NP-MRD: Showing NP-Card for (2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide (NP0298554)

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Record Information

Version

2.0

Created at

2022-09-10 09:52:35 UTC

Updated at

2022-09-10 09:52:35 UTC

NP-MRD ID

NP0298554

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide

Description

Amathamide C belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from reaction of proline at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. (2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide was first documented in 2011 (PMID: 21069234). Based on a literature review a small amount of articles have been published on Amathamide C.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
    6.3805    2.0548   -0.2979 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5856    1.5976    0.7815 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8060    0.4512    0.7071 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3179   -0.7599    1.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1264   -0.9482    1.6814 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.5366   -1.8922    0.9860 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2370   -1.8059    0.5495 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1651   -3.3956    0.4493 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.7018   -0.5550    0.1795 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3457   -0.5778   -0.2584 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6206    0.4162   -0.6500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7580    0.2068   -1.0660 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0471    0.5934   -2.4270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6935   -0.3387   -0.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2977   -0.6303    1.0056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1008   -0.5907   -0.4658 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8620    0.5875   -1.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1457    0.5806   -0.2003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2345   -0.8766    0.2341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8562   -1.1351    0.6186 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6041   -0.5076    1.9009 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4751    0.5591    0.2569 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9048    2.3158   -0.2036 Br  0  0  0  0  0  0  0  0  0  0  0  0
    7.4248    1.6780   -0.1835 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4047    3.1662   -0.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0154    1.6953   -1.2814 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9274   -2.8580    1.2644 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7955   -1.5490   -0.2854 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9498    1.4202   -0.6999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1558    1.6715   -2.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9277    0.0204   -2.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1911    0.2738   -3.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1144   -1.3677   -1.2864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3183    1.5443   -0.9123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1540    0.4809   -2.0664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1058    1.2629    0.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0372    0.7643   -0.8565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4307   -1.4687   -0.6803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9512   -1.0345    1.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1680    0.5035    1.8164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6019   -0.4530    2.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9650   -1.1000    2.5659 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
  4  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
  9 22  2  0
 22 23  1  0
 22  3  1  0
 20 16  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  6 27  1  0
 10 28  1  0
 11 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
 16 33  1  6
 17 34  1  0
 17 35  1  0
 18 36  1  0
 18 37  1  0
 19 38  1  0
 19 39  1  0
 21 40  1  0
 21 41  1  0
 21 42  1  0
M  END


  Mrv1652309102211522D          

 23 24  0  0  1  0            999 V2000
    3.4656    9.3027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    8.4777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801    8.0652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946    8.4777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946    9.3027    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.6091    8.0652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6091    7.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3235    6.8277    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.8946    6.8277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946    6.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801    5.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801    4.7652    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    4.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946    4.3527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6091    4.7652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946    3.5277    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5620    3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3071    2.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821    2.2581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2272    3.0428    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4425    3.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801    7.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    6.8277    0.0000 Br  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
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16 14  1  6  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
 16 20  1  0  0  0  0
 20 21  1  0  0  0  0
  9 22  2  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0298554

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(Br)C=C(Br)C(\C=C\N(C)C(=O)[C@@H]2CCCN2C)=C1Br

> <INCHI_IDENTIFIER>
InChI=1S/C16H19Br3N2O2/c1-20-7-4-5-13(20)16(22)21(2)8-6-10-11(17)9-12(18)15(23-3)14(10)19/h6,8-9,13H,4-5,7H2,1-3H3/b8-6+/t13-/m0/s1

> <INCHI_KEY>
ZQRHBJBZUREHPH-CFNZNRNTSA-N

> <FORMULA>
C16H19Br3N2O2

> <MOLECULAR_WEIGHT>
511.052

> <EXACT_MASS>
507.899667

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
40.66026236626708

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-N,1-dimethyl-N-[(E)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide

> <JCHEM_LOGP>
4.182716023666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.12821189183108

> <JCHEM_POLAR_SURFACE_AREA>
32.78

> <JCHEM_REFRACTIVITY>
103.76689999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-N,1-dimethyl-N-[(E)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       6.469  17.365   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.469  15.825   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.803  15.055   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.137  15.825   0.000  0.00  0.00           C+0
HETATM    5 Br   UNK     0       9.137  17.365   0.000  0.00  0.00          Br+0
HETATM    6  C   UNK     0      10.470  15.055   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.470  13.515   0.000  0.00  0.00           C+0
HETATM    8 Br   UNK     0      11.804  12.745   0.000  0.00  0.00          Br+0
HETATM    9  C   UNK     0       9.137  12.745   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.137  11.205   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.803  10.435   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       7.803   8.895   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       6.469   8.125   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.137   8.125   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.470   8.895   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.137   6.585   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.382   5.680   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.907   4.215   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.367   4.215   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       7.891   5.680   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       6.426   6.156   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.803  13.515   0.000  0.00  0.00           C+0
HETATM   23 Br   UNK     0       6.469  12.745   0.000  0.00  0.00          Br+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   20                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   16   21                                                  
CONECT   21   20                                                            
CONECT   22    9    3   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₉Br₃N₂O₂

Average Mass

511.0520 Da

Monoisotopic Mass

507.89967 Da

IUPAC Name

(2S)-N,1-dimethyl-N-[(E)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide

Traditional Name

(2S)-N,1-dimethyl-N-[(E)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide

CAS Registry Number

Not Available

SMILES

COC1=C(Br)C=C(Br)C(\C=C\N(C)C(=O)[C@@H]2CCCN2C)=C1Br

InChI Identifier

InChI=1S/C16H19Br3N2O2/c1-20-7-4-5-13(20)16(22)21(2)8-6-10-11(17)9-12(18)15(23-3)14(10)19/h6,8-9,13H,4-5,7H2,1-3H3/b8-6+/t13-/m0/s1

InChI Key

ZQRHBJBZUREHPH-CFNZNRNTSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from reaction of proline 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

Proline and derivatives

Alternative Parents

Substituents

Proline or derivatives
Alpha-amino acid amide
Phenoxy compound
Anisole
Phenol ether
Pyrrolidine carboxylic acid or derivatives
Methoxybenzene
Pyrrolidine-2-carboxamide
Styrene
Alkyl aryl ether
Halobenzene
Bromobenzene
Aryl bromide
Aryl halide
Monocyclic benzene moiety
Benzenoid
N-alkylpyrrolidine
Pyrrolidine
Tertiary carboxylic acid amide
Carboxamide group
Tertiary amine
Tertiary aliphatic amine
Azacycle
Organoheterocyclic compound
Ether
Amine
Organooxygen compound
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organonitrogen compound
Organohalogen compound
Organobromide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	4.18	ChemAxon
pKa (Strongest Basic)	8.13	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	32.78 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	103.77 m³·mol⁻¹	ChemAxon
Polarizability	40.66 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

29216090

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102579136

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Carroll AR, Duffy S, Sykes M, Avery VM: Wilsoniamines A and B: novel alkaloids from the temperate Australian bryozoan, Amathia wilsoni. Org Biomol Chem. 2011 Jan 21;9(2):604-9. doi: 10.1039/c0ob00538j. Epub 2010 Nov 10. [PubMed:21069234 ]
LOTUS database [Link]

Showing NP-Card for (2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide (NP0298554)

MOL for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

3D MOL for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

3D SDF for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

3D-SDF for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

PDB for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

3D PDB for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

SMILES for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

INCHI for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

Structure for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)

3D Structure for NP0298554 ((2s)-n,1-dimethyl-n-[(1e)-2-(2,4,6-tribromo-3-methoxyphenyl)ethenyl]pyrrolidine-2-carboxamide)