NP-MRD: Showing NP-Card for Vanoxonin (NP0021978)

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Record Information

Version

2.0

Created at

2021-01-06 07:12:53 UTC

Updated at

2021-07-15 17:37:48 UTC

NP-MRD ID

NP0021978

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Vanoxonin

Provided By

NPAtlas

Description

Vanoxonin is found in Saccharopolyspora and Saccharopolyspora hirsuta. Vanoxonin was first documented in 1983 (PMID: 6874588). Based on a literature review very few articles have been published on Vanoxonin.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105203D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306242105203D          

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    0.4121    2.9252    0.0644 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5237    0.5745   -1.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1665   -1.4471   -0.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8692   -0.2542   -0.7736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8720   -3.9128    2.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9108   -4.5477    3.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9686   -3.3139    2.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4192   -0.5109    0.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7280    0.0137   -0.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1758   -1.9016   -2.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8791   -0.1439   -2.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6882   -0.0649   -4.2679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5444    1.1274   -2.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3300   -0.4708   -4.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3968    4.9148   -0.6838 H   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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  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  2  0  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
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 23 17  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  5 34  1  0  0  0  0
  6 35  1  0  0  0  0
  6 36  1  0  0  0  0
  7 37  1  0  0  0  0
  7 38  1  0  0  0  0
  8 39  1  0  0  0  0
  8 40  1  0  0  0  0
  9 41  1  1  0  0  0
 10 42  1  0  0  0  0
 13 43  1  1  0  0  0
 14 44  1  0  0  0  0
 18 45  1  0  0  0  0
 19 46  1  0  0  0  0
 20 47  1  0  0  0  0
 22 48  1  0  0  0  0
 24 49  1  0  0  0  0
 25 50  1  1  0  0  0
 26 51  1  0  0  0  0
 26 52  1  0  0  0  0
 26 53  1  0  0  0  0
 27 54  1  0  0  0  0
 30 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0021978

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]ON(C(=O)C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)C1=C([H])C([H])=C([H])C(O[H])=C1O[H])[C@]([H])(O[H])C([H])([H])[H])C(=O)O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H25N3O9/c1-9(22)14(20-16(26)11-5-3-7-13(24)15(11)25)17(27)19-12(18(28)29)6-4-8-21(30)10(2)23/h3,5,7,9,12,14,22,24-25,30H,4,6,8H2,1-2H3,(H,19,27)(H,20,26)(H,28,29)/t9-,12+,14+/m1/s1

> <INCHI_KEY>
KCWDMHXDGAWLOA-LQJRIPTKSA-N

> <FORMULA>
C18H25N3O9

> <MOLECULAR_WEIGHT>
427.41

> <EXACT_MASS>
427.159079397

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.201216853285246

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S,3R)-2-[(2,3-dihydroxyphenyl)formamido]-3-hydroxybutanamido]-5-(N-hydroxyacetamido)pentanoic acid

> <ALOGPS_LOGP>
-0.14

> <JCHEM_LOGP>
-0.7904793336666668

> <ALOGPS_LOGS>
-2.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.051534229802563

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.309131677469194

> <JCHEM_PKA_STRONGEST_BASIC>
-2.937308003816467

> <JCHEM_POLAR_SURFACE_AREA>
196.73

> <JCHEM_REFRACTIVITY>
101.75289999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.57e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S,3R)-2-[(2,3-dihydroxyphenyl)formamido]-3-hydroxybutanamido]-5-(N-hydroxyacetamido)pentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 55  0  0  0  0  0  0  0  0999 V2000
    5.4440   -1.0891    0.6658 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9168   -0.4064    1.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7243   -1.0711    2.9035 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6336    0.9674    1.8391 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1531    1.5708    2.9796 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8374    1.7276    0.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6453    1.7957   -0.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4486    2.4330    0.4054 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2551    2.4971   -0.5106 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8547    1.1659   -0.9383 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4105    0.6589   -0.5820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1753    1.3670    0.1051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8326   -0.6779   -1.0045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1636   -0.9278   -0.4262 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4188   -1.9501    0.4749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253   -2.6849    0.7904 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6749   -2.2474    1.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7675   -3.3185    1.9659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9175   -3.6957    2.5966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0667   -3.0128    2.3671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0310   -1.9305    1.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2439   -1.2941    1.3052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8538   -1.5614    0.8472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8899   -0.4883   -0.0132 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8695   -0.8844   -2.4969 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8335    0.0784   -3.1746 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3774   -0.6611   -3.0610 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4985    3.3310   -1.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3710    2.9228   -2.8801 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8955    4.6585   -1.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7241   -1.0480   -0.1755 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6492   -2.1717    0.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3901   -0.6260    0.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2406    0.9759    3.7523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2076    2.7578    0.8441 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6537    1.2440    0.0563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9174    2.4651   -1.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3516    0.8255   -0.6623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1903    1.8639    1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7540    3.4532    0.7131 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4121    2.9252    0.0644 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5237    0.5745   -1.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1665   -1.4471   -0.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8692   -0.2542   -0.7736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8720   -3.9128    2.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9108   -4.5477    3.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9686   -3.3139    2.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4192   -0.5109    0.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7280    0.0137   -0.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1758   -1.9016   -2.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8791   -0.1439   -2.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6882   -0.0649   -4.2679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5444    1.1274   -2.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3300   -0.4708   -4.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3968    4.9148   -0.6838 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 13 25  1  0
 25 26  1  0
 25 27  1  0
  9 28  1  0
 28 29  2  0
 28 30  1  0
 23 17  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  1
 10 42  1  0
 13 43  1  1
 14 44  1  0
 18 45  1  0
 19 46  1  0
 20 47  1  0
 22 48  1  0
 24 49  1  0
 25 50  1  1
 26 51  1  0
 26 52  1  0
 26 53  1  0
 27 54  1  0
 30 55  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       5.444  -1.089   0.666  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.917  -0.406   1.861  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.724  -1.071   2.904  0.00  0.00           O+0
HETATM    4  N   UNK     0       4.634   0.967   1.839  0.00  0.00           N+0
HETATM    5  O   UNK     0       4.153   1.571   2.980  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.837   1.728   0.635  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.645   1.796  -0.267  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.449   2.433   0.405  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.255   2.497  -0.511  0.00  0.00           C+0
HETATM   10  N   UNK     0       0.855   1.166  -0.938  0.00  0.00           N+0
HETATM   11  C   UNK     0      -0.411   0.659  -0.582  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.175   1.367   0.105  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.833  -0.678  -1.004  0.00  0.00           C+0
HETATM   14  N   UNK     0      -2.164  -0.928  -0.426  0.00  0.00           N+0
HETATM   15  C   UNK     0      -2.419  -1.950   0.475  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.425  -2.685   0.790  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.675  -2.247   1.071  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.768  -3.318   1.966  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.918  -3.696   2.597  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.067  -3.013   2.367  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.031  -1.931   1.479  0.00  0.00           C+0
HETATM   22  O   UNK     0      -7.244  -1.294   1.305  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.854  -1.561   0.847  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.890  -0.488  -0.013  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.870  -0.884  -2.497  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.833   0.078  -3.175  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.377  -0.661  -3.061  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.498   3.331  -1.699  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.371   2.923  -2.880  0.00  0.00           O+0
HETATM   30  O   UNK     0       1.896   4.659  -1.542  0.00  0.00           O+0
HETATM   31  H   UNK     0       4.724  -1.048  -0.176  0.00  0.00           H+0
HETATM   32  H   UNK     0       5.649  -2.172   0.862  0.00  0.00           H+0
HETATM   33  H   UNK     0       6.390  -0.626   0.293  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.241   0.976   3.752  0.00  0.00           H+0
HETATM   35  H   UNK     0       5.208   2.758   0.844  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.654   1.244   0.056  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.917   2.465  -1.114  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.352   0.826  -0.662  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.190   1.864   1.318  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.754   3.453   0.713  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.412   2.925   0.064  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.524   0.575  -1.518  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.167  -1.447  -0.568  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.869  -0.254  -0.774  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.872  -3.913   2.195  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.911  -4.548   3.286  0.00  0.00           H+0
HETATM   47  H   UNK     0      -6.969  -3.314   2.866  0.00  0.00           H+0
HETATM   48  H   UNK     0      -7.419  -0.511   0.719  0.00  0.00           H+0
HETATM   49  H   UNK     0      -5.728   0.014  -0.184  0.00  0.00           H+0
HETATM   50  H   UNK     0      -1.176  -1.902  -2.777  0.00  0.00           H+0
HETATM   51  H   UNK     0      -2.879  -0.144  -2.959  0.00  0.00           H+0
HETATM   52  H   UNK     0      -1.688  -0.065  -4.268  0.00  0.00           H+0
HETATM   53  H   UNK     0      -1.544   1.127  -2.957  0.00  0.00           H+0
HETATM   54  H   UNK     0       0.330  -0.471  -4.027  0.00  0.00           H+0
HETATM   55  H   UNK     0       2.397   4.915  -0.684  0.00  0.00           H+0
CONECT    1    2   31   32   33                                             
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4   34                                                       
CONECT    6    4    7   35   36                                             
CONECT    7    6    8   37   38                                             
CONECT    8    7    9   39   40                                             
CONECT    9    8   10   28   41                                             
CONECT   10    9   11   42                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   25   43                                             
CONECT   14   13   15   44                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   23                                                  
CONECT   18   17   19   45                                                  
CONECT   19   18   20   46                                                  
CONECT   20   19   21   47                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21   48                                                       
CONECT   23   21   24   17                                                  
CONECT   24   23   49                                                       
CONECT   25   13   26   27   50                                             
CONECT   26   25   51   52   53                                             
CONECT   27   25   54                                                       
CONECT   28    9   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   55                                                       
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    1                                                            
CONECT   34    5                                                            
CONECT   35    6                                                            
CONECT   36    6                                                            
CONECT   37    7                                                            
CONECT   38    7                                                            
CONECT   39    8                                                            
CONECT   40    8                                                            
CONECT   41    9                                                            
CONECT   42   10                                                            
CONECT   43   13                                                            
CONECT   44   14                                                            
CONECT   45   18                                                            
CONECT   46   19                                                            
CONECT   47   20                                                            
CONECT   48   22                                                            
CONECT   49   24                                                            
CONECT   50   25                                                            
CONECT   51   26                                                            
CONECT   52   26                                                            
CONECT   53   26                                                            
CONECT   54   27                                                            
CONECT   55   30                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  110    0
END

RDKit          3D

55 55  0  0  0  0  0  0  0  0999 V2000
    5.4440   -1.0891    0.6658 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0310   -1.9305    1.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2439   -1.2941    1.3052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8538   -1.5614    0.8472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8899   -0.4883   -0.0132 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8695   -0.8844   -2.4969 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8335    0.0784   -3.1746 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3774   -0.6611   -3.0610 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4985    3.3310   -1.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3710    2.9228   -2.8801 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8955    4.6585   -1.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7241   -1.0480   -0.1755 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6492   -2.1717    0.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3901   -0.6260    0.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2406    0.9759    3.7523 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2076    2.7578    0.8441 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6537    1.2440    0.0563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9174    2.4651   -1.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3516    0.8255   -0.6623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1903    1.8639    1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7540    3.4532    0.7131 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4121    2.9252    0.0644 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5237    0.5745   -1.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1665   -1.4471   -0.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8692   -0.2542   -0.7736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8720   -3.9128    2.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9108   -4.5477    3.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9686   -3.3139    2.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4192   -0.5109    0.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7280    0.0137   -0.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1758   -1.9016   -2.7772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8791   -0.1439   -2.9592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6882   -0.0649   -4.2679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5444    1.1274   -2.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3300   -0.4708   -4.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3968    4.9148   -0.6838 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 13 25  1  0
 25 26  1  0
 25 27  1  0
  9 28  1  0
 28 29  2  0
 28 30  1  0
 23 17  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  1
 10 42  1  0
 13 43  1  1
 14 44  1  0
 18 45  1  0
 19 46  1  0
 20 47  1  0
 22 48  1  0
 24 49  1  0
 25 50  1  1
 26 51  1  0
 26 52  1  0
 26 53  1  0
 27 54  1  0
 30 55  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
N-(2,3-Dihydroxybenzoyl)threonyl-(N-omega-acetyl-N-omega-hydroxy)ornithine	MeSH

Chemical Formula

C₁₈H₂₅N₃O₉

Average Mass

427.4100 Da

Monoisotopic Mass

427.15908 Da

IUPAC Name

(2S)-2-[(2S,3R)-2-[(2,3-dihydroxyphenyl)formamido]-3-hydroxybutanamido]-5-(N-hydroxyacetamido)pentanoic acid

Traditional Name

(2S)-2-[(2S,3R)-2-[(2,3-dihydroxyphenyl)formamido]-3-hydroxybutanamido]-5-(N-hydroxyacetamido)pentanoic acid

CAS Registry Number

Not Available

SMILES

C[C@@H](O)[C@H](NC(=O)C1=C(O)C(O)=CC=C1)C(=O)N[C@@H](CCCN(O)C(C)=O)C(O)=O

InChI Identifier

InChI=1S/C18H25N3O9/c1-9(22)14(20-16(26)11-5-3-7-13(24)15(11)25)17(27)19-12(18(28)29)6-4-8-21(30)10(2)23/h3,5,7,9,12,14,22,24-25,30H,4,6,8H2,1-2H3,(H,19,27)(H,20,26)(H,28,29)/t9-,12+,14+/m1/s1

InChI Key

KCWDMHXDGAWLOA-LQJRIPTKSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Saccharopolyspora	NPAtlas	6874588
Saccharopolyspora hirsuta	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	-0.14	ALOGPS
logP	-0.79	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	3.31	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	196.73 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	101.75 m³·mol⁻¹	ChemAxon
Polarizability	41.2 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA020953

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

143444

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163530

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kanai F, Sawa T, Hamada M, Naganawa H, Takeuchi T, Umezawa H: Vanoxonin, a new inhibitor of thymidylate synthetase. J Antibiot (Tokyo). 1983 Jun;36(6):656-60. doi: 10.7164/antibiotics.36.656. [PubMed:6874588 ]

Showing NP-Card for Vanoxonin (NP0021978)

MOL for NP0021978 (Vanoxonin)

3D MOL for NP0021978 (Vanoxonin)

3D SDF for NP0021978 (Vanoxonin)

3D-SDF for NP0021978 (Vanoxonin)

PDB for NP0021978 (Vanoxonin)

3D PDB for NP0021978 (Vanoxonin)

SMILES for NP0021978 (Vanoxonin)

INCHI for NP0021978 (Vanoxonin)

Structure for NP0021978 (Vanoxonin)

3D Structure for NP0021978 (Vanoxonin)