NP-MRD: Showing NP-Card for n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid (NP0179074)

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Record Information

Version

2.0

Created at

2022-09-03 17:11:45 UTC

Updated at

2022-09-03 17:11:46 UTC

NP-MRD ID

NP0179074

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

N-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzene-1-carboximidic 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. N-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzene-1-carboximidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241503112D          

 33 34  0  0  0  0            999 V2000
   -3.0717   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3572   -2.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6427   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9283   -2.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2138   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5007   -2.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2152   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0719   -1.5504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2594   -1.4072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4844   -0.8360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9541   -0.2040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2596   -0.5538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0349   -0.8360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5652   -0.2040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4474   -1.5504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2599   -1.4072    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7902   -2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5080   -2.8144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6026   -1.8959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8848   -1.1207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6973   -0.9774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2276   -1.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9454   -2.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4757   -3.0166    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1935   -3.7919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7238   -4.4238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8508   -3.3031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3041   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0186   -2.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6721   -2.8932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8471   -2.8932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5650   -3.6684    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  1  0  0  0  0
 10 11  1  0  0  0  0
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 13 15  1  0  0  0  0
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 17 19  1  0  0  0  0
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 31 32  1  0  0  0  0
  7 32  1  0  0  0  0
 32 33  2  0  0  0  0
M  END

     RDKit          3D

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   -2.9185   -0.5343    0.1011 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0979    0.0252   -0.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2643   -1.2839    1.3077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4101   -1.7041    1.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6507   -1.2323    1.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7681   -0.3521    0.5288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9875    0.1528    0.0775 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2449   -0.1418    0.5868 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4396   -0.9170    1.5388 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5706    0.0747   -0.1319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6885    0.9487   -1.1526 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8009   -2.5333   -1.1806 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3042   -1.2309   -1.3811 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.4931   -0.6146   -0.6557 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0952   -1.5544    0.1774 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8870    2.7236    0.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1744    0.5171    1.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5944    0.5651    1.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5582   -1.3179    2.7980 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5809    0.0345    2.8205 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8060   -1.3407    1.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9390   -1.8637    1.3856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2342    0.2193   -0.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.3196   -2.4042    2.7721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4875   -1.6134    2.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
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 11 48  1  1
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 12 50  1  0
 12 51  1  0
M  END


  Mrv1533004241503112D          

 33 34  0  0  0  0            999 V2000
   -3.0717   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3572   -2.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6427   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9283   -2.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2138   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4757   -3.0166    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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    7.7238   -4.4238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3041   -2.3629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0186   -2.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0179074

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCC1C(O)C(C)OC(=O)C(NC(=O)C2=CC=CC(NC=O)=C2O)C(C)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H32N2O8/c1-4-5-6-7-9-16-19(27)14(3)33-23(31)18(13(2)32-22(16)30)25-21(29)15-10-8-11-17(20(15)28)24-12-26/h8,10-14,16,18-19,27-28H,4-7,9H2,1-3H3,(H,24,26)(H,25,29)

> <INCHI_KEY>
GTUQGSSCDLWNEE-UHFFFAOYSA-N

> <FORMULA>
C23H32N2O8

> <MOLECULAR_WEIGHT>
464.515

> <EXACT_MASS>
464.215865998

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.62300354642711

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-formamido-N-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxybenzamide

> <ALOGPS_LOGP>
2.17

> <JCHEM_LOGP>
3.076852033666667

> <ALOGPS_LOGS>
-3.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.674425127147092

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.510311568460766

> <JCHEM_PKA_STRONGEST_BASIC>
-1.8657047656151455

> <JCHEM_POLAR_SURFACE_AREA>
151.26

> <JCHEM_REFRACTIVITY>
118.94919999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-formamido-N-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxybenzamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -5.734  -4.411   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.400  -5.181   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.066  -4.411   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.733  -5.181   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.399  -4.411   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.935  -5.181   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.268  -4.411   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.001  -2.894   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.484  -2.627   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.771  -1.560   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.781  -0.381   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.218  -1.034   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.665  -1.560   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.655  -0.381   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.435  -2.894   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       7.952  -2.627   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       8.942  -3.806   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.415  -5.254   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.458  -3.539   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.985  -2.092   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.502  -1.824   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.491  -3.004   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.965  -4.451   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      13.955  -5.631   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      13.428  -7.078   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      14.418  -8.258   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      11.448  -4.719   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.921  -6.166   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.168  -4.411   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.501  -5.181   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.988  -5.401   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       3.448  -5.401   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.921  -6.848   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   32                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   29                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   23   19   28                                                  
CONECT   28   27                                                            
CONECT   29   15   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31    7   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

View in JSmol

Synonyms

Value	Source
N-(7-Hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzene-1-carboximidate	Generator

Chemical Formula

C₂₃H₃₂N₂O₈

Average Mass

464.5150 Da

Monoisotopic Mass

464.21587 Da

IUPAC Name

3-formamido-N-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxybenzamide

Traditional Name

3-formamido-N-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxybenzamide

CAS Registry Number

Not Available

SMILES

CCCCCCC1C(O)C(C)OC(=O)C(NC(=O)C2=CC=CC(NC=O)=C2O)C(C)OC1=O

InChI Identifier

InChI=1S/C23H32N2O8/c1-4-5-6-7-9-16-19(27)14(3)33-23(31)18(13(2)32-22(16)30)25-21(29)15-10-8-11-17(20(15)28)24-12-26/h8,10-14,16,18-19,27-28H,4-7,9H2,1-3H3,(H,24,26)(H,25,29)

InChI Key

GTUQGSSCDLWNEE-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

Alpha-amino acid ester
N-acyl-alpha amino acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Benzenoid
Carboxylic acid ester
Lactone
Secondary alcohol
Carboximidic acid
Carboximidic acid derivative
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
Alcohol
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
logP	2.17	ALOGPS
logP	3.08	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	7.51	ChemAxon
pKa (Strongest Basic)	-1.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.26 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	118.95 m³·mol⁻¹	ChemAxon
Polarizability	47.62 Å³	ChemAxon
Number of Rings	2	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

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

85055997

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid (NP0179074)

MOL for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D MOL for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D SDF for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D-SDF for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

PDB for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D PDB for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

SMILES for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

INCHI for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

Structure for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D Structure for NP0179074 (n-(7-hexyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)