NP-MRD: Showing NP-Card for Bactobolin D (NP0008979)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2020-12-09 06:27:13 UTC

Updated at

2021-07-15 17:01:58 UTC

NP-MRD ID

NP0008979

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Bactobolin D

Provided By

NPAtlas

Description

Bactobolin D is found in Burkholderia. Based on a literature review very few articles have been published on Bactobolin D.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106313D          

 53 54  0  0  0  0            999 V2000
    6.7699   -1.2250    0.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4686   -1.2510    0.7933 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8151   -2.5510    0.6272 N   0  0  2  0  0  0  0  0  0  0  0  0
    4.5460   -0.2131    0.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.0233    0.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670   -0.5340   -0.1880 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2886    0.4000   -0.7174 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9724    0.0377   -2.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1485    0.5287    0.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3173    0.3106    1.4197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1903    0.8891   -0.2100 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2568    0.9967    0.7289 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1808   -0.2022    0.7092 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8574   -1.1673   -0.4226 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8999   -2.2817   -0.2868 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5146   -3.4521   -0.8882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1799   -1.6870   -0.9005 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5000   -0.4991   -0.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8163   -0.0648   -0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6117    0.1640    0.6458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0341    1.3291    1.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2294    1.4658    1.8095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0322    2.2700    1.7059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9610    2.2935    0.7315 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0113    3.3703    1.2614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5755    2.7765   -0.5258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5155    3.0517   -1.8807 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.3687    4.3496   -0.1449 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.7101   -0.5478   -0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5930   -0.8881    0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0037   -2.2705   -0.2981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6371   -1.1028    1.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376   -3.3379    0.9360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6473   -2.6570   -0.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510   -1.5403   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8688    1.3826   -0.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3356   -0.8385   -2.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806    0.9122   -2.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9200   -0.1059   -2.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2717    1.0392   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7524    0.9244    1.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0707   -0.8298    1.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8792   -1.6681   -0.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0105   -0.7179   -1.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1452   -2.4080    0.7992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9937   -4.1995   -0.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8822   -1.3891   -1.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9843   -2.4377   -0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4186   -0.4866    0.6439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5819    4.3408    1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7737    3.0985    2.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1349    3.4792    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4131    2.1202   -0.8617 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
  2  4  1  0  0  0  0
  4  5  2  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
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  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  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 24 12  1  0  0  0  0
 20 13  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  2 32  1  1  0  0  0
  3 33  1  0  0  0  0
  3 34  1  0  0  0  0
  6 35  1  0  0  0  0
  7 36  1  6  0  0  0
  8 37  1  0  0  0  0
  8 38  1  0  0  0  0
  8 39  1  0  0  0  0
 11 40  1  0  0  0  0
 12 41  1  1  0  0  0
 13 42  1  1  0  0  0
 14 43  1  0  0  0  0
 14 44  1  0  0  0  0
 15 45  1  1  0  0  0
 16 46  1  0  0  0  0
 17 47  1  0  0  0  0
 17 48  1  0  0  0  0
 19 49  1  0  0  0  0
 25 50  1  0  0  0  0
 25 51  1  0  0  0  0
 25 52  1  0  0  0  0
 26 53  1  6  0  0  0
M  END

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
    6.7699   -1.2250    0.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4686   -1.2510    0.7933 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8151   -2.5510    0.6272 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5460   -0.2131    0.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.0233    0.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670   -0.5340   -0.1880 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2886    0.4000   -0.7174 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9724    0.0377   -2.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1485    0.5287    0.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3173    0.3106    1.4197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1903    0.8891   -0.2100 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2568    0.9967    0.7289 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1808   -0.2022    0.7092 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8574   -1.1673   -0.4226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8999   -2.2817   -0.2868 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5146   -3.4521   -0.8882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1799   -1.6870   -0.9005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5000   -0.4991   -0.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8163   -0.0648   -0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6117    0.1640    0.6458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0341    1.3291    1.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2294    1.4658    1.8095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0322    2.2700    1.7059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9610    2.2935    0.7315 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0113    3.3703    1.2614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5755    2.7765   -0.5258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5155    3.0517   -1.8807 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.3687    4.3496   -0.1449 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.7101   -0.5478   -0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5930   -0.8881    0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0037   -2.2705   -0.2981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6371   -1.1028    1.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376   -3.3379    0.9360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6473   -2.6570   -0.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510   -1.5403   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8688    1.3826   -0.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3356   -0.8385   -2.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806    0.9122   -2.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9200   -0.1059   -2.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2717    1.0392   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7524    0.9244    1.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0707   -0.8298    1.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8792   -1.6681   -0.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0105   -0.7179   -1.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1452   -2.4080    0.7992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9937   -4.1995   -0.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8822   -1.3891   -1.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9843   -2.4377   -0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4186   -0.4866    0.6439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5819    4.3408    1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7737    3.0985    2.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1349    3.4792    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4131    2.1202   -0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 26 28  1  0
 24 12  1  0
 20 13  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  1
  3 33  1  0
  3 34  1  0
  6 35  1  0
  7 36  1  6
  8 37  1  0
  8 38  1  0
  8 39  1  0
 11 40  1  0
 12 41  1  1
 13 42  1  1
 14 43  1  0
 14 44  1  0
 15 45  1  1
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 25 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  6
M  END


  Mrv1652306242106313D          

 53 54  0  0  0  0            999 V2000
    6.7699   -1.2250    0.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4686   -1.2510    0.7933 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8151   -2.5510    0.6272 N   0  0  2  0  0  0  0  0  0  0  0  0
    4.5460   -0.2131    0.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.0233    0.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670   -0.5340   -0.1880 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2886    0.4000   -0.7174 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9724    0.0377   -2.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1485    0.5287    0.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3173    0.3106    1.4197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1903    0.8891   -0.2100 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2568    0.9967    0.7289 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1808   -0.2022    0.7092 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8574   -1.1673   -0.4226 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8999   -2.2817   -0.2868 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5146   -3.4521   -0.8882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1799   -1.6870   -0.9005 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5000   -0.4991   -0.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8163   -0.0648   -0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6117    0.1640    0.6458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0341    1.3291    1.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2294    1.4658    1.8095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0322    2.2700    1.7059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9610    2.2935    0.7315 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0113    3.3703    1.2614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5755    2.7765   -0.5258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5155    3.0517   -1.8807 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.3687    4.3496   -0.1449 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.7101   -0.5478   -0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5930   -0.8881    0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0037   -2.2705   -0.2981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6371   -1.1028    1.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376   -3.3379    0.9360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6473   -2.6570   -0.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510   -1.5403   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8688    1.3826   -0.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3356   -0.8385   -2.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806    0.9122   -2.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9200   -0.1059   -2.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2717    1.0392   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7524    0.9244    1.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0707   -0.8298    1.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8792   -1.6681   -0.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0105   -0.7179   -1.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1452   -2.4080    0.7992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9937   -4.1995   -0.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8822   -1.3891   -1.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9843   -2.4377   -0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4186   -0.4866    0.6439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5819    4.3408    1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7737    3.0985    2.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1349    3.4792    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4131    2.1202   -0.8617 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
  2  4  1  0  0  0  0
  4  5  2  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
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  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  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 24 12  1  0  0  0  0
 20 13  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  2 32  1  1  0  0  0
  3 33  1  0  0  0  0
  3 34  1  0  0  0  0
  6 35  1  0  0  0  0
  7 36  1  6  0  0  0
  8 37  1  0  0  0  0
  8 38  1  0  0  0  0
  8 39  1  0  0  0  0
 11 40  1  0  0  0  0
 12 41  1  1  0  0  0
 13 42  1  1  0  0  0
 14 43  1  0  0  0  0
 14 44  1  0  0  0  0
 15 45  1  1  0  0  0
 16 46  1  0  0  0  0
 17 47  1  0  0  0  0
 17 48  1  0  0  0  0
 19 49  1  0  0  0  0
 25 50  1  0  0  0  0
 25 51  1  0  0  0  0
 25 52  1  0  0  0  0
 26 53  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0008979

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)O[C@](C([H])([H])[H])(C([H])(Cl)Cl)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@@]([H])(N([H])[H])C([H])([H])[H])C([H])([H])[H])[C@]2([H])C([H])([H])[C@]([H])(O[H])C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C17H25Cl2N3O6/c1-6(20)13(25)21-7(2)14(26)22-12-9-4-8(23)5-10(24)11(9)15(27)28-17(12,3)16(18)19/h6-9,12,16,23-24H,4-5,20H2,1-3H3,(H,21,25)(H,22,26)/t6-,7-,8-,9+,12+,17-/m0/s1

> <INCHI_KEY>
KHGMZWVYYCQZEC-AVMQSFCVSA-N

> <FORMULA>
C17H25Cl2N3O6

> <MOLECULAR_WEIGHT>
438.3

> <EXACT_MASS>
437.1120409

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
42.098315610882665

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-N-[(3S,4R,4aR,6S)-3-(dichloromethyl)-6,8-dihydroxy-3-methyl-1-oxo-3,4,4a,5,6,7-hexahydro-1H-2-benzopyran-4-yl]-2-[(2S)-2-aminopropanamido]propanamide

> <ALOGPS_LOGP>
-0.10

> <JCHEM_LOGP>
-1.2619566191077194

> <ALOGPS_LOGS>
-2.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.10438569488801

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.905662330906067

> <JCHEM_PKA_STRONGEST_BASIC>
8.015999976927032

> <JCHEM_POLAR_SURFACE_AREA>
150.98

> <JCHEM_REFRACTIVITY>
102.22269999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.81e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-N-[(3S,4R,4aR,6S)-3-(dichloromethyl)-6,8-dihydroxy-3-methyl-1-oxo-4a,5,6,7-tetrahydro-4H-2-benzopyran-4-yl]-2-[(2S)-2-aminopropanamido]propanamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
    6.7699   -1.2250    0.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4686   -1.2510    0.7933 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8151   -2.5510    0.6272 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5460   -0.2131    0.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.0233    0.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670   -0.5340   -0.1880 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2886    0.4000   -0.7174 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9724    0.0377   -2.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1485    0.5287    0.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3173    0.3106    1.4197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1903    0.8891   -0.2100 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2568    0.9967    0.7289 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1808   -0.2022    0.7092 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8574   -1.1673   -0.4226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8999   -2.2817   -0.2868 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5146   -3.4521   -0.8882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1799   -1.6870   -0.9005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5000   -0.4991   -0.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8163   -0.0648   -0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6117    0.1640    0.6458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0341    1.3291    1.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2294    1.4658    1.8095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0322    2.2700    1.7059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9610    2.2935    0.7315 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0113    3.3703    1.2614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5755    2.7765   -0.5258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5155    3.0517   -1.8807 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.3687    4.3496   -0.1449 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.7101   -0.5478   -0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5930   -0.8881    0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0037   -2.2705   -0.2981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6371   -1.1028    1.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376   -3.3379    0.9360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6473   -2.6570   -0.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510   -1.5403   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8688    1.3826   -0.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3356   -0.8385   -2.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806    0.9122   -2.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9200   -0.1059   -2.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2717    1.0392   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7524    0.9244    1.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0707   -0.8298    1.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8792   -1.6681   -0.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0105   -0.7179   -1.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1452   -2.4080    0.7992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9937   -4.1995   -0.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8822   -1.3891   -1.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9843   -2.4377   -0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4186   -0.4866    0.6439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5819    4.3408    1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7737    3.0985    2.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1349    3.4792    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4131    2.1202   -0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 26 28  1  0
 24 12  1  0
 20 13  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  1
  3 33  1  0
  3 34  1  0
  6 35  1  0
  7 36  1  6
  8 37  1  0
  8 38  1  0
  8 39  1  0
 11 40  1  0
 12 41  1  1
 13 42  1  1
 14 43  1  0
 14 44  1  0
 15 45  1  1
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 25 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  6
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       6.770  -1.225   0.031  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.469  -1.251   0.793  0.00  0.00           C+0
HETATM    3  N   UNK     0       4.815  -2.551   0.627  0.00  0.00           N+0
HETATM    4  C   UNK     0       4.546  -0.213   0.284  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.869   1.023   0.245  0.00  0.00           O+0
HETATM    6  N   UNK     0       3.267  -0.534  -0.188  0.00  0.00           N+0
HETATM    7  C   UNK     0       2.289   0.400  -0.717  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.972   0.038  -2.127  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.149   0.529   0.185  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.317   0.311   1.420  0.00  0.00           O+0
HETATM   11  N   UNK     0      -0.190   0.889  -0.210  0.00  0.00           N+0
HETATM   12  C   UNK     0      -1.257   0.997   0.729  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.181  -0.202   0.709  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.857  -1.167  -0.423  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.900  -2.282  -0.287  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.515  -3.452  -0.888  0.00  0.00           O+0
HETATM   17  C   UNK     0      -4.180  -1.687  -0.901  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.500  -0.499  -0.071  0.00  0.00           C+0
HETATM   19  O   UNK     0      -5.816  -0.065  -0.055  0.00  0.00           O+0
HETATM   20  C   UNK     0      -3.612   0.164   0.646  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.034   1.329   1.423  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.229   1.466   1.810  0.00  0.00           O+0
HETATM   23  O   UNK     0      -3.032   2.270   1.706  0.00  0.00           O+0
HETATM   24  C   UNK     0      -1.961   2.293   0.732  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.011   3.370   1.261  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.575   2.777  -0.526  0.00  0.00           C+0
HETATM   27 Cl   UNK     0      -1.516   3.052  -1.881  0.00  0.00          Cl+0
HETATM   28 Cl   UNK     0      -3.369   4.350  -0.145  0.00  0.00          Cl+0
HETATM   29  H   UNK     0       6.710  -0.548  -0.826  0.00  0.00           H+0
HETATM   30  H   UNK     0       7.593  -0.888   0.721  0.00  0.00           H+0
HETATM   31  H   UNK     0       7.004  -2.271  -0.298  0.00  0.00           H+0
HETATM   32  H   UNK     0       5.637  -1.103   1.895  0.00  0.00           H+0
HETATM   33  H   UNK     0       5.438  -3.338   0.936  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.647  -2.657  -0.401  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.951  -1.540  -0.172  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.869   1.383  -0.767  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.336  -0.839  -2.211  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.481   0.912  -2.653  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.920  -0.106  -2.687  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.272   1.039  -1.248  0.00  0.00           H+0
HETATM   41  H   UNK     0      -0.752   0.924   1.754  0.00  0.00           H+0
HETATM   42  H   UNK     0      -2.071  -0.830   1.644  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.879  -1.668  -0.290  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.010  -0.718  -1.412  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.145  -2.408   0.799  0.00  0.00           H+0
HETATM   46  H   UNK     0      -2.994  -4.199  -0.407  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.882  -1.389  -1.932  0.00  0.00           H+0
HETATM   48  H   UNK     0      -4.984  -2.438  -0.935  0.00  0.00           H+0
HETATM   49  H   UNK     0      -6.419  -0.487   0.644  0.00  0.00           H+0
HETATM   50  H   UNK     0      -1.582   4.341   1.293  0.00  0.00           H+0
HETATM   51  H   UNK     0      -0.774   3.099   2.306  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.135   3.479   0.614  0.00  0.00           H+0
HETATM   53  H   UNK     0      -3.413   2.120  -0.862  0.00  0.00           H+0
CONECT    1    2   29   30   31                                             
CONECT    2    1    3    4   32                                             
CONECT    3    2   33   34                                                  
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   35                                                  
CONECT    7    6    8    9   36                                             
CONECT    8    7   37   38   39                                             
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   40                                                  
CONECT   12   11   13   24   41                                             
CONECT   13   12   14   20   42                                             
CONECT   14   13   15   43   44                                             
CONECT   15   14   16   17   45                                             
CONECT   16   15   46                                                       
CONECT   17   15   18   47   48                                             
CONECT   18   17   19   20                                                  
CONECT   19   18   49                                                       
CONECT   20   18   21   13                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26   12                                             
CONECT   25   24   50   51   52                                             
CONECT   26   24   27   28   53                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    2                                                            
CONECT   33    3                                                            
CONECT   34    3                                                            
CONECT   35    6                                                            
CONECT   36    7                                                            
CONECT   37    8                                                            
CONECT   38    8                                                            
CONECT   39    8                                                            
CONECT   40   11                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
CONECT   43   14                                                            
CONECT   44   14                                                            
CONECT   45   15                                                            
CONECT   46   16                                                            
CONECT   47   17                                                            
CONECT   48   17                                                            
CONECT   49   19                                                            
CONECT   50   25                                                            
CONECT   51   25                                                            
CONECT   52   25                                                            
CONECT   53   26                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  108    0
END

RDKit          3D

53 54  0  0  0  0  0  0  0  0999 V2000
    6.7699   -1.2250    0.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4686   -1.2510    0.7933 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8151   -2.5510    0.6272 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5460   -0.2131    0.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.0233    0.2454 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2670   -0.5340   -0.1880 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2886    0.4000   -0.7174 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9724    0.0377   -2.1273 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1485    0.5287    0.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3173    0.3106    1.4197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1903    0.8891   -0.2100 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2568    0.9967    0.7289 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1808   -0.2022    0.7092 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8574   -1.1673   -0.4226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8999   -2.2817   -0.2868 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5146   -3.4521   -0.8882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1799   -1.6870   -0.9005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5000   -0.4991   -0.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8163   -0.0648   -0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6117    0.1640    0.6458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0341    1.3291    1.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2294    1.4658    1.8095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0322    2.2700    1.7059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9610    2.2935    0.7315 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0113    3.3703    1.2614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5755    2.7765   -0.5258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5155    3.0517   -1.8807 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.3687    4.3496   -0.1449 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.7101   -0.5478   -0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5930   -0.8881    0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0037   -2.2705   -0.2981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6371   -1.1028    1.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376   -3.3379    0.9360 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6473   -2.6570   -0.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510   -1.5403   -0.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8688    1.3826   -0.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3356   -0.8385   -2.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806    0.9122   -2.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9200   -0.1059   -2.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2717    1.0392   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7524    0.9244    1.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0707   -0.8298    1.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8792   -1.6681   -0.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0105   -0.7179   -1.4121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1452   -2.4080    0.7992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9937   -4.1995   -0.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8822   -1.3891   -1.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9843   -2.4377   -0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4186   -0.4866    0.6439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5819    4.3408    1.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7737    3.0985    2.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1349    3.4792    0.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4131    2.1202   -0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 26 28  1  0
 24 12  1  0
 20 13  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  1
  3 33  1  0
  3 34  1  0
  6 35  1  0
  7 36  1  6
  8 37  1  0
  8 38  1  0
  8 39  1  0
 11 40  1  0
 12 41  1  1
 13 42  1  1
 14 43  1  0
 14 44  1  0
 15 45  1  1
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 25 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  6
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(2S)-N-[(3S,4R,4AR,6S)-3-(dichloromethyl)-6,8-dihydroxy-3-methyl-1-oxo-3,4,4a,5,6,7-hexahydro-1H-2-benzopyran-4-yl]-2-{[(2S)-2-amino-1-hydroxypropylidene]amino}propanimidate	Generator

Chemical Formula

C₁₇H₂₅Cl₂N₃O₆

Average Mass

438.3000 Da

Monoisotopic Mass

437.11204 Da

IUPAC Name

(2S)-N-[(3S,4R,4aR,6S)-3-(dichloromethyl)-6,8-dihydroxy-3-methyl-1-oxo-3,4,4a,5,6,7-hexahydro-1H-2-benzopyran-4-yl]-2-[(2S)-2-aminopropanamido]propanamide

Traditional Name

(2S)-N-[(3S,4R,4aR,6S)-3-(dichloromethyl)-6,8-dihydroxy-3-methyl-1-oxo-4a,5,6,7-tetrahydro-4H-2-benzopyran-4-yl]-2-[(2S)-2-aminopropanamido]propanamide

CAS Registry Number

Not Available

SMILES

C[C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H]1[C@@H]2C[C@H](O)CC(O)=C2C(=O)O[C@]1(C)C(Cl)Cl

InChI Identifier

InChI=1S/C17H25Cl2N3O6/c1-6(20)13(25)21-7(2)14(26)22-12-9-4-8(23)5-10(24)11(9)15(27)28-17(12,3)16(18)19/h6-9,12,16,23-24H,4-5,20H2,1-3H3,(H,21,25)(H,22,26)/t6-,7-,8-,9+,12+,17-/m0/s1

InChI Key

KHGMZWVYYCQZEC-AVMQSFCVSA-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
Burkholderia	NPAtlas	20095633

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	-0.1	ALOGPS
logP	-1.3	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	8.91	ChemAxon
pKa (Strongest Basic)	8.02	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	150.98 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	102.22 m³·mol⁻¹	ChemAxon
Polarizability	42.1 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA012633

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78437773

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54751361

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Bactobolin D (NP0008979)

MOL for NP0008979 (Bactobolin D)

3D MOL for NP0008979 (Bactobolin D)

3D SDF for NP0008979 (Bactobolin D)

3D-SDF for NP0008979 (Bactobolin D)

PDB for NP0008979 (Bactobolin D)

3D PDB for NP0008979 (Bactobolin D)

SMILES for NP0008979 (Bactobolin D)

INCHI for NP0008979 (Bactobolin D)

Structure for NP0008979 (Bactobolin D)

3D Structure for NP0008979 (Bactobolin D)