NP-MRD: Showing NP-Card for plakortide R (NP0042194)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-06-20 23:55:04 UTC

Updated at

2021-06-30 00:17:08 UTC

NP-MRD ID

NP0042194

Secondary Accession Numbers

None

Natural Product Identification

Common Name

plakortide R

Provided By

JEOL Database JEOL Logo

Description

Plakortide R belongs to the class of organic compounds known as methyl esters. These are organic compounds containing a carboxyl group that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=H or organyl group and R'=methyl group. plakortide R is found in Plakinastrella mamillaris. plakortide R was first documented in 2013 (Festa, C., et al.). Based on a literature review very few articles have been published on Plakortide R.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212101553D          

 55 55  0  0  0  0            999 V2000
   -2.2359   -0.1252    6.7786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8643    0.3218    6.2978 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8044    0.3872    4.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0163   -0.3660    4.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0826   -0.2942    2.5341 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4392   -1.6071    1.9145 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4171   -2.8441    2.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5140    0.1290    2.1202 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7510    0.4564    0.6213 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7577    1.4925    0.0460 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7096    2.8300    0.7742 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1938    0.9233    0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0322    0.4042   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4679    0.8529   -0.5667 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7093    1.7512   -1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.6438   -1.4310 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9866   -2.0568   -1.0836 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6346   -2.9852   -2.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8984   -2.7718   -3.3885 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0322   -4.1102   -1.7375 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6583   -5.0428   -2.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0860   -0.5733   -1.4700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6062   -0.7868   -0.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0188    0.5620    6.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2620   -0.1540    7.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4778   -1.1270    6.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -0.3614    6.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6419    1.3158    6.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4729    1.0997    4.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6855   -1.0722    4.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6085    0.4951    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5727   -1.4760    0.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4451   -1.8085    2.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5087   -3.0666    3.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4213   -2.7358    1.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0453   -3.7140    1.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.0077    2.7193 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.6648    2.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2501    1.0601    0.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0016    1.6905   -1.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3891    2.7156    1.8132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6832    3.3286    0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0069    3.4949    0.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5394    1.7016    1.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1277   -0.0202   -0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7643    1.3996    0.3374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7472    2.0998   -1.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5323    1.2207   -2.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0577    2.6311   -1.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8537   -0.3690   -2.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0708   -2.1158   -0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5118   -2.4124   -0.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5450   -5.4145   -3.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9557   -4.5848   -3.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1616   -5.8884   -2.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 13  1  0  0  0  0
  3  2  1  0  0  0  0
 13 12  2  0  0  0  0
  2  1  1  0  0  0  0
 13 14  1  0  0  0  0
  9  8  1  1  0  0  0
 17 18  1  0  0  0  0
  9 23  1  0  0  0  0
 14 15  1  0  0  0  0
 16 17  1  0  0  0  0
 18 20  1  0  0  0  0
  9 12  1  0  0  0  0
 20 21  1  0  0  0  0
  8  5  1  0  0  0  0
 18 19  2  0  0  0  0
 23 22  1  0  0  0  0
  5  6  1  0  0  0  0
  5  4  1  0  0  0  0
  6  7  1  0  0  0  0
 22 16  1  0  0  0  0
  9 10  1  0  0  0  0
  4  3  2  0  0  0  0
 10 11  1  0  0  0  0
 16 50  1  6  0  0  0
 12 44  1  0  0  0  0
  8 37  1  0  0  0  0
  8 38  1  0  0  0  0
 17 51  1  0  0  0  0
 17 52  1  0  0  0  0
  5 31  1  6  0  0  0
  4 30  1  0  0  0  0
  3 29  1  0  0  0  0
  2 27  1  0  0  0  0
  2 28  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
 14 45  1  0  0  0  0
 14 46  1  0  0  0  0
 15 47  1  0  0  0  0
 15 48  1  0  0  0  0
 15 49  1  0  0  0  0
 21 53  1  0  0  0  0
 21 54  1  0  0  0  0
 21 55  1  0  0  0  0
  6 32  1  0  0  0  0
  6 33  1  0  0  0  0
  7 34  1  0  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
 10 39  1  0  0  0  0
 10 40  1  0  0  0  0
 11 41  1  0  0  0  0
 11 42  1  0  0  0  0
 11 43  1  0  0  0  0
M  END

     RDKit          3D

 55 55  0  0  0  0  0  0  0  0999 V2000
   -2.2359   -0.1252    6.7786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8643    0.3218    6.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8044    0.3872    4.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0163   -0.3660    4.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0826   -0.2942    2.5341 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4392   -1.6071    1.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4171   -2.8441    2.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5140    0.1290    2.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7510    0.4564    0.6213 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7577    1.4925    0.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7096    2.8300    0.7742 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1938    0.9233    0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0322    0.4042   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4679    0.8529   -0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093    1.7512   -1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.6438   -1.4310 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9866   -2.0568   -1.0836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6346   -2.9852   -2.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8984   -2.7718   -3.3885 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0322   -4.1102   -1.7375 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6583   -5.0428   -2.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0860   -0.5733   -1.4700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6062   -0.7868   -0.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0188    0.5620    6.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2620   -0.1540    7.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4778   -1.1270    6.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -0.3614    6.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6419    1.3158    6.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4729    1.0997    4.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6855   -1.0722    4.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6085    0.4951    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5727   -1.4760    0.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4451   -1.8085    2.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5087   -3.0666    3.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4213   -2.7358    1.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0453   -3.7140    1.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.0077    2.7193 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.6648    2.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2501    1.0601    0.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0016    1.6905   -1.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3891    2.7156    1.8132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6832    3.3286    0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0069    3.4949    0.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5394    1.7016    1.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1277   -0.0202   -0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7643    1.3996    0.3374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7472    2.0998   -1.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5323    1.2207   -2.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0577    2.6311   -1.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8537   -0.3690   -2.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0708   -2.1158   -0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5118   -2.4124   -0.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5450   -5.4145   -3.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9557   -4.5848   -3.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1616   -5.8884   -2.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 13  1  0
  3  2  1  0
 13 12  2  0
  2  1  1  0
 13 14  1  0
  9  8  1  1
 17 18  1  0
  9 23  1  0
 14 15  1  0
 16 17  1  0
 18 20  1  0
  9 12  1  0
 20 21  1  0
  8  5  1  0
 18 19  2  0
 23 22  1  0
  5  6  1  0
  5  4  1  0
  6  7  1  0
 22 16  1  0
  9 10  1  0
  4  3  2  0
 10 11  1  0
 16 50  1  6
 12 44  1  0
  8 37  1  0
  8 38  1  0
 17 51  1  0
 17 52  1  0
  5 31  1  6
  4 30  1  0
  3 29  1  0
  2 27  1  0
  2 28  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 15 49  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 11 43  1  0
M  END


  Mrv1652306212101553D          

 55 55  0  0  0  0            999 V2000
   -2.2359   -0.1252    6.7786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8643    0.3218    6.2978 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8044    0.3872    4.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0163   -0.3660    4.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0826   -0.2942    2.5341 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4392   -1.6071    1.9145 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4171   -2.8441    2.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5140    0.1290    2.1202 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7510    0.4564    0.6213 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7577    1.4925    0.0460 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7096    2.8300    0.7742 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1938    0.9233    0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0322    0.4042   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4679    0.8529   -0.5667 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7093    1.7512   -1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.6438   -1.4310 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9866   -2.0568   -1.0836 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6346   -2.9852   -2.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8984   -2.7718   -3.3885 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0322   -4.1102   -1.7375 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6583   -5.0428   -2.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0860   -0.5733   -1.4700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6062   -0.7868   -0.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0188    0.5620    6.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2620   -0.1540    7.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4778   -1.1270    6.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -0.3614    6.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6419    1.3158    6.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4729    1.0997    4.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6855   -1.0722    4.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6085    0.4951    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5727   -1.4760    0.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4451   -1.8085    2.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5087   -3.0666    3.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4213   -2.7358    1.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0453   -3.7140    1.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.0077    2.7193 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.6648    2.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2501    1.0601    0.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0016    1.6905   -1.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3891    2.7156    1.8132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6832    3.3286    0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0069    3.4949    0.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5394    1.7016    1.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1277   -0.0202   -0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7643    1.3996    0.3374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7472    2.0998   -1.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5323    1.2207   -2.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0577    2.6311   -1.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8537   -0.3690   -2.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0708   -2.1158   -0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5118   -2.4124   -0.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5450   -5.4145   -3.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9557   -4.5848   -3.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1616   -5.8884   -2.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 13  1  0  0  0  0
  3  2  1  0  0  0  0
 13 12  2  0  0  0  0
  2  1  1  0  0  0  0
 13 14  1  0  0  0  0
  9  8  1  1  0  0  0
 17 18  1  0  0  0  0
  9 23  1  0  0  0  0
 14 15  1  0  0  0  0
 16 17  1  0  0  0  0
 18 20  1  0  0  0  0
  9 12  1  0  0  0  0
 20 21  1  0  0  0  0
  8  5  1  0  0  0  0
 18 19  2  0  0  0  0
 23 22  1  0  0  0  0
  5  6  1  0  0  0  0
  5  4  1  0  0  0  0
  6  7  1  0  0  0  0
 22 16  1  0  0  0  0
  9 10  1  0  0  0  0
  4  3  2  0  0  0  0
 10 11  1  0  0  0  0
 16 50  1  6  0  0  0
 12 44  1  0  0  0  0
  8 37  1  0  0  0  0
  8 38  1  0  0  0  0
 17 51  1  0  0  0  0
 17 52  1  0  0  0  0
  5 31  1  6  0  0  0
  4 30  1  0  0  0  0
  3 29  1  0  0  0  0
  2 27  1  0  0  0  0
  2 28  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
 14 45  1  0  0  0  0
 14 46  1  0  0  0  0
 15 47  1  0  0  0  0
 15 48  1  0  0  0  0
 15 49  1  0  0  0  0
 21 53  1  0  0  0  0
 21 54  1  0  0  0  0
 21 55  1  0  0  0  0
  6 32  1  0  0  0  0
  6 33  1  0  0  0  0
  7 34  1  0  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
 10 39  1  0  0  0  0
 10 40  1  0  0  0  0
 11 41  1  0  0  0  0
 11 42  1  0  0  0  0
 11 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0042194

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(=C(\[H])[C@]([H])(C([H])([H])C([H])([H])[H])C([H])([H])[C@@]1(OO[C@@]([H])(C(=C1[H])C([H])([H])C([H])([H])[H])C([H])([H])C(=O)OC([H])([H])[H])C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H32O4/c1-6-10-11-15(7-2)13-19(9-4)14-16(8-3)17(22-23-19)12-18(20)21-5/h10-11,14-15,17H,6-9,12-13H2,1-5H3/b11-10+/t15-,17+,19-/m0/s1

> <INCHI_KEY>
SVIKESJVLMSASY-SEQSLPPWSA-N

> <FORMULA>
C19H32O4

> <MOLECULAR_WEIGHT>
324.461

> <EXACT_MASS>
324.23005951

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
38.31051462914157

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[(3R,6S)-4,6-diethyl-6-[(2R,3E)-2-ethylhex-3-en-1-yl]-3,6-dihydro-1,2-dioxin-3-yl]acetate

> <ALOGPS_LOGP>
5.52

> <JCHEM_LOGP>
5.1631341163333335

> <ALOGPS_LOGS>
-4.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.867655450273058

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
93.32490000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.73e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(3R,6S)-4,6-diethyl-6-[(2R,3E)-2-ethylhex-3-en-1-yl]-3H-1,2-dioxin-3-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 55  0  0  0  0  0  0  0  0999 V2000
   -2.2359   -0.1252    6.7786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8643    0.3218    6.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8044    0.3872    4.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0163   -0.3660    4.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0826   -0.2942    2.5341 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4392   -1.6071    1.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4171   -2.8441    2.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5140    0.1290    2.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7510    0.4564    0.6213 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7577    1.4925    0.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7096    2.8300    0.7742 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1938    0.9233    0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0322    0.4042   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4679    0.8529   -0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093    1.7512   -1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.6438   -1.4310 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9866   -2.0568   -1.0836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6346   -2.9852   -2.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8984   -2.7718   -3.3885 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0322   -4.1102   -1.7375 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6583   -5.0428   -2.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0860   -0.5733   -1.4700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6062   -0.7868   -0.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0188    0.5620    6.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2620   -0.1540    7.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4778   -1.1270    6.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -0.3614    6.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6419    1.3158    6.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4729    1.0997    4.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6855   -1.0722    4.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6085    0.4951    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5727   -1.4760    0.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4451   -1.8085    2.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5087   -3.0666    3.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4213   -2.7358    1.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0453   -3.7140    1.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.0077    2.7193 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.6648    2.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2501    1.0601    0.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0016    1.6905   -1.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3891    2.7156    1.8132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6832    3.3286    0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0069    3.4949    0.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5394    1.7016    1.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1277   -0.0202   -0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7643    1.3996    0.3374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7472    2.0998   -1.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5323    1.2207   -2.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0577    2.6311   -1.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8537   -0.3690   -2.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0708   -2.1158   -0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5118   -2.4124   -0.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5450   -5.4145   -3.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9557   -4.5848   -3.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1616   -5.8884   -2.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 13  1  0
  3  2  1  0
 13 12  2  0
  2  1  1  0
 13 14  1  0
  9  8  1  1
 17 18  1  0
  9 23  1  0
 14 15  1  0
 16 17  1  0
 18 20  1  0
  9 12  1  0
 20 21  1  0
  8  5  1  0
 18 19  2  0
 23 22  1  0
  5  6  1  0
  5  4  1  0
  6  7  1  0
 22 16  1  0
  9 10  1  0
  4  3  2  0
 10 11  1  0
 16 50  1  6
 12 44  1  0
  8 37  1  0
  8 38  1  0
 17 51  1  0
 17 52  1  0
  5 31  1  6
  4 30  1  0
  3 29  1  0
  2 27  1  0
  2 28  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 15 49  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 11 43  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.236  -0.125   6.779  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.864   0.322   6.298  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.804   0.387   4.799  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.016  -0.366   4.049  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.083  -0.294   2.534  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.439  -1.607   1.915  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.417  -2.844   2.159  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.514   0.129   2.120  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.751   0.456   0.621  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.758   1.492   0.046  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.710   2.830   0.774  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.194   0.923   0.467  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.032   0.404  -0.453  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.468   0.853  -0.567  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.709   1.751  -1.772  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.527  -0.644  -1.431  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.987  -2.057  -1.084  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.635  -2.985  -2.212  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.898  -2.772  -3.389  0.00  0.00           O+0
HETATM   20  O   UNK     0       3.032  -4.110  -1.738  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.658  -5.043  -2.752  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.086  -0.573  -1.470  0.00  0.00           O+0
HETATM   23  O   UNK     0       1.606  -0.787  -0.101  0.00  0.00           O+0
HETATM   24  H   UNK     0      -3.019   0.562   6.440  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.262  -0.154   7.873  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.478  -1.127   6.408  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.103  -0.361   6.693  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.642   1.316   6.702  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.473   1.100   4.319  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.686  -1.072   4.538  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.609   0.495   2.213  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.573  -1.476   0.835  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.445  -1.809   2.307  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.509  -3.067   3.226  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.421  -2.736   1.742  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.045  -3.714   1.681  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.795   1.008   2.719  0.00  0.00           H+0
HETATM   38  H   UNK     0       2.212  -0.665   2.423  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.250   1.060   0.016  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.002   1.690  -1.006  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.389   2.716   1.813  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.683   3.329   0.764  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.007   3.495   0.281  0.00  0.00           H+0
HETATM   44  H   UNK     0       3.539   1.702   1.143  0.00  0.00           H+0
HETATM   45  H   UNK     0       6.128  -0.020  -0.619  0.00  0.00           H+0
HETATM   46  H   UNK     0       5.764   1.400   0.337  0.00  0.00           H+0
HETATM   47  H   UNK     0       6.747   2.100  -1.778  0.00  0.00           H+0
HETATM   48  H   UNK     0       5.532   1.221  -2.712  0.00  0.00           H+0
HETATM   49  H   UNK     0       5.058   2.631  -1.747  0.00  0.00           H+0
HETATM   50  H   UNK     0       3.854  -0.369  -2.439  0.00  0.00           H+0
HETATM   51  H   UNK     0       5.071  -2.116  -0.941  0.00  0.00           H+0
HETATM   52  H   UNK     0       3.512  -2.412  -0.162  0.00  0.00           H+0
HETATM   53  H   UNK     0       3.545  -5.415  -3.275  0.00  0.00           H+0
HETATM   54  H   UNK     0       1.956  -4.585  -3.455  0.00  0.00           H+0
HETATM   55  H   UNK     0       2.162  -5.888  -2.268  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    3    1   27   28                                             
CONECT    3    2    4   29                                                  
CONECT    4    5    3   30                                                  
CONECT    5    8    6    4   31                                             
CONECT    6    5    7   32   33                                             
CONECT    7    6   34   35   36                                             
CONECT    8    9    5   37   38                                             
CONECT    9    8   23   12   10                                             
CONECT   10    9   11   39   40                                             
CONECT   11   10   41   42   43                                             
CONECT   12   13    9   44                                                  
CONECT   13   16   12   14                                                  
CONECT   14   13   15   45   46                                             
CONECT   15   14   47   48   49                                             
CONECT   16   13   17   22   50                                             
CONECT   17   18   16   51   52                                             
CONECT   18   17   20   19                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   53   54   55                                             
CONECT   22   23   16                                                       
CONECT   23    9   22                                                       
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    2                                                            
CONECT   28    2                                                            
CONECT   29    3                                                            
CONECT   30    4                                                            
CONECT   31    5                                                            
CONECT   32    6                                                            
CONECT   33    6                                                            
CONECT   34    7                                                            
CONECT   35    7                                                            
CONECT   36    7                                                            
CONECT   37    8                                                            
CONECT   38    8                                                            
CONECT   39   10                                                            
CONECT   40   10                                                            
CONECT   41   11                                                            
CONECT   42   11                                                            
CONECT   43   11                                                            
CONECT   44   12                                                            
CONECT   45   14                                                            
CONECT   46   14                                                            
CONECT   47   15                                                            
CONECT   48   15                                                            
CONECT   49   15                                                            
CONECT   50   16                                                            
CONECT   51   17                                                            
CONECT   52   17                                                            
CONECT   53   21                                                            
CONECT   54   21                                                            
CONECT   55   21                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  110    0
END

RDKit          3D

55 55  0  0  0  0  0  0  0  0999 V2000
   -2.2359   -0.1252    6.7786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8643    0.3218    6.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8044    0.3872    4.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0163   -0.3660    4.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0826   -0.2942    2.5341 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4392   -1.6071    1.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4171   -2.8441    2.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5140    0.1290    2.1202 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7510    0.4564    0.6213 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7577    1.4925    0.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7096    2.8300    0.7742 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1938    0.9233    0.4670 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0322    0.4042   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4679    0.8529   -0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093    1.7512   -1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.6438   -1.4310 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9866   -2.0568   -1.0836 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6346   -2.9852   -2.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8984   -2.7718   -3.3885 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0322   -4.1102   -1.7375 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6583   -5.0428   -2.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0860   -0.5733   -1.4700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6062   -0.7868   -0.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0188    0.5620    6.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2620   -0.1540    7.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4778   -1.1270    6.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -0.3614    6.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6419    1.3158    6.7023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4729    1.0997    4.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6855   -1.0722    4.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6085    0.4951    2.2127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5727   -1.4760    0.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4451   -1.8085    2.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5087   -3.0666    3.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4213   -2.7358    1.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0453   -3.7140    1.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.0077    2.7193 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.6648    2.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2501    1.0601    0.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0016    1.6905   -1.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3891    2.7156    1.8132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6832    3.3286    0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0069    3.4949    0.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5394    1.7016    1.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1277   -0.0202   -0.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7643    1.3996    0.3374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7472    2.0998   -1.7776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5323    1.2207   -2.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0577    2.6311   -1.7466 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8537   -0.3690   -2.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0708   -2.1158   -0.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5118   -2.4124   -0.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5450   -5.4145   -3.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9557   -4.5848   -3.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1616   -5.8884   -2.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 13  1  0
  3  2  1  0
 13 12  2  0
  2  1  1  0
 13 14  1  0
  9  8  1  1
 17 18  1  0
  9 23  1  0
 14 15  1  0
 16 17  1  0
 18 20  1  0
  9 12  1  0
 20 21  1  0
  8  5  1  0
 18 19  2  0
 23 22  1  0
  5  6  1  0
  5  4  1  0
  6  7  1  0
 22 16  1  0
  9 10  1  0
  4  3  2  0
 10 11  1  0
 16 50  1  6
 12 44  1  0
  8 37  1  0
  8 38  1  0
 17 51  1  0
 17 52  1  0
  5 31  1  6
  4 30  1  0
  3 29  1  0
  2 27  1  0
  2 28  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 15 49  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 11 43  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₉H₃₂O₄

Average Mass

324.4610 Da

Monoisotopic Mass

324.23006 Da

IUPAC Name

methyl 2-[(3R,6S)-4,6-diethyl-6-[(2R,3E)-2-ethylhex-3-en-1-yl]-3,6-dihydro-1,2-dioxin-3-yl]acetate

Traditional Name

methyl [(3R,6S)-4,6-diethyl-6-[(2R,3E)-2-ethylhex-3-en-1-yl]-3H-1,2-dioxin-3-yl]acetate

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])[C@]([H])(C([H])([H])C([H])([H])[H])C([H])([H])[C@@]1(OO[C@@]([H])(C(=C1[H])C([H])([H])C([H])([H])[H])C([H])([H])C(=O)OC([H])([H])[H])C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])[H]

InChI Identifier

InChI=1S/C19H32O4/c1-6-10-11-15(7-2)13-19(9-4)14-16(8-3)17(22-23-19)12-18(20)21-5/h10-11,14-15,17H,6-9,12-13H2,1-5H3/b11-10+/t15-,17+,19-/m0/s1

InChI Key

SVIKESJVLMSASY-SEQSLPPWSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Plakinastrella mamillaris	JEOL database	Festa, C., et al, Tetrahedron 69, 3706 (2013)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methyl esters. These are organic compounds containing a carboxyl group that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=H or organyl group and R'=methyl group.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acid derivatives

Direct Parent

Methyl esters

Alternative Parents

Substituents

Methyl ester
Dialkyl peroxide
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	5.52	ALOGPS
logP	5.16	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	93.32 m³·mol⁻¹	ChemAxon
Polarizability	38.31 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

29215616

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71658055

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Festa, C., et al. (2013). Festa, C., et al, Tetrahedron 69, 3706 (2013). Tetrahedron.

Showing NP-Card for plakortide R (NP0042194)

MOL for NP0042194 (plakortide R)

3D MOL for NP0042194 (plakortide R)

3D SDF for NP0042194 (plakortide R)

3D-SDF for NP0042194 (plakortide R)

PDB for NP0042194 (plakortide R)

3D PDB for NP0042194 (plakortide R)

SMILES for NP0042194 (plakortide R)

INCHI for NP0042194 (plakortide R)

Structure for NP0042194 (plakortide R)

3D Structure for NP0042194 (plakortide R)