NP-MRD: Showing NP-Card for 2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid (NP0287701)

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Record Information

Version

2.0

Created at

2022-09-09 17:00:26 UTC

Updated at

2022-09-09 17:00:26 UTC

NP-MRD ID

NP0287701

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid

Description

2-{[(6-Amino-7-oxo-5,6,7,7a-tetrahydro-1H-inden-1-yl)(hydroxy)methylidene]amino}-3-(C-hydroxycarbonimidoyl)propanoic acid belongs to the class of organic compounds known as asparagine and derivatives. Asparagine and derivatives are compounds containing asparagine or a derivative thereof resulting from reaction of asparagine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. 2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid is found in Pantoea agglomerans. Based on a literature review very few articles have been published on 2-{[(6-amino-7-oxo-5,6,7,7a-tetrahydro-1H-inden-1-yl)(hydroxy)methylidene]amino}-3-(C-hydroxycarbonimidoyl)propanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    3.8497   -0.9892    2.2209 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1604    0.0013    2.1523 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0868    0.6620    1.0311 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5065    1.9794    0.9645 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5552   -0.0065   -0.1554 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3133    0.7139   -0.6851 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2577    0.7603    0.2787 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6017   -0.2390    0.7223 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9055   -1.4940    0.2569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4595   -0.0682    1.7101 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4457    1.3907    2.1110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3436    2.0651    1.4125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0284    1.1213    0.4954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6502    1.2120   -0.6308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2814    0.1235   -1.4072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3297   -1.1634   -0.6096 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4355   -2.2916   -1.5134 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1680   -1.2753    0.3083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5362   -2.2910    0.2691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8667   -0.1786    1.1834 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9180    0.0922   -1.9618 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7317   -0.0233   -2.9082 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6282   -0.3810   -2.1432 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0036    2.2798    0.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3024    0.0320   -0.9686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3552   -1.0793    0.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6510    1.7748   -0.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1936   -2.2004    0.9267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3710   -0.7064    2.6014 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1972    1.8307    2.8562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6013    3.1185    1.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7281    2.2153   -1.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7182   -0.0462   -2.3480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3200    0.4495   -1.6606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2362   -1.1499    0.0318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7467   -3.1613   -1.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6657   -2.3588   -2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5210   -0.1164    2.0938 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2354   -0.6024   -3.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10 20  1  0
 20 18  1  0
 18 19  2  0
 10  8  1  0
  8  9  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  6 21  1  0
 21 23  1  0
 21 22  2  0
 18 16  1  0
 20 13  1  0
 17 36  1  0
 17 37  1  0
 16 35  1  1
 15 33  1  0
 15 34  1  0
 14 32  1  0
 12 31  1  0
 11 30  1  0
 10 29  1  1
 20 38  1  1
  9 28  1  0
  6 27  1  6
  5 25  1  0
  5 26  1  0
  4 24  1  0
  2  1  1  0
 23 39  1  0
M  END


  Mrv1652309092219002D          

 22 23  0  0  0  0            999 V2000
    4.0456   -2.6727    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7600   -2.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4745   -2.6727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7600   -1.4352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4745   -1.0227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4745   -0.1977    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1890    0.2148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9035   -0.1977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1890    1.0398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5215    1.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7765    2.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6015    2.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1535    2.9225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9605    2.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2154    1.9663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0224    1.7948    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6634    1.3532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9183    0.5686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8564    1.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1890   -1.4352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9035   -1.0227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1890   -2.2602    0.0000 O   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  1  0  0  0  0
  6  5  1  4  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  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 12 19  1  0  0  0  0
  9 19  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287701

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC1CC=C2C=CC(C2C1=O)C(O)=NC(CC(O)=N)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H17N3O5/c15-8-4-2-6-1-3-7(11(6)12(8)19)13(20)17-9(14(21)22)5-10(16)18/h1-3,7-9,11H,4-5,15H2,(H2,16,18)(H,17,20)(H,21,22)

> <INCHI_KEY>
SOPAHPGXYDUTGN-UHFFFAOYSA-N

> <FORMULA>
C14H17N3O5

> <MOLECULAR_WEIGHT>
307.306

> <EXACT_MASS>
307.116820659

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
29.39578101009785

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[(6-amino-7-oxo-5,6,7,7a-tetrahydro-1H-inden-1-yl)(hydroxy)methylidene]amino}-3-(C-hydroxycarbonimidoyl)propanoic acid

> <JCHEM_LOGP>
-5.617952956417861

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.594123534050585

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.681223453346644

> <JCHEM_PKA_STRONGEST_BASIC>
12.589847282818818

> <JCHEM_POLAR_SURFACE_AREA>
157.05999999999997

> <JCHEM_REFRACTIVITY>
88.13879999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(C-hydroxycarbonimidoyl)propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  N   UNK     0       7.552  -4.989   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       8.885  -4.219   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.219  -4.989   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.885  -2.679   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.219  -1.909   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      10.219  -0.369   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      11.553   0.401   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      12.886  -0.369   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      11.553   1.941   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.307   2.846   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.783   4.311   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.323   4.311   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.353   5.455   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.860   5.135   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.335   3.670   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      16.842   3.350   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      14.305   2.526   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      14.781   1.061   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      12.799   2.846   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.553  -2.679   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.886  -1.909   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      11.553  -4.219   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   20                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12    9                                                  
CONECT   20    5   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
2-{[(6-amino-7-oxo-5,6,7,7a-tetrahydro-1H-inden-1-yl)(hydroxy)methylidene]amino}-3-(C-hydroxycarbonimidoyl)propanoate	Generator

Chemical Formula

C₁₄H₁₇N₃O₅

Average Mass

307.3060 Da

Monoisotopic Mass

307.11682 Da

IUPAC Name

2-{[(6-amino-7-oxo-5,6,7,7a-tetrahydro-1H-inden-1-yl)(hydroxy)methylidene]amino}-3-(C-hydroxycarbonimidoyl)propanoic acid

Traditional Name

2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(C-hydroxycarbonimidoyl)propanoic acid

CAS Registry Number

Not Available

SMILES

NC1CC=C2C=CC(C2C1=O)C(O)=NC(CC(O)=N)C(O)=O

InChI Identifier

InChI=1S/C14H17N3O5/c15-8-4-2-6-1-3-7(11(6)12(8)19)13(20)17-9(14(21)22)5-10(16)18/h1-3,7-9,11H,4-5,15H2,(H2,16,18)(H,17,20)(H,21,22)

InChI Key

SOPAHPGXYDUTGN-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
Pantoea agglomerans	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Asparagine and derivatives

Alternative Parents

Substituents

Asparagine or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Delta amino acid or derivatives
Cyclohexenone
Fatty acyl
Fatty amide
Amino acid
Secondary carboxylic acid amide
Primary carboxylic acid amide
Ketone
Carboxamide group
Monocarboxylic acid or derivatives
Carboxylic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Carbonyl group
Amine
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	-5.6	ChemAxon
pKa (Strongest Acidic)	-1.7	ChemAxon
pKa (Strongest Basic)	12.59	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	157.06 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	88.14 m³·mol⁻¹	ChemAxon
Polarizability	29.4 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

162945039

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid (NP0287701)

MOL for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

3D MOL for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

3D SDF for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

3D-SDF for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

PDB for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

3D PDB for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

SMILES for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

INCHI for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

Structure for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)

3D Structure for NP0287701 (2-{[(6-amino-7-oxo-1,5,6,7a-tetrahydroinden-1-yl)(hydroxy)methylidene]amino}-3-(c-hydroxycarbonimidoyl)propanoic acid)