NP-MRD: Showing NP-Card for 7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid (NP0241947)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 02:08:29 UTC

Updated at

2022-09-07 02:08:29 UTC

NP-MRD ID

NP0241947

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid

Description

7-[6-(Acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4,4a,4b,5,6,7,8,8a,10a-dodecahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 7-[6-(Acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4,4a,4b,5,6,7,8,8a,10a-dodecahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171513512D          

 39 41  0  0  0  0            999 V2000
   -5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   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
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    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    3.3000    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
    0.7145    4.5375    0.0000 C   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
    0.0000    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 O   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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    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
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   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
   -2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 16 15  1  4  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
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  5 32  1  0  0  0  0
  9 32  1  0  0  0  0
 32 33  1  0  0  0  0
  6 34  1  0  0  0  0
  2 34  1  0  0  0  0
 34 35  1  0  0  0  0
  3 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
M  END

     RDKit          3D

 73 75  0  0  0  0  0  0  0  0999 V2000
    2.1216   -5.8001    0.4725 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0067   -5.1300    0.7075 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8916   -3.7708    0.4354 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1939   -2.7709    1.3294 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6042   -3.0816    2.4767 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0400   -1.3629    0.9496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3647   -1.0440    0.5288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1393   -1.9423    0.3249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6820    0.4130    0.3975 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6644    0.9852    1.8208 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4201    1.0234   -0.4018 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0023    2.0267   -1.3974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1992    2.6005   -1.4256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1530    2.1816   -0.3698 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9834    0.6747   -0.2444 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1873    0.1681    0.4962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3016    0.1763   -0.5425 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5173   -0.3032   -0.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1513   -1.4526   -0.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4477   -1.9122    0.1598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6036   -2.1416   -1.3084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4100    1.4897   -1.2340 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8689    1.9407   -1.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5655    2.5797   -0.6375 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5559    3.6449   -1.5362 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2612   -0.0060   -1.1438 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9092   -1.0055   -0.2603 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2638   -0.7009    0.1878 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583    0.4555   -0.0027 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2161    0.6617    0.4839 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8235    1.8155    0.2997 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1722    2.0502    0.7718 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7760    3.1965    0.5885 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1234    3.4207    1.0643 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7483    2.5035    1.6724 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7781    4.6210    0.8817 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1383   -5.8156    1.2647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2192   -5.1811    1.4972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0334   -7.1744    1.5393 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2199   -6.8361    0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9629   -5.2587    0.0547 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3837   -0.6835    1.7626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6349    1.3922    2.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3832    0.2234    2.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1475    1.7663    1.8845 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1254    1.5463    0.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7094    2.3140   -2.1545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4660    3.3274   -2.1692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8274    2.6943    0.5663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9712    0.2416   -1.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0835   -0.8145    0.9458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4345    0.9521    1.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9730   -0.5757   -1.3201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2075   -2.6914    0.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8852   -1.0373    0.7045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1608   -2.2445   -0.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1941    1.4280   -2.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2482    1.7238   -0.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9393    3.0431   -1.2439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4912    1.4627   -1.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0585    2.9075    0.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0148    4.3799   -1.1566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5308   -0.4869   -1.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9653    0.5311   -1.7801 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9829   -1.9628   -0.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8023   -1.4765    0.7055 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3601    1.2681   -0.5165 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7432   -0.1167    0.9976 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2999    2.6224   -0.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6895    1.2508    1.2901 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2606    3.9963    0.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3787    4.8147    0.0906 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3912   -7.7352    0.7903 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 33 34  1  0
 34 36  1  0
 34 35  2  0
 27  6  1  0
  6  4  1  0
  4  5  2  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 37  1  0
 37 39  1  0
 37 38  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  1
 14 24  1  0
 24 25  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 24 22  1  0
  9 15  1  0
  9 11  1  0
 23 58  1  0
 23 59  1  0
 23 60  1  0
 22 57  1  6
 17 53  1  6
 16 51  1  0
 16 52  1  0
 15 50  1  6
 14 49  1  1
 13 48  1  0
 12 47  1  0
 11 46  1  1
 26 63  1  0
 26 64  1  0
 27 65  1  6
 28 66  1  0
 29 67  1  0
 30 68  1  0
 31 69  1  0
 32 70  1  0
 33 71  1  0
 36 72  1  0
  6 42  1  1
  1 40  1  0
  1 41  1  0
 39 73  1  0
 10 43  1  0
 10 44  1  0
 10 45  1  0
 24 61  1  1
 25 62  1  0
 20 54  1  0
 20 55  1  0
 20 56  1  0
M  END


  Mrv1533004171513512D          

 39 41  0  0  0  0            999 V2000
   -5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   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
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    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    3.3000    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
    0.7145    4.5375    0.0000 C   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
    0.0000    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 O   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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    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
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   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
   -2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 16 15  1  4  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
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  5 32  1  0  0  0  0
  9 32  1  0  0  0  0
 32 33  1  0  0  0  0
  6 34  1  0  0  0  0
  2 34  1  0  0  0  0
 34 35  1  0  0  0  0
  3 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0241947

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(CC2C(C=CC3CC(C=CC=CC=CC(O)=O)C(C(=O)OC(=C)C(O)=O)C(=O)C23C)C1O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C29H34O10/c1-15-22(39-17(3)30)14-21-20(25(15)33)12-11-19-13-18(9-7-5-6-8-10-23(31)32)24(26(34)29(19,21)4)28(37)38-16(2)27(35)36/h5-12,15,18-22,24-25,33H,2,13-14H2,1,3-4H3,(H,31,32)(H,35,36)

> <INCHI_KEY>
HWOQCCLLSGFOCF-UHFFFAOYSA-N

> <FORMULA>
C29H34O10

> <MOLECULAR_WEIGHT>
542.581

> <EXACT_MASS>
542.215197295

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
56.85527145468373

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4,4a,4b,5,6,7,8,8a,10a-dodecahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid

> <ALOGPS_LOGP>
3.06

> <JCHEM_LOGP>
2.8806349683333323

> <ALOGPS_LOGS>
-5.01

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.716958200966098

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6237636560664863

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9942498129113497

> <JCHEM_POLAR_SURFACE_AREA>
164.49999999999997

> <JCHEM_REFRACTIVITY>
142.87599999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.30e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0     -10.669   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.336   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.002   6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.668   6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000  10.780   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  11.550   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.334  13.090   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -2.667  10.780   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -5.335   3.080   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -9.336   3.850   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -10.669   4.620   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0     -10.669  -0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   34                                                  
CONECT    3    2    4   36                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   32                                                  
CONECT    6    5    7   34                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   32                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   21                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   11   22   30                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   21   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    5    9   33                                             
CONECT   33   32                                                            
CONECT   34    6    2   35                                                  
CONECT   35   34                                                            
CONECT   36    3   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

View in JSmol

Synonyms

Value	Source
7-[6-(Acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4,4a,4b,5,6,7,8,8a,10a-dodecahydrophenanthren-2-yl]hepta-2,4,6-trienoate	Generator

Chemical Formula

C₂₉H₃₄O₁₀

Average Mass

542.5810 Da

Monoisotopic Mass

542.21520 Da

IUPAC Name

7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4,4a,4b,5,6,7,8,8a,10a-dodecahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid

Traditional Name

7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid

CAS Registry Number

Not Available

SMILES

CC1C(CC2C(C=CC3CC(C=CC=CC=CC(O)=O)C(C(=O)OC(=C)C(O)=O)C(=O)C23C)C1O)OC(C)=O

InChI Identifier

InChI=1S/C29H34O10/c1-15-22(39-17(3)30)14-21-20(25(15)33)12-11-19-13-18(9-7-5-6-8-10-23(31)32)24(26(34)29(19,21)4)28(37)38-16(2)27(35)36/h5-12,15,18-22,24-25,33H,2,13-14H2,1,3-4H3,(H,31,32)(H,35,36)

InChI Key

HWOQCCLLSGFOCF-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Hydrophenanthrene
Phenanthrene
Tetracarboxylic acid or derivatives
1,3-dicarbonyl compound
Cyclic alcohol
Enol ester
Carboxylic acid ester
Ketone
Secondary alcohol
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.06	ALOGPS
logP	2.88	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	3.62	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	164.5 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	142.88 m³·mol⁻¹	ChemAxon
Polarizability	56.86 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

74327654

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid (NP0241947)

MOL for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

3D MOL for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

3D SDF for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

3D-SDF for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

PDB for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

3D PDB for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

SMILES for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

INCHI for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

Structure for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)

3D Structure for NP0241947 (7-[6-(acetyloxy)-3-{[(1-carboxyeth-1-en-1-yl)oxy]carbonyl}-8-hydroxy-4a,7-dimethyl-4-oxo-1,2,3,4b,5,6,7,8,8a,10a-decahydrophenanthren-2-yl]hepta-2,4,6-trienoic acid)