NP-MRD: Showing NP-Card for (+)-Atticin (NP0075128)

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Record Information

Version

2.0

Created at

2022-04-28 20:26:03 UTC

Updated at

2022-04-28 20:26:03 UTC

NP-MRD ID

NP0075128

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Atticin

Description

(2S,3S,4S,4aS,5S,8R,8aR)-5-formyl-4,8-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)-8a-methyl-decahydronaphthalen-2-yl (3S)-4-(acetyloxy)-3-hydroxy-2-methylidenebutanoate belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton. (+)-Atticin is found in Centaurea attica ssp.attica. Based on a literature review very few articles have been published on (2S,3S,4S,4aS,5S,8R,8aR)-5-formyl-4,8-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)-8a-methyl-decahydronaphthalen-2-yl (3S)-4-(acetyloxy)-3-hydroxy-2-methylidenebutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222262D          

 33 34  0  0  1  0            999 V2000
    2.8579   -2.4750    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
    3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  1  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
    1.4289   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    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    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   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    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  1  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
    5.7158    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.6500    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
    0.7145   -1.2375    0.0000 O   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
    4.2868   -0.8250    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  2  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 11 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 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  2  0  0  0  0
 21 23  1  0  0  0  0
 18 24  1  6  0  0  0
 10 25  1  6  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
 29 30  1  0  0  0  0
  9 31  1  6  0  0  0
  4 32  1  6  0  0  0
  3 33  1  6  0  0  0
M  END

     RDKit          3D

 65 66  0  0  0  0  0  0  0  0999 V2000
    2.4909    1.2401    2.9989 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7749    0.8286    1.7761 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7435    0.2859    0.9113 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0565   -0.0981   -0.2433 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4185    0.1587    1.2727 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5933   -0.3508    0.4908 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1554   -1.6443    1.0342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0554   -2.3233    0.0160 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2709   -3.0911   -0.9882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0337   -1.3376   -0.5215 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0810   -1.9146   -1.3962 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6588   -2.4366   -2.6908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5541   -3.6280   -2.9171 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8795   -2.9070   -0.5854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0022   -3.9323    0.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8607   -3.3385    0.8360 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0652   -4.3425    1.3341 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3925   -0.0714   -1.0753 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4084   -0.3338   -1.9873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7171    0.5694    0.1300 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3652    1.9532   -0.1302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5641    2.5035   -1.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7957    2.8272    0.8931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5787    2.3992    2.0490 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4644    4.1554    0.6632 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0894    4.9870    1.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1786    0.9373    1.3097 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0200    1.3673    2.3300 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3200    1.8283    0.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6946    1.7304   -0.3114 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1818    2.4192   -1.4010 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5981    2.3426   -1.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3713    3.1468   -2.0438 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2404    1.6474    3.6606 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4815    1.1750    3.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1203   -0.6456   -0.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2922   -2.3218    1.2193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7005   -1.5257    1.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5833   -4.1535   -1.0865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2141   -3.1633   -0.5899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1729   -2.6530   -1.9771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5874   -0.9551    0.3976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8082   -1.0746   -1.6169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4257   -1.7568   -3.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5913   -3.4316   -1.2367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4597   -2.3550    0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7097   -4.6679   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6407   -4.4634    0.8240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997   -2.7832    1.7167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1943   -4.4118    0.8984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2167    0.5132   -1.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409   -0.2938   -2.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4849    0.5041    0.9818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9817    1.9114   -2.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3163    3.5545   -1.5070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6159    4.3525    2.4348 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7185    5.7839    1.2796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7688    5.4381    2.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5692   -0.0751    0.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3588    0.6332    2.8929 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7433    1.4241   -0.7586 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1052    2.8818    0.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6973    2.0510   -2.8925 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1240    1.6017   -1.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1133    3.3290   -1.7260 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 23  1  0
 23 24  2  0
 23 21  1  0
 21 22  2  3
 21 20  1  0
 20 18  1  0
 18 19  1  0
 18 10  1  0
 10 11  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16  8  1  0
  8  9  1  6
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  2  0
 11 12  1  0
 12 13  2  0
  6 20  1  0
  8 10  1  0
 26 56  1  0
 26 57  1  0
 26 58  1  0
 22 54  1  0
 22 55  1  0
 20 53  1  1
 18 51  1  6
 19 52  1  0
 10 42  1  1
 11 43  1  6
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  1
 17 50  1  0
  9 39  1  0
  9 40  1  0
  9 41  1  0
  7 37  1  0
  7 38  1  0
  6 36  1  6
  1 34  1  0
  1 35  1  0
 27 59  1  6
 28 60  1  0
 29 61  1  0
 29 62  1  0
 32 63  1  0
 32 64  1  0
 32 65  1  0
 12 44  1  0
M  END


  Mrv1652304282222262D          

 33 34  0  0  1  0            999 V2000
    2.8579   -2.4750    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
    3.5724   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  1  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
    1.4289   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    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    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   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    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  1  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
    5.7158    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.6500    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
    0.7145   -1.2375    0.0000 O   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
    4.2868   -0.8250    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  2  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 11 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 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  2  0  0  0  0
 21 23  1  0  0  0  0
 18 24  1  6  0  0  0
 10 25  1  6  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
 29 30  1  0  0  0  0
  9 31  1  6  0  0  0
  4 32  1  6  0  0  0
  3 33  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0075128

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(=C)[C@H]1[C@@H](O)[C@H]2[C@H](CC[C@@H](O)[C@]2(C)C[C@@H]1OC(=O)C(=C)[C@H](O)COC(C)=O)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O10/c1-11(15(26)10-32-13(3)25)22(30)33-16-8-23(4)17(27)7-6-14(9-24)19(23)20(28)18(16)12(2)21(29)31-5/h9,14-20,26-28H,1-2,6-8,10H2,3-5H3/t14-,15-,16+,17-,18-,19-,20-,23+/m1/s1

> <INCHI_KEY>
DIHJNCJEIOMBSV-MEHCSJBBSA-N

> <FORMULA>
C23H32O10

> <MOLECULAR_WEIGHT>
468.499

> <EXACT_MASS>
468.19954723

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.07818182898441

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S,4S,4aS,5S,8R,8aR)-5-formyl-4,8-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)-8a-methyl-decahydronaphthalen-2-yl (3S)-4-(acetyloxy)-3-hydroxy-2-methylidenebutanoate

> <ALOGPS_LOGP>
0.43

> <JCHEM_LOGP>
-0.17754435633333351

> <ALOGPS_LOGS>
-2.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.322277049898595

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.46086825136313

> <JCHEM_PKA_STRONGEST_BASIC>
-2.933392191511711

> <JCHEM_POLAR_SURFACE_AREA>
156.66000000000003

> <JCHEM_REFRACTIVITY>
113.5013

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.73e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,4aS,5S,8R,8aR)-5-formyl-4,8-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)-8a-methyl-octahydro-1H-naphthalen-2-yl (3S)-4-(acetyloxy)-3-hydroxy-2-methylidenebutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.667  -6.160   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.669   3.080   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      13.337   3.080   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.003   0.770   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.002   4.620   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.667   3.080   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -0.000   3.080   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       8.002  -1.540   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   33                                                  
CONECT    4    3    5   12   32                                             
CONECT    5    4    6    9                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    5   10   31                                                  
CONECT   10    9   11   25                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11    4                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   18                                                            
CONECT   25   10   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29                                                            
CONECT   31    9                                                            
CONECT   32    4                                                            
CONECT   33    3                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

View in JSmol

Synonyms

Value	Source
(2S,3S,4S,4AS,5S,8R,8ar)-5-formyl-4,8-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)-8a-methyl-decahydronaphthalen-2-yl (3S)-4-(acetyloxy)-3-hydroxy-2-methylidenebutanoic acid	Generator

Chemical Formula

C₂₃H₃₂O₁₀

Average Mass

468.4990 Da

Monoisotopic Mass

468.19955 Da

IUPAC Name

(2S,3S,4S,4aS,5S,8R,8aR)-5-formyl-4,8-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)-8a-methyl-decahydronaphthalen-2-yl (3S)-4-(acetyloxy)-3-hydroxy-2-methylidenebutanoate

Traditional Name

(2S,3S,4S,4aS,5S,8R,8aR)-5-formyl-4,8-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)-8a-methyl-octahydro-1H-naphthalen-2-yl (3S)-4-(acetyloxy)-3-hydroxy-2-methylidenebutanoate

CAS Registry Number

Not Available

SMILES

COC(=O)C(=C)[C@H]1[C@@H](O)[C@H]2[C@H](CC[C@@H](O)[C@]2(C)C[C@@H]1OC(=O)C(=C)[C@H](O)COC(C)=O)C=O

InChI Identifier

InChI=1S/C23H32O10/c1-11(15(26)10-32-13(3)25)22(30)33-16-8-23(4)17(27)7-6-14(9-24)19(23)20(28)18(16)12(2)21(29)31-5/h9,14-20,26-28H,1-2,6-8,10H2,3-5H3/t14-,15-,16+,17-,18-,19-,20-,23+/m1/s1

InChI Key

DIHJNCJEIOMBSV-MEHCSJBBSA-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
Centaurea attica ssp.attica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids

Alternative Parents

Substituents

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Beta-hydroxy acid
Fatty acyl
Hydroxy acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Alcohol
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	0.43	ALOGPS
logP	-0.18	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	13.46	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	156.66 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	113.5 m³·mol⁻¹	ChemAxon
Polarizability	47.08 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

163002515

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Atticin (NP0075128)

MOL for NP0075128 ((+)-Atticin)

3D MOL for NP0075128 ((+)-Atticin)

3D SDF for NP0075128 ((+)-Atticin)

3D-SDF for NP0075128 ((+)-Atticin)

PDB for NP0075128 ((+)-Atticin)

3D PDB for NP0075128 ((+)-Atticin)

SMILES for NP0075128 ((+)-Atticin)

INCHI for NP0075128 ((+)-Atticin)

Structure for NP0075128 ((+)-Atticin)

3D Structure for NP0075128 ((+)-Atticin)