NP-MRD: Showing NP-Card for (2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid (NP0231136)

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Record Information

Version

2.0

Created at

2022-09-06 11:51:13 UTC

Updated at

2022-09-06 11:51:13 UTC

NP-MRD ID

NP0231136

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid

Description

(2R)-4-[(E)-2-{[(1S)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. (2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid is found in Phytolacca acinosa. Based on a literature review very few articles have been published on (2R)-4-[(E)-2-{[(1S)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 41  0  0  0  0  0  0  0  0999 V2000
   -4.9471    3.6684    0.3798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7744    3.3240    0.6418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8334    4.2604    1.0032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4183    1.9036    0.5573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2617    1.0079    0.2265 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0105   -0.3855    0.1184 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3497   -0.9122   -1.2553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1918   -2.1116   -1.5275 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8350   -0.0448   -2.1976 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6291   -0.8446    0.4182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6996    0.2358    0.7962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3151   -0.1549    1.1076 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1019   -1.4064    1.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4330   -1.7950    1.3582 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4887   -1.8180    0.3549 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5961   -0.3993   -0.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6289   -0.1896   -1.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5713    1.2910   -1.5821 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4952    1.6007   -2.5591 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7355   -2.3128    0.9849 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7936   -2.6210    2.2173 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9019   -2.4649    0.2580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0518    1.5061    0.8630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1475    5.1339    1.3916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7753   -0.8961    0.7803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6571   -0.2963   -2.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6801   -1.5574    1.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1630   -1.4364   -0.4079 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4137    0.6006    1.3911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6605   -2.1462    0.7705 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6719   -2.0745    2.3244 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2073   -2.5036   -0.4767 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839    0.2378    0.7448 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5887   -0.1436   -0.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6309   -0.4373   -0.7845 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4216   -0.8311   -2.0595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7639    1.8763   -0.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5300    1.4937   -1.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1113    2.2988   -2.2174 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8376   -2.9186   -0.6391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3058    2.2628    1.1513 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11 23  2  0
 23  4  1  0
  4  5  2  0
  5  6  1  0
  6 10  1  0
  6  7  1  0
  7  9  1  0
  7  8  2  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
 15 20  1  0
 20 22  1  0
 20 21  2  0
 10 11  1  0
 19 39  1  0
 18 37  1  0
 18 38  1  0
 17 35  1  0
 17 36  1  0
 16 33  1  0
 16 34  1  0
 15 32  1  6
 14 31  1  0
 13 30  1  0
 12 29  1  0
 23 41  1  0
  6 25  1  1
 10 27  1  0
 10 28  1  0
  9 26  1  0
  3 24  1  0
 22 40  1  0
M  END


  Mrv1652309062213512D          

 23 23  0  0  1  0            999 V2000
   12.0138    5.8559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    5.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7763    6.5704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7763    5.1414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    4.4270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7763    3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.1888    2.9980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7763    2.2836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0138    2.9980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5388    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3013    5.1414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4763    5.1414    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0638    4.4270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2388    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8263    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888    2.9980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4763    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3013    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0638    2.9980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    5.1414    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  6 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
 13 14  1  0  0  0  0
 15 14  1  6  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
 15 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 11 23  2  0  0  0  0
  4 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0231136

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCCC[C@H](N\C=C\C1=CC(=N[C@H](C1)C(O)=O)C(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H18N2O7/c17-5-1-2-9(12(18)19)15-4-3-8-6-10(13(20)21)16-11(7-8)14(22)23/h3-4,6,9,11,15,17H,1-2,5,7H2,(H,18,19)(H,20,21)(H,22,23)/b4-3+/t9-,11+/m0/s1

> <INCHI_KEY>
QOCJNRPNBHJDDW-NCDNIOQDSA-N

> <FORMULA>
C14H18N2O7

> <MOLECULAR_WEIGHT>
326.305

> <EXACT_MASS>
326.111400928

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
31.929616444745335

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-4-[(E)-2-{[(1S)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid

> <JCHEM_LOGP>
-2.898723879319887

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
3.250490086497687

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.189613629855749

> <JCHEM_PKA_STRONGEST_BASIC>
8.72384115654447

> <JCHEM_POLAR_SURFACE_AREA>
156.51999999999998

> <JCHEM_REFRACTIVITY>
78.3321

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-4-[(E)-2-{[(1S)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  O   UNK     0      22.426  10.931   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      20.886  10.931   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      20.116  12.265   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      20.116   9.597   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      20.886   8.264   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      20.116   6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.886   5.596   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      20.116   4.263   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      22.426   5.596   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      18.576   6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.806   8.264   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.266   8.264   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.496   9.597   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      13.956   9.597   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      13.186   8.264   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.646   8.264   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.876   6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.566   5.596   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      13.956   6.930   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      15.496   6.930   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      13.186   5.596   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      18.576   9.597   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   23                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    6   11                                                       
CONECT   11   10   12   23                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   15   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   11    4                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Value	Source
(2R)-4-[(e)-2-{[(1S)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylate	Generator

Chemical Formula

C₁₄H₁₈N₂O₇

Average Mass

326.3050 Da

Monoisotopic Mass

326.11140 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OCCC[C@H](N\C=C\C1=CC(=N[C@H](C1)C(O)=O)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C14H18N2O7/c17-5-1-2-9(12(18)19)15-4-3-8-6-10(13(20)21)16-11(7-8)14(22)23/h3-4,6,9,11,15,17H,1-2,5,7H2,(H,18,19)(H,20,21)(H,22,23)/b4-3+/t9-,11+/m0/s1

InChI Key

QOCJNRPNBHJDDW-NCDNIOQDSA-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
Phytolacca acinosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

L-alpha-amino acids

Alternative Parents

Substituents

L-alpha-amino acid
Dihydropyridinecarboxylic acid derivative
Tricarboxylic acid or derivatives
Dihydropyridine
Hydropyridine
Amino acid
Ketimine
Allylamine
Carboxylic acid
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Secondary aliphatic amine
Secondary amine
Enamine
Hydrocarbon derivative
Organonitrogen compound
Imine
Organooxygen compound
Primary alcohol
Alcohol
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Carbonyl group
Amine
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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

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

4444617

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281191

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid (NP0231136)

MOL for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

3D MOL for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

3D SDF for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

3D-SDF for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

PDB for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

3D PDB for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

SMILES for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

INCHI for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

Structure for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)

3D Structure for NP0231136 ((2r)-4-[(1e)-2-{[(1s)-1-carboxy-4-hydroxybutyl]amino}ethenyl]-2,3-dihydropyridine-2,6-dicarboxylic acid)