NP-MRD: Showing NP-Card for (1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid (NP0309749)

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Record Information

Version

2.0

Created at

2022-09-11 04:33:50 UTC

Updated at

2022-09-11 04:33:51 UTC

NP-MRD ID

NP0309749

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid

Description

(1R,3S,4S,5S,6R,7R)-1-[(7E)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]Octane-3,4,5-tricarboxylic acid belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. (1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid is found in Amauroascus niger. Based on a literature review very few articles have been published on (1R,3S,4S,5S,6R,7R)-1-[(7E)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]Octane-3,4,5-tricarboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112206332D          

 50 52  0  0  1  0            999 V2000
   -7.8720    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1576    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4431    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7286    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0141    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2997    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5852    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8707    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1563    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4418    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4418    1.3067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7273    0.0692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0128    0.4817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6688    0.0169    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5458   -0.7988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4571    0.2601    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0183   -0.3446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8226   -0.1611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3837   -0.7658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1881   -0.5823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4312    0.2061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2356    0.3897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4787    1.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7967   -0.2151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7492   -1.1870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5060   -1.9754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5535   -1.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1147   -1.6082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4801   -2.0294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2844   -1.8458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.6024   -3.2389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7981   -3.4225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6335    2.3626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4528    3.1675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303    1.8655    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1514    2.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8317    2.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2117    3.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0745    1.3044    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8425    1.6058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6666    1.5688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9654    2.4216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
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 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
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 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 16 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 37 41  1  0  0  0  0
 41 42  1  1  0  0  0
 41 43  1  6  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 41 46  1  0  0  0  0
 13 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
 46 50  1  0  0  0  0
 16 50  1  0  0  0  0
M  END

     RDKit          3D

100102  0  0  0  0  0  0  0  0999 V2000
   10.9066   -0.7180    0.8896 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3943   -1.9819   -1.2165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8032   -1.4106   -0.9744 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7217   -0.0637   -0.6106 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2149    0.9973   -1.3280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0930    2.4123   -0.8850 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4848   -2.2393    0.0641 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -6.9347   -2.0091    0.2348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3407   -0.6441    0.6344 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.4409    2.1572   -0.5035 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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 32 33  2  0
 33 34  1  0
 34 35  2  0
 16 50  1  0
 50 46  1  0
 46 47  1  6
 47 49  1  0
 47 48  2  0
 46 41  1  0
 41 42  1  1
 41 37  1  0
 37 36  1  0
 37 38  1  0
 38 40  1  0
 38 39  2  0
 41 43  1  0
 43 45  1  0
 43 44  2  0
 46 13  1  0
 36 16  1  0
 35 30  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  2 54  1  0
  2 55  1  0
  3 56  1  0
  3 57  1  0
  4 58  1  0
  4 59  1  0
  5 60  1  0
  5 61  1  0
  6 62  1  0
  6 63  1  0
  7 64  1  0
  7 65  1  0
  8 66  1  0
  8 67  1  0
  9 68  1  0
  9 69  1  0
 13 70  1  6
 14 71  1  1
 15 72  1  0
 17 73  1  0
 17 74  1  0
 18 75  1  0
 18 76  1  0
 19 77  1  0
 19 78  1  0
 20 79  1  6
 23 80  1  0
 23 81  1  0
 23 82  1  0
 25 83  1  6
 26 84  1  0
 26 85  1  0
 26 86  1  0
 27 87  1  0
 27 88  1  0
 28 89  1  0
 29 90  1  0
 31 91  1  0
 32 92  1  0
 33 93  1  0
 34 94  1  0
 35 95  1  0
 49100  1  0
 42 98  1  0
 37 96  1  6
 40 97  1  0
 45 99  1  0
M  END


  Mrv1652309112206332D          

 50 52  0  0  1  0            999 V2000
   -7.8720    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1576    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4431    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7286    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0141    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2997    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5852    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8707    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1563    0.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4418    0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4418    1.3067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7273    0.0692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0128    0.4817    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6688    0.0169    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5458   -0.7988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4571    0.2601    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0183   -0.3446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8226   -0.1611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3837   -0.7658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1881   -0.5823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4312    0.2061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2356    0.3897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4787    1.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7967   -0.2151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7492   -1.1870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5060   -1.9754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5535   -1.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1147   -1.6082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9190   -1.4246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4801   -2.0294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2844   -1.8458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8456   -2.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6024   -3.2389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7981   -3.4225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2370   -2.8177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7586    1.0281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3461    1.7426    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8108    2.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6335    2.3626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4528    3.1675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303    1.8655    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1514    2.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8317    2.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3173    3.2785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2117    3.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0745    1.3044    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8425    1.6058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6666    1.5688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9654    2.4216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8219    0.9737    0.0000 O   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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 16 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 37 41  1  0  0  0  0
 41 42  1  1  0  0  0
 41 43  1  6  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 41 46  1  0  0  0  0
 13 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
 46 50  1  0  0  0  0
 16 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0309749

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCC(=O)O[C@@H]1[C@@H](O)[C@@]2(CCCC(OC(C)=O)C(C)C\C=C\C3=CC=CC=C3)O[C@]1(C(O)=O)[C@@](O)([C@H](O2)C(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C36H50O14/c1-4-5-6-7-8-9-13-21-27(38)48-29-28(39)34(49-30(31(40)41)35(46,32(42)43)36(29,50-34)33(44)45)22-15-20-26(47-24(3)37)23(2)16-14-19-25-17-11-10-12-18-25/h10-12,14,17-19,23,26,28-30,39,46H,4-9,13,15-16,20-22H2,1-3H3,(H,40,41)(H,42,43)(H,44,45)/b19-14+/t23?,26?,28-,29-,30-,34-,35-,36-/m1/s1

> <INCHI_KEY>
WDLYATMIWWDJQY-GWDLGUPBSA-N

> <FORMULA>
C36H50O14

> <MOLECULAR_WEIGHT>
706.782

> <EXACT_MASS>
706.32005629

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
74.98757248240226

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3S,4S,5S,6R,7R)-1-[(7E)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid

> <JCHEM_LOGP>
5.855885311666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
4.256655972627013

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.422632013666025

> <JCHEM_PKA_STRONGEST_BASIC>
-4.033597207297459

> <JCHEM_POLAR_SURFACE_AREA>
223.42

> <JCHEM_REFRACTIVITY>
174.6792000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
23

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,4S,5S,6R,7R)-1-[(7E)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0     -14.694   0.129   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -13.361   0.899   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.027   0.129   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.693   0.899   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.360   0.129   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.026   0.899   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.692   0.129   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.359   0.899   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.025   0.129   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.691   0.899   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.691   2.439   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -1.358   0.129   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.024   0.899   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.248   0.032   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.019  -1.491   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.720   0.486   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.767  -0.643   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.269  -0.301   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.316  -1.430   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.818  -1.087   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.272   0.385   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.773   0.727   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.227   2.199   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.820  -0.402   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.865  -2.216   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.411  -3.687   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.367  -1.873   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.414  -3.002   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.915  -2.659   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.963  -3.788   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      15.464  -3.446   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      16.512  -4.574   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.058  -6.046   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.556  -6.389   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      13.509  -5.260   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.283   1.919   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       2.513   3.253   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.380   4.525   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       4.916   4.410   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       2.712   5.913   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       0.990   3.482   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -0.283   4.350   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       1.552   4.916   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       0.592   6.120   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       2.262   6.283   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -0.139   2.435   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -1.573   2.997   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -3.111   2.928   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      -1.802   4.520   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       1.534   1.818   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   46                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   36   50                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   30                                                       
CONECT   36   16   37                                                       
CONECT   37   36   38   41                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   37   42   43   46                                             
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   41   13   47   50                                             
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   46   16                                                       
MASTER        0    0    0    0    0    0    0    0   50    0  104    0
END

View in JSmol

Synonyms

Value	Source
(1R,3S,4S,5S,6R,7R)-1-[(7E)-4-(Acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylate	Generator

Chemical Formula

C₃₆H₅₀O₁₄

Average Mass

706.7820 Da

Monoisotopic Mass

706.32006 Da

IUPAC Name

(1R,3S,4S,5S,6R,7R)-1-[(7E)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid

Traditional Name

(1R,3S,4S,5S,6R,7R)-1-[(7E)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCC(=O)O[C@@H]1[C@@H](O)[C@@]2(CCCC(OC(C)=O)C(C)C\C=C\C3=CC=CC=C3)O[C@]1(C(O)=O)[C@@](O)([C@H](O2)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C36H50O14/c1-4-5-6-7-8-9-13-21-27(38)48-29-28(39)34(49-30(31(40)41)35(46,32(42)43)36(29,50-34)33(44)45)22-15-20-26(47-24(3)37)23(2)16-14-19-25-17-11-10-12-18-25/h10-12,14,17-19,23,26,28-30,39,46H,4-9,13,15-16,20-22H2,1-3H3,(H,40,41)(H,42,43)(H,44,45)/b19-14+/t23?,26?,28-,29-,30-,34-,35-,36-/m1/s1

InChI Key

WDLYATMIWWDJQY-GWDLGUPBSA-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
Amauroascus niger	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Styrene
Ketal
Oxepane
Fatty acid ester
Fatty acyl
Benzenoid
Monosaccharide
Hydroxy acid
Monocyclic benzene moiety
Alpha-hydroxy acid
Meta-dioxane
Tetrahydrofuran
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	5.86	ChemAxon
pKa (Strongest Acidic)	3.42	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	223.42 Å²	ChemAxon
Rotatable Bond Count	23	ChemAxon
Refractivity	174.68 m³·mol⁻¹	ChemAxon
Polarizability	74.99 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	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

4952785

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6450164

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid (NP0309749)

MOL for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

3D MOL for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

3D SDF for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

3D-SDF for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

PDB for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

3D PDB for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

SMILES for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

INCHI for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

Structure for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)

3D Structure for NP0309749 ((1r,3s,4s,5s,6r,7r)-1-[(7e)-4-(acetyloxy)-5-methyl-8-phenyloct-7-en-1-yl]-6-(decanoyloxy)-4,7-dihydroxy-2,8-dioxabicyclo[3.2.1]octane-3,4,5-tricarboxylic acid)