NP-MRD: Showing NP-Card for n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid (NP0239476)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 23:05:06 UTC

Updated at

2022-09-06 23:05:06 UTC

NP-MRD ID

NP0239476

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid

Description

N-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-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-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid is found in Streptomyces argillaceus. Based on a literature review very few articles have been published on N-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzene-1-carboximidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072201052D          

 36 37  0  0  0  0            999 V2000
    1.7576   -4.7675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4755   -3.9922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6630   -3.8490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3808   -3.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4316   -2.9305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8441   -3.6449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3138   -4.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6194   -3.9271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3946   -3.6449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8071   -2.9305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6196   -3.0737    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1499   -2.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8677   -1.6665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9624   -2.5850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2445   -3.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0570   -3.5035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5873   -2.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3051   -2.0963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8354   -1.4643    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5533   -0.6891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0836   -0.0571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4927   -1.9530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2105   -1.1778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6639   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3783   -1.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0319   -1.5877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2069   -1.5877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9247   -0.8125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5749   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1396   -1.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540   -2.9430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685   -1.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685   -0.8805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2830   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9975   -1.7055    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  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  4  0  0  0
 18 22  2  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END

     RDKit          3D

 70 71  0  0  0  0  0  0  0  0999 V2000
   -4.0251   -4.6576   -0.8926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9586   -3.8201    0.3575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8237   -2.8069    0.1475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7654   -1.9852    1.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7057   -0.9131    1.3969 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3417   -1.4669    1.5094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0578   -1.7236    2.7044 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5300   -1.7358    0.5306 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4974   -1.8297   -0.8289 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5695   -0.9874   -1.5339 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7988   -1.0292   -0.9984 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8866   -1.0667   -0.5244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3775   -2.3135   -0.0389 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8521    0.0514   -0.3591 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5652    1.3362   -0.7599 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4831    2.3708   -0.6054 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7080    2.1394   -0.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0175    0.8666    0.3618 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3077    0.6211    0.9522 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.3341    0.6239    0.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5961    0.3924    0.7167 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0986   -0.1464    0.2024 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4203   -1.4176    0.6145 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9276    0.3430   -1.7952 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4534    1.0433   -2.7361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1243    0.8927   -1.1734 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6070    0.8476    0.1145 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8841    2.3061    0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8836    0.0872    0.2838 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9663    0.9425    0.6965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1357    1.0567   -0.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2519    0.3906   -1.0865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2374    1.9230    0.4039 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7280    1.4540    1.7821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8769    3.3682    0.5214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4009    3.9780   -0.7597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0374   -5.1305   -1.0361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1894   -3.9542   -1.7581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8570   -5.4067   -0.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7401   -4.4847    1.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9281   -3.2945    0.5242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1275   -2.1890   -0.6995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9210   -3.4205   -0.0453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7419   -1.4936    1.5218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6002   -2.6444    2.2620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9227   -0.3291    2.3497 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7985   -2.8970   -1.0830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4745   -1.7222   -1.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6367   -1.4264   -2.6041 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3335   -2.4305    0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6277    1.5688   -1.1980 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2721    3.3790   -0.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4526    2.9167    0.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2618    0.8046   -0.8701 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4454    0.6806    0.2187 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3112   -1.6226    1.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2011    0.5330    0.8256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0020    2.7968    0.9496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1569    2.9182   -0.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7224    2.3776    1.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2552   -0.3634   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1127    1.8722   -0.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7885    1.6995    1.9370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0602    1.9485    2.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5303    0.3439    1.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1849    3.5886    1.3609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8356    3.8981    0.7972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6976    3.3195   -1.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3106    4.0613   -0.7373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9089    4.9675   -0.9525 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 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  2  0
 31 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 29 27  1  0
 27 28  1  0
 27 26  1  0
 26 24  1  0
 24 25  2  0
 24 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  2  0
 10 11  1  0
 11 12  2  3
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 18 22  2  0
 22 23  1  0
  6  5  1  0
 22 14  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  2 40  1  0
  2 41  1  0
  3 42  1  0
  3 43  1  0
  4 44  1  0
  4 45  1  0
  5 46  1  1
 29 61  1  6
 33 62  1  6
 34 63  1  0
 34 64  1  0
 34 65  1  0
 35 66  1  0
 35 67  1  0
 36 68  1  0
 36 69  1  0
 36 70  1  0
 27 57  1  1
 28 58  1  0
 28 59  1  0
 28 60  1  0
 10 49  1  6
  9 47  1  0
  9 48  1  0
 13 50  1  0
 15 51  1  0
 16 52  1  0
 17 53  1  0
 20 54  1  0
 21 55  1  0
 23 56  1  0
M  END


  Mrv1652309072201052D          

 36 37  0  0  0  0            999 V2000
    1.7576   -4.7675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4755   -3.9922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6630   -3.8490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3808   -3.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4316   -2.9305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8441   -3.6449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3138   -4.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6194   -3.9271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3946   -3.6449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8071   -2.9305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6196   -3.0737    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1499   -2.4418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8677   -1.6665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9624   -2.5850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2445   -3.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0570   -3.5035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5873   -2.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3051   -2.0963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8354   -1.4643    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5533   -0.6891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0836   -0.0571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4927   -1.9530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2105   -1.1778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6639   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3783   -1.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0319   -1.5877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2069   -1.5877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9247   -0.8125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5749   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1396   -1.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540   -2.9430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685   -1.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685   -0.8805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2830   -2.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9975   -1.7055    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  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  4  0  0  0
 18 22  2  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0239476

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC1C(OC(=O)C(C)CC)C(C)OC(=O)C(COC1=O)N=C(O)C1=CC=CC(N=CO)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H34N2O9/c1-5-7-9-17-21(36-23(31)14(3)6-2)15(4)35-25(33)19(12-34-24(17)32)27-22(30)16-10-8-11-18(20(16)29)26-13-28/h8,10-11,13-15,17,19,21,29H,5-7,9,12H2,1-4H3,(H,26,28)(H,27,30)

> <INCHI_KEY>
AZVOLHUZWCOOKC-UHFFFAOYSA-N

> <FORMULA>
C25H34N2O9

> <MOLECULAR_WEIGHT>
506.552

> <EXACT_MASS>
506.226430683

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
53.737345366600266

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzene-1-carboximidic acid

> <JCHEM_LOGP>
6.097416677

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.312760702068852

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3348132440359843

> <JCHEM_PKA_STRONGEST_BASIC>
0.14300936657931151

> <JCHEM_POLAR_SURFACE_AREA>
164.30999999999997

> <JCHEM_REFRACTIVITY>
129.5591

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       3.281  -8.899   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.754  -7.452   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.238  -7.185   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.711  -5.738   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.806  -5.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.576  -6.804   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.586  -7.984   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -3.023  -7.331   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -4.470  -6.804   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.240  -5.470   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -6.757  -5.738   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -7.746  -4.558   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -7.220  -3.111   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -9.263  -4.825   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.790  -6.272   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -11.306  -6.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -12.296  -5.360   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -11.770  -3.913   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0     -12.759  -2.733   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0     -12.233  -1.286   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0     -13.223  -0.107   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0     -10.253  -3.646   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -9.726  -2.199   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.973  -3.954   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -6.306  -3.184   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -3.793  -2.964   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.253  -2.964   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.726  -1.517   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.073  -3.954   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.261  -3.184   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.594  -3.954   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       1.594  -5.494   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.928  -3.184   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.928  -1.644   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.262  -3.954   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.595  -3.184   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   29                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   24                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   18   14   23                                                  
CONECT   23   22                                                            
CONECT   24   10   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    5   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   74    0
END

View in JSmol

Synonyms

Value	Source
N-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzene-1-carboximidate	Generator

Chemical Formula

C₂₅H₃₄N₂O₉

Average Mass

506.5520 Da

Monoisotopic Mass

506.22643 Da

IUPAC Name

N-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzene-1-carboximidic acid

Traditional Name

N-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid

CAS Registry Number

Not Available

SMILES

CCCCC1C(OC(=O)C(C)CC)C(C)OC(=O)C(COC1=O)N=C(O)C1=CC=CC(N=CO)=C1O

InChI Identifier

InChI=1S/C25H34N2O9/c1-5-7-9-17-21(36-23(31)14(3)6-2)15(4)35-25(33)19(12-34-24(17)32)27-22(30)16-10-8-11-18(20(16)29)26-13-28/h8,10-11,13-15,17,19,21,29H,5-7,9,12H2,1-4H3,(H,26,28)(H,27,30)

InChI Key

AZVOLHUZWCOOKC-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
Streptomyces argillaceus	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

N-acyl-alpha amino acid or derivatives
Alpha-amino acid ester
Tricarboxylic acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
Phenol
Fatty acid ester
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	6.1	ChemAxon
pKa (Strongest Acidic)	3.33	ChemAxon
pKa (Strongest Basic)	0.14	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	164.31 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	129.56 m³·mol⁻¹	ChemAxon
Polarizability	53.74 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

162870411

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-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid (NP0239476)

MOL for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D MOL for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D SDF for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D-SDF for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

PDB for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D PDB for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

SMILES for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

INCHI for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

Structure for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)

3D Structure for NP0239476 (n-{7-butyl-9-methyl-8-[(2-methylbutanoyl)oxy]-2,6-dioxo-1,5-dioxonan-3-yl}-2-hydroxy-3-[(hydroxymethylidene)amino]benzenecarboximidic acid)