NP-MRD: Showing NP-Card for (9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate (NP0243155)

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Record Information

Version

2.0

Created at

2022-09-07 03:38:38 UTC

Updated at

2022-09-07 03:38:38 UTC

NP-MRD ID

NP0243155

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate

Description

15-Hydroxyleptocarpin, also known as ac-asp-ile-val-pro-cys-OH, belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety. 15-Hydroxyleptocarpin is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, 15-hydroxyleptocarpin has been detected, but not quantified in, fats and oils. (9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate is found in Helianthus annuus, Heliomeris multiflora and Tithonia rotundifolia. This could make 15-hydroxyleptocarpin a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061309172D          

 27 29  0  0  0  0            999 V2000
    3.5024   -2.0749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6566   -1.7230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7485   -1.0048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3210   -0.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3153   -2.2158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8599    1.8673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7057    1.5154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2747   -0.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7626    2.7825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8437   -1.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0553   -0.2390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0470    2.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5186    1.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1444    1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8031    0.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1773    0.8818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6160    0.4594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5592   -0.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8552   -0.0370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4618    0.1074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2910    3.4161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2936    0.5809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7463   -0.6670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4888   -0.5654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9103    0.7862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0876   -0.1742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6489    0.2482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
 10  2  1  0  0  0  0
 10  5  2  0  0  0  0
 11  3  2  0  0  0  0
 12  6  2  0  0  0  0
 12  9  1  0  0  0  0
 13  7  1  0  0  0  0
 13 12  1  0  0  0  0
 14  6  1  0  0  0  0
 15  8  1  0  0  0  0
 16  7  1  0  0  0  0
 17 11  1  0  0  0  0
 17 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 10  1  0  0  0  0
 19 11  1  0  0  0  0
 20  4  1  0  0  0  0
 20  8  1  0  0  0  0
 20 16  1  0  0  0  0
 21  9  1  0  0  0  0
 22 13  1  0  0  0  0
 23 18  2  0  0  0  0
 24 19  2  0  0  0  0
 25 14  1  0  0  0  0
 25 19  1  0  0  0  0
 26 15  1  0  0  0  0
 26 18  1  0  0  0  0
 27 16  1  0  0  0  0
 27 20  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    1.6070   -2.7235   -1.7933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7532   -2.2039   -0.9564 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4348   -2.5540    0.4246 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1550   -3.3181    1.1524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7718   -1.9154    0.7937 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3481   -1.5699   -0.4249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6240   -1.0133   -0.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1964   -0.1512    0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5943    0.3602   -0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3490   -0.0047    1.1050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5221    0.3352    1.4177 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4113    0.1338    2.5139 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3546    1.8693    1.3510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0682    2.1580    0.6686 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8184    3.3566    0.0225 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0444    2.1069   -0.7344 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1829    2.3911   -1.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1763    1.4593   -1.2840 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5372    0.1336   -0.6400 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9647   -0.0550   -0.7376 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8092   -0.1805    0.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2897   -0.1235    1.4647 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2229   -0.3679    0.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7549   -0.4232   -1.2926 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0444   -0.4900    1.1042 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5853   -0.4450    2.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1796   -1.0353   -1.2225 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2219   -3.5632   -1.4813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7373   -2.3564   -2.7981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4350   -2.6307   -0.9031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2435   -1.3206   -1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0416   -0.1306   -0.8890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6424    1.4340   -0.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1866   -0.9627    1.3409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5916   -0.0784    1.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9254    0.9557    2.6784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2438    2.2419    2.4139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2373    2.3688    0.9653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1833    1.8526    1.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5686    1.4378   -2.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8691    2.9945   -2.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0024    2.8643   -1.1117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0232    1.2609   -2.3617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0390    2.1433   -1.1384 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3778    0.1206    0.4537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9575   -0.6339   -2.0480 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4998   -1.2580   -1.4264 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2711    0.4988   -1.6075 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1299   -0.6333    0.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1224    0.5440    2.7337 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8734   -1.2869    2.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4503   -0.6431    3.1749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4024   -0.9489   -2.2977 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 23  2  0
 23 24  1  0
 23 21  1  0
 21 22  2  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  6
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 11  1  0
 11 12  1  0
 11  8  1  0
  8  9  1  0
  9 10  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 27  1  0
 27 19  1  0
 14 16  1  0
 27  6  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
 25 49  1  0
 24 46  1  0
 24 47  1  0
 24 48  1  0
 19 45  1  1
 18 43  1  0
 18 44  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 14 39  1  1
 13 37  1  0
 13 38  1  0
 11 35  1  1
 12 36  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
  7 31  1  0
  6 30  1  6
  1 28  1  0
  1 29  1  0
 27 53  1  6
M  END


  Mrv0541 05061309172D          

 27 29  0  0  0  0            999 V2000
    3.5024   -2.0749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6566   -1.7230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7485   -1.0048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3210   -0.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3153   -2.2158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8599    1.8673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7057    1.5154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2747   -0.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7626    2.7825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8437   -1.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0553   -0.2390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0470    2.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5186    1.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1444    1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8031    0.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1773    0.8818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6160    0.4594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5592   -0.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8552   -0.0370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4618    0.1074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2910    3.4161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2936    0.5809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7463   -0.6670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4888   -0.5654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9103    0.7862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0876   -0.1742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6489    0.2482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
 10  2  1  0  0  0  0
 10  5  2  0  0  0  0
 11  3  2  0  0  0  0
 12  6  2  0  0  0  0
 12  9  1  0  0  0  0
 13  7  1  0  0  0  0
 13 12  1  0  0  0  0
 14  6  1  0  0  0  0
 15  8  1  0  0  0  0
 16  7  1  0  0  0  0
 17 11  1  0  0  0  0
 17 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 10  1  0  0  0  0
 19 11  1  0  0  0  0
 20  4  1  0  0  0  0
 20  8  1  0  0  0  0
 20 16  1  0  0  0  0
 21  9  1  0  0  0  0
 22 13  1  0  0  0  0
 23 18  2  0  0  0  0
 24 19  2  0  0  0  0
 25 14  1  0  0  0  0
 25 19  1  0  0  0  0
 26 15  1  0  0  0  0
 26 18  1  0  0  0  0
 27 16  1  0  0  0  0
 27 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0243155

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)OC1CC2(C)OC2CC(O)\C(CO)=C/C2OC(=O)C(=C)C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O7/c1-5-10(2)18(23)26-15-8-20(4)16(27-20)7-13(22)12(9-21)6-14-17(15)11(3)19(24)25-14/h5-6,13-17,21-22H,3,7-9H2,1-2,4H3/b10-5-,12-6-

> <INCHI_KEY>
WRYLLOROOPMFIC-ZIIBAIFASA-N

> <FORMULA>
C20H26O7

> <MOLECULAR_WEIGHT>
378.4162

> <EXACT_MASS>
378.167853186

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
39.186172380504686

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9Z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate

> <ALOGPS_LOGP>
0.56

> <JCHEM_LOGP>
1.125990337333334

> <ALOGPS_LOGS>
-2.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.36361935863475

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.213378118693682

> <JCHEM_PKA_STRONGEST_BASIC>
-2.766061259279562

> <JCHEM_POLAR_SURFACE_AREA>
105.59

> <JCHEM_REFRACTIVITY>
97.31039999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.13e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(9Z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       6.538  -3.873   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.559  -3.216   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.731  -1.876   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.199  -1.317   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.055  -4.136   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.938   3.486   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.917   2.829   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.979  -0.062   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.890   5.194   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.042  -2.953   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.303  -0.446   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.421   3.748   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.435   2.566   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.470   2.040   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.966   1.120   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.931   1.646   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.483   0.858   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.511  -1.508   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.796  -0.069   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.462   0.200   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.877   6.377   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       8.015   1.084   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       6.993  -1.245   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      13.979  -1.055   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      12.899   1.468   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       9.497  -0.325   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       4.945   0.463   0.000  0.00  0.00           O+0
CONECT    1    5                                                            
CONECT    2   10                                                            
CONECT    3   11                                                            
CONECT    4   20                                                            
CONECT    5    1   10                                                       
CONECT    6   12   14                                                       
CONECT    7   13   16                                                       
CONECT    8   15   20                                                       
CONECT    9   12   21                                                       
CONECT   10    2    5   18                                                  
CONECT   11    3   17   19                                                  
CONECT   12    6    9   13                                                  
CONECT   13    7   12   22                                                  
CONECT   14    6   17   25                                                  
CONECT   15    8   17   26                                                  
CONECT   16    7   20   27                                                  
CONECT   17   11   14   15                                                  
CONECT   18   10   23   26                                                  
CONECT   19   11   24   25                                                  
CONECT   20    4    8   16   27                                             
CONECT   21    9                                                            
CONECT   22   13                                                            
CONECT   23   18                                                            
CONECT   24   19                                                            
CONECT   25   14   19                                                       
CONECT   26   15   18                                                       
CONECT   27   16   20                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
Ac-asp-ile-val-pro-cys-OH	HMDB
(9Z)-8-Hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₆O₇

Average Mass

378.4162 Da

Monoisotopic Mass

378.16785 Da

IUPAC Name

(9Z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(9Z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)OC1CC2(C)OC2CC(O)\C(CO)=C/C2OC(=O)C(=C)C12

InChI Identifier

InChI=1S/C20H26O7/c1-5-10(2)18(23)26-15-8-20(4)16(27-20)7-13(22)12(9-21)6-14-17(15)11(3)19(24)25-14/h5-6,13-17,21-22H,3,7-9H2,1-2,4H3/b10-5-,12-6-

InChI Key

WRYLLOROOPMFIC-ZIIBAIFASA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Helianthus annuus	LOTUS Database	35616633
Heliomeris multiflora	LOTUS Database	35616633
Tithonia rotundifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Germacranolides and derivatives

Alternative Parents

Substituents

Germacranolide
Sesquiterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Gamma butyrolactone
Fatty acyl
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Secondary alcohol
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Primary alcohol
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	0.56	ALOGPS
logP	1.13	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	6.21	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	105.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	97.31 m³·mol⁻¹	ChemAxon
Polarizability	39.19 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0036694

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB015627

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

131752040

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate (NP0243155)

MOL for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

PDB for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

Structure for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0243155 ((9z)-8-hydroxy-9-(hydroxymethyl)-4-methyl-14-methylidene-13-oxo-5,12-dioxatricyclo[9.3.0.0⁴,⁶]tetradec-9-en-2-yl (2z)-2-methylbut-2-enoate)