NP-MRD: Showing NP-Card for Strobilurin E (NP0011230)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-01-05 20:59:42 UTC

Updated at

2021-07-15 17:08:20 UTC

NP-MRD ID

NP0011230

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Strobilurin E

Provided By

NPAtlas

Description

Methyl (2E,3Z)-6-[(2S,5'R)-3',3'-dimethyl-5'-(2-methylprop-1-en-1-yl)-3H-spiro[1,4-benzodioxine-2,2'-[1,4]dioxolane]-7-yl]-2-(methoxymethylidene)-3-methylhexa-3,5-dienoate belongs to the class of organic compounds known as styrenes. These are organic compounds containing an ethenylbenzene moiety. Strobilurin E is found in Crepidotus. Strobilurin E was first documented in 1990 (PMID: 2312406). Based on a literature review very few articles have been published on methyl (2E,3Z)-6-[(2S,5'R)-3',3'-dimethyl-5'-(2-methylprop-1-en-1-yl)-3H-spiro[1,4-benzodioxine-2,2'-[1,4]dioxolane]-7-yl]-2-(methoxymethylidene)-3-methylhexa-3,5-dienoate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107443D          

 65 67  0  0  0  0            999 V2000
    8.8733    0.8506   -0.9597 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6562    0.1378   -1.0283 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4972    0.8156   -0.7314 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3393    0.2257   -0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2797    1.1528   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5511    2.4251   -0.3611 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0249    1.1053    0.4342 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1148    2.1541    0.5950 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -1.1775   -0.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9207   -1.7901   -0.0664 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5783   -2.0067    0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1815   -1.6987    0.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -2.6524    0.8756 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9189   -2.4124    1.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1321   -3.4627    1.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2243   -3.3487    1.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.1427    1.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154   -1.0625    0.9872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2596   -1.2403    0.8072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7094    0.1726    0.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1275    0.1721    0.6189 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6559   -0.6316    1.7738 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2115   -1.9584    1.6175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6242    1.4845    0.6679 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7026    1.8117   -0.6838 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5963    2.9650   -0.9216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9023    2.8399   -0.8315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5039    1.5265   -0.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8148    3.9879   -1.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2362    0.6966   -1.2829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5385   -0.3786   -0.7195 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3401   -0.6888   -1.5848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4498   -1.5556   -0.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8317    1.6932   -1.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0412    1.2956    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7003    0.1571   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4487    1.8970   -0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191    2.5062    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145    1.9634    0.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5122    3.0418    0.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2601   -1.9870   -1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6015   -1.2354    0.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9070   -2.8237    0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9090   -3.0680    0.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7213   -0.7906    0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7481   -3.6286    1.0580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6275   -4.4259    1.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7983   -4.1797    2.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8029   -0.4019    0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.2390    2.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7269   -0.5383    1.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835    2.0000   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1693    3.9185   -1.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5706    0.8815   -1.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9109    1.0312    0.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5249    1.6772   -0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3119    4.7196   -1.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7663    3.6290   -1.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9737    4.4849   -0.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5972   -0.5332   -2.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0468   -1.7487   -1.4585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4947    0.0039   -1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0904   -1.5397   -1.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1477   -1.5402    0.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8984   -2.5367   -0.7108 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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  3  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 19 14  1  0  0  0  0
 31 21  1  0  0  0  0
 23 17  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  1 36  1  0  0  0  0
  3 37  1  0  0  0  0
  8 38  1  0  0  0  0
  8 39  1  0  0  0  0
  8 40  1  0  0  0  0
 10 41  1  0  0  0  0
 10 42  1  0  0  0  0
 10 43  1  0  0  0  0
 11 44  1  0  0  0  0
 12 45  1  0  0  0  0
 13 46  1  0  0  0  0
 15 47  1  0  0  0  0
 16 48  1  0  0  0  0
 19 49  1  0  0  0  0
 22 50  1  0  0  0  0
 22 51  1  0  0  0  0
 25 52  1  6  0  0  0
 26 53  1  0  0  0  0
 28 54  1  0  0  0  0
 28 55  1  0  0  0  0
 28 56  1  0  0  0  0
 29 57  1  0  0  0  0
 29 58  1  0  0  0  0
 29 59  1  0  0  0  0
 32 60  1  0  0  0  0
 32 61  1  0  0  0  0
 32 62  1  0  0  0  0
 33 63  1  0  0  0  0
 33 64  1  0  0  0  0
 33 65  1  0  0  0  0
M  END

     RDKit          3D

 65 67  0  0  0  0  0  0  0  0999 V2000
    8.8733    0.8506   -0.9597 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6562    0.1378   -1.0283 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4972    0.8156   -0.7314 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3393    0.2257   -0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2797    1.1528   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5511    2.4251   -0.3611 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0249    1.1053    0.4342 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1148    2.1541    0.5950 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -1.1775   -0.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9207   -1.7901   -0.0664 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5783   -2.0067    0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1815   -1.6987    0.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -2.6524    0.8756 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9189   -2.4124    1.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1321   -3.4627    1.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2243   -3.3487    1.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.1427    1.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154   -1.0625    0.9872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2596   -1.2403    0.8072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7094    0.1726    0.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1275    0.1721    0.6189 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6559   -0.6316    1.7738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2115   -1.9584    1.6175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6242    1.4845    0.6679 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7026    1.8117   -0.6838 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5963    2.9650   -0.9216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9023    2.8399   -0.8315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5039    1.5265   -0.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8148    3.9879   -1.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2362    0.6966   -1.2829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5385   -0.3786   -0.7195 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3401   -0.6888   -1.5848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4498   -1.5556   -0.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8317    1.6932   -1.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0412    1.2956    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7003    0.1571   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4487    1.8970   -0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191    2.5062    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145    1.9634    0.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5122    3.0418    0.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2601   -1.9870   -1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6015   -1.2354    0.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9070   -2.8237    0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9090   -3.0680    0.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7213   -0.7906    0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7481   -3.6286    1.0580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6275   -4.4259    1.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7983   -4.1797    2.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8029   -0.4019    0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.2390    2.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7269   -0.5383    1.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835    2.0000   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1693    3.9185   -1.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5706    0.8815   -1.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9109    1.0312    0.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5249    1.6772   -0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3119    4.7196   -1.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7663    3.6290   -1.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9737    4.4849   -0.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5972   -0.5332   -2.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0468   -1.7487   -1.4585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4947    0.0039   -1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0904   -1.5397   -1.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1477   -1.5402    0.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8984   -2.5367   -0.7108 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
  5  7  1  0
  7  8  1  0
  4  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 21 20  1  6
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  3
 27 28  1  0
 27 29  1  0
 25 30  1  0
 30 31  1  0
 31 32  1  6
 31 33  1  0
 19 14  1  0
 31 21  1  0
 23 17  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  8 38  1  0
  8 39  1  0
  8 40  1  0
 10 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  0
 12 45  1  0
 13 46  1  0
 15 47  1  0
 16 48  1  0
 19 49  1  0
 22 50  1  0
 22 51  1  0
 25 52  1  6
 26 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
 29 58  1  0
 29 59  1  0
 32 60  1  0
 32 61  1  0
 32 62  1  0
 33 63  1  0
 33 64  1  0
 33 65  1  0
M  END


  Mrv1652306242107443D          

 65 67  0  0  0  0            999 V2000
    8.8733    0.8506   -0.9597 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6562    0.1378   -1.0283 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4972    0.8156   -0.7314 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3393    0.2257   -0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2797    1.1528   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5511    2.4251   -0.3611 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0249    1.1053    0.4342 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1148    2.1541    0.5950 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -1.1775   -0.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9207   -1.7901   -0.0664 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5783   -2.0067    0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1815   -1.6987    0.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -2.6524    0.8756 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9189   -2.4124    1.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1321   -3.4627    1.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2243   -3.3487    1.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.1427    1.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154   -1.0625    0.9872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2596   -1.2403    0.8072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7094    0.1726    0.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1275    0.1721    0.6189 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6559   -0.6316    1.7738 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2115   -1.9584    1.6175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6242    1.4845    0.6679 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7026    1.8117   -0.6838 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5963    2.9650   -0.9216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9023    2.8399   -0.8315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5039    1.5265   -0.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8148    3.9879   -1.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2362    0.6966   -1.2829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5385   -0.3786   -0.7195 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3401   -0.6888   -1.5848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4498   -1.5556   -0.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8317    1.6932   -1.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0412    1.2956    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7003    0.1571   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4487    1.8970   -0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191    2.5062    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145    1.9634    0.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5122    3.0418    0.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2601   -1.9870   -1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6015   -1.2354    0.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9070   -2.8237    0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9090   -3.0680    0.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7213   -0.7906    0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7481   -3.6286    1.0580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6275   -4.4259    1.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7983   -4.1797    2.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8029   -0.4019    0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.2390    2.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7269   -0.5383    1.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835    2.0000   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1693    3.9185   -1.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5706    0.8815   -1.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9109    1.0312    0.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5249    1.6772   -0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3119    4.7196   -1.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7663    3.6290   -1.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9737    4.4849   -0.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5972   -0.5332   -2.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0468   -1.7487   -1.4585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4947    0.0039   -1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0904   -1.5397   -1.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1477   -1.5402    0.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8984   -2.5367   -0.7108 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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  3  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 19 14  1  0  0  0  0
 31 21  1  0  0  0  0
 23 17  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  1 36  1  0  0  0  0
  3 37  1  0  0  0  0
  8 38  1  0  0  0  0
  8 39  1  0  0  0  0
  8 40  1  0  0  0  0
 10 41  1  0  0  0  0
 10 42  1  0  0  0  0
 10 43  1  0  0  0  0
 11 44  1  0  0  0  0
 12 45  1  0  0  0  0
 13 46  1  0  0  0  0
 15 47  1  0  0  0  0
 16 48  1  0  0  0  0
 19 49  1  0  0  0  0
 22 50  1  0  0  0  0
 22 51  1  0  0  0  0
 25 52  1  6  0  0  0
 26 53  1  0  0  0  0
 28 54  1  0  0  0  0
 28 55  1  0  0  0  0
 28 56  1  0  0  0  0
 29 57  1  0  0  0  0
 29 58  1  0  0  0  0
 29 59  1  0  0  0  0
 32 60  1  0  0  0  0
 32 61  1  0  0  0  0
 32 62  1  0  0  0  0
 33 63  1  0  0  0  0
 33 64  1  0  0  0  0
 33 65  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011230

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(OC([H])([H])[H])=C(/C(=O)OC([H])([H])[H])\C(=C(\[H])/C(/[H])=C(\[H])C1=C([H])C([H])=C2OC([H])([H])[C@@]3(O[C@@]([H])(OC3(C([H])([H])[H])C([H])([H])[H])C([H])=C(C([H])([H])[H])C([H])([H])[H])OC2=C1[H])\C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O7/c1-17(2)13-23-32-25(4,5)26(33-23)16-30-21-12-11-19(14-22(21)31-26)10-8-9-18(3)20(15-28-6)24(27)29-7/h8-15,23H,16H2,1-7H3/b10-8+,18-9-,20-15+/t23-,26+/m1/s1

> <INCHI_KEY>
UKZBFRLDRGPOEJ-JZMZRJBLSA-N

> <FORMULA>
C26H32O7

> <MOLECULAR_WEIGHT>
456.535

> <EXACT_MASS>
456.21480337

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
51.196889213364614

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2E,3Z,5E)-6-[(2S,5'R)-3',3'-dimethyl-5'-(2-methylprop-1-en-1-yl)-3H-spiro[1,4-benzodioxine-2,2'-[1,4]dioxolane]-7-yl]-2-(methoxymethylidene)-3-methylhexa-3,5-dienoate

> <ALOGPS_LOGP>
4.50

> <JCHEM_LOGP>
5.536554139333333

> <ALOGPS_LOGS>
-5.41

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.000220724435554

> <JCHEM_POLAR_SURFACE_AREA>
72.45000000000002

> <JCHEM_REFRACTIVITY>
126.9941

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.78e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2E,3Z,5E)-6-[(2S,5'R)-3',3'-dimethyl-5'-(2-methylprop-1-en-1-yl)-3H-spiro[1,4-benzodioxine-2,2'-[1,4]dioxolane]-7-yl]-2-(methoxymethylidene)-3-methylhexa-3,5-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 65 67  0  0  0  0  0  0  0  0999 V2000
    8.8733    0.8506   -0.9597 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6562    0.1378   -1.0283 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4972    0.8156   -0.7314 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3393    0.2257   -0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2797    1.1528   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5511    2.4251   -0.3611 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0249    1.1053    0.4342 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1148    2.1541    0.5950 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -1.1775   -0.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9207   -1.7901   -0.0664 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5783   -2.0067    0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1815   -1.6987    0.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -2.6524    0.8756 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9189   -2.4124    1.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1321   -3.4627    1.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2243   -3.3487    1.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.1427    1.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154   -1.0625    0.9872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2596   -1.2403    0.8072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7094    0.1726    0.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1275    0.1721    0.6189 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6559   -0.6316    1.7738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2115   -1.9584    1.6175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6242    1.4845    0.6679 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7026    1.8117   -0.6838 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5963    2.9650   -0.9216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9023    2.8399   -0.8315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5039    1.5265   -0.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8148    3.9879   -1.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2362    0.6966   -1.2829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5385   -0.3786   -0.7195 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3401   -0.6888   -1.5848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4498   -1.5556   -0.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8317    1.6932   -1.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0412    1.2956    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7003    0.1571   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4487    1.8970   -0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191    2.5062    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145    1.9634    0.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5122    3.0418    0.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2601   -1.9870   -1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6015   -1.2354    0.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9070   -2.8237    0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9090   -3.0680    0.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7213   -0.7906    0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7481   -3.6286    1.0580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6275   -4.4259    1.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7983   -4.1797    2.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8029   -0.4019    0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.2390    2.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7269   -0.5383    1.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835    2.0000   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1693    3.9185   -1.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5706    0.8815   -1.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9109    1.0312    0.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5249    1.6772   -0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3119    4.7196   -1.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7663    3.6290   -1.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9737    4.4849   -0.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5972   -0.5332   -2.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0468   -1.7487   -1.4585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4947    0.0039   -1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0904   -1.5397   -1.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1477   -1.5402    0.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8984   -2.5367   -0.7108 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
  5  7  1  0
  7  8  1  0
  4  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 21 20  1  6
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  3
 27 28  1  0
 27 29  1  0
 25 30  1  0
 30 31  1  0
 31 32  1  6
 31 33  1  0
 19 14  1  0
 31 21  1  0
 23 17  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  8 38  1  0
  8 39  1  0
  8 40  1  0
 10 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  0
 12 45  1  0
 13 46  1  0
 15 47  1  0
 16 48  1  0
 19 49  1  0
 22 50  1  0
 22 51  1  0
 25 52  1  6
 26 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
 29 58  1  0
 29 59  1  0
 32 60  1  0
 32 61  1  0
 32 62  1  0
 33 63  1  0
 33 64  1  0
 33 65  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       8.873   0.851  -0.960  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.656   0.138  -1.028  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.497   0.816  -0.731  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.339   0.226  -0.269  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.280   1.153  -0.042  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.551   2.425  -0.361  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.025   1.105   0.434  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.115   2.154   0.595  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.529  -1.178  -0.010  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.921  -1.790  -0.066  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.578  -2.007   0.329  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.182  -1.699   0.487  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.336  -2.652   0.876  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.919  -2.412   1.053  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.132  -3.463   1.507  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.224  -3.349   1.703  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.831  -2.143   1.438  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.115  -1.063   0.987  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.260  -1.240   0.807  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.709   0.173   0.712  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.127   0.172   0.619  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.656  -0.632   1.774  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.212  -1.958   1.617  0.00  0.00           O+0
HETATM   24  O   UNK     0      -3.624   1.484   0.668  0.00  0.00           O+0
HETATM   25  C   UNK     0      -3.703   1.812  -0.684  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.596   2.965  -0.922  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.902   2.840  -0.832  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.504   1.527  -0.487  0.00  0.00           C+0
HETATM   29  C   UNK     0      -6.815   3.988  -1.067  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.236   0.697  -1.283  0.00  0.00           O+0
HETATM   31  C   UNK     0      -3.539  -0.379  -0.720  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.340  -0.689  -1.585  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.450  -1.556  -0.638  0.00  0.00           C+0
HETATM   34  H   UNK     0       8.832   1.693  -1.672  0.00  0.00           H+0
HETATM   35  H   UNK     0       9.041   1.296   0.050  0.00  0.00           H+0
HETATM   36  H   UNK     0       9.700   0.157  -1.245  0.00  0.00           H+0
HETATM   37  H   UNK     0       6.449   1.897  -0.857  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.019   2.506   1.642  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.115   1.963   0.179  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.512   3.042   0.022  0.00  0.00           H+0
HETATM   41  H   UNK     0       7.260  -1.987  -1.083  0.00  0.00           H+0
HETATM   42  H   UNK     0       7.601  -1.235   0.592  0.00  0.00           H+0
HETATM   43  H   UNK     0       6.907  -2.824   0.414  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.909  -3.068   0.505  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.721  -0.791   0.273  0.00  0.00           H+0
HETATM   46  H   UNK     0       2.748  -3.629   1.058  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.628  -4.426   1.716  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.798  -4.180   2.054  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.803  -0.402   0.452  0.00  0.00           H+0
HETATM   50  H   UNK     0      -3.143  -0.239   2.694  0.00  0.00           H+0
HETATM   51  H   UNK     0      -4.727  -0.538   1.936  0.00  0.00           H+0
HETATM   52  H   UNK     0      -2.684   2.000  -1.098  0.00  0.00           H+0
HETATM   53  H   UNK     0      -4.169   3.918  -1.172  0.00  0.00           H+0
HETATM   54  H   UNK     0      -6.571   0.882  -1.388  0.00  0.00           H+0
HETATM   55  H   UNK     0      -5.911   1.031   0.313  0.00  0.00           H+0
HETATM   56  H   UNK     0      -7.525   1.677  -0.070  0.00  0.00           H+0
HETATM   57  H   UNK     0      -6.312   4.720  -1.753  0.00  0.00           H+0
HETATM   58  H   UNK     0      -7.766   3.629  -1.504  0.00  0.00           H+0
HETATM   59  H   UNK     0      -6.974   4.485  -0.075  0.00  0.00           H+0
HETATM   60  H   UNK     0      -2.597  -0.533  -2.647  0.00  0.00           H+0
HETATM   61  H   UNK     0      -2.047  -1.749  -1.458  0.00  0.00           H+0
HETATM   62  H   UNK     0      -1.495   0.004  -1.352  0.00  0.00           H+0
HETATM   63  H   UNK     0      -5.090  -1.540  -1.567  0.00  0.00           H+0
HETATM   64  H   UNK     0      -5.148  -1.540   0.209  0.00  0.00           H+0
HETATM   65  H   UNK     0      -3.898  -2.537  -0.711  0.00  0.00           H+0
CONECT    1    2   34   35   36                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   37                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7   38   39   40                                             
CONECT    9    4   10   11                                                  
CONECT   10    9   41   42   43                                             
CONECT   11    9   12   44                                                  
CONECT   12   11   13   45                                                  
CONECT   13   12   14   46                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16   47                                                  
CONECT   16   15   17   48                                                  
CONECT   17   16   18   23                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   14   49                                                  
CONECT   20   18   21                                                       
CONECT   21   20   22   24   31                                             
CONECT   22   21   23   50   51                                             
CONECT   23   22   17                                                       
CONECT   24   21   25                                                       
CONECT   25   24   26   30   52                                             
CONECT   26   25   27   53                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27   54   55   56                                             
CONECT   29   27   57   58   59                                             
CONECT   30   25   31                                                       
CONECT   31   30   32   33   21                                             
CONECT   32   31   60   61   62                                             
CONECT   33   31   63   64   65                                             
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    1                                                            
CONECT   37    3                                                            
CONECT   38    8                                                            
CONECT   39    8                                                            
CONECT   40    8                                                            
CONECT   41   10                                                            
CONECT   42   10                                                            
CONECT   43   10                                                            
CONECT   44   11                                                            
CONECT   45   12                                                            
CONECT   46   13                                                            
CONECT   47   15                                                            
CONECT   48   16                                                            
CONECT   49   19                                                            
CONECT   50   22                                                            
CONECT   51   22                                                            
CONECT   52   25                                                            
CONECT   53   26                                                            
CONECT   54   28                                                            
CONECT   55   28                                                            
CONECT   56   28                                                            
CONECT   57   29                                                            
CONECT   58   29                                                            
CONECT   59   29                                                            
CONECT   60   32                                                            
CONECT   61   32                                                            
CONECT   62   32                                                            
CONECT   63   33                                                            
CONECT   64   33                                                            
CONECT   65   33                                                            
MASTER        0    0    0    0    0    0    0    0   65    0  134    0
END

RDKit          3D

65 67  0  0  0  0  0  0  0  0999 V2000
    8.8733    0.8506   -0.9597 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6562    0.1378   -1.0283 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4972    0.8156   -0.7314 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3393    0.2257   -0.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2797    1.1528   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5511    2.4251   -0.3611 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0249    1.1053    0.4342 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1148    2.1541    0.5950 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5289   -1.1775   -0.0095 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9207   -1.7901   -0.0664 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5783   -2.0067    0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1815   -1.6987    0.4868 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3360   -2.6524    0.8756 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9189   -2.4124    1.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1321   -3.4627    1.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2243   -3.3487    1.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8306   -2.1427    1.4385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154   -1.0625    0.9872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2596   -1.2403    0.8072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7094    0.1726    0.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1275    0.1721    0.6189 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6559   -0.6316    1.7738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2115   -1.9584    1.6175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6242    1.4845    0.6679 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7026    1.8117   -0.6838 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5963    2.9650   -0.9216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9023    2.8399   -0.8315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5039    1.5265   -0.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8148    3.9879   -1.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2362    0.6966   -1.2829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5385   -0.3786   -0.7195 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3401   -0.6888   -1.5848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4498   -1.5556   -0.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8317    1.6932   -1.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0412    1.2956    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7003    0.1571   -1.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4487    1.8970   -0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191    2.5062    1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145    1.9634    0.1786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5122    3.0418    0.0219 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2601   -1.9870   -1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6015   -1.2354    0.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9070   -2.8237    0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9090   -3.0680    0.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7213   -0.7906    0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7481   -3.6286    1.0580 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6275   -4.4259    1.7164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7983   -4.1797    2.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8029   -0.4019    0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.2390    2.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7269   -0.5383    1.9355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6835    2.0000   -1.0977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1693    3.9185   -1.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5706    0.8815   -1.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9109    1.0312    0.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5249    1.6772   -0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3119    4.7196   -1.7528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7663    3.6290   -1.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9737    4.4849   -0.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5972   -0.5332   -2.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0468   -1.7487   -1.4585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4947    0.0039   -1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0904   -1.5397   -1.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1477   -1.5402    0.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8984   -2.5367   -0.7108 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
  5  7  1  0
  7  8  1  0
  4  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 21 20  1  6
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  3
 27 28  1  0
 27 29  1  0
 25 30  1  0
 30 31  1  0
 31 32  1  6
 31 33  1  0
 19 14  1  0
 31 21  1  0
 23 17  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  8 38  1  0
  8 39  1  0
  8 40  1  0
 10 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  0
 12 45  1  0
 13 46  1  0
 15 47  1  0
 16 48  1  0
 19 49  1  0
 22 50  1  0
 22 51  1  0
 25 52  1  6
 26 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
 29 58  1  0
 29 59  1  0
 32 60  1  0
 32 61  1  0
 32 62  1  0
 33 63  1  0
 33 64  1  0
 33 65  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Methyl (2E,3Z)-6-[(2S,5'r)-3',3'-dimethyl-5'-(2-methylprop-1-en-1-yl)-3H-spiro[1,4-benzodioxine-2,2'-[1,4]dioxolane]-7-yl]-2-(methoxymethylidene)-3-methylhexa-3,5-dienoic acid	Generator

Chemical Formula

C₂₆H₃₂O₇

Average Mass

456.5350 Da

Monoisotopic Mass

456.21480 Da

IUPAC Name

methyl (2E,3Z,5E)-6-[(2S,5'R)-3',3'-dimethyl-5'-(2-methylprop-1-en-1-yl)-3H-spiro[1,4-benzodioxine-2,2'-[1,4]dioxolane]-7-yl]-2-(methoxymethylidene)-3-methylhexa-3,5-dienoate

Traditional Name

methyl (2E,3Z,5E)-6-[(2S,5'R)-3',3'-dimethyl-5'-(2-methylprop-1-en-1-yl)-3H-spiro[1,4-benzodioxine-2,2'-[1,4]dioxolane]-7-yl]-2-(methoxymethylidene)-3-methylhexa-3,5-dienoate

CAS Registry Number

Not Available

SMILES

CO\C=C(\C(=O)OC)/C(/C)=C\C=C\C1=CC2=C(OC[C@@]3(O[C@@H](OC3(C)C)C=C(C)C)O2)C=C1

InChI Identifier

InChI=1S/C26H32O7/c1-17(2)13-23-32-25(4,5)26(33-23)16-30-21-12-11-19(14-22(21)31-26)10-8-9-18(3)20(15-28-6)24(27)29-7/h8-15,23H,16H2,1-7H3/b10-8+,18-9-,20-15+/t23-,26+/m1/s1

InChI Key

UKZBFRLDRGPOEJ-JZMZRJBLSA-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
Crepidotus	NPAtlas	2312406

Species Where Detected

Species Name	Source	Reference
Crepidotus fulvotomentosus strain 80145	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as styrenes. These are organic compounds containing an ethenylbenzene moiety.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Styrenes

Direct Parent

Styrenes

Alternative Parents

Substituents

Styrene
Alkyl aryl ether
Ketal
Fatty acid ester
Para-dioxin
Fatty acyl
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Meta-dioxolane
Carboxylic acid ester
Oxacycle
Acetal
Carboxylic acid derivative
Organoheterocyclic compound
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxide
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
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	4.5	ALOGPS
logP	5.54	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	72.45 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	126.99 m³·mol⁻¹	ChemAxon
Polarizability	51.2 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

NPAtlas ID

NPA020701

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9266857

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11091713

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Weber W, Anke T, Steffan B, Steglich W: Antibiotics from basidiomycetes. XXXII. Strobilurin E: a new cytostatic and antifungal (E)-beta-methoxyacrylate antibiotic from Crepidotus fulvotomentosus Peck. J Antibiot (Tokyo). 1990 Feb;43(2):207-12. doi: 10.7164/antibiotics.43.207. [PubMed:2312406 ]

Showing NP-Card for Strobilurin E (NP0011230)

MOL for NP0011230 (Strobilurin E)

3D MOL for NP0011230 (Strobilurin E)

3D SDF for NP0011230 (Strobilurin E)

3D-SDF for NP0011230 (Strobilurin E)

PDB for NP0011230 (Strobilurin E)

3D PDB for NP0011230 (Strobilurin E)

SMILES for NP0011230 (Strobilurin E)

INCHI for NP0011230 (Strobilurin E)

Structure for NP0011230 (Strobilurin E)

3D Structure for NP0011230 (Strobilurin E)