NP-MRD: Showing NP-Card for (7S,11S,12S,14R)-4',14-dimethoxyamentol (NP0006349)

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Record Information

Version

2.0

Created at

2020-12-09 03:23:20 UTC

Updated at

2021-07-15 16:54:32 UTC

NP-MRD ID

NP0006349

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(7S,11S,12S,14R)-4',14-dimethoxyamentol

Provided By

NPAtlas

Description

2-[(2E)-3-{[(1S,4'R,4aS,7aS)-4'-methoxy-4a,5',5',7a-tetramethyl-5,6,7,7a-tetrahydro-4aH-spiro[cyclopenta[c]pyran-1,2'-oxolane]-3-yl]methyl}but-2-en-1-yl]-4-methoxy-6-methylphenol belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. (7S,11S,12S,14R)-4',14-dimethoxyamentol is found in Cystophora. Based on a literature review very few articles have been published on 2-[(2E)-3-{[(1S,4'R,4aS,7aS)-4'-methoxy-4a,5',5',7a-tetramethyl-5,6,7,7a-tetrahydro-4aH-spiro[cyclopenta[c]pyran-1,2'-oxolane]-3-yl]methyl}but-2-en-1-yl]-4-methoxy-6-methylphenol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652307012119043D          

 76 79  0  0  0  0            999 V2000
    7.3898    1.1741   -1.5484 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2981    0.2154   -0.5164 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1553    0.1771    0.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -0.7389    1.2757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9011   -0.7786    2.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7756   -1.7703    3.1339 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779    0.1005    1.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6931    0.1126    2.5773 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9721    1.0327    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9070    2.0216    0.5051 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7750    1.3919   -0.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4745    1.8407   -1.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917    2.9504   -1.9903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3650    1.2701   -2.2205 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3497    0.1836   -1.5325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4000   -1.0285   -2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1476   -2.0645   -1.2939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2380   -2.7466   -0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6481   -3.1285   -2.2547 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0847   -2.8173   -2.5469 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3612   -1.4943   -1.8519 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4020   -1.5531   -0.6746 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9214   -2.6062    0.2772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2815   -0.1980   -0.0214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5679   -0.2012    1.4449 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9255    0.4982    1.4953 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1525    1.1664    2.6716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3636    0.7503    3.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7746    1.4556    0.3281 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1187    1.9609   -0.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9509    2.6196    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2095    0.6699   -0.6301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0020    0.3216   -0.3258 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1188    1.0472    0.0561 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3417    1.1391   -2.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5480    0.9589   -2.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3046    2.8913   -0.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321    0.5836    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3758    2.7123   -2.0404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0043    3.1199   -3.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    3.8529   -1.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7914    0.8705   -3.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3160    2.0956   -2.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761   -1.2261   -3.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547   -3.7637   -0.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7390   -2.8746   -0.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5046   -4.1486   -1.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0344   -3.0534   -3.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7820   -3.6078   -2.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2035   -2.6587   -3.6547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4092   -1.4065   -1.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0276   -0.6939   -2.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0983   -3.5235   -0.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8775   -2.3610    0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1343   -2.9361    1.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5846   -1.1742    1.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8395    0.5100    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7541   -0.1983    1.2964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3500   -0.3290    3.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5960    1.3031    4.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2120    0.9617    2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9805    2.3145   -1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8501    1.1391   -0.1463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4208    2.8408    0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9093    3.4386    0.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9403    2.3758    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4706    3.0711    1.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2129    1.7730   -0.7398 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 24 33  1  1  0  0  0
  9 34  2  0  0  0  0
 34  3  1  0  0  0  0
 33 15  1  0  0  0  0
 22 17  1  0  0  0  0
 32 24  1  0  0  0  0
  1 35  1  0  0  0  0
  1 36  1  0  0  0  0
  1 37  1  0  0  0  0
  4 38  1  0  0  0  0
  6 39  1  0  0  0  0
  6 40  1  0  0  0  0
  6 41  1  0  0  0  0
  8 42  1  0  0  0  0
 10 43  1  0  0  0  0
 10 44  1  0  0  0  0
 11 45  1  0  0  0  0
 13 46  1  0  0  0  0
 13 47  1  0  0  0  0
 13 48  1  0  0  0  0
 14 49  1  0  0  0  0
 14 50  1  0  0  0  0
 16 51  1  0  0  0  0
 18 52  1  0  0  0  0
 18 53  1  0  0  0  0
 18 54  1  0  0  0  0
 19 55  1  0  0  0  0
 19 56  1  0  0  0  0
 20 57  1  0  0  0  0
 20 58  1  0  0  0  0
 21 59  1  0  0  0  0
 21 60  1  0  0  0  0
 23 61  1  0  0  0  0
 23 62  1  0  0  0  0
 23 63  1  0  0  0  0
 25 64  1  0  0  0  0
 25 65  1  0  0  0  0
 26 66  1  6  0  0  0
 28 67  1  0  0  0  0
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 30 70  1  0  0  0  0
 30 71  1  0  0  0  0
 30 72  1  0  0  0  0
 31 73  1  0  0  0  0
 31 74  1  0  0  0  0
 31 75  1  0  0  0  0
 34 76  1  0  0  0  0
M  END

     RDKit          3D

 76 79  0  0  0  0  0  0  0  0999 V2000
    7.3898    1.1741   -1.5484 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2981    0.2154   -0.5164 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1553    0.1771    0.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -0.7389    1.2757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9011   -0.7786    2.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7756   -1.7703    3.1339 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779    0.1005    1.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6931    0.1126    2.5773 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9721    1.0327    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9070    2.0216    0.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7750    1.3919   -0.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4745    1.8407   -1.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917    2.9504   -1.9903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3650    1.2701   -2.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3497    0.1836   -1.5325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4000   -1.0285   -2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1476   -2.0645   -1.2939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2380   -2.7466   -0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6481   -3.1285   -2.2547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0847   -2.8173   -2.5469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3612   -1.4943   -1.8519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4020   -1.5531   -0.6746 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9214   -2.6062    0.2772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2815   -0.1980   -0.0214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5679   -0.2012    1.4449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9255    0.4982    1.4953 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1525    1.1664    2.6716 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1187    1.9609   -0.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0020    0.3216   -0.3258 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1188    1.0472    0.0561 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5480    0.9589   -2.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1895    2.2109   -1.1752 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8114   -1.4510    1.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7492   -2.2364    3.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9801   -1.2755    4.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4666   -2.6085    2.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5649   -0.5567    3.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4778    2.3275    1.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3046    2.8913   -0.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321    0.5836    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3758    2.7123   -2.0404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0043    3.1199   -3.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0983   -3.5235   -0.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1343   -2.9361    1.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5846   -1.1742    1.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8395    0.5100    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7541   -0.1983    1.2964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3500   -0.3290    3.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5960    1.3031    4.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2120    0.9617    2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9805    2.3145   -1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8501    1.1391   -0.1463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4208    2.8408    0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9093    3.4386    0.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9403    2.3758    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4706    3.0711    1.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2129    1.7730   -0.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  1  0
 29 30  1  6
 29 31  1  0
 29 32  1  0
 24 33  1  1
  9 34  2  0
 34  3  1  0
 33 15  1  0
 22 17  1  0
 32 24  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  0
  6 39  1  0
  6 40  1  0
  6 41  1  0
  8 42  1  0
 10 43  1  0
 10 44  1  0
 11 45  1  0
 13 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 16 51  1  0
 18 52  1  0
 18 53  1  0
 18 54  1  0
 19 55  1  0
 19 56  1  0
 20 57  1  0
 20 58  1  0
 21 59  1  0
 21 60  1  0
 23 61  1  0
 23 62  1  0
 23 63  1  0
 25 64  1  0
 25 65  1  0
 26 66  1  6
 28 67  1  0
 28 68  1  0
 28 69  1  0
 30 70  1  0
 30 71  1  0
 30 72  1  0
 31 73  1  0
 31 74  1  0
 31 75  1  0
 34 76  1  0
M  END


  Mrv1652307012119043D          

 76 79  0  0  0  0            999 V2000
    7.3898    1.1741   -1.5484 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2981    0.2154   -0.5164 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1553    0.1771    0.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -0.7389    1.2757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9011   -0.7786    2.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7756   -1.7703    3.1339 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779    0.1005    1.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6931    0.1126    2.5773 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9721    1.0327    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9070    2.0216    0.5051 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7750    1.3919   -0.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4745    1.8407   -1.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917    2.9504   -1.9903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3650    1.2701   -2.2205 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3497    0.1836   -1.5325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4000   -1.0285   -2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1476   -2.0645   -1.2939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2380   -2.7466   -0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6481   -3.1285   -2.2547 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0847   -2.8173   -2.5469 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3612   -1.4943   -1.8519 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4020   -1.5531   -0.6746 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9214   -2.6062    0.2772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2815   -0.1980   -0.0214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5679   -0.2012    1.4449 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9255    0.4982    1.4953 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1525    1.1664    2.6716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3636    0.7503    3.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7746    1.4556    0.3281 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1187    1.9609   -0.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9509    2.6196    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2095    0.6699   -0.6301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0020    0.3216   -0.3258 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1188    1.0472    0.0561 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3417    1.1391   -2.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5480    0.9589   -2.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1895    2.2109   -1.1752 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8114   -1.4510    1.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7492   -2.2364    3.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9801   -1.2755    4.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4666   -2.6085    2.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5649   -0.5567    3.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4778    2.3275    1.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3046    2.8913   -0.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321    0.5836    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3758    2.7123   -2.0404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0043    3.1199   -3.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    3.8529   -1.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7914    0.8705   -3.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3160    2.0956   -2.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761   -1.2261   -3.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547   -3.7637   -0.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777   -2.2408    0.6749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7390   -2.8746   -0.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5046   -4.1486   -1.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0344   -3.0534   -3.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7820   -3.6078   -2.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2035   -2.6587   -3.6547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4092   -1.4065   -1.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0276   -0.6939   -2.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0983   -3.5235   -0.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8775   -2.3610    0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1343   -2.9361    1.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5846   -1.1742    1.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8395    0.5100    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7541   -0.1983    1.2964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3500   -0.3290    3.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5960    1.3031    4.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2120    0.9617    2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9805    2.3145   -1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8501    1.1391   -0.1463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4208    2.8408    0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9093    3.4386    0.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9403    2.3758    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4706    3.0711    1.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2129    1.7730   -0.7398 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 24 33  1  1  0  0  0
  9 34  2  0  0  0  0
 34  3  1  0  0  0  0
 33 15  1  0  0  0  0
 22 17  1  0  0  0  0
 32 24  1  0  0  0  0
  1 35  1  0  0  0  0
  1 36  1  0  0  0  0
  1 37  1  0  0  0  0
  4 38  1  0  0  0  0
  6 39  1  0  0  0  0
  6 40  1  0  0  0  0
  6 41  1  0  0  0  0
  8 42  1  0  0  0  0
 10 43  1  0  0  0  0
 10 44  1  0  0  0  0
 11 45  1  0  0  0  0
 13 46  1  0  0  0  0
 13 47  1  0  0  0  0
 13 48  1  0  0  0  0
 14 49  1  0  0  0  0
 14 50  1  0  0  0  0
 16 51  1  0  0  0  0
 18 52  1  0  0  0  0
 18 53  1  0  0  0  0
 18 54  1  0  0  0  0
 19 55  1  0  0  0  0
 19 56  1  0  0  0  0
 20 57  1  0  0  0  0
 20 58  1  0  0  0  0
 21 59  1  0  0  0  0
 21 60  1  0  0  0  0
 23 61  1  0  0  0  0
 23 62  1  0  0  0  0
 23 63  1  0  0  0  0
 25 64  1  0  0  0  0
 25 65  1  0  0  0  0
 26 66  1  6  0  0  0
 28 67  1  0  0  0  0
 28 68  1  0  0  0  0
 28 69  1  0  0  0  0
 30 70  1  0  0  0  0
 30 71  1  0  0  0  0
 30 72  1  0  0  0  0
 31 73  1  0  0  0  0
 31 74  1  0  0  0  0
 31 75  1  0  0  0  0
 34 76  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0006349

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C([H])=C(OC([H])([H])[H])C([H])=C1C([H])([H])C(\[H])=C(/C([H])([H])[H])C([H])([H])C1=C([H])[C@]2(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]2(C([H])([H])[H])[C@]2(OC(C([H])([H])[H])(C([H])([H])[H])[C@]([H])(OC([H])([H])[H])C2([H])[H])O1)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C29H42O5/c1-19(10-11-21-16-22(31-7)15-20(2)25(21)30)14-23-17-27(5)12-9-13-28(27,6)29(33-23)18-24(32-8)26(3,4)34-29/h10,15-17,24,30H,9,11-14,18H2,1-8H3/b19-10+/t24-,27+,28+,29+/m1/s1

> <INCHI_KEY>
PLIQXOWNZPNPRH-CDTDPFSWSA-N

> <FORMULA>
C29H42O5

> <MOLECULAR_WEIGHT>
470.65

> <EXACT_MASS>
470.303224452

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
52.9834691732437

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(2E)-3-{[(1S,4'R,4aS,7aS)-4'-methoxy-4a,5',5',7a-tetramethyl-5,6,7,7a-tetrahydro-4aH-spiro[cyclopenta[c]pyran-1,2'-oxolane]-3-yl]methyl}but-2-en-1-yl]-4-methoxy-6-methylphenol

> <ALOGPS_LOGP>
5.81

> <JCHEM_LOGP>
6.6157043873333325

> <ALOGPS_LOGS>
-5.88

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.110272545189398

> <JCHEM_PKA_STRONGEST_BASIC>
-3.858143213228177

> <JCHEM_POLAR_SURFACE_AREA>
57.150000000000006

> <JCHEM_REFRACTIVITY>
137.20700000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.20e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2E)-3-[(1S,4'R,4aS,7aS)-4'-methoxy-4a,5',5',7a-tetramethyl-6,7-dihydro-5H-spiro[cyclopenta[c]pyran-1,2'-oxolane]-3-ylmethyl]but-2-en-1-yl]-4-methoxy-6-methylphenol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 76 79  0  0  0  0  0  0  0  0999 V2000
    7.3898    1.1741   -1.5484 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2981    0.2154   -0.5164 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1553    0.1771    0.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -0.7389    1.2757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9011   -0.7786    2.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7756   -1.7703    3.1339 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779    0.1005    1.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6931    0.1126    2.5773 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9721    1.0327    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9070    2.0216    0.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7750    1.3919   -0.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4745    1.8407   -1.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917    2.9504   -1.9903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3650    1.2701   -2.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3497    0.1836   -1.5325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4000   -1.0285   -2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1476   -2.0645   -1.2939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2380   -2.7466   -0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6481   -3.1285   -2.2547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0847   -2.8173   -2.5469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3612   -1.4943   -1.8519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4020   -1.5531   -0.6746 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9214   -2.6062    0.2772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2815   -0.1980   -0.0214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5679   -0.2012    1.4449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9255    0.4982    1.4953 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1525    1.1664    2.6716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3636    0.7503    3.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7746    1.4556    0.3281 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1187    1.9609   -0.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9509    2.6196    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2095    0.6699   -0.6301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0020    0.3216   -0.3258 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1188    1.0472    0.0561 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3417    1.1391   -2.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5480    0.9589   -2.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1895    2.2109   -1.1752 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8114   -1.4510    1.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7492   -2.2364    3.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9801   -1.2755    4.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4666   -2.6085    2.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5649   -0.5567    3.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4778    2.3275    1.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3046    2.8913   -0.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321    0.5836    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3758    2.7123   -2.0404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0043    3.1199   -3.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    3.8529   -1.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7914    0.8705   -3.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3160    2.0956   -2.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761   -1.2261   -3.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547   -3.7637   -0.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777   -2.2408    0.6749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7390   -2.8746   -0.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5046   -4.1486   -1.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0344   -3.0534   -3.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7820   -3.6078   -2.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2035   -2.6587   -3.6547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4092   -1.4065   -1.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0276   -0.6939   -2.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0983   -3.5235   -0.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8775   -2.3610    0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1343   -2.9361    1.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5846   -1.1742    1.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8395    0.5100    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7541   -0.1983    1.2964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3500   -0.3290    3.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5960    1.3031    4.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2120    0.9617    2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9805    2.3145   -1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8501    1.1391   -0.1463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4208    2.8408    0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9093    3.4386    0.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9403    2.3758    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4706    3.0711    1.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2129    1.7730   -0.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  1  0
 29 30  1  6
 29 31  1  0
 29 32  1  0
 24 33  1  1
  9 34  2  0
 34  3  1  0
 33 15  1  0
 22 17  1  0
 32 24  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  0
  6 39  1  0
  6 40  1  0
  6 41  1  0
  8 42  1  0
 10 43  1  0
 10 44  1  0
 11 45  1  0
 13 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 16 51  1  0
 18 52  1  0
 18 53  1  0
 18 54  1  0
 19 55  1  0
 19 56  1  0
 20 57  1  0
 20 58  1  0
 21 59  1  0
 21 60  1  0
 23 61  1  0
 23 62  1  0
 23 63  1  0
 25 64  1  0
 25 65  1  0
 26 66  1  6
 28 67  1  0
 28 68  1  0
 28 69  1  0
 30 70  1  0
 30 71  1  0
 30 72  1  0
 31 73  1  0
 31 74  1  0
 31 75  1  0
 34 76  1  0
M  END

HEADER    PROTEIN                                 01-JUL-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-JUL-21         0                                  
HETATM    1  C   UNK     0       7.390   1.174  -1.548  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.298   0.215  -0.516  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.155   0.177   0.265  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.027  -0.739   1.276  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.901  -0.779   2.047  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.776  -1.770   3.134  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.878   0.101   1.821  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.693   0.113   2.577  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.972   1.033   0.815  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.907   2.022   0.505  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.775   1.392  -0.224  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.474   1.841  -1.435  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.292   2.950  -1.990  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.365   1.270  -2.220  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.350   0.184  -1.533  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.400  -1.028  -2.067  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.148  -2.064  -1.294  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.238  -2.747  -0.288  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.648  -3.128  -2.255  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.085  -2.817  -2.547  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.361  -1.494  -1.852  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.402  -1.553  -0.675  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.921  -2.606   0.277  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.281  -0.198  -0.021  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.568  -0.201   1.445  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.926   0.498   1.495  0.00  0.00           C+0
HETATM   27  O   UNK     0      -4.152   1.166   2.672  0.00  0.00           O+0
HETATM   28  C   UNK     0      -5.364   0.750   3.237  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.775   1.456   0.328  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.119   1.961  -0.151  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.951   2.620   0.775  0.00  0.00           C+0
HETATM   32  O   UNK     0      -3.209   0.670  -0.630  0.00  0.00           O+0
HETATM   33  O   UNK     0      -1.002   0.322  -0.326  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.119   1.047   0.056  0.00  0.00           C+0
HETATM   35  H   UNK     0       8.342   1.139  -2.082  0.00  0.00           H+0
HETATM   36  H   UNK     0       6.548   0.959  -2.259  0.00  0.00           H+0
HETATM   37  H   UNK     0       7.189   2.211  -1.175  0.00  0.00           H+0
HETATM   38  H   UNK     0       6.811  -1.451   1.489  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.749  -2.236   3.138  0.00  0.00           H+0
HETATM   40  H   UNK     0       4.980  -1.276   4.106  0.00  0.00           H+0
HETATM   41  H   UNK     0       5.467  -2.608   2.915  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.565  -0.557   3.338  0.00  0.00           H+0
HETATM   43  H   UNK     0       2.478   2.328   1.503  0.00  0.00           H+0
HETATM   44  H   UNK     0       3.305   2.891  -0.017  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.232   0.584   0.258  0.00  0.00           H+0
HETATM   46  H   UNK     0       3.376   2.712  -2.040  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.004   3.120  -3.070  0.00  0.00           H+0
HETATM   48  H   UNK     0       2.139   3.853  -1.391  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.791   0.871  -3.162  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.316   2.096  -2.542  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.076  -1.226  -3.001  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.655  -3.764  -0.140  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.178  -2.241   0.675  0.00  0.00           H+0
HETATM   54  H   UNK     0       0.739  -2.875  -0.779  0.00  0.00           H+0
HETATM   55  H   UNK     0      -1.505  -4.149  -1.839  0.00  0.00           H+0
HETATM   56  H   UNK     0      -1.034  -3.053  -3.184  0.00  0.00           H+0
HETATM   57  H   UNK     0      -3.782  -3.608  -2.273  0.00  0.00           H+0
HETATM   58  H   UNK     0      -3.204  -2.659  -3.655  0.00  0.00           H+0
HETATM   59  H   UNK     0      -4.409  -1.407  -1.524  0.00  0.00           H+0
HETATM   60  H   UNK     0      -3.028  -0.694  -2.534  0.00  0.00           H+0
HETATM   61  H   UNK     0      -3.098  -3.523  -0.354  0.00  0.00           H+0
HETATM   62  H   UNK     0      -3.878  -2.361   0.741  0.00  0.00           H+0
HETATM   63  H   UNK     0      -2.134  -2.936   1.010  0.00  0.00           H+0
HETATM   64  H   UNK     0      -2.585  -1.174   1.928  0.00  0.00           H+0
HETATM   65  H   UNK     0      -1.839   0.510   1.934  0.00  0.00           H+0
HETATM   66  H   UNK     0      -4.754  -0.198   1.296  0.00  0.00           H+0
HETATM   67  H   UNK     0      -5.350  -0.329   3.450  0.00  0.00           H+0
HETATM   68  H   UNK     0      -5.596   1.303   4.163  0.00  0.00           H+0
HETATM   69  H   UNK     0      -6.212   0.962   2.527  0.00  0.00           H+0
HETATM   70  H   UNK     0      -4.981   2.314  -1.184  0.00  0.00           H+0
HETATM   71  H   UNK     0      -5.850   1.139  -0.146  0.00  0.00           H+0
HETATM   72  H   UNK     0      -5.421   2.841   0.448  0.00  0.00           H+0
HETATM   73  H   UNK     0      -2.909   3.439   0.020  0.00  0.00           H+0
HETATM   74  H   UNK     0      -1.940   2.376   1.088  0.00  0.00           H+0
HETATM   75  H   UNK     0      -3.471   3.071   1.664  0.00  0.00           H+0
HETATM   76  H   UNK     0       5.213   1.773  -0.740  0.00  0.00           H+0
CONECT    1    2   35   36   37                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   34                                                  
CONECT    4    3    5   38                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   39   40   41                                             
CONECT    7    5    8    9                                                  
CONECT    8    7   42                                                       
CONECT    9    7   10   34                                                  
CONECT   10    9   11   43   44                                             
CONECT   11   10   12   45                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   46   47   48                                             
CONECT   14   12   15   49   50                                             
CONECT   15   14   16   33                                                  
CONECT   16   15   17   51                                                  
CONECT   17   16   18   19   22                                             
CONECT   18   17   52   53   54                                             
CONECT   19   17   20   55   56                                             
CONECT   20   19   21   57   58                                             
CONECT   21   20   22   59   60                                             
CONECT   22   21   23   24   17                                             
CONECT   23   22   61   62   63                                             
CONECT   24   22   25   33   32                                             
CONECT   25   24   26   64   65                                             
CONECT   26   25   27   29   66                                             
CONECT   27   26   28                                                       
CONECT   28   27   67   68   69                                             
CONECT   29   26   30   31   32                                             
CONECT   30   29   70   71   72                                             
CONECT   31   29   73   74   75                                             
CONECT   32   29   24                                                       
CONECT   33   24   15                                                       
CONECT   34    9    3   76                                                  
CONECT   35    1                                                            
CONECT   36    1                                                            
CONECT   37    1                                                            
CONECT   38    4                                                            
CONECT   39    6                                                            
CONECT   40    6                                                            
CONECT   41    6                                                            
CONECT   42    8                                                            
CONECT   43   10                                                            
CONECT   44   10                                                            
CONECT   45   11                                                            
CONECT   46   13                                                            
CONECT   47   13                                                            
CONECT   48   13                                                            
CONECT   49   14                                                            
CONECT   50   14                                                            
CONECT   51   16                                                            
CONECT   52   18                                                            
CONECT   53   18                                                            
CONECT   54   18                                                            
CONECT   55   19                                                            
CONECT   56   19                                                            
CONECT   57   20                                                            
CONECT   58   20                                                            
CONECT   59   21                                                            
CONECT   60   21                                                            
CONECT   61   23                                                            
CONECT   62   23                                                            
CONECT   63   23                                                            
CONECT   64   25                                                            
CONECT   65   25                                                            
CONECT   66   26                                                            
CONECT   67   28                                                            
CONECT   68   28                                                            
CONECT   69   28                                                            
CONECT   70   30                                                            
CONECT   71   30                                                            
CONECT   72   30                                                            
CONECT   73   31                                                            
CONECT   74   31                                                            
CONECT   75   31                                                            
CONECT   76   34                                                            
MASTER        0    0    0    0    0    0    0    0   76    0  158    0
END

RDKit          3D

76 79  0  0  0  0  0  0  0  0999 V2000
    7.3898    1.1741   -1.5484 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2981    0.2154   -0.5164 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1553    0.1771    0.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0272   -0.7389    1.2757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9011   -0.7786    2.0471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7756   -1.7703    3.1339 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8779    0.1005    1.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6931    0.1126    2.5773 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9721    1.0327    0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9070    2.0216    0.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7750    1.3919   -0.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4745    1.8407   -1.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2917    2.9504   -1.9903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3650    1.2701   -2.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3497    0.1836   -1.5325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4000   -1.0285   -2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1476   -2.0645   -1.2939 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2380   -2.7466   -0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6481   -3.1285   -2.2547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0847   -2.8173   -2.5469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3612   -1.4943   -1.8519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4020   -1.5531   -0.6746 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9214   -2.6062    0.2772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2815   -0.1980   -0.0214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5679   -0.2012    1.4449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9255    0.4982    1.4953 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1525    1.1664    2.6716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3636    0.7503    3.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7746    1.4556    0.3281 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1187    1.9609   -0.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9509    2.6196    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2095    0.6699   -0.6301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0020    0.3216   -0.3258 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1188    1.0472    0.0561 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3417    1.1391   -2.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5480    0.9589   -2.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1895    2.2109   -1.1752 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8114   -1.4510    1.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7492   -2.2364    3.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9801   -1.2755    4.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4666   -2.6085    2.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5649   -0.5567    3.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4778    2.3275    1.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3046    2.8913   -0.0167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321    0.5836    0.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3758    2.7123   -2.0404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0043    3.1199   -3.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1389    3.8529   -1.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7914    0.8705   -3.1618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3160    2.0956   -2.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761   -1.2261   -3.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6547   -3.7637   -0.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777   -2.2408    0.6749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7390   -2.8746   -0.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5046   -4.1486   -1.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0344   -3.0534   -3.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7820   -3.6078   -2.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2035   -2.6587   -3.6547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4092   -1.4065   -1.5239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0276   -0.6939   -2.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0983   -3.5235   -0.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8775   -2.3610    0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1343   -2.9361    1.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5846   -1.1742    1.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8395    0.5100    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7541   -0.1983    1.2964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3500   -0.3290    3.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5960    1.3031    4.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2120    0.9617    2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9805    2.3145   -1.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8501    1.1391   -0.1463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4208    2.8408    0.4484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9093    3.4386    0.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9403    2.3758    1.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4706    3.0711    1.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2129    1.7730   -0.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
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 14 15  1  0
 15 16  2  0
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 17 19  1  0
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  9 34  2  0
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 22 17  1  0
 32 24  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  0
  6 39  1  0
  6 40  1  0
  6 41  1  0
  8 42  1  0
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 34 76  1  0
M  END

View in JSmol View NMR Assignments View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₉H₄₂O₅

Average Mass

470.6500 Da

Monoisotopic Mass

470.30322 Da

IUPAC Name

2-[(2E)-3-{[(1S,4'R,4aS,7aS)-4'-methoxy-4a,5',5',7a-tetramethyl-5,6,7,7a-tetrahydro-4aH-spiro[cyclopenta[c]pyran-1,2'-oxolane]-3-yl]methyl}but-2-en-1-yl]-4-methoxy-6-methylphenol

Traditional Name

2-[(2E)-3-[(1S,4'R,4aS,7aS)-4'-methoxy-4a,5',5',7a-tetramethyl-6,7-dihydro-5H-spiro[cyclopenta[c]pyran-1,2'-oxolane]-3-ylmethyl]but-2-en-1-yl]-4-methoxy-6-methylphenol

CAS Registry Number

Not Available

SMILES

CO[C@@H]1C[C@@]2(OC1(C)C)OC(C\C(C)=C\CC1=C(O)C(C)=CC(OC)=C1)=C[C@]1(C)CCC[C@]21C

InChI Identifier

InChI=1S/C29H42O5/c1-19(10-11-21-16-22(31-7)15-20(2)25(21)30)14-23-17-27(5)12-9-13-28(27,6)29(33-23)18-24(32-8)26(3,4)34-29/h10,15-17,24,30H,9,11-14,18H2,1-8H3/b19-10+/t24-,27+,28+,29+/m1/s1

InChI Key

PLIQXOWNZPNPRH-CDTDPFSWSA-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
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
Cystophora	NPAtlas	16678228

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Methoxyphenol
4-alkoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
O-cresol
Alkyl aryl ether
Ketal
Toluene
Monocyclic benzene moiety
Monosaccharide
Oxolane
Acetal
Oxacycle
Dialkyl ether
Ether
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	5.81	ALOGPS
logP	6.62	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	10.11	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	57.15 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	137.21 m³·mol⁻¹	ChemAxon
Polarizability	52.98 Å³	ChemAxon
Number of Rings	4	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

NPAtlas ID

NPA015434

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10481395

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21778648

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (7S,11S,12S,14R)-4',14-dimethoxyamentol (NP0006349)

MOL for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

3D MOL for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

3D SDF for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

3D-SDF for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

PDB for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

3D PDB for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

SMILES for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

INCHI for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

Structure for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)

3D Structure for NP0006349 ((7S,11S,12S,14R)-4',14-dimethoxyamentol)