NP-MRD: Showing NP-Card for (z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium (NP0168991)

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Record Information

Version

2.0

Created at

2022-09-03 04:52:41 UTC

Updated at

2022-09-03 04:52:41 UTC

NP-MRD ID

NP0168991

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium

Description

Fragin belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen. (z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium is found in Pseudomonas fragi. (z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium was first documented in 2018 (PMID: 29602945). Based on a literature review a small amount of articles have been published on Fragin (PMID: 31945256) (PMID: 34594316) (PMID: 34659189) (PMID: 32212725).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 45  0  0  0  0  0  0  0  0999 V2000
    6.0318   -1.3699    0.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6231   -0.3827   -1.0469 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3035    0.9707   -0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1765    0.9096    0.5205 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9507    0.3866   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8065    0.3214    0.8247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5854   -0.2130    0.0850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5161   -0.2582    1.1109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2389   -1.0960    2.2288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5124    0.3697    0.9552 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6341    1.0761    0.7807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6200    0.5131   -0.2290 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1198   -0.8396    0.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1069   -1.9222    0.2394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1919   -1.2968   -0.8637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7141    1.4423   -0.3480 N   0  0  0  0  0  4  0  0  0  0  0  0
   -5.7555    1.1798   -1.2005 O   0  0  0  0  0  1  0  0  0  0  0  0
   -4.7538    2.5169    0.3187 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8180    3.3705    0.1706 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4795   -0.9077    0.9058 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7050   -2.1215   -0.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1614   -1.9702    0.3836 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7983   -0.7533   -1.6567 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5347   -0.2336   -1.6969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1959    1.4841   -0.0734 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9331    1.5951   -1.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9591    1.9331    0.8736 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4531    0.2986    1.4096 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0593   -0.6117   -0.6008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6766    1.1010   -0.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5829    1.3566    1.1419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0678   -0.2991    1.7011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3200    0.5169   -0.6795 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8477   -1.2129   -0.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2159   -2.1152    2.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2247    1.3404    1.7291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3745    2.1393    0.4198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0783    0.4041   -1.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6328   -0.7499    1.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6269   -2.8947   -0.0211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7168   -2.0683    1.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2924   -1.8406   -0.4803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2075   -2.4197   -0.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1987   -1.0075   -0.5029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9910   -0.9254   -1.8814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7109    4.2840   -0.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 12 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  2 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  9 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  6
 13 39  1  0
 14 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 15 45  1  0
 19 46  1  0
M  CHG  2  16   1  17  -1
M  END


  Mrv1652309032206522D          

 19 18  0  0  0  0            999 V2000
    1.0461    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    2.6664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618    1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4763    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9052    0.1914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4763    0.1914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9052    1.8414    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    8.9052    2.6664    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    9.6197    1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3342    1.8414    0.0000 O   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  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  4  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
M  CHG  2  16   1  17  -1
M  END
> <DATABASE_ID>
NP0168991

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(O)=NCC(C(C)C)[N+](\[O-])=N\O

> <INCHI_IDENTIFIER>
InChI=1S/C13H27N3O3/c1-4-5-6-7-8-9-13(17)14-10-12(11(2)3)16(19)15-18/h11-12,18H,4-10H2,1-3H3,(H,14,17)/b16-15-

> <INCHI_KEY>
SXMAXSCAVUEAAA-NXVVXOECSA-N

> <FORMULA>
C13H27N3O3

> <MOLECULAR_WEIGHT>
273.377

> <EXACT_MASS>
273.205241741

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
31.37839259633853

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(Z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium

> <ALOGPS_LOGP>
3.26

> <JCHEM_LOGP>
3.5215578631241216

> <ALOGPS_LOGS>
-3.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
6.310054415143283

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.279337805916185

> <JCHEM_PKA_STRONGEST_BASIC>
3.2021099006129687

> <JCHEM_POLAR_SURFACE_AREA>
91.25

> <JCHEM_REFRACTIVITY>
76.38090000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.76e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(Z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       1.953   2.667   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.286   3.437   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.287   2.667   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.621   3.437   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.955   2.667   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.288   3.437   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      11.288   4.977   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0      12.622   2.667   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      13.956   3.437   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.289   2.667   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.289   1.127   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.623   0.357   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.956   0.357   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      16.623   3.437   0.000  0.00  0.00           N+1
HETATM   17  O   UNK     0      16.623   4.977   0.000  0.00  0.00           O-1
HETATM   18  N   UNK     0      17.957   2.667   0.000  0.00  0.00           N+0
HETATM   19  O   UNK     0      19.290   3.437   0.000  0.00  0.00           O+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                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   12   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₂₇N₃O₃

Average Mass

273.3770 Da

Monoisotopic Mass

273.20524 Da

IUPAC Name

(Z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium

Traditional Name

(Z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium

CAS Registry Number

Not Available

SMILES

CCCCCCCC(O)=NCC(C(C)C)[N+](\[O-])=N\O

InChI Identifier

InChI=1S/C13H27N3O3/c1-4-5-6-7-8-9-13(17)14-10-12(11(2)3)16(19)15-18/h11-12,18H,4-10H2,1-3H3,(H,14,17)/b16-15-

InChI Key

SXMAXSCAVUEAAA-NXVVXOECSA-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
Pseudomonas fragi	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Amines

Direct Parent

Trialkylamines

Alternative Parents

Substituents

Tertiary aliphatic amine
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidic acid derivative
Carboximidic acid
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	3.26	ALOGPS
logP	3.52	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	4.28	ChemAxon
pKa (Strongest Basic)	3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	91.25 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	76.38 m³·mol⁻¹	ChemAxon
Polarizability	31.38 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00011938

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

135502789

PDB ID

Not Available

ChEBI ID

156352

Good Scents ID

Not Available

References

General References

Jenul C, Sieber S, Daeppen C, Mathew A, Lardi M, Pessi G, Hoepfner D, Neuburger M, Linden A, Gademann K, Eberl L: Biosynthesis of fragin is controlled by a novel quorum sensing signal. Nat Commun. 2018 Mar 30;9(1):1297. doi: 10.1038/s41467-018-03690-2. [PubMed:29602945 ]
Sieber S, Daeppen C, Jenul C, Mannancherril V, Eberl L, Gademann K: Biosynthesis and Structure-Activity Relationship Investigations of the Diazeniumdiolate Antifungal Agent Fragin. Chembiochem. 2020 Jun 2;21(11):1587-1592. doi: 10.1002/cbic.201900755. Epub 2020 Mar 4. [PubMed:31945256 ]
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LOTUS database [Link]

Showing NP-Card for (z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium (NP0168991)

MOL for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

3D MOL for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

3D SDF for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

3D-SDF for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

PDB for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

3D PDB for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

SMILES for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

INCHI for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

Structure for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)

3D Structure for NP0168991 ((z)-(hydroxyimino)({1-[(1-hydroxyoctylidene)amino]-3-methylbutan-2-yl})oxidoazanium)