NP-MRD: Showing NP-Card for n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid (NP0328983)

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Record Information

Version

2.0

Created at

2022-09-12 12:55:36 UTC

Updated at

2022-09-12 12:55:37 UTC

NP-MRD ID

NP0328983

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid

Description

Antimycin A 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. n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid is found in Streptomyces fimicarius. n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid was first documented in 2022 (PMID: 35892626). Based on a literature review a small amount of articles have been published on Antimycin A (PMID: 36057400) (PMID: 36012337) (PMID: 35966537) (PMID: 35736101).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122214552D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309122214552D          

 39 40  0  0  1  0            999 V2000
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    7.5814   -7.8983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5099   -6.1438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0402   -6.7758    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7346   -6.4259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9594   -6.1438    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4291   -6.7758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5469   -5.4293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7344   -5.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4523   -6.3478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9826   -6.9798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6398   -6.4911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3576   -7.2663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8879   -7.8983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5452   -7.4096    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  2  0  0  0  0
 15 16  1  4  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  4  0  0  0
 21 25  2  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
  7 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0328983

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCC1[C@@H](OC(=O)CC(C)C)[C@H](C)OC(=O)[C@@H](N=C(O)C2=CC=CC(N=CO)=C2O)[C@@H](C)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H40N2O9/c1-6-7-8-9-11-20-25(39-22(32)14-16(2)3)18(5)38-28(36)23(17(4)37-27(20)35)30-26(34)19-12-10-13-21(24(19)33)29-15-31/h10,12-13,15-18,20,23,25,33H,6-9,11,14H2,1-5H3,(H,29,31)(H,30,34)/t17-,18+,20?,23+,25+/m1/s1

> <INCHI_KEY>
UIFFUZWRFRDZJC-RBVQMQRASA-N

> <FORMULA>
C28H40N2O9

> <MOLECULAR_WEIGHT>
548.633

> <EXACT_MASS>
548.273380876

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
59.311344333330936

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(3S,4R,8R,9S)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzene-1-carboximidic acid

> <JCHEM_LOGP>
7.1471618496666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.351971855183726

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2877397377417656

> <JCHEM_PKA_STRONGEST_BASIC>
0.028330233565097562

> <JCHEM_POLAR_SURFACE_AREA>
164.30999999999997

> <JCHEM_REFRACTIVITY>
143.15400000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-[(3S,4R,8R,9S)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       0.220  -6.308   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.220  -7.848   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.554  -8.618   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.887  -7.848   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.221  -8.618   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.555  -7.848   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.888  -8.618   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.068  -7.628   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.541  -6.181   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       9.608  -7.628   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.788  -8.618   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.121  -7.848   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.055 -10.135   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      12.572 -10.402   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      13.098 -11.849   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      12.109 -13.029   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      14.615 -12.117   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.605 -10.937   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.122 -11.204   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.648 -12.652   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.658 -13.831   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      17.185 -15.278   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      16.195 -16.458   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      16.722 -17.905   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      15.142 -13.564   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      14.152 -14.744   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.285 -11.468   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.275 -12.648   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       8.838 -11.995   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.391 -11.468   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.401 -12.648   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.621 -10.135   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.104 -10.402   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.578 -11.849   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.567 -13.029   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.061 -12.117   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.534 -13.564   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.524 -14.744   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.018 -13.831   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   32                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   21   17   26                                                  
CONECT   26   25                                                            
CONECT   27   13   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    7   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   80    0
END

View in JSmol

Synonyms

Value	Source
Antimycin a1	MeSH

Chemical Formula

C₂₈H₄₀N₂O₉

Average Mass

548.6330 Da

Monoisotopic Mass

548.27338 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCC1[C@@H](OC(=O)CC(C)C)[C@H](C)OC(=O)[C@@H](N=C(O)C2=CC=CC(N=CO)=C2O)[C@@H](C)OC1=O

InChI Identifier

InChI=1S/C28H40N2O9/c1-6-7-8-9-11-20-25(39-22(32)14-16(2)3)18(5)38-28(36)23(17(4)37-27(20)35)30-26(34)19-12-10-13-21(24(19)33)29-15-31/h10,12-13,15-18,20,23,25,33H,6-9,11,14H2,1-5H3,(H,29,31)(H,30,34)/t17-,18+,20?,23+,25+/m1/s1

InChI Key

UIFFUZWRFRDZJC-RBVQMQRASA-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
Streptomyces fimicarius	LOTUS Database	35616633

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

Alpha-amino acid ester
N-acyl-alpha amino acid or derivatives
Tricarboxylic acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
Fatty acid ester
Phenol
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Oxacycle
Carboximidic acid derivative
Carboximidic acid
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organic oxygen 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

C00016357

Chemspider ID

17346333

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Antimycin A

METLIN ID

Not Available

PubChem Compound

16218979

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

de Haan LR, Reiniers MJ, Reeskamp LF, Belkouz A, Ao L, Cheng S, Ding B, van Golen RF, Heger M: Experimental Conditions That Influence the Utility of 2'7'-Dichlorodihydrofluorescein Diacetate (DCFH2-DA) as a Fluorogenic Biosensor for Mitochondrial Redox Status. Antioxidants (Basel). 2022 Jul 22;11(8). pii: antiox11081424. doi: 10.3390/antiox11081424. [PubMed:35892626 ]
Pan J, Zhang G, Hu Y, Jiang H, Tang X, Zhang D: MiR-6918-5p prevents renal tubular cell apoptosis by targeting MBD2 in ischemia/reperfusion-induced AKI. Life Sci. 2022 Nov 1;308:120921. doi: 10.1016/j.lfs.2022.120921. Epub 2022 Aug 31. [PubMed:36057400 ]
Zuberek M, Paciorek P, Rakowski M, Grzelak A: How to Use Respiratory Chain Inhibitors in Toxicology Studies-Whole-Cell Measurements. Int J Mol Sci. 2022 Aug 13;23(16). pii: ijms23169076. doi: 10.3390/ijms23169076. [PubMed:36012337 ]
Dikalov SI, Dikalova AE, Kirilyuk IA: Coupling of phagocytic NADPH oxidase activity and mitochondrial superoxide production. Front Cardiovasc Med. 2022 Jul 28;9:942736. doi: 10.3389/fcvm.2022.942736. eCollection 2022. [PubMed:35966537 ]
Paul SK, Chakraborty M, Rahman M, Gupta DR, Mahmud NU, Rahat AAM, Sarker A, Hannan MA, Rahman MM, Akanda AM, Ahmed JU, Islam T: Marine Natural Product Antimycin A Suppresses Wheat Blast Disease Caused by Magnaporthe oryzae Triticum. J Fungi (Basel). 2022 Jun 9;8(6). pii: jof8060618. doi: 10.3390/jof8060618. [PubMed:35736101 ]
LOTUS database [Link]

Showing NP-Card for n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid (NP0328983)

MOL for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D MOL for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D SDF for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D-SDF for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

PDB for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D PDB for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

SMILES for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

INCHI for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

Structure for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D Structure for NP0328983 (n-[(3s,4r,8r,9s)-7-hexyl-4,9-dimethyl-8-[(3-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl]-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)