NP-MRD: Showing NP-Card for Aralionine A (NP0051093)

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Record Information

Version

2.0

Created at

2022-04-27 22:31:37 UTC

Updated at

2022-04-27 22:31:37 UTC

NP-MRD ID

NP0051093

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Aralionine A

Description

Aralionine A belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. Aralionine A is found in Araliorhamnus vaginata. Based on a literature review very few articles have been published on Aralionine A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282200312D          

 43 46  0  0  1  0            999 V2000
    0.7385   -0.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1581    0.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3955    1.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1904    1.5252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7374    0.9105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5284    0.1145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8275    2.1128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6443    2.3785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4695    2.1170    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0490    1.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8469    1.5216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2520    0.6391    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0714   -0.1742    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6226   -0.9292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2079   -1.6128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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 38 43  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282200312D          

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    4.1865   -3.3842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7532   -1.8121    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3598   -0.8918    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0229   -0.1766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5297   -0.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5888   -2.2193    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4519   -2.0861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2830   -1.8998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9016   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1426    0.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8766   -0.1259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4820    1.3664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0620    2.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4670    2.7953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2920    2.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7119    2.0938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3069    1.3751    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  1 18  1  0  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 16 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  1  6  0  0  0
 12 36  1  6  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 38 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0051093

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)[C@H](N(C)C)C(=O)N[C@H]1[C@H](OC2=CC=C(C=C2)\C=C/NC(=O)[C@@H](NC1=O)C(=O)C1=CC=CC=C1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C34H38N4O5/c1-5-22(2)29(38(3)4)34(42)37-28-31(25-14-10-7-11-15-25)43-26-18-16-23(17-19-26)20-21-35-32(40)27(36-33(28)41)30(39)24-12-8-6-9-13-24/h6-22,27-29,31H,5H2,1-4H3,(H,35,40)(H,36,41)(H,37,42)/b21-20-/t22-,27-,28-,29-,31+/m0/s1

> <INCHI_KEY>
JGTFUPZKTHJDJO-NLPARSELSA-N

> <FORMULA>
C34H38N4O5

> <MOLECULAR_WEIGHT>
582.701

> <EXACT_MASS>
582.28422034

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
61.2668505280907

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S)-N-[(3R,4S,7S,10Z)-7-benzoyl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-methylpentanamide

> <ALOGPS_LOGP>
3.62

> <JCHEM_LOGP>
4.298518588999999

> <ALOGPS_LOGS>
-5.27

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.124600279140589

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.496032160529696

> <JCHEM_PKA_STRONGEST_BASIC>
7.354644977730298

> <JCHEM_POLAR_SURFACE_AREA>
116.84

> <JCHEM_REFRACTIVITY>
164.26929999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.09e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S)-N-[(3R,4S,7S,10Z)-7-benzoyl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-methylpentanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       1.379  -0.287   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.295   0.859   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.738   2.341   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.222   2.847   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.243   1.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.853   0.214   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.411   3.944   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.936   4.440   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       6.476   3.952   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       7.558   2.745   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.048   2.840   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.937   1.193   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       7.600  -0.325   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       6.762  -1.735   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.855  -3.011   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.255  -2.249   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.685  -2.280   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.228  -1.667   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.396  -3.792   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.561  -4.799   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.272  -6.312   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.817  -6.817   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.652  -5.810   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.941  -4.298   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       5.740  -3.894   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       7.424  -4.668   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.815  -6.317   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.873  -3.383   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       8.138  -1.665   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       9.376  -0.330   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.589  -0.647   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.432  -4.143   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.044  -3.894   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.595  -3.546   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.016  -5.652   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.599   1.022   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      10.970  -0.235   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      10.233   2.551   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.449   3.876   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.205   5.218   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      11.745   5.234   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      12.529   3.908   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      11.773   2.567   0.000  0.00  0.00           C+0
CONECT    1    2    6   18                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   36                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   25                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17    1                                                       
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   16   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   32                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   28   33   35                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   32                                                            
CONECT   36   12   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   43                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   38                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₃₈N₄O₅

Average Mass

582.7010 Da

Monoisotopic Mass

582.28422 Da

IUPAC Name

(2S,3S)-N-[(3R,4S,7S,10Z)-7-benzoyl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-methylpentanamide

Traditional Name

(2S,3S)-N-[(3R,4S,7S,10Z)-7-benzoyl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-methylpentanamide

CAS Registry Number

Not Available

SMILES

CC[C@H](C)[C@H](N(C)C)C(=O)N[C@H]1[C@H](OC2=CC=C(C=C2)\C=C/NC(=O)[C@@H](NC1=O)C(=O)C1=CC=CC=C1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C34H38N4O5/c1-5-22(2)29(38(3)4)34(42)37-28-31(25-14-10-7-11-15-25)43-26-18-16-23(17-19-26)20-21-35-32(40)27(36-33(28)41)30(39)24-12-8-6-9-13-24/h6-22,27-29,31H,5H2,1-4H3,(H,35,40)(H,36,41)(H,37,42)/b21-20-/t22-,27-,28-,29-,31+/m0/s1

InChI Key

JGTFUPZKTHJDJO-NLPARSELSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Araliorhamnus vaginata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Cyclic alpha peptide
Isoleucine or derivatives
N-acyl-alpha amino acid or derivatives
Alkyl-phenylketone
Macrolactam
Alpha-amino acid amide
Alpha-amino acid or derivatives
Phenylketone
Benzoyl
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Monocyclic benzene moiety
Fatty amide
Fatty acyl
Benzenoid
1,3-dicarbonyl compound
N-acyl-amine
Amino acid or derivatives
Carboxamide group
Ketone
Lactam
Tertiary aliphatic amine
Tertiary amine
Secondary carboxylic acid amide
Azacycle
Ether
Oxacycle
Organoheterocyclic compound
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Amine
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

cyclic peptide (CHEBI:2801 )

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	3.62	ALOGPS
logP	4.3	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	10.5	ChemAxon
pKa (Strongest Basic)	7.35	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	116.84 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	164.27 m³·mol⁻¹	ChemAxon
Polarizability	61.27 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00001994

Chemspider ID

4444904

KEGG Compound ID

C09999

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281583

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Aralionine A (NP0051093)

MOL for NP0051093 (Aralionine A)

3D MOL for NP0051093 (Aralionine A)

3D SDF for NP0051093 (Aralionine A)

3D-SDF for NP0051093 (Aralionine A)

PDB for NP0051093 (Aralionine A)

3D PDB for NP0051093 (Aralionine A)

SMILES for NP0051093 (Aralionine A)

INCHI for NP0051093 (Aralionine A)

Structure for NP0051093 (Aralionine A)

3D Structure for NP0051093 (Aralionine A)