NP-MRD: Showing NP-Card for 10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate (NP0159355)

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Record Information

Version

2.0

Created at

2022-09-02 17:05:43 UTC

Updated at

2022-09-02 17:05:43 UTC

NP-MRD ID

NP0159355

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate

Description

10-[(Acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-2H,3H,3aH,4H,5H,6H,7H,8H,9H,11aH-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. 10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate is found in Centaurea paui. Based on a literature review very few articles have been published on 10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-2H,3H,3aH,4H,5H,6H,7H,8H,9H,11aH-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022219052D          

 32 33  0  0  0  0            999 V2000
    3.3428   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6784   -1.7362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131   -1.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2775   -0.3443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6900    0.3702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5429   -0.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0950    0.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 15 21  2  0  0  0  0
 21 22  1  4  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 22 28  1  0  0  0  0
  6 28  1  0  0  0  0
  2 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

 60 61  0  0  0  0  0  0  0  0999 V2000
    1.0932    2.6377   -0.8899 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2291    1.6710   -1.1316 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7912    0.2860   -1.3303 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1946   -0.3421   -0.0545 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6261   -0.5249    0.0796 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4175    0.1445    0.9496 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8604    0.9964    1.6882 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8471   -0.0996    1.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4227   -1.0041    0.2581 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6520    0.6685    2.0054 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9647    0.2135    1.9499 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5898    2.1621    1.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1068    2.3346    0.4309 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4856   -1.4924    0.4540 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1447   -2.6531   -0.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2711   -3.1016   -1.5471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5348   -3.4859    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7878   -4.7351    0.6230 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8251   -2.6383    1.7853 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8463   -1.3065    1.1465 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0197   -1.3801    0.2687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9236   -0.5240   -0.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0086   -1.0540   -1.0592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2751   -1.0079   -0.6195 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2248   -0.1724   -0.2349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5744   -0.7045    0.2081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0449    1.0455   -0.2235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0435    0.9191    0.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7797    1.7250    0.1870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2122    1.9933   -1.1883 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8746    1.3065   -2.1816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3454    2.1653   -3.0508 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1702    2.5035   -0.8255 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7759    3.6794   -0.7301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0225   -0.2441   -1.9150 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6534    0.4561   -2.0411 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0367    0.4621    0.7386 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9038   -1.5935   -0.4704 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4905   -1.1763    0.3425 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2852    0.5348    3.0446 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0115   -0.6402    2.4481 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5671    2.5634    1.8062 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2495    2.6964    2.4299 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3760    3.2804    0.3687 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1502   -1.9086    1.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7590   -2.4880   -2.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0477   -4.0808   -1.8699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8620   -0.5594    1.9447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1432   -2.4057   -0.1743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7733   -2.0876   -1.3881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9380   -0.4670   -2.0210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5009   -0.9678    1.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8709   -1.5449   -0.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3152    0.1049    0.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6294    1.1736    1.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6198    1.4104   -0.6945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1083    1.4069    0.9434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1429    2.7520    0.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2780    3.0814   -1.4493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5983    1.6667   -3.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
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 21 20  1  0
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 17 15  1  0
 15 16  2  3
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 14  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
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 30 29  1  0
 29 28  1  0
 30 31  1  0
 31 32  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
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  8  9  2  3
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 10 11  1  0
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 28 22  1  0
 14 20  1  0
 26 52  1  0
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 21 49  1  0
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 16 46  1  0
 16 47  1  0
 14 45  1  1
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 30 59  1  6
 29 57  1  0
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 28 55  1  0
 28 56  1  0
 32 60  1  0
  9 38  1  0
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 12 42  1  0
 12 43  1  0
 13 44  1  0
M  END


  Mrv1652309022219052D          

 32 33  0  0  0  0            999 V2000
    3.3428   -1.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6784   -1.7362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131   -1.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2775   -0.3443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6900    0.3702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5429   -0.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0950    0.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
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 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
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 18 20  2  0  0  0  0
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 29 30  1  0  0  0  0
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M  END
> <DATABASE_ID>
NP0159355

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1=CC2OC(=O)C(=C)C2C(CC(=C)C(CC1)OO)OC(=O)C(=C)C(O)CO

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O10/c1-11-7-18(30-21(26)12(2)16(25)9-23)20-13(3)22(27)31-19(20)8-15(10-29-14(4)24)5-6-17(11)32-28/h8,16-20,23,25,28H,1-3,5-7,9-10H2,4H3

> <INCHI_KEY>
VQJJEVWMPNOJOZ-UHFFFAOYSA-N

> <FORMULA>
C22H28O10

> <MOLECULAR_WEIGHT>
452.456

> <EXACT_MASS>
452.168247102

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
44.37685813707751

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-2H,3H,3aH,4H,5H,6H,7H,8H,9H,11aH-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate

> <ALOGPS_LOGP>
0.57

> <JCHEM_LOGP>
0.8230132223333336

> <ALOGPS_LOGS>
-2.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.53839573783818

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.70475619203369

> <JCHEM_PKA_STRONGEST_BASIC>
-2.967081778194194

> <JCHEM_POLAR_SURFACE_AREA>
148.82

> <JCHEM_REFRACTIVITY>
110.13

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.10e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3aH,4H,5H,7H,8H,9H,11aH-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       6.240  -2.786   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.001   0.770   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       2.667  -1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.866  -3.241   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.144  -2.050   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.518  -0.643   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.288   0.691   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.013  -0.804   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.044   0.341   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.668   0.770   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   15   22                                                       
CONECT   22   21   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   22    6                                                  
CONECT   29    2   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Value	Source
10-[(Acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-2H,3H,3ah,4H,5H,6H,7H,8H,9H,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoic acid	Generator

Chemical Formula

C₂₂H₂₈O₁₀

Average Mass

452.4560 Da

Monoisotopic Mass

452.16825 Da

IUPAC Name

10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-2H,3H,3aH,4H,5H,6H,7H,8H,9H,11aH-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate

Traditional Name

10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3aH,4H,5H,7H,8H,9H,11aH-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1=CC2OC(=O)C(=C)C2C(CC(=C)C(CC1)OO)OC(=O)C(=C)C(O)CO

InChI Identifier

InChI=1S/C22H28O10/c1-11-7-18(30-21(26)12(2)16(25)9-23)20-13(3)22(27)31-19(20)8-15(10-29-14(4)24)5-6-17(11)32-28/h8,16-20,23,25,28H,1-3,5-7,9-10H2,4H3

InChI Key

VQJJEVWMPNOJOZ-UHFFFAOYSA-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
Centaurea paui	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Germacrane sesquiterpenoid
Sesquiterpenoid
Tricarboxylic acid or derivatives
Beta-hydroxy acid
Fatty acid ester
Gamma butyrolactone
Hydroxy acid
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Tetrahydrofuran
Enoate ester
Secondary alcohol
1,2-diol
Hydroperoxide
Lactone
Carboxylic acid ester
Organoheterocyclic compound
Peroxol
Carboxylic acid derivative
Oxacycle
Alkyl hydroperoxide
Alcohol
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Organic oxygen compound
Primary 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	0.57	ALOGPS
logP	0.82	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	11.7	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	148.82 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	110.13 m³·mol⁻¹	ChemAxon
Polarizability	44.38 Å³	ChemAxon
Number of Rings	2	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163029226

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate (NP0159355)

MOL for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

3D MOL for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

3D SDF for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

3D-SDF for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

PDB for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

3D PDB for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

SMILES for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

INCHI for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

Structure for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)

3D Structure for NP0159355 (10-[(acetyloxy)methyl]-7-hydroperoxy-3,6-dimethylidene-2-oxo-3ah,4h,5h,7h,8h,9h,11ah-cyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylidenebutanoate)