NP-MRD: Showing NP-Card for Oximidine I (NP0003910)

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Record Information

Version

2.0

Created at

2020-12-09 01:27:34 UTC

Updated at

2021-07-15 16:47:42 UTC

NP-MRD ID

NP0003910

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Oximidine I

Provided By

NPAtlas

Description

Oximidine I is found in Pseudomonas and Pseudomonas sp. Q52002.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117513D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306242117513D          

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    2.1835    1.3109    1.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2316   -0.6698    2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7484   -1.6015    1.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1615   -1.3561    1.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3395    1.1263    0.1878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3714    1.1059    0.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4854   -3.3876   -2.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0110   -4.8763   -0.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2067   -3.8806    1.5927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6797   -1.6058    2.3036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7793    0.1483    2.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1173    2.2026    1.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4247    1.3355   -1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2485    2.4215   -2.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8060    4.2892   -1.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5033    3.7225   -1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5188    1.6687   -1.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5448    1.6104   -3.1126 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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
 12 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
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 13  1  0  0  0  0
 23 17  1  0  0  0  0
 30 28  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  4 36  1  0  0  0  0
  5 37  1  0  0  0  0
  6 38  1  0  0  0  0
  9 39  1  0  0  0  0
 10 40  1  0  0  0  0
 10 41  1  0  0  0  0
 11 42  1  0  0  0  0
 12 43  1  0  0  0  0
 13 44  1  1  0  0  0
 19 45  1  0  0  0  0
 20 46  1  0  0  0  0
 21 47  1  0  0  0  0
 22 48  1  0  0  0  0
 24 49  1  0  0  0  0
 25 50  1  0  0  0  0
 26 51  1  0  0  0  0
 27 52  1  0  0  0  0
 28 53  1  1  0  0  0
 30 54  1  1  0  0  0
 31 55  1  6  0  0  0
 32 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0003910

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=C([H])C([H])=C1[H])\C([H])=C(\[H])/C(/[H])=C([H])\[C@@]1([H])O[C@@]1([H])[C@]([H])(O[H])[C@@]([H])(OC2=O)C(\[H])=C(/[H])C([H])([H])N([H])C(=O)C(\[H])=C(\[H])/C(/[H])=N\OC([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H24N2O7/c1-30-25-14-6-12-19(27)24-13-5-11-17-21(28)22-18(31-22)10-3-2-7-15-8-4-9-16(26)20(15)23(29)32-17/h2-12,14,17-18,21-22,26,28H,13H2,1H3,(H,24,27)/b7-2-,10-3-,11-5+,12-6-,25-14-/t17-,18+,21+,22+/m0/s1

> <INCHI_KEY>
MJQHXIHJXNEHLK-KZIRSVARSA-N

> <FORMULA>
C23H24N2O7

> <MOLECULAR_WEIGHT>
440.452

> <EXACT_MASS>
440.158351121

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
44.94955130777258

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z,4Z)-N-[(2E)-3-[(4S,5R,6S,8R,9Z,11Z)-5,17-dihydroxy-2-oxo-3,7-dioxatricyclo[11.4.0.0^{6,8}]heptadeca-1(17),9,11,13,15-pentaen-4-yl]prop-2-en-1-yl]-4-(methoxyimino)but-2-enamide

> <ALOGPS_LOGP>
2.79

> <JCHEM_LOGP>
2.3023160296666667

> <ALOGPS_LOGS>
-4.10

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.034589206522693

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.66426967240799

> <JCHEM_PKA_STRONGEST_BASIC>
3.7848801167159856

> <JCHEM_POLAR_SURFACE_AREA>
129.98000000000002

> <JCHEM_REFRACTIVITY>
120.35770000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.50e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,4Z)-N-[(2E)-3-[(4S,5R,6S,8R,9Z,11Z)-5,17-dihydroxy-2-oxo-3,7-dioxatricyclo[11.4.0.0^{6,8}]heptadeca-1(17),9,11,13,15-pentaen-4-yl]prop-2-en-1-yl]-4-(methoxyimino)but-2-enamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
    8.5524   -1.1794   -0.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7041    0.6999   -0.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9985    1.6551    0.1356 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7781    1.5298    0.8892 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3451    2.7598    1.1777 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0407    0.4593    1.3227 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3073   -0.6055    1.7540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8753   -0.6050    1.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5594    0.3844    0.4154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7849    0.5682   -0.2140 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2834   -0.6135   -0.6434 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4137   -1.1827   -1.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6535   -1.2461   -2.3398 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5034   -1.7947   -0.2525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8270   -3.0998   -0.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2090   -3.7594   -1.6774 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8107   -3.8539    0.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4570   -3.2796    1.0866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1329   -2.0059    1.4394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1382   -1.2068    0.7787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0279    0.1503    1.3201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1603    1.3540    0.7870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4551    1.6382   -0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7703    2.4004   -1.4224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5655    3.1580   -1.2607 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0272    3.0264    0.0553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2584    2.8542   -1.0977 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5759    1.5782   -1.3655 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1574    0.9602   -2.4810 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3966   -0.3621    0.0877 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3611   -0.8829   -1.3744 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7319   -2.1444   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5808   -1.0162    0.3376 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6183    0.9760   -0.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3708    2.6842   -0.0747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1835    1.3109    1.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2316   -0.6698    2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7484   -1.6015    1.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1615   -1.3561    1.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3395    1.1263    0.1878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3714    1.1059    0.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4854   -3.3876   -2.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0110   -4.8763   -0.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2067   -3.8806    1.5927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6797   -1.6058    2.3036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7793    0.1483    2.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1173    2.2026    1.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4247    1.3355   -1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2485    2.4215   -2.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8060    4.2892   -1.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5033    3.7225   -1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5188    1.6687   -1.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5448    1.6104   -3.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 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
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 13  1  0
 23 17  1  0
 30 28  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  4 36  1  0
  5 37  1  0
  6 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  1
 19 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 24 49  1  0
 25 50  1  0
 26 51  1  0
 27 52  1  0
 28 53  1  1
 30 54  1  1
 31 55  1  6
 32 56  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       8.552  -1.179  -0.665  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.339  -1.272  -1.392  0.00  0.00           O+0
HETATM    3  N   UNK     0       6.210  -1.586  -0.692  0.00  0.00           N+0
HETATM    4  C   UNK     0       5.438  -0.705  -0.191  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.704   0.700  -0.324  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.999   1.655   0.136  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.778   1.530   0.889  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.345   2.760   1.178  0.00  0.00           O+0
HETATM    9  N   UNK     0       3.041   0.459   1.323  0.00  0.00           N+0
HETATM   10  C   UNK     0       2.307  -0.606   1.754  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.875  -0.605   1.212  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.559   0.384   0.415  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.785   0.568  -0.214  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.283  -0.614  -0.643  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.414  -1.183  -1.066  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.654  -1.246  -2.340  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.503  -1.795  -0.253  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.827  -3.100  -0.624  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.209  -3.759  -1.677  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.811  -3.854   0.045  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.457  -3.280   1.087  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.133  -2.006   1.439  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.138  -1.207   0.779  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.028   0.150   1.320  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.160   1.354   0.787  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.455   1.638  -0.559  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.770   2.400  -1.422  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.566   3.158  -1.261  0.00  0.00           C+0
HETATM   29  O   UNK     0      -2.027   3.026   0.055  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.258   2.854  -1.098  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.576   1.578  -1.365  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.157   0.960  -2.481  0.00  0.00           O+0
HETATM   33  H   UNK     0       8.397  -0.362   0.088  0.00  0.00           H+0
HETATM   34  H   UNK     0       9.361  -0.883  -1.374  0.00  0.00           H+0
HETATM   35  H   UNK     0       8.732  -2.144  -0.171  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.581  -1.016   0.338  0.00  0.00           H+0
HETATM   37  H   UNK     0       6.618   0.976  -0.892  0.00  0.00           H+0
HETATM   38  H   UNK     0       5.371   2.684  -0.075  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.184   1.311   1.958  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.232  -0.670   2.887  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.748  -1.601   1.406  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.162  -1.356   1.460  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.339   1.126   0.188  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.371   1.106   0.558  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.485  -3.388  -2.230  0.00  0.00           H+0
HETATM   46  H   UNK     0      -5.011  -4.876  -0.307  0.00  0.00           H+0
HETATM   47  H   UNK     0      -6.207  -3.881   1.593  0.00  0.00           H+0
HETATM   48  H   UNK     0      -5.680  -1.606   2.304  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.779   0.148   2.426  0.00  0.00           H+0
HETATM   50  H   UNK     0      -4.117   2.203   1.585  0.00  0.00           H+0
HETATM   51  H   UNK     0      -5.425   1.335  -1.061  0.00  0.00           H+0
HETATM   52  H   UNK     0      -4.248   2.422  -2.459  0.00  0.00           H+0
HETATM   53  H   UNK     0      -2.806   4.289  -1.500  0.00  0.00           H+0
HETATM   54  H   UNK     0      -0.503   3.723  -1.151  0.00  0.00           H+0
HETATM   55  H   UNK     0       0.519   1.669  -1.615  0.00  0.00           H+0
HETATM   56  H   UNK     0      -1.545   1.610  -3.113  0.00  0.00           H+0
CONECT    1    2   33   34   35                                             
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   36                                                  
CONECT    5    4    6   37                                                  
CONECT    6    5    7   38                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   39                                                  
CONECT   10    9   11   40   41                                             
CONECT   11   10   12   42                                                  
CONECT   12   11   13   43                                                  
CONECT   13   12   14   31   44                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   23                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   45                                                       
CONECT   20   18   21   46                                                  
CONECT   21   20   22   47                                                  
CONECT   22   21   23   48                                                  
CONECT   23   22   24   17                                                  
CONECT   24   23   25   49                                                  
CONECT   25   24   26   50                                                  
CONECT   26   25   27   51                                                  
CONECT   27   26   28   52                                                  
CONECT   28   27   29   30   53                                             
CONECT   29   28   30                                                       
CONECT   30   29   31   28   54                                             
CONECT   31   30   32   13   55                                             
CONECT   32   31   56                                                       
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    4                                                            
CONECT   37    5                                                            
CONECT   38    6                                                            
CONECT   39    9                                                            
CONECT   40   10                                                            
CONECT   41   10                                                            
CONECT   42   11                                                            
CONECT   43   12                                                            
CONECT   44   13                                                            
CONECT   45   19                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
CONECT   48   22                                                            
CONECT   49   24                                                            
CONECT   50   25                                                            
CONECT   51   26                                                            
CONECT   52   27                                                            
CONECT   53   28                                                            
CONECT   54   30                                                            
CONECT   55   31                                                            
CONECT   56   32                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  116    0
END

RDKit          3D

56 58  0  0  0  0  0  0  0  0999 V2000
    8.5524   -1.1794   -0.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3388   -1.2722   -1.3922 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2097   -1.5860   -0.6924 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376   -0.7048   -0.1905 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7041    0.6999   -0.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9985    1.6551    0.1356 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7781    1.5298    0.8892 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3451    2.7598    1.1777 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0407    0.4593    1.3227 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3073   -0.6055    1.7540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8753   -0.6050    1.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5594    0.3844    0.4154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7849    0.5682   -0.2140 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2834   -0.6135   -0.6434 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4137   -1.1827   -1.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6535   -1.2461   -2.3398 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5034   -1.7947   -0.2525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8270   -3.0998   -0.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2090   -3.7594   -1.6774 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8107   -3.8539    0.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4570   -3.2796    1.0866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1329   -2.0059    1.4394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1382   -1.2068    0.7787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0279    0.1503    1.3201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1603    1.3540    0.7870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4551    1.6382   -0.5593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7703    2.4004   -1.4224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5655    3.1580   -1.2607 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0272    3.0264    0.0553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2584    2.8542   -1.0977 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5759    1.5782   -1.3655 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1574    0.9602   -2.4810 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3966   -0.3621    0.0877 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3611   -0.8829   -1.3744 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7319   -2.1444   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5808   -1.0162    0.3376 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6183    0.9760   -0.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3708    2.6842   -0.0747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1835    1.3109    1.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2316   -0.6698    2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7484   -1.6015    1.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1615   -1.3561    1.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3395    1.1263    0.1878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3714    1.1059    0.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4854   -3.3876   -2.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0110   -4.8763   -0.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2067   -3.8806    1.5927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6797   -1.6058    2.3036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7793    0.1483    2.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1173    2.2026    1.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4247    1.3355   -1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2485    2.4215   -2.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8060    4.2892   -1.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5033    3.7225   -1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5188    1.6687   -1.6146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5448    1.6104   -3.1126 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 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
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 13  1  0
 23 17  1  0
 30 28  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  4 36  1  0
  5 37  1  0
  6 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  1
 19 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 24 49  1  0
 25 50  1  0
 26 51  1  0
 27 52  1  0
 28 53  1  1
 30 54  1  1
 31 55  1  6
 32 56  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₃H₂₄N₂O₇

Average Mass

440.4520 Da

Monoisotopic Mass

440.15835 Da

IUPAC Name

(2Z,4Z)-N-[(2E)-3-[(4S,5R,6S,8R,9Z,11Z)-5,17-dihydroxy-2-oxo-3,7-dioxatricyclo[11.4.0.0^{6,8}]heptadeca-1(17),9,11,13,15-pentaen-4-yl]prop-2-en-1-yl]-4-(methoxyimino)but-2-enamide

Traditional Name

(2Z,4Z)-N-[(2E)-3-[(4S,5R,6S,8R,9Z,11Z)-5,17-dihydroxy-2-oxo-3,7-dioxatricyclo[11.4.0.0^{6,8}]heptadeca-1(17),9,11,13,15-pentaen-4-yl]prop-2-en-1-yl]-4-(methoxyimino)but-2-enamide

CAS Registry Number

Not Available

SMILES

CO\N=C/C=C\C(=O)NC\C=C\[C@@H]1OC(=O)C2=C(C=CC=C2O)\C=C/C=C\[C@H]2O[C@H]2[C@@H]1O

InChI Identifier

InChI=1S/C23H24N2O7/c1-30-25-14-6-12-19(27)24-13-5-11-17-21(28)22-18(31-22)10-3-2-7-15-8-4-9-16(26)20(15)23(29)32-17/h2-12,14,17-18,21-22,26,28H,13H2,1H3,(H,24,27)/b7-2-,10-3-,11-5+,12-6-,25-14-/t17-,18+,21+,22+/m0/s1

InChI Key

MJQHXIHJXNEHLK-KZIRSVARSA-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
Pseudomonas	NPAtlas	11674097
Pseudomonas sp. Q52002	Bacteria	KNApSAcK

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	2.79	ALOGPS
logP	2.3	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	9.66	ChemAxon
pKa (Strongest Basic)	3.78	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	129.98 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	120.36 m³·mol⁻¹	ChemAxon
Polarizability	44.95 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

Showing NP-Card for Oximidine I (NP0003910)

MOL for NP0003910 (Oximidine I)

3D MOL for NP0003910 (Oximidine I)

3D SDF for NP0003910 (Oximidine I)

3D-SDF for NP0003910 (Oximidine I)

PDB for NP0003910 (Oximidine I)

3D PDB for NP0003910 (Oximidine I)

SMILES for NP0003910 (Oximidine I)

INCHI for NP0003910 (Oximidine I)

Structure for NP0003910 (Oximidine I)

3D Structure for NP0003910 (Oximidine I)