenyl-2-[(2S)-3-phenyl-2-(phenylformamido)propanamido]propyl acetate; methane

Traditional Name

(2S)-3-phenyl-2-[(2S)-3-phenyl-2-(phenylformamido)propanamido]propyl acetate; methane

CAS Registry Number

Not Available

SMILES

C.CC(=O)OC[C@H](CC1=CC=CC=C1)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C27H28N2O4.CH4/c1-20(30)33-19-24(17-21-11-5-2-6-12-21)28-27(32)25(18-22-13-7-3-8-14-22)29-26(31)23-15-9-4-10-16-23;/h2-16,24-25H,17-19H2,1H3,(H,28,32)(H,29,31);1H4/t24-,25-;/m0./s1

InChI Key

DMEQPARTZXHZCA-DKIIUIKKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C3D6O, experimental)	Not Available	Université de Rennes	Solenn Ferron	2024-04-23	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, C3D6O, experimental)	Not Available	Université de Rennes	Solenn Ferron	2024-04-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C3D6O, experimental)	Not Available	Université de Rennes	Solenn Ferron	2024-04-23	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
flavicans		Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Phenylalanine and derivatives

Alternative Parents

Substituents

Phenylalanine or derivatives
N-acyl-alpha amino acid or derivatives
Hippuric acid or derivatives
Alpha-amino acid amide
Amphetamine or derivatives
Benzoic acid or derivatives
Benzamide
Benzoyl
Fatty acyl
Benzenoid
Fatty amide
Monocyclic benzene moiety
Secondary carboxylic acid amide
Carboxylic acid ester
Carboxamide group
Monocarboxylic acid or derivatives
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Saturated hydrocarbon
Hydrocarbon
Aromatic homomonocyclic compound

Molecular Framework

Not Available

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	3.99	ChemAxon
pKa (Strongest Acidic)	13.82	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	84.5 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	126.43 m³·mol⁻¹	ChemAxon
Polarizability	48.05 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ferron S, Ismed F, Elyashberg ME, Buevich AV, Arifa N, Boustie J, Uriac P, Le Pogam P, Le Devehat F: CASE-DFT Structure Elucidation of Proton-Deficient Chlorodepsidones from the Indonesian Lichen Teloschistes flavicans and Structure Revision of Flavicansone. J Nat Prod. 2024 Sep 27;87(9):2148-2159. doi: 10.1021/acs.jnatprod.4c00277. Epub 2024 May 23. [PubMed:38780134 ]
Zhou K, Han L, Li W, Liu S, Chen T, Chen J, Lv J, Zhou X, Li Q, Meng X, Li H, Qin L: Pipersarmenoids, new amide alkaloids from Piper sarmentosum. Fitoterapia. 2024 Sep;177:106090. doi: 10.1016/j.fitote.2024.106090. Epub 2024 Jun 19. [PubMed:38906388 ]
Jiang FY, Yue SR, Tan YY, Tang N, Xu YS, Zhang BJ, Mao YJ, Xue ZS, Lu AP, Liu BC, Wang RR: Gynostemma pentaphyllum Extract Alleviates NASH in Mice: Exploration of Inflammation and Gut Microbiota. Nutrients. 2024 Jun 6;16(11):1782. doi: 10.3390/nu16111782. [PubMed:38892715 ]
Balkrishna A, Verma S, Priya Rani M, Nain P, Varshney A: Exploring the potential of Mustard (Brassica spp.) seeds through 'Kolhu' traditional method of extraction and novel identification of an anti-cancer dipeptide, Aurantiamide acetate (Asperglaucide) on ultra-performance liquid chromatography-mass spectrometry coupled with quadrupole time-of-flight (UPLC/MS-QToF) analytical platform. Food Chem. 2024 Jul 15;446:138870. doi: 10.1016/j.foodchem.2024.138870. Epub 2024 Feb 28. [PubMed:38430771 ]
Ngnokam Jouogo DC, Eckhardt P, Tamokou JD, Matsuete Takongmo G, Voutquenne-Nazabadioko L, Opatz T, Tapondjou LA, Ngnokam D, Teponno RB: A new phenolic glycoside from the leaves of Flacourtia flavescens Willd. Nat Prod Res. 2024 Aug;38(16):2737-2747. doi: 10.1080/14786419.2023.2232078. Epub 2023 Jul 5. [PubMed:37405859 ]

Showing NP-Card for aurantiamide acetate (NP0332835)

MOL for NP0332835 (aurantiamide acetate)

3D MOL for NP0332835 (aurantiamide acetate)

3D SDF for NP0332835 (aurantiamide acetate)

3D-SDF for NP0332835 (aurantiamide acetate)

PDB for NP0332835 (aurantiamide acetate)

3D PDB for NP0332835 (aurantiamide acetate)

SMILES for NP0332835 (aurantiamide acetate)

INCHI for NP0332835 (aurantiamide acetate)

Structure for NP0332835 (aurantiamide acetate)

3D Structure for NP0332835 (aurantiamide acetate)