NP-MRD: Showing NP-Card for 3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid (NP0234942)

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Record Information

Version

2.0

Created at

2022-09-06 17:17:49 UTC

Updated at

2022-09-06 17:17:49 UTC

NP-MRD ID

NP0234942

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid

Description

3-(2,3-Dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-N-[4-(N-hydroxyacetamido)butyl]propanimidic acid belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. Based on a literature review very few articles have been published on 3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-N-[4-(N-hydroxyacetamido)butyl]propanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062219172D          

 42 44  0  0  0  0            999 V2000
   -3.0298   -8.7727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3154   -8.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6009   -8.7727    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6009   -9.5977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8864   -8.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 29 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309062219172D          

 42 44  0  0  0  0            999 V2000
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    4.8293  -10.0102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5830   -9.6746    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1351  -10.2877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9555  -10.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2911   -9.4478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1116   -9.3616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5965  -10.0290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2609  -10.7827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7459  -11.4501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4405  -10.8689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1049  -11.6226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7226  -11.0022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9156  -10.8307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3025  -11.3827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  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
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  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  1  0  0  0  0
 22 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 13  1  4  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  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
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 32 38  1  0  0  0  0
 38 39  1  0  0  0  0
 31 40  1  0  0  0  0
 40 41  1  0  0  0  0
 29 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0234942

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(=NC1C(O)=NC(COC(=O)C1=CC=CC(O)=C1O)C(O)=NCCCCN(O)C(C)=O)C1=CC=CC(O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H32N4O11/c1-14-21(30-26(42-14)16-7-5-9-19(33)22(16)35)25(38)29-18(24(37)28-11-3-4-12-31(40)15(2)32)13-41-27(39)17-8-6-10-20(34)23(17)36/h5-10,14,18,21,33-36,40H,3-4,11-13H2,1-2H3,(H,28,37)(H,29,38)

> <INCHI_KEY>
UEUUKYCTOZDARB-UHFFFAOYSA-N

> <FORMULA>
C27H32N4O11

> <MOLECULAR_WEIGHT>
588.57

> <EXACT_MASS>
588.206757866

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
59.63593024878976

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-N-[4-(N-hydroxyacetamido)butyl]propanimidic acid

> <JCHEM_LOGP>
0.9191376841379612

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
2.963774190370913

> <JCHEM_PKA_STRONGEST_ACIDIC>
-5.058106074275

> <JCHEM_PKA_STRONGEST_BASIC>
11.48826158335696

> <JCHEM_POLAR_SURFACE_AREA>
234.52999999999994

> <JCHEM_REFRACTIVITY>
146.60290000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-N-[4-(N-hydroxyacetamido)butyl]propanimidic 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  C   UNK     0      -5.656 -16.376   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.322 -15.606   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.322 -14.066   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0      -2.988 -16.376   0.000  0.00  0.00           N+0
HETATM    5  O   UNK     0      -2.988 -17.916   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.655 -15.606   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.321 -16.376   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.013 -15.606   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.346 -16.376   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       3.680 -15.606   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       5.014 -16.376   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.014 -17.916   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.347 -15.606   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.347 -14.066   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.681 -13.296   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.681 -11.756   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.347 -10.986   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.015 -10.986   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.015  -9.446   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.348  -8.676   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.682  -9.446   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.682 -10.986   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.016 -11.756   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.348 -11.756   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.348 -13.296   0.000  0.00  0.00           O+0
HETATM   26  N   UNK     0       7.681 -16.376   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       7.681 -17.916   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.347 -18.686   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.015 -18.686   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0      10.422 -18.059   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      11.452 -19.204   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.984 -19.043   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.610 -17.636   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      15.142 -17.475   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      16.047 -18.721   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      15.420 -20.128   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      16.326 -21.374   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      13.889 -20.289   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      13.262 -21.696   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      10.682 -20.537   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       9.176 -20.217   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       8.031 -21.248   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   18   25                                                  
CONECT   25   24                                                            
CONECT   26   13   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   41                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   40                                                  
CONECT   32   31   33   38                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   32   39                                                  
CONECT   39   38                                                            
CONECT   40   31   41                                                       
CONECT   41   40   29   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

View in JSmol

Synonyms

Value	Source
3-(2,3-Dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-N-[4-(N-hydroxyacetamido)butyl]propanimidate	Generator

Chemical Formula

C₂₇H₃₂N₄O₁₁

Average Mass

588.5700 Da

Monoisotopic Mass

588.20676 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1OC(=NC1C(O)=NC(COC(=O)C1=CC=CC(O)=C1O)C(O)=NCCCCN(O)C(C)=O)C1=CC=CC(O)=C1O

InChI Identifier

InChI=1S/C27H32N4O11/c1-14-21(30-26(42-14)16-7-5-9-19(33)22(16)35)25(38)29-18(24(37)28-11-3-4-12-31(40)15(2)32)13-41-27(39)17-8-6-10-20(34)23(17)36/h5-10,14,18,21,33-36,40H,3-4,11-13H2,1-2H3,(H,28,37)(H,29,38)

InChI Key

UEUUKYCTOZDARB-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids and derivatives

Alternative Parents

Substituents

N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
M-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Salicylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Catechol
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
Phenol
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Acetamide
Oxazoline
Vinylogous acid
Acetohydroxamic acid
Carboxamide group
Carboxylic acid ester
Hydroxamic acid
Secondary carboxylic acid amide
Azacycle
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
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

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

162885973

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid (NP0234942)

MOL for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

3D MOL for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

3D SDF for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

3D-SDF for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

PDB for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

3D PDB for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

SMILES for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

INCHI for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

Structure for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)

3D Structure for NP0234942 (3-(2,3-dihydroxybenzoyloxy)-2-({[2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazol-4-yl](hydroxy)methylidene}amino)-n-[4-(n-hydroxyacetamido)butyl]propanimidic acid)