NP-MRD: Showing NP-Card for 14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone (NP0300329)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 12:40:23 UTC

Updated at

2022-09-10 12:40:23 UTC

NP-MRD ID

NP0300329

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone

Description

5Alpha-Ethoxy-6beta-hydroxy-5,6-dihydrophysalin B belongs to the class of organic compounds known as physalins and derivatives. These are steroidal constituents of Physalis plants which possess an unusual 13,14-seco-16,24-cyclo-steroidal ring skeleton (where the bond that is normally present between the 13 and 14 positions in other steroids is broken while a new bond between positions 16 and 24 is formed). 5Alpha-Ethoxy-6beta-hydroxy-5,6-dihydrophysalin B is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, 5alpha-ethoxy-6beta-hydroxy-5,6-dihydrophysalin b has been detected, but not quantified in, fruits. 14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone is found in Physalis minima. This could make 5alpha-ethoxy-6beta-hydroxy-5,6-dihydrophysalin b a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241207522D          

 41 48  0  0  0  0            999 V2000
   -3.5758   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5758   -0.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8601   -1.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1457   -0.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1457   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8601    0.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4300   -1.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7157   -0.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7157   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4300    0.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0027    0.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0027    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7157    1.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4300    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7101    1.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4245    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4245    0.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1374    1.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1374    2.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4245    2.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7101    2.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1374    3.1814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545    1.9472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545    2.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0896    2.5705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4164    1.8382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8601    1.1212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1457    0.7129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5874    0.5364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5819    0.8825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0092   -0.2868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5758    3.1814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7101   -0.1144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4245    1.9472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7101    3.1814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2162    2.0520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1457   -1.7693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4300   -2.1830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7305   -2.3539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7305   -3.1814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  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
  4  7  1  0  0  0  0
  4 38  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 28  1  0  0  0  0
  6 27  2  0  0  0  0
  7  8  1  0  0  0  0
  7 39  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 10 14  1  0  0  0  0
 11 17  1  0  0  0  0
 11 30  1  0  0  0  0
 11 34  1  0  0  0  0
 12 13  1  0  0  0  0
 12 15  1  0  0  0  0
 12 26  1  0  0  0  0
 12 29  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 15 21  1  0  0  0  0
 15 30  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 17 31  2  0  0  0  0
 18 19  1  0  0  0  0
 18 23  1  0  0  0  0
 18 35  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 21 25  1  0  0  0  0
 21 36  1  0  0  0  0
 22 24  1  0  0  0  0
 23 24  1  0  0  0  0
 23 33  1  0  0  0  0
 24 32  2  0  0  0  0
 25 26  1  0  0  0  0
 26 37  2  0  0  0  0
 33 34  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END

     RDKit          3D

 77 84  0  0  0  0  0  0  0  0999 V2000
    5.8401    1.4700    1.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6296    0.1335    0.5187 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7088    0.0973   -0.3718 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3977    0.2748   -0.4470 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1432    0.1308   -1.9939 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1933   -0.8437   -2.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1426   -1.9676   -1.7812 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405   -2.0664   -0.7272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6831   -3.2526   -0.5647 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6634   -0.9220    0.1083 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1786   -1.1844    1.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1408   -0.8036    0.0147 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5612   -1.7355    0.9922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7988   -2.2355    0.9291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6790   -1.9673   -0.2306 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0649   -2.3069   -1.4038 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9034   -2.8514   -0.1541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8998   -3.9462    0.4443 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8994   -2.2270   -0.8251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5258   -0.8800   -1.1657 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1971   -0.9013   -2.6227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7196   -0.0406   -0.9340 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9746    0.2834    0.5261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7054    1.0394    0.9693 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0103    1.4445    2.4214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4386    2.2253    0.1780 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2003    2.3951   -0.6041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9929    2.2536   -0.0007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7321    0.8725    0.2095 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4160    0.2330   -0.8201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3399   -0.6194   -0.2751 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6715   -0.0415    1.0577 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3704    0.5879    1.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0275    0.7719    2.5845 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7105    0.6039    0.0281 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6140    1.5120    0.8300 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8742    1.6092   -0.0455 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4300    2.3209   -1.1740 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5420    2.3483   -0.8537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2152    3.3922   -1.0030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7349    1.2040   -1.6124 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9109    2.3150    0.5694 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1294    1.5588    2.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8564    1.4443    1.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6389    0.1095   -0.0856 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8627   -0.7108    1.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2175   -0.3937   -2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2709    1.1168   -2.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8759   -0.6693   -3.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8329   -2.7959   -1.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4908   -1.6650    2.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6794   -0.3109    1.9498 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9870   -1.9711    1.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9015   -1.2300   -0.9891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2470   -2.6082    1.0395 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6602   -1.2540    2.0245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3470   -2.0848    1.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7773   -3.3812    0.9523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8938   -3.2737   -1.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8155   -1.9202   -2.9035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1742   -0.8162   -3.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5518   -0.1059   -2.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6183   -0.5971   -1.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0723   -0.6378    1.1139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8553    0.9230    0.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1023    1.6191    2.5542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7227    0.6433    3.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4109    2.3466    2.7005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5504    3.1647    0.8007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2303    3.4573   -1.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3014    1.7847   -1.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9723   -0.7582    1.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273    0.9941   -1.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8140    1.1886    1.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626    2.5286    0.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5385    2.2828    0.4766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    3.2964   -1.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  4  3  1  6
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  6
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  1
 24 32  1  0
 32 33  1  0
 33 34  2  0
 33 29  1  0
 29 30  1  0
 31 30  1  6
 29 28  1  6
 28 27  1  0
 27 26  1  0
 26 39  1  0
 39 40  2  0
 39 41  1  0
 29 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 10  4  1  0
 35 12  1  0
 37  4  1  0
 31 15  1  0
 31 20  1  0
 41 22  1  0
 26 24  1  0
 31 32  1  0
  1 42  1  0
  1 43  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  5 47  1  0
  5 48  1  0
  6 49  1  0
  7 50  1  0
 11 51  1  0
 11 52  1  0
 11 53  1  0
 12 54  1  6
 13 55  1  0
 13 56  1  0
 14 57  1  0
 14 58  1  0
 16 59  1  0
 21 60  1  0
 21 61  1  0
 21 62  1  0
 22 63  1  6
 23 64  1  0
 23 65  1  0
 25 66  1  0
 25 67  1  0
 25 68  1  0
 32 72  1  1
 27 70  1  0
 27 71  1  0
 26 69  1  1
 35 73  1  6
 36 74  1  0
 36 75  1  0
 37 76  1  1
 38 77  1  0
M  END


  Mrv0541 02241207522D          

 41 48  0  0  0  0            999 V2000
   -3.5758   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5758   -0.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8601   -1.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1457   -0.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1457   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8601    0.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4300   -1.3556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7157   -0.9419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7157   -0.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4300    0.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0027    0.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0027    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7157    1.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4300    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7101    1.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4245    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4245    0.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1374    1.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1374    2.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4245    2.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7101    2.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1374    3.1814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545    1.9472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545    2.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0896    2.5705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4164    1.8382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8601    1.1212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1457    0.7129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5874    0.5364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5819    0.8825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0092   -0.2868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5758    3.1814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545    1.1212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7101   -0.1144    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4245    1.9472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7101    3.1814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2162    2.0520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1457   -1.7693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4300   -2.1830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7305   -2.3539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7305   -3.1814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  6  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
  4  7  1  0  0  0  0
  4 38  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  5 28  1  0  0  0  0
  6 27  2  0  0  0  0
  7  8  1  0  0  0  0
  7 39  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 10 14  1  0  0  0  0
 11 17  1  0  0  0  0
 11 30  1  0  0  0  0
 11 34  1  0  0  0  0
 12 13  1  0  0  0  0
 12 15  1  0  0  0  0
 12 26  1  0  0  0  0
 12 29  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 15 21  1  0  0  0  0
 15 30  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 17 31  2  0  0  0  0
 18 19  1  0  0  0  0
 18 23  1  0  0  0  0
 18 35  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 21 25  1  0  0  0  0
 21 36  1  0  0  0  0
 22 24  1  0  0  0  0
 23 24  1  0  0  0  0
 23 33  1  0  0  0  0
 24 32  2  0  0  0  0
 25 26  1  0  0  0  0
 26 37  2  0  0  0  0
 33 34  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0300329

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC12CC=CC(=O)C1(C)C1CCC3(O)C(=O)OC4(C)C5CC6(C)C7C(=O)C(OC347)(OCC6C(=O)O5)C1CC2O

> <INCHI_IDENTIFIER>
InChI=1S/C30H36O11/c1-5-37-28-9-6-7-17(31)25(28,3)14-8-10-27(36)23(35)40-26(4)19-12-24(2)16(22(34)39-19)13-38-29(15(14)11-18(28)32)21(33)20(24)30(26,27)41-29/h6-7,14-16,18-20,32,36H,5,8-13H2,1-4H3

> <INCHI_KEY>
GCRPDPKXRPYCEV-UHFFFAOYSA-N

> <FORMULA>
C30H36O11

> <MOLECULAR_WEIGHT>
572.6002

> <EXACT_MASS>
572.225761994

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_AVERAGE_POLARIZABILITY>
56.36371943147399

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone

> <ALOGPS_LOGP>
1.51

> <JCHEM_LOGP>
1.756231060333333

> <ALOGPS_LOGS>
-2.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.528177316491435

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.676481151155816

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2665814887028555

> <JCHEM_POLAR_SURFACE_AREA>
154.89

> <JCHEM_REFRACTIVITY>
137.24099999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.15e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -6.675  -0.214   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.675  -1.758   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.339  -2.530   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.005  -1.758   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.005  -0.214   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.339   0.556   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.669  -2.530   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.336  -1.758   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.336  -0.214   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.669   0.556   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.005   0.556   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.005   2.093   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.336   2.860   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.669   2.093   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.326   2.860   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.659   2.093   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.659   0.556   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.990   2.860   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.990   4.399   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.659   5.166   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.326   4.399   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.990   5.939   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.328   3.635   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.328   5.166   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.167   4.798   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.777   3.431   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -5.339   2.093   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -4.005   1.331   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.096   1.001   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       1.086   1.647   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       3.751  -0.535   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       6.675   5.939   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.328   2.093   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       1.326  -0.214   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       2.659   3.635   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.326   5.939   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -2.270   3.830   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -4.005  -3.303   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -2.669  -4.075   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -5.097  -4.394   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -5.097  -5.939   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7   38                                             
CONECT    5    4    6   10   28                                             
CONECT    6    1    5   27                                                  
CONECT    7    4    8   39                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    5    9   14                                                  
CONECT   11    9   17   30   34                                             
CONECT   12   13   15   26   29                                             
CONECT   13   12   14                                                       
CONECT   14   10   13                                                       
CONECT   15   12   16   21   30                                             
CONECT   16   15   17   18                                                  
CONECT   17   11   16   31                                                  
CONECT   18   16   19   23   35                                             
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   15   20   25   36                                             
CONECT   22   20   24                                                       
CONECT   23   18   24   33                                                  
CONECT   24   22   23   32                                                  
CONECT   25   21   26                                                       
CONECT   26   12   25   37                                                  
CONECT   27    6                                                            
CONECT   28    5                                                            
CONECT   29   12                                                            
CONECT   30   11   15                                                       
CONECT   31   17                                                            
CONECT   32   24                                                            
CONECT   33   23   34                                                       
CONECT   34   11   33                                                       
CONECT   35   18                                                            
CONECT   36   21                                                            
CONECT   37   26                                                            
CONECT   38    4   40                                                       
CONECT   39    7                                                            
CONECT   40   38   41                                                       
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   96    0
END

View in JSmol

Synonyms

Value	Source
5a-Ethoxy-6b-hydroxy-5,6-dihydrophysalin b	Generator
5Α-ethoxy-6β-hydroxy-5,6-dihydrophysalin b	Generator

Chemical Formula

C₃₀H₃₆O₁₁

Average Mass

572.6002 Da

Monoisotopic Mass

572.22576 Da

IUPAC Name

14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone

Traditional Name

14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone

CAS Registry Number

Not Available

SMILES

CCOC12CC=CC(=O)C1(C)C1CCC3(O)C(=O)OC4(C)C5CC6(C)C7C(=O)C(OC347)(OCC6C(=O)O5)C1CC2O

InChI Identifier

InChI=1S/C30H36O11/c1-5-37-28-9-6-7-17(31)25(28,3)14-8-10-27(36)23(35)40-26(4)19-12-24(2)16(22(34)39-19)13-38-29(15(14)11-18(28)32)21(33)20(24)30(26,27)41-29/h6-7,14-16,18-20,32,36H,5,8-13H2,1-4H3

InChI Key

GCRPDPKXRPYCEV-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Physalis minima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as physalins and derivatives. These are steroidal constituents of Physalis plants which possess an unusual 13,14-seco-16,24-cyclo-steroidal ring skeleton (where the bond that is normally present between the 13 and 14 positions in other steroids is broken while a new bond between positions 16 and 24 is formed).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Physalins and derivatives

Direct Parent

Physalins and derivatives

Alternative Parents

Not Available

Substituents

Not Available

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.51	ALOGPS
logP	1.76	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	9.68	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	154.89 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	137.24 m³·mol⁻¹	ChemAxon
Polarizability	56.36 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0029626

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB000796

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

131750889

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone (NP0300329)

MOL for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D MOL for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D SDF for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D-SDF for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

PDB for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D PDB for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

SMILES for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

INCHI for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

Structure for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D Structure for NP0300329 (14-ethoxy-5,15-dihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)