NP-MRD: Showing NP-Card for (3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate (NP0213982)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 13:08:46 UTC

Updated at

2022-09-05 13:08:46 UTC

NP-MRD ID

NP0213982

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate

Description

(3S,4aR,6aR,8S,10R,10aR,10bS)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-dodecahydro-1H-naphtho[2,1-b]pyran-10-yl (2R)-2-methylbutanoate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on (3S,4aR,6aR,8S,10R,10aR,10bS)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-dodecahydro-1H-naphtho[2,1-b]pyran-10-yl (2R)-2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052215082D          

 33 35  0  0  1  0            999 V2000
    0.2481   -2.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303   -1.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5303   -1.4570    0.0000 C   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
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    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    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  2  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
   -1.5269    2.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966    3.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    3.3000    0.0000 C   0  0  1  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
    0.7145    4.5375    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
    1.4289    4.1250    0.0000 O   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    2.0625    0.0000 C   0  0  1  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
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  2  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
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.6500    0.0000 C   0  0  1  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  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
  3 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 32  1  0  0  0  0
  7 32  1  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END

     RDKit          3D

 75 77  0  0  0  0  0  0  0  0999 V2000
    5.3389    1.3586    1.9906 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0656    1.5100    1.7076 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6493    1.6269    0.2538 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7554    2.5001   -0.3666 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4095    2.4086    0.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2698    1.7995   -0.6283 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3549    0.3559   -0.4230 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6467   -0.0539   -1.0563 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9470    0.5101   -2.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6755    0.3568   -0.2182 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8199   -1.5318   -1.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7756   -1.9465   -1.8036 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8945   -2.4528   -0.5360 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6033   -1.8981   -0.0919 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4415   -2.9323   -0.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452   -4.0274    0.8588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6949   -3.6173   -1.4074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7756   -2.4694    0.4567 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3174   -3.4180    1.2889 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5223   -4.0503    1.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0315   -5.0611    1.9858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0938   -3.6943   -0.0229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5441   -1.1173    1.0246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0969   -0.2137   -0.1405 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3937    1.0653    0.2354 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4476    1.8294   -0.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1753    1.2495   -1.0592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6465    3.2107    0.2805 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8621    3.1719    1.7795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8623    3.8526   -0.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0284    5.2464    0.1762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2068   -0.5488   -0.7111 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0642   -0.6732   -2.2251 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0711    1.3185    1.2035 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6710    1.2722    3.0107 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3483    1.5475    2.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2903    3.3009   -1.0154 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3074    3.0748    0.4056 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4947    1.8976   -0.9049 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5485    3.4656   -0.1580 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9613    2.5595    1.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3994    2.3665   -0.3448 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5158    2.1530   -1.6688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5239    0.2151    0.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5747   -0.2088   -3.0137 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6246    1.4132   -2.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1346    0.7975   -3.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7468   -3.3225   -1.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4518   -2.9397    0.3241 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7564   -1.6208    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9219   -4.5390    0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7836   -4.7223    1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3833   -3.5259    1.7704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0227   -3.4068   -2.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7190   -4.7457   -1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7351   -3.3796   -1.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4787   -2.3304   -0.4163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2101   -5.7506    2.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5167   -4.6240    2.8755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7982   -5.7243    1.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9504   -1.0278    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5663   -0.7038    1.2850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9113   -0.4724   -0.8948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7795    3.8701    0.0455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9402    2.9906    1.9391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4951    4.0928    2.2638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3012    2.3135    2.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7689    3.9239   -1.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7888    3.2710   -0.1406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4782    5.9864   -0.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1028    5.5642    0.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7414    5.3449    1.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9286   -1.1992   -2.3674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1584    0.3585   -2.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8610   -1.2003   -2.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
 31 30  1  0
 30 28  1  0
 28 29  1  0
 28 26  1  0
 26 27  2  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 18 15  1  0
 15 16  1  0
 15 17  1  0
 15 14  1  0
 14 13  1  0
 13 11  1  0
 11 12  2  0
 11  8  1  0
  8  9  1  6
  8 10  1  0
 10  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7 32  1  0
 32 33  1  6
  3  2  1  1
  2  1  2  3
 32 24  1  0
 32 14  1  0
  7  8  1  0
 31 70  1  0
 31 71  1  0
 31 72  1  0
 30 68  1  0
 30 69  1  0
 28 64  1  1
 29 65  1  0
 29 66  1  0
 29 67  1  0
 24 63  1  6
 23 61  1  0
 23 62  1  0
 18 57  1  6
 21 58  1  0
 21 59  1  0
 21 60  1  0
 16 51  1  0
 16 52  1  0
 16 53  1  0
 17 54  1  0
 17 55  1  0
 17 56  1  0
 14 50  1  1
 13 48  1  0
 13 49  1  0
  9 45  1  0
  9 46  1  0
  9 47  1  0
  4 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  6 43  1  0
  7 44  1  1
 33 73  1  0
 33 74  1  0
 33 75  1  0
  2 36  1  0
  1 34  1  0
  1 35  1  0
M  END


  Mrv1652309052215082D          

 33 35  0  0  1  0            999 V2000
    0.2481   -2.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303   -1.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5303   -1.4570    0.0000 C   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
    0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    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    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  2  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
   -1.5269    2.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966    3.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    3.3000    0.0000 C   0  0  1  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
    0.7145    4.5375    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
    1.4289    4.1250    0.0000 O   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    2.0625    0.0000 C   0  0  1  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
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  2  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
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.6500    0.0000 C   0  0  1  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  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
  3 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 32  1  0  0  0  0
  7 32  1  0  0  0  0
 14 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0213982

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)C(=O)O[C@@H]1C[C@H](OC(C)=O)C(C)(C)[C@H]2CC(=O)[C@]3(C)O[C@@](C)(CC[C@H]3[C@]12C)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C27H42O6/c1-10-16(3)23(30)32-22-15-21(31-17(4)28)24(5,6)19-14-20(29)27(9)18(26(19,22)8)12-13-25(7,11-2)33-27/h11,16,18-19,21-22H,2,10,12-15H2,1,3-9H3/t16-,18+,19-,21+,22-,25-,26+,27-/m1/s1

> <INCHI_KEY>
GPVCYNCHZGERJR-NEDRTXQDSA-N

> <FORMULA>
C27H42O6

> <MOLECULAR_WEIGHT>
462.627

> <EXACT_MASS>
462.298139072

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
51.63247511780986

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4aR,6aR,8S,10R,10aR,10bS)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-dodecahydro-1H-naphtho[2,1-b]pyran-10-yl (2R)-2-methylbutanoate

> <JCHEM_LOGP>
5.023111330999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.009478069010346

> <JCHEM_PKA_STRONGEST_BASIC>
-4.286198544679265

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
125.10479999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4aR,6aR,8S,10R,10aR,10bS)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2R)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       0.463  -4.167   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.990  -2.720   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.000  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.990  -2.720   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.001   0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334   3.850   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      -2.850   5.123   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.860   6.837   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.000   6.160   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.000   7.700   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  10.010   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.667   7.700   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.667   3.080   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.001   5.390   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.000   3.080   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   10                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   32                                                  
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8    3                                                       
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   32                                                  
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24                                                       
CONECT   24   23   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30                                                            
CONECT   32   24    7   14   33                                             
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
(3S,4AR,6ar,8S,10R,10ar,10BS)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-dodecahydro-1H-naphtho[2,1-b]pyran-10-yl (2R)-2-methylbutanoic acid	Generator

Chemical Formula

C₂₇H₄₂O₆

Average Mass

462.6270 Da

Monoisotopic Mass

462.29814 Da

IUPAC Name

(3S,4aR,6aR,8S,10R,10aR,10bS)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-dodecahydro-1H-naphtho[2,1-b]pyran-10-yl (2R)-2-methylbutanoate

Traditional Name

(3S,4aR,6aR,8S,10R,10aR,10bS)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2R)-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)C(=O)O[C@@H]1C[C@H](OC(C)=O)C(C)(C)[C@H]2CC(=O)[C@]3(C)O[C@@](C)(CC[C@H]3[C@]12C)C=C

InChI Identifier

InChI=1S/C27H42O6/c1-10-16(3)23(30)32-22-15-21(31-17(4)28)24(5,6)19-14-20(29)27(9)18(26(19,22)8)12-13-25(7,11-2)33-27/h11,16,18-19,21-22H,2,10,12-15H2,1,3-9H3/t16-,18+,19-,21+,22-,25-,26+,27-/m1/s1

InChI Key

GPVCYNCHZGERJR-NEDRTXQDSA-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 triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Naphthopyran
Naphthalene
Fatty acid ester
Dicarboxylic acid or derivatives
Oxane
Pyran
Fatty acyl
Ketone
Carboxylic acid ester
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	5.02	ChemAxon
pKa (Strongest Acidic)	18.01	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	125.1 m³·mol⁻¹	ChemAxon
Polarizability	51.63 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

162961790

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate (NP0213982)

MOL for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

3D MOL for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

3D SDF for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

3D-SDF for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

PDB for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

3D PDB for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

SMILES for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

INCHI for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

Structure for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)

3D Structure for NP0213982 ((3s,4ar,6ar,8s,10r,10ar,10bs)-8-(acetyloxy)-3-ethenyl-3,4a,7,7,10a-pentamethyl-5-oxo-octahydronaphtho[2,1-b]pyran-10-yl (2r)-2-methylbutanoate)