NP-MRD: Showing NP-Card for Geometricin A (NP0069899)

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Record Information

Version

2.0

Created at

2022-04-28 15:12:26 UTC

Updated at

2022-04-28 15:12:26 UTC

NP-MRD ID

NP0069899

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Geometricin A

Description

(2Z,6E,8E,10S,11R,12R,13S,15S)-11,13-dihydroxy-15-[(2R,3R,5R,7S,8S,9S)-9-hydroxy-4,4,8-trimethyl-7-[(2E)-3-(2-methyl-1,3-oxazol-4-yl)prop-2-en-1-yl]-3-(phosphonooxy)-1,6-dioxaspiro[4.5]Decan-2-yl]-15-methoxy-3,7,8,10,12-pentamethylpentadeca-2,6,8-trienimidic acid belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. Geometricin A is found in Luffariella geometrica. Based on a literature review very few articles have been published on (2Z,6E,8E,10S,11R,12R,13S,15S)-11,13-dihydroxy-15-[(2R,3R,5R,7S,8S,9S)-9-hydroxy-4,4,8-trimethyl-7-[(2E)-3-(2-methyl-1,3-oxazol-4-yl)prop-2-en-1-yl]-3-(phosphonooxy)-1,6-dioxaspiro[4.5]Decan-2-yl]-15-methoxy-3,7,8,10,12-pentamethylpentadeca-2,6,8-trienimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282217122D          

 54 56  0  0  1  0            999 V2000
    6.4542    3.5955    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6940    2.8061    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1302    2.2038    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3267    2.3909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0869    3.1803    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6507    3.7826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4633    2.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7569    3.0664    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9440    3.8699    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7660    3.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4039    4.4935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5938    4.3376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0537    4.9613    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3237    5.7408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2436    4.8054    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9735    4.0258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7035    5.4290    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9735    6.2085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    5.2731    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6467    5.8967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3767    6.6763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9168    7.2999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6467    8.0795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1868    8.7031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9168    9.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4569   10.1063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2670    9.9504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5371    9.1708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3472    9.0149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9970    8.5472    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1868   10.8859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7269    7.1440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4334    6.8322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3767    4.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6740    5.2731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4841    5.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9969    2.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3390    3.2432    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    2.8367    3.9011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    2.5852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6810    3.7409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9281    1.9586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1211    1.8895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3699    1.4144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4975    2.6190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0180    4.1978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8215    4.0107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3853    4.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1888    4.4260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8124    4.9661    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.5188    4.5398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3317    3.7363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5097    3.6660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2788    4.8608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  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
  5 10  1  6  0  0  0
  9 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 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  1  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  2  0  0  0  0
 28 30  1  0  0  0  0
 26 31  1  0  0  0  0
 22 32  1  0  0  0  0
 21 33  1  0  0  0  0
 19 34  1  1  0  0  0
 11 35  1  6  0  0  0
 35 36  1  0  0  0  0
  8 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
  7 42  1  0  0  0  0
  7 43  1  0  0  0  0
  3 44  1  1  0  0  0
  2 45  1  1  0  0  0
  1 46  1  1  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 49 53  2  0  0  0  0
 51 54  1  0  0  0  0
M  END

     RDKit          3D

117119  0  0  0  0  0  0  0  0999 V2000
   -0.5958   -1.6132   -1.1530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0861   -0.8893   -0.1060 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2231   -1.4724    1.1043 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4127   -0.8587    2.1862 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0731   -0.8057    2.0732 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3997   -0.2465    3.3972 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912    0.2621    1.1051 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1913    1.6240    1.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8910    0.0656    0.5190 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9070   -1.1489   -0.1874 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2003    0.4059    1.1770 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4832   -0.2559    2.4307 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1692    0.4869    0.0871 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3370   -0.0577   -0.0189 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8584   -0.9000    1.0379 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1597    0.1759   -1.2587 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6889    0.9657   -2.3981 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3568   -0.3669   -1.3233 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2173   -0.1740   -2.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5166    0.5110   -2.0936 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2673    1.8318   -1.5259 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4750    2.0458   -0.2655 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7439    2.9316   -2.0775 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5410    3.0322   -3.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9663    4.3333   -3.6996 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.8989    2.0760   -3.9434 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6859   -1.5510    1.5873 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2201   -0.2793    1.5456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6272   -0.4123    1.4145 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0923   -0.7356    2.8155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1417    0.5069    3.6758 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6673    0.1447    4.9126 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1415    1.4391    3.0162 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.5282    1.1153    3.5926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0969    1.4191    1.5317 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.4794    1.0703    0.9783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5267    1.0248   -0.4864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2992    1.7885   -1.2422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3083    1.7026   -2.6944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5733    0.8778   -3.5046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9118    1.1447   -4.7461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8269    2.0978   -4.7962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4320    2.6415   -6.0638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0668    2.4376   -3.5258 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0694    0.7621    0.9277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7172   -1.5977    0.4798 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4084   -1.2114   -0.9262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9715   -2.3991    0.6231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5640   -2.5197    0.9574 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1070   -3.3445   -0.0182 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3636   -4.9786    0.2696 P   0  0  2  0  0  5  0  0  0  0  0  0
   -4.0121   -5.2067    1.6132 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9325   -5.8658    0.2031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4266   -5.6268   -0.9011 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4175   -2.0388   -0.9683 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4437   -0.8727   -2.0169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8897   -2.5615    1.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7714    0.1903    2.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6542   -1.4145    3.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5001   -1.7801    1.9557 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8298   -1.0053    3.8704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8565    0.1510    0.2261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0983    1.8066    1.5524 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4115    1.6132    2.7229 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6907    2.4521    1.1314 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9272    0.8132   -0.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6050   -1.0918   -1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0495    1.5152    1.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8933    0.3154    3.2533 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2053   -1.2795    2.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5182    0.0501    2.7869 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8285    1.1330   -0.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1587   -1.6553    1.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5601   -0.4480    1.7570 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5601   -1.6558    0.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3867    1.8239   -2.5804 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6712    1.3282   -2.3878 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7677    0.3256   -3.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7982   -0.9647   -0.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5022   -1.1516   -2.9770 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7171    0.4876   -3.2216 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8149   -0.1437   -1.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
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    9.3597    1.1458    0.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0685    2.8185    0.3183 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5421    2.5669   -0.5192 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5126    3.9059   -1.5817 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9490    4.4983   -4.0054 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.2629    5.0922   -3.7012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5521   -1.8722    2.6756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1142   -1.1602    2.7934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4488   -1.4652    3.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1791    1.0223    3.7653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9359   -0.1796    5.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9117    2.4591    3.4459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8028    0.0658    3.4834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4187    1.2989    4.7045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2915    1.8507    3.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9603    2.5005    1.2055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9267    0.1998    1.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1364    1.9471    1.2675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8973    0.3262   -1.0195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9316    2.4915   -0.6982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8520    0.1477   -3.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.4528    2.2427   -6.2302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8135    2.3122   -6.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1080   -0.1342   -1.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6201   -1.8057   -1.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.9745   -3.0416    1.5291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0335   -3.0637   -0.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0227   -3.2294    1.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1393   -5.2644    0.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8699   -5.9023   -1.6600 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
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 21 22  1  0
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 29 28  1  1
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 31 32  1  0
 31 33  1  0
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 33 35  1  0
 35 36  1  0
 36 37  1  0
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 38 39  1  0
 39 40  2  0
 40 41  1  0
 41 42  1  0
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 42 44  2  0
 35 45  1  0
 29 46  1  0
 46 47  1  6
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 51 50  1  6
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  1 55  1  0
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 31 94  1  1
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 33 96  1  1
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 35100  1  6
 36101  1  0
 36102  1  0
 37103  1  0
 38104  1  0
 40105  1  0
 43106  1  0
 43107  1  0
 43108  1  0
 47109  1  0
 47110  1  0
 47111  1  0
 48112  1  0
 48113  1  0
 48114  1  0
 49115  1  1
 53116  1  0
 54117  1  0
M  END


  Mrv1652304282217122D          

 54 56  0  0  1  0            999 V2000
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    6.1302    2.2038    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3267    2.3909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0869    3.1803    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6507    3.7826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4633    2.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7569    3.0664    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9440    3.8699    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7660    3.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4039    4.4935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5938    4.3376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0537    4.9613    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3237    5.7408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2670    9.9504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5371    9.1708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3472    9.0149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9970    8.5472    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1868   10.8859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7269    7.1440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4334    6.8322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3767    4.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6740    5.2731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4841    5.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9969    2.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3390    3.2432    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    2.8367    3.9011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    2.5852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6810    3.7409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9281    1.9586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1211    1.8895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3699    1.4144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4975    2.6190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0180    4.1978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8215    4.0107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3853    4.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1888    4.4260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8124    4.9661    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.5188    4.5398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3317    3.7363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5097    3.6660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2788    4.8608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  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
  5 10  1  6  0  0  0
  9 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 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  1  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  2  0  0  0  0
 28 30  1  0  0  0  0
 26 31  1  0  0  0  0
 22 32  1  0  0  0  0
 21 33  1  0  0  0  0
 19 34  1  1  0  0  0
 11 35  1  6  0  0  0
 35 36  1  0  0  0  0
  8 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
  7 42  1  0  0  0  0
  7 43  1  0  0  0  0
  3 44  1  1  0  0  0
  2 45  1  1  0  0  0
  1 46  1  1  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 49 53  2  0  0  0  0
 51 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069899

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H](C[C@H](O)[C@@H](C)[C@H](O)[C@@H](C)\C=C(/C)\C(\C)=C\CC\C(C)=C/C(N)=O)[C@H]1O[C@]2(C[C@H](O)[C@H](C)[C@H](C\C=C\C3=COC(C)=N3)O2)C(C)(C)[C@H]1OP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C39H63N2O12P/c1-22(17-34(40)44)13-11-14-23(2)24(3)18-25(4)35(45)27(6)30(42)19-33(49-10)36-37(53-54(46,47)48)38(8,9)39(52-36)20-31(43)26(5)32(51-39)16-12-15-29-21-50-28(7)41-29/h12,14-15,17-18,21,25-27,30-33,35-37,42-43,45H,11,13,16,19-20H2,1-10H3,(H2,40,44)(H2,46,47,48)/b15-12+,22-17-,23-14+,24-18+/t25-,26-,27+,30-,31-,32-,33-,35+,36+,37-,39+/m0/s1

> <INCHI_KEY>
GNMWTNFLWQSTKW-QYGNYFKXSA-N

> <FORMULA>
C39H63N2O12P

> <MOLECULAR_WEIGHT>
782.909

> <EXACT_MASS>
782.411862475

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
117

> <JCHEM_AVERAGE_POLARIZABILITY>
84.12138802262804

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3R,5R,7S,8S,9S)-2-[(1S,3S,4R,5R,6S,7E,9E,13Z)-14-carbamoyl-3,5-dihydroxy-1-methoxy-4,6,8,9,13-pentamethyltetradeca-7,9,13-trien-1-yl]-9-hydroxy-4,4,8-trimethyl-7-[(2E)-3-(2-methyl-1,3-oxazol-4-yl)prop-2-en-1-yl]-1,6-dioxaspiro[4.5]decan-3-yl]oxy}phosphonic acid

> <ALOGPS_LOGP>
3.11

> <JCHEM_LOGP>
3.4085547944422734

> <ALOGPS_LOGS>
-4.38

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.175528950718004

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2776506809044323

> <JCHEM_PKA_STRONGEST_BASIC>
0.58690883261

> <JCHEM_POLAR_SURFACE_AREA>
224.26

> <JCHEM_REFRACTIVITY>
205.84720000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.30e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3R,5R,7S,8S,9S)-2-[(1S,3S,4R,5R,6S,7E,9E,13Z)-14-carbamoyl-3,5-dihydroxy-1-methoxy-4,6,8,9,13-pentamethyltetradeca-7,9,13-trien-1-yl]-9-hydroxy-4,4,8-trimethyl-7-[(2E)-3-(2-methyl-1,3-oxazol-4-yl)prop-2-en-1-yl]-1,6-dioxaspiro[4.5]decan-3-yl]oxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      12.048   6.712   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.495   5.238   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.443   4.114   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.943   4.463   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.496   5.936   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.548   7.061   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.331   4.928   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.013   5.724   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.362   7.224   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.897   7.355   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.354   8.388   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.842   8.097   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.834   9.261   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.338  10.716   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.321   8.970   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.817   7.515   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.313  10.134   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.817  11.589   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.199   9.843   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.207  11.007   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.703  12.462   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.711  13.627   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.207  15.082   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.215  16.246   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.711  17.701   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.720  18.865   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.232  18.574   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.736  17.119   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.248  16.828   0.000  0.00  0.00           O+0
HETATM   30  N   UNK     0      -3.728  15.955   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      -2.215  20.320   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.224  13.335   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.809  12.753   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.703   8.388   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       6.858   9.843   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       8.370  10.134   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.594   5.125   0.000  0.00  0.00           O+0
HETATM   38  P   UNK     0       4.366   6.054   0.000  0.00  0.00           P+0
HETATM   39  O   UNK     0       5.295   7.282   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       3.437   4.826   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       3.138   6.983   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       9.199   3.656   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.693   3.527   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      11.891   2.640   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      13.995   4.889   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      13.100   7.836   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      14.600   7.487   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      15.653   8.611   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      17.152   8.262   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0      18.317   9.270   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      19.635   8.474   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      19.286   6.974   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      17.751   6.843   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      21.054   9.073   0.000  0.00  0.00           C+0
CONECT    1    2    6   46                                                  
CONECT    2    1    3   45                                                  
CONECT    3    2    4   44                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   10                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   42   43                                             
CONECT    8    7    9   37                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    5                                                       
CONECT   11    9   12   35                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   34                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   33                                                  
CONECT   22   21   23   32                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   26                                                            
CONECT   32   22                                                            
CONECT   33   21                                                            
CONECT   34   19                                                            
CONECT   35   11   36                                                       
CONECT   36   35                                                            
CONECT   37    8   38                                                       
CONECT   38   37   39   40   41                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   38                                                            
CONECT   42    7                                                            
CONECT   43    7                                                            
CONECT   44    3                                                            
CONECT   45    2                                                            
CONECT   46    1   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50   53                                                  
CONECT   50   49   51                                                       
CONECT   51   50   52   54                                                  
CONECT   52   51   53                                                       
CONECT   53   52   49                                                       
CONECT   54   51                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  112    0
END

View in JSmol

Synonyms

Value	Source
(2Z,6E,8E,10S,11R,12R,13S,15S)-11,13-Dihydroxy-15-[(2R,3R,5R,7S,8S,9S)-9-hydroxy-4,4,8-trimethyl-7-[(2E)-3-(2-methyl-1,3-oxazol-4-yl)prop-2-en-1-yl]-3-(phosphonooxy)-1,6-dioxaspiro[4.5]decan-2-yl]-15-methoxy-3,7,8,10,12-pentamethylpentadeca-2,6,8-trienimidate	Generator

Chemical Formula

C₃₉H₆₃N₂O₁₂P

Average Mass

782.9090 Da

Monoisotopic Mass

782.41186 Da

IUPAC Name

{[(2R,3R,5R,7S,8S,9S)-2-[(1S,3S,4R,5R,6S,7E,9E,13Z)-14-carbamoyl-3,5-dihydroxy-1-methoxy-4,6,8,9,13-pentamethyltetradeca-7,9,13-trien-1-yl]-9-hydroxy-4,4,8-trimethyl-7-[(2E)-3-(2-methyl-1,3-oxazol-4-yl)prop-2-en-1-yl]-1,6-dioxaspiro[4.5]decan-3-yl]oxy}phosphonic acid

Traditional Name

[(2R,3R,5R,7S,8S,9S)-2-[(1S,3S,4R,5R,6S,7E,9E,13Z)-14-carbamoyl-3,5-dihydroxy-1-methoxy-4,6,8,9,13-pentamethyltetradeca-7,9,13-trien-1-yl]-9-hydroxy-4,4,8-trimethyl-7-[(2E)-3-(2-methyl-1,3-oxazol-4-yl)prop-2-en-1-yl]-1,6-dioxaspiro[4.5]decan-3-yl]oxyphosphonic acid

CAS Registry Number

Not Available

SMILES

CO[C@@H](C[C@H](O)[C@@H](C)[C@H](O)[C@@H](C)\C=C(/C)\C(\C)=C\CC\C(C)=C/C(N)=O)[C@H]1O[C@]2(C[C@H](O)[C@H](C)[C@H](C\C=C\C3=COC(C)=N3)O2)C(C)(C)[C@H]1OP(O)(O)=O

InChI Identifier

InChI=1S/C39H63N2O12P/c1-22(17-34(40)44)13-11-14-23(2)24(3)18-25(4)35(45)27(6)30(42)19-33(49-10)36-37(53-54(46,47)48)38(8,9)39(52-36)20-31(43)26(5)32(51-39)16-12-15-29-21-50-28(7)41-29/h12,14-15,17-18,21,25-27,30-33,35-37,42-43,45H,11,13,16,19-20H2,1-10H3,(H2,40,44)(H2,46,47,48)/b15-12+,22-17-,23-14+,24-18+/t25-,26-,27+,30-,31-,32-,33-,35+,36+,37-,39+/m0/s1

InChI Key

GNMWTNFLWQSTKW-QYGNYFKXSA-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
Luffariella geometrica	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Aromatic monoterpenoids

Alternative Parents

Substituents

Aromatic monoterpenoid
Ketal
Monoalkyl phosphate
2,4-disubstituted 1,3-oxazole
Alkyl phosphate
Phosphoric acid ester
Oxane
Organic phosphoric acid derivative
Monosaccharide
Heteroaromatic compound
Tetrahydrofuran
Oxazole
Azole
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboximidic acid derivative
Carboximidic acid
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.11	ALOGPS
logP	3.41	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	1.28	ChemAxon
pKa (Strongest Basic)	0.59	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	224.26 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	205.85 m³·mol⁻¹	ChemAxon
Polarizability	84.12 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163025527

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Geometricin A (NP0069899)

MOL for NP0069899 (Geometricin A)

3D MOL for NP0069899 (Geometricin A)

3D SDF for NP0069899 (Geometricin A)

3D-SDF for NP0069899 (Geometricin A)

PDB for NP0069899 (Geometricin A)

3D PDB for NP0069899 (Geometricin A)

SMILES for NP0069899 (Geometricin A)

INCHI for NP0069899 (Geometricin A)

Structure for NP0069899 (Geometricin A)

3D Structure for NP0069899 (Geometricin A)