NP-MRD: Showing NP-Card for (+)-Beesioside I (NP0080195)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 01:14:53 UTC

Updated at

2022-04-29 01:14:53 UTC

NP-MRD ID

NP0080195

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Beesioside I

Description

Beesioside I belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus. (+)-Beesioside I is found in Beesia calthaefolia. Based on a literature review very few articles have been published on Beesioside I.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203142D          

 51 58  0  0  1  0            999 V2000
   13.2554    3.4159    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.7543    2.7589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.4348    1.9983    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.6163    1.8947    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1174    2.5517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4369    3.3123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2968    1.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4784    1.0305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9793    1.6908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1647    1.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7845    0.8060    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3119    0.1362    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.1569    0.2603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9090   -0.0788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2997   -0.5523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9758   -0.6373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1460   -0.7403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5852   -0.0873    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.9235    0.6905    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3865    1.3450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5891    1.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1016    0.5167    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7033   -0.1335    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3324   -0.8859    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5147   -0.7876    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3494    0.0362    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4663    0.2017    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4907    0.9387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3979    1.6577    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2295    1.8932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9117    1.3893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5879    1.3295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6214    0.4513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1302    2.4381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8626    3.2185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3499    2.1704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9106    2.7058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2732   -0.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9547   -1.3934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1993   -2.1813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0040   -2.3634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6393   -2.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7255   -1.6112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2938   -2.3143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6869   -3.0397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7911   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1572   -0.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2606    1.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9338    1.3413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.5728    2.8625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    4.1766    0.0000 O   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
  4  7  1  6  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  6  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 25  1  6  0  0  0
 22 26  1  0  0  0  0
 26 27  1  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  1  0  0  0  0
 22 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 27 33  1  0  0  0  0
 29 34  1  1  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
 27 38  1  1  0  0  0
 25 39  1  6  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 24 43  1  6  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 23 47  1  1  0  0  0
 19 48  1  6  0  0  0
 11 48  1  6  0  0  0
  3 49  1  1  0  0  0
  2 50  1  6  0  0  0
  1 51  1  1  0  0  0
M  END

     RDKit          3D

111118  0  0  0  0  0  0  0  0999 V2000
   -2.2531    0.8552    5.4242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1615    1.5546    4.1337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8950    2.7857    4.1083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3703    0.8541    2.9256 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2938    1.4711    1.6973 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7611    1.6445    1.1905 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5415    0.7636    1.9093 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5571    1.1829    2.7748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4007    0.2697    3.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7289    2.4277    2.8688 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5914    1.4631   -0.2535 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7000    1.3908   -1.1768 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6031    2.3927   -2.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0915    1.4268   -0.6612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4843   -0.0151   -0.4535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2390   -0.7589   -0.9576 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7429   -1.9735   -1.7082 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6581   -2.8653   -2.1961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5874   -1.5425   -2.8921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5759   -2.7497   -0.8872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5406   -1.1380    0.1132 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2336   -0.9058    0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6014    0.3016   -0.2914 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0218    0.0101   -1.6050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6149   -0.3965   -1.7045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2306   -0.3902   -0.4887 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1514   -1.6529   -0.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6718   -0.3042   -0.5167 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3875   -0.0115   -1.8201 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7350    0.5824   -1.6530 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5703    0.0442   -0.5171 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3737   -1.0115   -0.9218 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7211   -0.6759   -0.9625 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1633   -0.6473   -2.3168 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3085    0.1462   -2.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4106   -0.7016   -1.7162 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.5956    0.0419   -1.6683 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0450   -1.0668   -0.3184 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.9189   -2.0567    0.1659 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6172   -1.5375   -0.1452 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3226   -1.3273    1.2152 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7859   -0.2002    0.7334 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4575    0.4742    1.9396 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7034   -1.6554    1.0395 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4185    0.4392    0.5290 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6880    0.7059    1.7815 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4138   -0.0790    1.9549 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4993   -0.1378    0.8056 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5078    0.9207    0.6057 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9080    2.1056   -0.1704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7025    0.1311   -1.8204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9507   -0.0061    5.2910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2610    0.4307    5.6699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6556    1.5404    6.1729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9968    2.5480    1.9015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1228    2.6719    1.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0649   -0.7650    3.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4733    0.4230    3.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2689    0.4730    4.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9637    2.3556   -0.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6117    2.7810   -2.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2108    1.9472   -3.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0026    3.2811   -2.0210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7822    1.8094   -1.4802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2894    2.0974    0.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7056   -0.2834    0.5896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3130   -0.3235   -1.1334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0704   -2.4544   -3.0467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0336   -3.2747   -1.3794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1610   -3.7766   -2.6446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2914   -0.5033   -3.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4040   -2.1825   -3.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6737   -1.6240   -2.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0740   -3.1356   -0.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6635   -1.7955   -0.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0594   -0.9922    1.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2972    0.8586   -2.3040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6292   -0.8375   -2.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5006   -1.3909   -2.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1281    0.2835   -2.4700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1023   -2.2474    0.5459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1725   -2.3263   -1.2677 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4584   -0.9284   -2.4429 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8255    0.7303   -2.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3196    0.3350   -2.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6928    1.6935   -1.6538 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2809    0.8955   -0.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8365    0.3758   -0.6337 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5661    0.5465   -3.2996 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1444    1.0101   -1.6180 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6122   -1.5796   -2.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4302    1.0079   -1.5656 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1728   -0.1636    0.3170 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8281   -1.7800   -0.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5064   -2.6169   -0.3797 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7404   -0.4703    1.4811 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9878    1.4613    2.1315 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4441   -0.2022    2.8162 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5348    0.6748    1.7139 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4697   -2.2991    0.1727 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0248   -1.8391    1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6971   -1.9841    1.4047 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6572    1.4541    0.0808 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3475    0.3904    2.6445 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4562    1.7712    1.9775 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0057    0.2598    2.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7615   -1.1361    2.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0844   -1.1068    0.9387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0809    2.0732   -1.2366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2686    3.0893    0.2553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1932    2.1711   -0.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8 10  2  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 49  1  0
 49 50  1  6
 49 48  1  0
 48 47  1  0
 47 46  1  0
 46 45  1  0
 45 28  1  0
 28 27  1  1
 26 27  1  1
 26 25  1  0
 25 24  1  0
 23 24  1  6
 23 22  1  0
 22 21  1  0
 16 21  1  1
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  1  6
 12 51  1  0
 12 11  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 17 20  1  1
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 31 42  1  0
 42 43  1  1
 42 44  1  0
 11  6  1  0
 40 33  1  0
 23 49  1  0
 11 23  1  0
 26 48  1  0
 51 16  1  0
 42 45  1  0
 26 28  1  0
  9 57  1  0
  9 58  1  0
  9 59  1  0
  6 56  1  6
  5 55  1  1
  1 52  1  0
  1 53  1  0
  1 54  1  0
 50109  1  0
 50110  1  0
 50111  1  0
 48108  1  1
 47106  1  0
 47107  1  0
 46104  1  0
 46105  1  0
 45103  1  6
 27 81  1  0
 27 82  1  0
 25 79  1  0
 25 80  1  0
 24 77  1  0
 24 78  1  0
 22 75  1  0
 22 76  1  0
 15 66  1  0
 15 67  1  0
 14 64  1  0
 14 65  1  0
 13 61  1  0
 13 62  1  0
 13 63  1  0
 11 60  1  6
 18 68  1  0
 18 69  1  0
 18 70  1  0
 19 71  1  0
 19 72  1  0
 19 73  1  0
 20 74  1  0
 29 83  1  0
 29 84  1  0
 30 85  1  0
 30 86  1  0
 31 87  1  1
 33 88  1  1
 35 89  1  0
 35 90  1  0
 36 91  1  6
 37 92  1  0
 38 93  1  1
 39 94  1  0
 40 95  1  6
 41 96  1  0
 43 97  1  0
 43 98  1  0
 43 99  1  0
 44100  1  0
 44101  1  0
 44102  1  0
M  END


  Mrv1652304292203142D          

 51 58  0  0  1  0            999 V2000
   13.2554    3.4159    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.7543    2.7589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.4348    1.9983    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.6163    1.8947    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1174    2.5517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4369    3.3123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2968    1.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4784    1.0305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9793    1.6908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1647    1.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7845    0.8060    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3119    0.1362    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.1569    0.2603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9090   -0.0788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2997   -0.5523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9758   -0.6373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1460   -0.7403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5852   -0.0873    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.9235    0.6905    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3865    1.3450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5891    1.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1016    0.5167    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7033   -0.1335    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3324   -0.8859    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5147   -0.7876    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3494    0.0362    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4663    0.2017    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4907    0.9387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3979    1.6577    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2295    1.8932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9117    1.3893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5879    1.3295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6214    0.4513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1302    2.4381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8626    3.2185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3499    2.1704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9106    2.7058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2732   -0.6004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9547   -1.3934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1993   -2.1813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0040   -2.3634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6393   -2.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7255   -1.6112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2938   -2.3143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6869   -3.0397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7911   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1572   -0.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2606    1.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9338    1.3413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.5728    2.8625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749    4.1766    0.0000 O   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
  4  7  1  6  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  6  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 25  1  6  0  0  0
 22 26  1  0  0  0  0
 26 27  1  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  1  0  0  0  0
 22 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 27 33  1  0  0  0  0
 29 34  1  1  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
 27 38  1  1  0  0  0
 25 39  1  6  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 24 43  1  6  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 23 47  1  1  0  0  0
 19 48  1  6  0  0  0
 11 48  1  6  0  0  0
  3 49  1  1  0  0  0
  2 50  1  6  0  0  0
  1 51  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0080195

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1[C@@H](OC(C)=O)[C@@]2(C)[C@@H]3CC[C@@H]4[C@]5(C[C@@]35CC[C@@]22CO[C@]3(CC[C@](C)(O3)[C@@H]12)C(C)(C)O)CC[C@H](O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O)C4(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C39H60O12/c1-20(40)48-28-29-34(7)13-16-39(51-34,33(5,6)45)47-19-38(29)15-14-37-18-36(37)12-11-25(50-31-27(44)26(43)22(42)17-46-31)32(3,4)23(36)9-10-24(37)35(38,8)30(28)49-21(2)41/h22-31,42-45H,9-19H2,1-8H3/t22-,23+,24+,25+,26+,27-,28-,29-,30-,31+,34+,35-,36-,37+,38+,39+/m1/s1

> <INCHI_KEY>
UZSZTNKGIQMEOL-QGODIXMOSA-N

> <FORMULA>
C39H60O12

> <MOLECULAR_WEIGHT>
720.897

> <EXACT_MASS>
720.408477372

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
111

> <JCHEM_AVERAGE_POLARIZABILITY>
78.82031703693167

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3R,4S,5S,6R,9R,11S,14R,16S,19S,22S)-3-(acetyloxy)-22-(2-hydroxypropan-2-yl)-1,5,10,10-tetramethyl-11-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-21,25-dioxaheptacyclo[20.2.1.0^{2,19}.0^{5,19}.0^{6,16}.0^{9,14}.0^{14,16}]pentacosan-4-yl acetate

> <ALOGPS_LOGP>
2.88

> <JCHEM_LOGP>
2.193858993999999

> <ALOGPS_LOGS>
-4.92

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.115128480331332

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.214518389640016

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5133443686302837

> <JCHEM_POLAR_SURFACE_AREA>
170.44

> <JCHEM_REFRACTIVITY>
179.92710000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.68e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3R,4S,5S,6R,9R,11S,14R,16S,19S,22S)-3-(acetyloxy)-22-(2-hydroxypropan-2-yl)-1,5,10,10-tetramethyl-11-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-21,25-dioxaheptacyclo[20.2.1.0^{2,19}.0^{5,19}.0^{6,16}.0^{9,14}.0^{14,16}]pentacosan-4-yl 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      24.743   6.376   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.675   5.150   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      25.078   3.730   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      23.551   3.537   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      22.619   4.763   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      23.216   6.183   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      22.954   2.117   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      21.426   1.924   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.495   3.156   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.974   2.932   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.264   1.505   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      19.249   0.254   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.826   0.486   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      22.230  -0.147   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.093  -1.031   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      18.622  -1.190   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.073  -1.382   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.026  -0.163   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.657   1.289   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.655   2.511   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.166   2.275   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.256   0.964   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.380  -0.249   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.687  -1.654   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.161  -1.470   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.852   0.068   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.204   0.376   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.249   1.752   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      10.076   3.094   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      11.628   3.534   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      12.902   2.593   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.564   2.482   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.627   0.842   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.576   4.551   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.077   6.008   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       8.120   4.051   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      11.033   5.051   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.843  -1.121   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      11.115  -2.601   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      11.572  -4.072   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      13.074  -4.412   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      10.527  -5.203   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      14.421  -3.008   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      13.615  -4.320   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      14.349  -5.674   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      12.677  -5.541   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      15.227  -1.535   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      17.287   2.708   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      26.010   2.504   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      27.203   5.343   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      25.340   7.796   0.000  0.00  0.00           O+0
CONECT    1    2    6   51                                                  
CONECT    2    1    3   50                                                  
CONECT    3    2    4   49                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   19   48                                             
CONECT   12   11   13   16                                                  
CONECT   13   12    8   14   15                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   12   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   11   20   48                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   26   31                                             
CONECT   23   22   18   24   47                                             
CONECT   24   23   25   43                                                  
CONECT   25   24   26   39                                                  
CONECT   26   25   22   27                                                  
CONECT   27   26   28   33   38                                             
CONECT   28   27   29                                                       
CONECT   29   28   30   32   34                                             
CONECT   30   29   31                                                       
CONECT   31   30   22                                                       
CONECT   32   29   33                                                       
CONECT   33   32   27                                                       
CONECT   34   29   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34                                                            
CONECT   38   27                                                            
CONECT   39   25   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   24   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   23                                                            
CONECT   48   19   11                                                       
CONECT   49    3                                                            
CONECT   50    2                                                            
CONECT   51    1                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  116    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₆₀O₁₂

Average Mass

720.8970 Da

Monoisotopic Mass

720.40848 Da

IUPAC Name

(1S,2R,3R,4S,5S,6R,9R,11S,14R,16S,19S,22S)-3-(acetyloxy)-22-(2-hydroxypropan-2-yl)-1,5,10,10-tetramethyl-11-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-21,25-dioxaheptacyclo[20.2.1.0^{2,19}.0^{5,19}.0^{6,16}.0^{9,14}.0^{14,16}]pentacosan-4-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1[C@@H](OC(C)=O)[C@@]2(C)[C@@H]3CC[C@@H]4[C@]5(C[C@@]35CC[C@@]22CO[C@]3(CC[C@](C)(O3)[C@@H]12)C(C)(C)O)CC[C@H](O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O)C4(C)C

InChI Identifier

InChI=1S/C39H60O12/c1-20(40)48-28-29-34(7)13-16-39(51-34,33(5,6)45)47-19-38(29)15-14-37-18-36(37)12-11-25(50-31-27(44)26(43)22(42)17-46-31)32(3,4)23(36)9-10-24(37)35(38,8)30(28)49-21(2)41/h22-31,42-45H,9-19H2,1-8H3/t22-,23+,24+,25+,26+,27-,28-,29-,30-,31+,34+,35-,36-,37+,38+,39+/m1/s1

InChI Key

UZSZTNKGIQMEOL-QGODIXMOSA-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
Beesia calthifolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Cucurbitacin glycosides

Alternative Parents

Substituents

Cucurbitacin glycoside skeleton
Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
Steroid ester
Glycosyl compound
O-glycosyl compound
Ketal
1,3-dioxepane
Dioxepane
Oxane
Dicarboxylic acid or derivatives
Monosaccharide
Tertiary alcohol
Tetrahydrofuran
Secondary alcohol
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Polyol
Acetal
Alcohol
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
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
logP	2.88	ALOGPS
logP	2.19	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	170.44 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	179.93 m³·mol⁻¹	ChemAxon
Polarizability	78.82 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	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00045234

Chemspider ID

10269241

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15908521

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Beesioside I (NP0080195)

MOL for NP0080195 ((+)-Beesioside I)

3D MOL for NP0080195 ((+)-Beesioside I)

3D SDF for NP0080195 ((+)-Beesioside I)

3D-SDF for NP0080195 ((+)-Beesioside I)

PDB for NP0080195 ((+)-Beesioside I)

3D PDB for NP0080195 ((+)-Beesioside I)

SMILES for NP0080195 ((+)-Beesioside I)

INCHI for NP0080195 ((+)-Beesioside I)

Structure for NP0080195 ((+)-Beesioside I)

3D Structure for NP0080195 ((+)-Beesioside I)