NP-MRD: Showing NP-Card for (+)-Peritassine A (NP0081130)

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Record Information

Version

2.0

Created at

2022-04-29 02:05:49 UTC

Updated at

2022-04-29 02:05:49 UTC

NP-MRD ID

NP0081130

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Peritassine A

Description

[(1S,3R,13R,14S,17R,18S,19R,20R,21S,22R,23R,24S,25S)-18,19,21,22,24-pentakis(acetyloxy)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-9-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]Pentacosa-7,9,11-trien-20-yl]methyl acetate belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (+)-Peritassine A is found in Tripterygium wilfordii . Based on a literature review very few articles have been published on [(1S,3R,13R,14S,17R,18S,19R,20R,21S,22R,23R,24S,25S)-18,19,21,22,24-pentakis(acetyloxy)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-9-azapentacyclo[15.7.1.0¹,²⁰.0³,²³.0⁷,¹²]Pentacosa-7,9,11-trien-20-yl]methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292204052D          

 57 61  0  0  1  0            999 V2000
    0.3242   -1.5479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0983   -0.7787    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4690   -0.0356    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3145   -0.0204    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6606   -0.8391    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1462   -1.6109    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9782   -2.7341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5074   -3.6968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7842   -4.5540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2103   -4.1626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5213   -0.9554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0169   -0.2750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6694    0.5029    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9848    0.2260    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4926   -0.2829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1533   -0.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6976   -0.1246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7769   -1.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1879    1.2101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3577    0.8874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8469    2.0209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9666    1.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7914    1.3562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2201    0.6124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5602    1.4930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3305   -0.2432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1221   -1.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5133   -1.7206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6538   -1.9402    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7056   -1.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8747   -2.1190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9709   -1.0594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0045   -2.8476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1996   -2.6802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7093   -1.6210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048   -1.4023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7131   -0.6041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0729    0.0794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    0.4438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8936    0.7254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4887    1.4334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0471   -1.9586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4392   -2.7942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3771   -3.7079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6746   -3.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2374   -1.4740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1453   -1.4506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8561   -2.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8285   -2.6517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8672   -3.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4211    0.0508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0716    0.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5870   -1.7400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4743   -1.7265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0765   -2.3460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0561   -1.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
  4 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
  4 20  1  6  0  0  0
 19 21  1  6  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  2 32  1  1  0  0  0
 29 33  1  6  0  0  0
 28 34  1  6  0  0  0
 27 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 26 38  1  0  0  0  0
 12 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 11 43  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
  5 47  1  1  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
  3 52  1  6  0  0  0
  3 53  1  0  0  0  0
  1 54  1  6  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 55 57  1  0  0  0  0
M  END

     RDKit          3D

104108  0  0  0  0  0  0  0  0999 V2000
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   -3.4000   -0.3891   -1.1743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8216   -0.1292   -2.4650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2737    0.1539   -2.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6828    1.3026   -1.4267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0098    4.1462   -1.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0328    4.8825   -2.3540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2063    3.6280   -2.8278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3468    2.0162    2.7670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7835    0.3115    3.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7648    1.0432    3.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8895   -0.2879    3.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
 38 37  1  0
 37 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  2  0
 41 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 47 49  2  0
 45 50  1  0
 50 51  1  0
 51 52  1  0
 52 53  1  0
 52 54  2  0
 50  6  1  0
  6  5  1  1
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
  7 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 12 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 18 23  1  0
 23 24  1  6
 24 25  1  0
 25 26  1  6
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 31 36  2  0
 36 35  1  0
 35 34  2  0
 34 33  1  0
 33 32  2  0
 23 55  1  0
 55 56  1  0
 55 57  1  1
 36 37  1  0
 55 44  1  0
 23  6  1  0
 32 31  1  0
 25 17  1  0
 38 85  1  0
 38 86  1  0
 38 87  1  0
 37 84  1  1
 39 88  1  6
 40 89  1  0
 40 90  1  0
 40 91  1  0
 44 92  1  6
 45 93  1  1
 48 94  1  0
 48 95  1  0
 48 96  1  0
 50 97  1  6
 53 98  1  0
 53 99  1  0
 53100  1  0
  5 61  1  0
  5 62  1  0
  1 58  1  0
  1 59  1  0
  1 60  1  0
  7 63  1  6
 10 64  1  0
 10 65  1  0
 10 66  1  0
 12 67  1  6
 15 68  1  0
 15 69  1  0
 15 70  1  0
 17 71  1  1
 18 72  1  1
 21 73  1  0
 21 74  1  0
 21 75  1  0
 26 76  1  0
 26 77  1  0
 26 78  1  0
 27 79  1  0
 27 80  1  0
 35 83  1  0
 34 82  1  0
 32 81  1  0
 56101  1  0
 56102  1  0
 56103  1  0
 57104  1  0
M  END


  Mrv1652304292204052D          

 57 61  0  0  1  0            999 V2000
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    0.0983   -0.7787    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4690   -0.0356    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3145   -0.0204    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6606   -0.8391    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1462   -1.6109    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9782   -2.7341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5074   -3.6968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7842   -4.5540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2103   -4.1626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5213   -0.9554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0169   -0.2750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6694    0.5029    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9848    0.2260    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4926   -0.2829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1533   -0.7925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6976   -0.1246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7769   -1.3918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1879    1.2101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3577    0.8874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8469    2.0209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9666    1.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7914    1.3562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2201    0.6124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5602    1.4930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3305   -0.2432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1221   -1.0414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5133   -1.7206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6538   -1.9402    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7056   -1.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8747   -2.1190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9709   -1.0594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0045   -2.8476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1996   -2.6802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7093   -1.6210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048   -1.4023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7131   -0.6041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0729    0.0794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    0.4438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8936    0.7254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4887    1.4334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0471   -1.9586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4392   -2.7942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3771   -3.7079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6746   -3.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2374   -1.4740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1453   -1.4506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8561   -2.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8285   -2.6517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8672   -3.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4211    0.0508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0716    0.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5870   -1.7400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4743   -1.7265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0765   -2.3460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0561   -1.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
  4 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
  4 20  1  6  0  0  0
 19 21  1  6  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  2 32  1  1  0  0  0
 29 33  1  6  0  0  0
 28 34  1  6  0  0  0
 27 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 26 38  1  0  0  0  0
 12 39  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 11 43  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
  5 47  1  1  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
  3 52  1  6  0  0  0
  3 53  1  0  0  0  0
  1 54  1  6  0  0  0
 54 55  1  0  0  0  0
 55 56  2  0  0  0  0
 55 57  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0081130

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@H](C)C(=O)O[C@@H]2[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@]3(COC(C)=O)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@@H]4[C@H](OC(C)=O)[C@]3(O[C@@]4(C)COC(=O)C3=C1C=CN=C3)[C@@]2(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C38H47NO18/c1-16-17(2)33(46)56-30-28(52-20(5)42)32(55-23(8)45)37(15-49-18(3)40)31(54-22(7)44)27(51-19(4)41)26-29(53-21(6)43)38(37,36(30,10)48)57-35(26,9)14-50-34(47)25-13-39-12-11-24(16)25/h11-13,16-17,26-32,48H,14-15H2,1-10H3/t16-,17+,26-,27-,28-,29+,30-,31-,32+,35+,36+,37-,38+/m1/s1

> <INCHI_KEY>
XVCIECFQBMGYAF-BUZDURJNSA-N

> <FORMULA>
C38H47NO18

> <MOLECULAR_WEIGHT>
805.783

> <EXACT_MASS>
805.279313677

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
77.83975320827787

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1S,3R,13R,14S,17R,18S,19R,20R,21S,22R,23R,24S,25S)-18,19,21,22,24-pentakis(acetyloxy)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-9-azapentacyclo[15.7.1.0^{1,20}.0^{3,23}.0^{7,12}]pentacosa-7(12),8,10-trien-20-yl]methyl acetate

> <ALOGPS_LOGP>
2.00

> <JCHEM_LOGP>
-0.37286204866666395

> <ALOGPS_LOGS>
-3.41

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.73527641239195

> <JCHEM_PKA_STRONGEST_BASIC>
3.179110538287778

> <JCHEM_POLAR_SURFACE_AREA>
252.74999999999991

> <JCHEM_REFRACTIVITY>
183.1945

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.12e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,3R,13R,14S,17R,18S,19R,20R,21S,22R,23R,24S,25S)-18,19,21,22,24-pentakis(acetyloxy)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-9-azapentacyclo[15.7.1.0^{1,20}.0^{3,23}.0^{7,12}]pentacosa-7(12),8,10-trien-20-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       0.605  -2.889   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.183  -1.454   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.875  -0.066   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.454  -0.038   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.100  -1.566   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.140  -3.007   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.956  -5.114   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.232  -6.974   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.747  -8.543   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.138  -7.803   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.706  -1.783   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.631  -0.513   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.983   0.939   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.705   0.422   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.719  -0.421   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.888  -1.511   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.456  -1.020   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.141  -2.820   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.084   2.259   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.534   1.656   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.447   3.772   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.538   2.983   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.077   2.532   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.877   1.143   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.570   2.741   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.084  -0.454   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.695  -1.944   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.558  -3.212   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.954  -3.622   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.184  -3.104   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.611  -3.935   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       1.812  -1.978   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.877  -5.351   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.781  -4.816   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.791  -3.026   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.276  -2.618   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0      10.665  -1.128   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0       9.470   0.148   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.133   0.591   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       9.172   1.243   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      10.337   2.496   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      10.627   0.042   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       5.749  -3.837   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       4.742  -5.567   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       4.489  -7.223   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       3.091  -5.822   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.163  -2.716   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       6.061  -2.522   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       7.051  -4.264   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       8.901  -4.789   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       6.864  -5.902   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      -0.784   0.086   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       0.120   1.417   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      -1.099  -3.273   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      -2.756  -3.346   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      -3.859  -4.522   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0      -3.677  -2.066   0.000  0.00  0.00           C+0
CONECT    1    2    6   54                                                  
CONECT    2    1    3   32                                                  
CONECT    3    2    4   52   53                                             
CONECT    4    3    5   14   20                                             
CONECT    5    4    6   11   47                                             
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    5   12   43                                                  
CONECT   12   11   13   39                                                  
CONECT   13   12   14   19                                                  
CONECT   14   13    4   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   13   20   21   22                                             
CONECT   20   19    4                                                       
CONECT   21   19                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   38                                                  
CONECT   27   26   28   35                                                  
CONECT   28   27   29   34                                                  
CONECT   29   28   30   33                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    2                                                       
CONECT   33   29                                                            
CONECT   34   28                                                            
CONECT   35   27   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   26                                                       
CONECT   39   12   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   11   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47    5   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
CONECT   52    3                                                            
CONECT   53    3                                                            
CONECT   54    1   55                                                       
CONECT   55   54   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  122    0
END

View in JSmol

Synonyms

Value	Source
[(1S,3R,13R,14S,17R,18S,19R,20R,21S,22R,23R,24S,25S)-18,19,21,22,24-Pentakis(acetyloxy)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-9-azapentacyclo[15.7.1.0,.0,.0,]pentacosa-7,9,11-trien-20-yl]methyl acetic acid	Generator

Chemical Formula

C₃₈H₄₇NO₁₈

Average Mass

805.7830 Da

Monoisotopic Mass

805.27931 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@H](C)C(=O)O[C@@H]2[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@]3(COC(C)=O)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@@H]4[C@H](OC(C)=O)[C@]3(O[C@@]4(C)COC(=O)C3=C1C=CN=C3)[C@@]2(C)O

InChI Identifier

InChI=1S/C38H47NO18/c1-16-17(2)33(46)56-30-28(52-20(5)42)32(55-23(8)45)37(15-49-18(3)40)31(54-22(7)44)27(51-19(4)41)26-29(53-21(6)43)38(37,36(30,10)48)57-35(26,9)14-50-34(47)25-13-39-12-11-24(16)25/h11-13,16-17,26-32,48H,14-15H2,1-10H3/t16-,17+,26-,27-,28-,29+,30-,31-,32+,35+,36+,37-,38+/m1/s1

InChI Key

XVCIECFQBMGYAF-BUZDURJNSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Tripterygium wilfordii	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Agarofuran
Pyridine carboxylic acid
Oxepane
Pyridine
Monosaccharide
Heteroaromatic compound
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Lactone
Carboxylic acid ester
Oxacycle
Azacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2	ALOGPS
logP	-0.37	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	12.74	ChemAxon
pKa (Strongest Basic)	3.18	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	252.75 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	183.19 m³·mol⁻¹	ChemAxon
Polarizability	77.84 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162891613

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Peritassine A (NP0081130)

MOL for NP0081130 ((+)-Peritassine A)

3D MOL for NP0081130 ((+)-Peritassine A)

3D SDF for NP0081130 ((+)-Peritassine A)

3D-SDF for NP0081130 ((+)-Peritassine A)

PDB for NP0081130 ((+)-Peritassine A)

3D PDB for NP0081130 ((+)-Peritassine A)

SMILES for NP0081130 ((+)-Peritassine A)

INCHI for NP0081130 ((+)-Peritassine A)

Structure for NP0081130 ((+)-Peritassine A)

3D Structure for NP0081130 ((+)-Peritassine A)