NP-MRD: Showing NP-Card for Harzianolide (NP0012140)

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Record Information

Version

2.0

Created at

2021-01-05 21:36:46 UTC

Updated at

2021-07-15 17:10:56 UTC

NP-MRD ID

NP0012140

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Harzianolide

Provided By

NPAtlas

Description

Harzianolide is found in Trichoderma harzianum. Harzianolide was first documented in 2009 (PMID: 19413806). Based on a literature review a small amount of articles have been published on HARZIANOLIDE (PMID: 22196692) (PMID: 22948254) (PMID: 24080397) (PMID: 26637047).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117023D          

 34 34  0  0  0  0            999 V2000
    5.1097    2.0611   -0.1613 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7907    1.6989    0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453    0.5067    0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9374    0.1669    0.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4436   -1.0272    0.6482 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1243   -1.4790    1.1895 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7192   -1.8608    0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8808   -1.3667   -0.3651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182   -0.2721    0.3167 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8386    0.9170   -0.5605 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5886    1.9596    0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5972    1.4587   -0.9040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3603   -2.0469   -1.5783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4494   -1.7959   -2.1965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3925   -2.9883   -1.8838 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3562   -2.9388   -0.9521 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2647    1.5389   -1.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9552    1.8239    0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1109    3.1471   -0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2682    2.4449    0.9792 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7989   -0.2211   -0.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3679    0.8802    1.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9937   -1.7614    0.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3522   -0.7263    1.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3615   -2.4156    1.7744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6359   -0.6866    0.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1392    0.0373    1.2441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4442    0.6858   -1.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5149    1.5513    0.6927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9499    2.3905    1.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9315    2.7806   -0.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3486    2.1070   -0.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847   -2.6787   -1.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2392   -3.8909   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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 16 33  1  0  0  0  0
 16 34  1  0  0  0  0
M  END

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
    5.1097    2.0611   -0.1613 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7907    1.6989    0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453    0.5067    0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9374    0.1669    0.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4436   -1.0272    0.6482 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1243   -1.4790    1.1895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7192   -1.8608    0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5886    1.9596    0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5972    1.4587   -0.9040 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3925   -2.9883   -1.8838 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9552    1.8239    0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1109    3.1471   -0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2682    2.4449    0.9792 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7989   -0.2211   -0.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3679    0.8802    1.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9937   -1.7614    0.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3522   -0.7263    1.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3615   -2.4156    1.7744 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2392   -3.8909   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
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 12 32  1  0
 16 33  1  0
 16 34  1  0
M  END


  Mrv1652306242117023D          

 34 34  0  0  0  0            999 V2000
    5.1097    2.0611   -0.1613 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7907    1.6989    0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453    0.5067    0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9374    0.1669    0.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4436   -1.0272    0.6482 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1243   -1.4790    1.1895 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7192   -1.8608    0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8808   -1.3667   -0.3651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182   -0.2721    0.3167 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8386    0.9170   -0.5605 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5886    1.9596    0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5972    1.4587   -0.9040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3603   -2.0469   -1.5783 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3925   -2.9883   -1.8838 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3562   -2.9388   -0.9521 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.9315    2.7806   -0.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3486    2.1070   -0.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847   -2.6787   -1.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2392   -3.8909   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
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 12 32  1  0  0  0  0
 16 33  1  0  0  0  0
 16 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0012140

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]([H])(C([H])([H])[H])C([H])([H])C1=C(C([H])([H])C(\[H])=C(/[H])\C(\[H])=C(/[H])C([H])([H])[H])C([H])([H])OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H18O3/c1-3-4-5-6-7-11-9-16-13(15)12(11)8-10(2)14/h3-6,10,14H,7-9H2,1-2H3/b4-3+,6-5+/t10-/m1/s1

> <INCHI_KEY>
KELRJXQJITUJOU-VNKDHWASSA-N

> <FORMULA>
C13H18O3

> <MOLECULAR_WEIGHT>
222.284

> <EXACT_MASS>
222.12559444

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
24.970535478595785

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(2E,4E)-hexa-2,4-dien-1-yl]-3-[(2R)-2-hydroxypropyl]-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
2.78

> <JCHEM_LOGP>
2.098992434333333

> <ALOGPS_LOGS>
-2.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.587952207234814

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.199973759315384

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5441679613413584

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
66.0732

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.09e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(2E,4E)-hexa-2,4-dien-1-yl]-3-[(2R)-2-hydroxypropyl]-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 34 34  0  0  0  0  0  0  0  0999 V2000
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    3.7907    1.6989    0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453    0.5067    0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9374    0.1669    0.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1243   -1.4790    1.1895 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5886    1.9596    0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5972    1.4587   -0.9040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3603   -2.0469   -1.5783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4494   -1.7959   -2.1965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3925   -2.9883   -1.8838 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3562   -2.9388   -0.9521 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2647    1.5389   -1.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9552    1.8239    0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1109    3.1471   -0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2682    2.4449    0.9792 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7989   -0.2211   -0.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3679    0.8802    1.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9937   -1.7614    0.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3522   -0.7263    1.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3615   -2.4156    1.7744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6359   -0.6866    0.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1392    0.0373    1.2441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4442    0.6858   -1.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5149    1.5513    0.6927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9499    2.3905    1.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9315    2.7806   -0.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3486    2.1070   -0.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847   -2.6787   -1.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2392   -3.8909   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
  8 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16  7  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  6
 11 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 16 33  1  0
 16 34  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       5.110   2.061  -0.161  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.791   1.699   0.414  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.245   0.507   0.257  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.937   0.167   0.834  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.444  -1.027   0.648  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.124  -1.479   1.190  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.719  -1.861   0.025  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.881  -1.367  -0.365  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.618  -0.272   0.317  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.839   0.917  -0.561  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.589   1.960   0.222  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.597   1.459  -0.904  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.360  -2.047  -1.578  0.00  0.00           C+0
HETATM   14  O   UNK     0      -3.449  -1.796  -2.196  0.00  0.00           O+0
HETATM   15  O   UNK     0      -1.393  -2.988  -1.884  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.356  -2.939  -0.952  0.00  0.00           C+0
HETATM   17  H   UNK     0       5.265   1.539  -1.129  0.00  0.00           H+0
HETATM   18  H   UNK     0       5.955   1.824   0.510  0.00  0.00           H+0
HETATM   19  H   UNK     0       5.111   3.147  -0.388  0.00  0.00           H+0
HETATM   20  H   UNK     0       3.268   2.445   0.979  0.00  0.00           H+0
HETATM   21  H   UNK     0       3.799  -0.221  -0.319  0.00  0.00           H+0
HETATM   22  H   UNK     0       1.368   0.880   1.412  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.994  -1.761   0.073  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.352  -0.726   1.831  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.362  -2.416   1.774  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.636  -0.687   0.564  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.139   0.037   1.244  0.00  0.00           H+0
HETATM   28  H   UNK     0      -3.444   0.686  -1.461  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.515   1.551   0.693  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.950   2.390   1.039  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.932   2.781  -0.468  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.349   2.107  -0.198  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.585  -2.679  -1.505  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.239  -3.891  -0.377  0.00  0.00           H+0
CONECT    1    2   17   18   19                                             
CONECT    2    1    3   20                                                  
CONECT    3    2    4   21                                                  
CONECT    4    3    5   22                                                  
CONECT    5    4    6   23                                                  
CONECT    6    5    7   24   25                                             
CONECT    7    6    8   16                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10   26   27                                             
CONECT   10    9   11   12   28                                             
CONECT   11   10   29   30   31                                             
CONECT   12   10   32                                                       
CONECT   13    8   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    7   33   34                                             
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    2                                                            
CONECT   21    3                                                            
CONECT   22    4                                                            
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    6                                                            
CONECT   26    9                                                            
CONECT   27    9                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   11                                                            
CONECT   31   11                                                            
CONECT   32   12                                                            
CONECT   33   16                                                            
CONECT   34   16                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   68    0
END

RDKit          3D

34 34  0  0  0  0  0  0  0  0999 V2000
    5.1097    2.0611   -0.1613 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7907    1.6989    0.4140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2453    0.5067    0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9374    0.1669    0.8343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4436   -1.0272    0.6482 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1243   -1.4790    1.1895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7192   -1.8608    0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8808   -1.3667   -0.3651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182   -0.2721    0.3167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8386    0.9170   -0.5605 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5886    1.9596    0.2215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5972    1.4587   -0.9040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3603   -2.0469   -1.5783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4494   -1.7959   -2.1965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3925   -2.9883   -1.8838 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3562   -2.9388   -0.9521 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2647    1.5389   -1.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9552    1.8239    0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1109    3.1471   -0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2682    2.4449    0.9792 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7989   -0.2211   -0.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3679    0.8802    1.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9937   -1.7614    0.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3522   -0.7263    1.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3615   -2.4156    1.7744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6359   -0.6866    0.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1392    0.0373    1.2441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4442    0.6858   -1.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5149    1.5513    0.6927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9499    2.3905    1.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9315    2.7806   -0.4677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3486    2.1070   -0.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847   -2.6787   -1.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2392   -3.8909   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
  8 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16  7  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  9 26  1  0
  9 27  1  0
 10 28  1  6
 11 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 16 33  1  0
 16 34  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₃H₁₈O₃

Average Mass

222.2840 Da

Monoisotopic Mass

222.12559 Da

IUPAC Name

4-[(2E,4E)-hexa-2,4-dien-1-yl]-3-[(2R)-2-hydroxypropyl]-2,5-dihydrofuran-2-one

Traditional Name

4-[(2E,4E)-hexa-2,4-dien-1-yl]-3-[(2R)-2-hydroxypropyl]-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

C\C=C\C=C\CC1=C(CC(C)O)C(=O)OC1

InChI Identifier

InChI=1S/C13H18O3/c1-3-4-5-6-7-11-9-16-13(15)12(11)8-10(2)14/h3-6,10,14H,7-9H2,1-2H3/b4-3+,6-5+

InChI Key

KELRJXQJITUJOU-VNKDHWASSA-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
Trichoderma harzianum	NPAtlas	24080397

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.78	ALOGPS
logP	2.1	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	13.2	ChemAxon
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	66.07 m³·mol⁻¹	ChemAxon
Polarizability	24.97 Å³	ChemAxon
Number of Rings	1	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

NPAtlas ID

NPA007432

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

31119711

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15719532

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Vinale F, Girona IA, Nigro M, Mazzei P, Piccolo A, Ruocco M, Woo S, Rosa DR, Herrera CL, Lorito M: Cerinolactone, a hydroxy-lactone derivative from Trichoderma cerinum. J Nat Prod. 2012 Jan 27;75(1):103-6. doi: 10.1021/np200577t. Epub 2011 Dec 23. [PubMed:22196692 ]
Fukuda T, Uchida R, Ohte S, Inoue H, Yamazaki H, Matsuda D, Nonaka K, Masuma R, Katagiri T, Tomoda H: Trichocyalides A and B, new inhibitors of alkaline phosphatase activity in bone morphogenetic protein-stimulated myoblasts, produced by Trichoderma sp. FKI-5513. J Antibiot (Tokyo). 2012 Nov;65(11):565-9. doi: 10.1038/ja.2012.70. Epub 2012 Sep 5. [PubMed:22948254 ]
Cai F, Yu G, Wang P, Wei Z, Fu L, Shen Q, Chen W: Harzianolide, a novel plant growth regulator and systemic resistance elicitor from Trichoderma harzianum. Plant Physiol Biochem. 2013 Dec;73:106-13. doi: 10.1016/j.plaphy.2013.08.011. Epub 2013 Sep 5. [PubMed:24080397 ]
Tata A, Perez C, Campos ML, Bayfield MA, Eberlin MN, Ifa DR: Imprint Desorption Electrospray Ionization Mass Spectrometry Imaging for Monitoring Secondary Metabolites Production during Antagonistic Interaction of Fungi. Anal Chem. 2015 Dec 15;87(24):12298-305. doi: 10.1021/acs.analchem.5b03614. Epub 2015 Dec 4. [PubMed:26637047 ]
Vinale F, Ghisalberti EL, Sivasithamparam K, Marra R, Ritieni A, Ferracane R, Woo S, Lorito M: Factors affecting the production of Trichoderma harzianum secondary metabolites during the interaction with different plant pathogens. Lett Appl Microbiol. 2009 Jun;48(6):705-11. doi: 10.1111/j.1472-765X.2009.02599.x. Epub 2009 Mar 30. [PubMed:19413806 ]

Showing NP-Card for Harzianolide (NP0012140)

MOL for NP0012140 (Harzianolide)

3D MOL for NP0012140 (Harzianolide)

3D SDF for NP0012140 (Harzianolide)

3D-SDF for NP0012140 (Harzianolide)

PDB for NP0012140 (Harzianolide)

3D PDB for NP0012140 (Harzianolide)

SMILES for NP0012140 (Harzianolide)

INCHI for NP0012140 (Harzianolide)

Structure for NP0012140 (Harzianolide)

3D Structure for NP0012140 (Harzianolide)