NP-MRD: Showing NP-Card for (1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde (NP0208536)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 05:34:46 UTC

Updated at

2022-09-05 05:34:46 UTC

NP-MRD ID

NP0208536

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde

Description

(1S,3R,5S,7R,10R,12R,14R,15S,18R,19R,20R,22S,23R)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]Pentacosane-14-carbaldehyde belongs to the class of organic compounds known as cardenolide glycosides and derivatives. Cardenolide glycosides and derivatives are compounds containing a carbohydrate glycosidically bound to the cardenolide moiety. (1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde is found in Asclepias curassavica. Based on a literature review very few articles have been published on (1S,3R,5S,7R,10R,12R,14R,15S,18R,19R,20R,22S,23R)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]Pentacosane-14-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052207342D          

 39 45  0  0  1  0            999 V2000
   -5.8483   -1.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0675   -1.0917    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9081   -0.2822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1274   -0.0155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    0.7939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5061   -0.5583    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3467    0.2511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7254   -0.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -0.8344    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3234   -0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021   -1.1106    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5427   -0.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1640    0.2417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8615   -1.9200    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2402   -2.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5405   -2.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6999   -1.3867    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0786   -0.8439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2380   -0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0188    0.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6401   -0.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8832    0.4778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4591   -0.2120    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8609    0.5085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141    1.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1188    1.8182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0203    2.6373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8394    1.4165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6800    0.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8060   -0.9606    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6154   -1.1200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2012   -1.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806   -1.1200    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4067   -1.9417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6422   -2.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2635   -1.6439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0442   -1.9106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6655   -1.3678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4462   -1.6345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 17 33  1  0  0  0  0
 21 33  1  0  0  0  0
 33 34  1  1  0  0  0
 14 35  1  0  0  0  0
 35 36  1  0  0  0  0
  9 36  1  0  0  0  0
 36 37  1  1  0  0  0
 38 37  1  6  0  0  0
  6 38  1  0  0  0  0
 38 39  1  0  0  0  0
  2 39  1  0  0  0  0
M  END

     RDKit          3D

 77 83  0  0  0  0  0  0  0  0999 V2000
    8.3558    0.9756    0.2157 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4285   -0.2028    0.3643 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9845   -0.7749   -0.9547 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0825   -1.9383   -0.6151 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2374   -3.0412   -1.0630 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9687   -1.5819    0.3405 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0165   -2.4130    1.4666 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7921   -1.7562   -0.3430 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8833   -0.8171    0.0652 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5000   -1.0510   -0.5578 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5907   -0.0384    0.1295 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7240   -0.3106    1.5956 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6163   -1.4553    2.0520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0011    1.3745   -0.1389 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2092    2.2981    0.7261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2534    2.0477    0.7725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6846    0.6280    0.6252 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8484   -0.1790   -0.3298 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3188   -1.6051   -0.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7446   -1.6743   -0.7707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6842   -0.7828    0.0010 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9572   -1.5272    1.2873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8791   -0.5176   -0.8594 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1000   -0.1212   -0.1709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6578    1.0677   -0.2516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8598    1.1203    0.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6256    2.1065    0.6962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0396   -0.0916    1.1486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9872   -0.9173    0.7265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3869    0.6021   -1.7419 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7752    0.1256   -2.9164 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4341    1.4154   -0.9154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1392    0.5882    0.2877 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8112    1.0808    1.4269 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4608    1.6484    0.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3369    0.5338   -0.4044 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6508    0.7650   -0.1016 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1537   -0.1699    0.8147 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4218    0.1289    1.2142 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7832    1.1643    1.2418 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1841    0.7503   -0.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7587    1.8542   -0.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0389   -1.0127    0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8804   -1.2269   -1.4347 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4858   -0.0439   -1.6003 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5111   -3.2221    1.1819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6961   -0.8447    1.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1365   -2.0560   -0.2391 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5082   -0.9208   -1.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9183    0.4556    2.3346 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7173    1.5893   -1.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6634    2.3905    1.7558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3555    3.3344    0.2970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    2.3945    1.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8005    2.7340    0.0614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5860    0.1500    1.6453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9165    0.1890   -1.3531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1377   -2.1200    0.6593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7175   -2.1575   -1.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0638   -2.7449   -0.5645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7657   -1.5825   -1.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2327   -0.8897    2.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5441   -2.4240    1.1026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9381   -1.9353    1.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0388   -1.4191   -1.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3263    1.9698   -0.8191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4593   -1.7638    0.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4985   -1.2417    1.6652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1758    1.2777   -2.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8722    0.7383   -3.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5355    1.6773   -1.5104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8693    2.3808   -0.5690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8519    2.0550    1.4227 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7216    2.5534   -0.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6201    1.9346    1.1271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2489    0.5290   -1.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4933   -0.0566    1.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  1
 12 13  2  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  1
 21 23  1  0
 23 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 33 34  1  1
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  1  0
 14 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39  2  1  0
 38  6  1  0
 36  9  1  0
 18 11  1  0
 33 21  1  0
 29 24  1  0
 33 17  1  0
  1 40  1  0
  1 41  1  0
  1 42  1  0
  2 43  1  1
  3 44  1  0
  3 45  1  0
  7 46  1  0
  9 47  1  1
 10 48  1  0
 10 49  1  0
 12 50  1  0
 14 51  1  6
 15 52  1  0
 15 53  1  0
 16 54  1  0
 16 55  1  0
 17 56  1  1
 18 57  1  6
 19 58  1  0
 19 59  1  0
 20 60  1  0
 20 61  1  0
 22 62  1  0
 22 63  1  0
 22 64  1  0
 23 65  1  6
 30 69  1  6
 31 70  1  0
 32 71  1  0
 32 72  1  0
 34 73  1  0
 25 66  1  0
 29 67  1  0
 29 68  1  0
 35 74  1  0
 35 75  1  0
 36 76  1  6
 38 77  1  1
M  END


  Mrv1652309052207342D          

 39 45  0  0  1  0            999 V2000
   -5.8483   -1.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0675   -1.0917    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9081   -0.2822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1274   -0.0155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    0.7939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5061   -0.5583    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3467    0.2511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7254   -0.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -0.8344    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3234   -0.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021   -1.1106    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5427   -0.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1640    0.2417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8615   -1.9200    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2402   -2.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5405   -2.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6999   -1.3867    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0786   -0.8439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2380   -0.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0188    0.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6401   -0.3106    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8832    0.4778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4591   -0.2120    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8609    0.5085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5141    1.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1188    1.8182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0203    2.6373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8394    1.4165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6800    0.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8060   -0.9606    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6154   -1.1200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2012   -1.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4806   -1.1200    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4067   -1.9417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6422   -2.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2635   -1.6439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0442   -1.9106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6655   -1.3678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4462   -1.6345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 17 33  1  0  0  0  0
 21 33  1  0  0  0  0
 33 34  1  1  0  0  0
 14 35  1  0  0  0  0
 35 36  1  0  0  0  0
  9 36  1  0  0  0  0
 36 37  1  1  0  0  0
 38 37  1  6  0  0  0
  6 38  1  0  0  0  0
 38 39  1  0  0  0  0
  2 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0208536

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC(=O)[C@]2(O)O[C@@H]3C[C@@]4(C=O)[C@@H](CC[C@@H]5[C@@H]4CC[C@]4(C)[C@H]([C@H](O)C[C@]54O)C4=CC(=O)OC4)C[C@H]3O[C@@H]2O1

> <INCHI_IDENTIFIER>
InChI=1S/C29H38O10/c1-14-7-22(32)29(35)25(37-14)38-20-9-16-3-4-18-17(27(16,13-30)11-21(20)39-29)5-6-26(2)24(15-8-23(33)36-12-15)19(31)10-28(18,26)34/h8,13-14,16-21,24-25,31,34-35H,3-7,9-12H2,1-2H3/t14-,16+,17+,18-,19-,20-,21-,24+,25+,26-,27-,28+,29+/m1/s1

> <INCHI_KEY>
HKHWPATYIZTJPO-LAIIKORZSA-N

> <FORMULA>
C29H38O10

> <MOLECULAR_WEIGHT>
546.613

> <EXACT_MASS>
546.246497424

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
57.09796716138923

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,5S,7R,10R,12R,14R,15S,18R,19R,20R,22S,23R)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2,5-dihydrofuran-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0^{3,12}.0^{5,10}.0^{15,23}.0^{18,22}]pentacosane-14-carbaldehyde

> <JCHEM_LOGP>
1.3745862279999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.664463538296149

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.824605354188491

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9014291587035155

> <JCHEM_POLAR_SURFACE_AREA>
148.82

> <JCHEM_REFRACTIVITY>
134.13979999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,5S,7R,10R,12R,14R,15S,18R,19R,20R,22S,23R)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2H-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0^{3,12}.0^{5,10}.0^{15,23}.0^{18,22}]pentacosane-14-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.917  -2.536   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.459  -2.038   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.162  -0.527   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.704  -0.029   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -7.407   1.482   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -6.545  -1.042   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -6.247   0.469   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -5.087  -0.544   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -3.928  -1.558   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.470  -1.060   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.311  -2.073   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.013  -0.562   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.173   0.451   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.608  -3.584   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.448  -4.597   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.009  -4.099   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.307  -2.588   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.147  -1.575   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.444  -0.064   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.902   0.433   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.061  -0.580   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.515   0.892   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.590  -0.396   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.340   0.949   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.693   2.347   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.822   3.394   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.638   4.923   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       7.167   2.644   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.869   1.133   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.238  -1.793   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.749  -2.091   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.109  -2.841   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.764  -2.091   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.626  -3.625   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -3.065  -4.082   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.225  -3.069   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -5.683  -3.566   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -6.842  -2.553   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -8.300  -3.051   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   39                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8   38                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   36                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   14   18                                             
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   35                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   33                                                  
CONECT   18   17   11   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   33                                             
CONECT   22   21                                                            
CONECT   23   21   24   30                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   24                                                       
CONECT   30   23   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   17   21   34                                             
CONECT   34   33                                                            
CONECT   35   14   36                                                       
CONECT   36   35    9   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37    6   39                                                  
CONECT   39   38    2                                                       
MASTER        0    0    0    0    0    0    0    0   39    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₃₈O₁₀

Average Mass

546.6130 Da

Monoisotopic Mass

546.24650 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC(=O)[C@]2(O)O[C@@H]3C[C@@]4(C=O)[C@@H](CC[C@@H]5[C@@H]4CC[C@]4(C)[C@H]([C@H](O)C[C@]54O)C4=CC(=O)OC4)C[C@H]3O[C@@H]2O1

InChI Identifier

InChI=1S/C29H38O10/c1-14-7-22(32)29(35)25(37-14)38-20-9-16-3-4-18-17(27(16,13-30)11-21(20)39-29)5-6-26(2)24(15-8-23(33)36-12-15)19(31)10-28(18,26)34/h8,13-14,16-21,24-25,31,34-35H,3-7,9-12H2,1-2H3/t14-,16+,17+,18-,19-,20-,21-,24+,25+,26-,27-,28+,29+/m1/s1

InChI Key

HKHWPATYIZTJPO-LAIIKORZSA-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
Asclepias curassavica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cardenolide glycosides and derivatives. Cardenolide glycosides and derivatives are compounds containing a carbohydrate glycosidically bound to the cardenolide moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Cardenolide glycosides and derivatives

Alternative Parents

Substituents

Cardanolide-glycoside
19-oxosteroid
16-hydroxysteroid
16-alpha-hydroxysteroid
14-hydroxysteroid
Hydroxysteroid
Oxosteroid
Para-dioxane
2-furanone
Oxane
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Hemiacetal
Secondary alcohol
Ketone
Lactone
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Polyol
Monocarboxylic acid or derivatives
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Aldehyde
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source

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

163040978

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde (NP0208536)

MOL for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

3D MOL for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

3D SDF for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

3D-SDF for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

PDB for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

3D PDB for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

SMILES for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

INCHI for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

Structure for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)

3D Structure for NP0208536 ((1s,3r,5s,7r,10r,12r,14r,15s,18r,19r,20r,22s,23r)-10,20,22-trihydroxy-7,18-dimethyl-9-oxo-19-(5-oxo-2h-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.0³,¹².0⁵,¹⁰.0¹⁵,²³.0¹⁸,²²]pentacosane-14-carbaldehyde)