NP-MRD: Showing NP-Card for 7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde (NP0168573)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 04:24:30 UTC

Updated at

2022-09-03 04:24:30 UTC

NP-MRD ID

NP0168573

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde

Description

5-[(6-{[(4,6-Dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-2-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. 7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde is found in Draba nemorosa. Based on a literature review very few articles have been published on 5-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-2-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032206242D          

 49 55  0  0  0  0            999 V2000
   -3.9355   -6.5230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4673   -5.8923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2794   -6.0375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8113   -5.4068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6234   -5.5520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5310   -4.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7188   -4.4856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4385   -3.7097    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1870   -5.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3749   -4.9711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0946   -4.1952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2825   -4.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0022   -3.2741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901   -3.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098   -2.3529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -2.2077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -1.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069   -1.1414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -0.5107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -1.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -1.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -0.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -1.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0646   -0.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7474    0.3984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7742    1.2229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3987   -0.1080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1184   -0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -2.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -2.7639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -2.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4850   -3.0585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705   -2.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -3.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -3.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -2.6932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9660   -3.4691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -2.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582   -3.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1539   -3.6143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9385   -4.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4067   -5.1662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507   -4.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0310   -5.4566    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 28 33  1  0  0  0  0
 27 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 22 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 19 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 16 43  1  0  0  0  0
 14 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 12 48  1  0  0  0  0
 48 49  1  0  0  0  0
M  END

     RDKit          3D

101107  0  0  0  0  0  0  0  0999 V2000
    8.0058    1.5387    0.7307 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3512    0.8621   -0.5603 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6671    0.4796   -0.6478 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0398   -0.5829    0.1344 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4656   -0.2092    1.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0674   -1.7162    0.1931 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6266   -1.3069    0.2427 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8821   -2.4395   -0.1615 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3887   -0.2689   -0.8387 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1028    0.2154   -0.8219 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4066   -0.0597   -1.9972 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0006    0.4834   -1.9577 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2682   -0.0448   -0.9242 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3048    0.7807   -0.4056 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6097    0.0709    0.5817 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2559   -0.0651    0.3001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1243   -1.5039    0.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6381   -1.4389   -0.2939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2867   -1.3260    1.0423 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9986   -2.6806    1.6824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1878   -2.7383    2.8841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7980   -1.2475    1.0506 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4385   -2.2985    0.2140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2171   -1.8956   -0.9680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4739   -0.4879   -1.2662 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8679   -0.2603   -2.6850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8941   -0.0663   -1.4375 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.9060   -0.5014   -0.5034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8746   -1.2096    0.5736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2184   -1.3712    1.1703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4872   -2.0209    2.2359 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0821   -0.6887    0.3486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3624   -0.1234   -0.6815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7904    1.4722   -1.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8589    1.6603   -0.2834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8081    0.5408   -0.4105 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7408    1.1739   -1.0407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4073    0.0999    0.9373 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5637    1.1650    1.5941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6888    0.5426    2.6175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6331   -0.3232    1.9513 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9862   -0.9455    3.0554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6368    0.5826    1.3210 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8887    2.0599    0.1802 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2882    1.8466    1.4968 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969    2.5185   -0.6020 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1522    3.9113   -0.5579 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9885    1.9944   -2.0008 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7871    2.4756   -2.5585 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6090    1.1932    1.6011 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0214    2.6390    0.6015 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9486    1.2567    0.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1994    1.6208   -1.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9749   -1.0034   -0.3448 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9634   -1.0037    1.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2815   -2.2925    1.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2391   -2.4180   -0.6484 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2576   -1.0081    1.2237 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8869   -3.0624    0.6035 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6266   -0.7792   -1.7963 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9524    0.4170   -2.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3597   -1.1707   -2.0710 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5370    0.1617   -2.9379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5470    1.0474   -1.1852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761    0.4552   -0.6772 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4552   -1.8924   -0.8022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0518   -2.1527    0.9132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8258   -2.4268   -0.7507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7273   -0.6004   -0.9707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6582   -3.5311    1.1560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0095   -1.5581    2.1335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0824   -2.9812    0.8601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6054   -3.0193   -0.0623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7339   -2.4381   -1.8553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2107   -2.4358   -0.9663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0152   -0.9545   -2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5486    0.7899   -2.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6474   -0.4263   -3.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2705   -0.2834   -2.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0365   -1.6479    1.0538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7424   -0.4392   -1.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4526    1.0001   -0.5777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7506    1.9533   -1.2686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2721    1.7555   -2.3829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4125    2.6525   -0.2810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4321    1.5546    0.6601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8916    2.0887   -1.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3651    0.0819    1.5550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0580    1.7035    0.7767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2141    1.9139    2.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3127   -0.0407    3.3170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1420    1.3276    3.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5323   -0.1921    3.5200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0666    1.5288    0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0612    0.9428    2.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1345    2.8901    0.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4867    1.5757    2.0112 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0061    2.1421   -0.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4194    4.2071    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8031    2.3613   -2.6594 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4427    1.8442   -3.2582 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  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 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  1
 20 21  2  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  6
 25 27  1  0
 27 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  6
 36 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  1
 41 43  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 30 32  1  0
 32 33  1  0
 14 44  1  0
 44 45  1  0
 44 46  1  0
 46 47  1  0
 46 48  1  0
 48 49  1  0
  9  2  1  0
 48 12  1  0
 43 16  1  0
 33 28  1  0
 41 19  1  0
 38 22  1  0
 36 25  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
  2 53  1  6
  4 54  1  6
  5 55  1  0
  6 56  1  0
  6 57  1  0
  7 58  1  1
  8 59  1  0
  9 60  1  6
 11 61  1  0
 11 62  1  0
 12 63  1  6
 14 64  1  6
 16 65  1  6
 17 66  1  0
 17 67  1  0
 18 68  1  0
 18 69  1  0
 20 70  1  0
 22 71  1  1
 23 72  1  0
 23 73  1  0
 24 74  1  0
 24 75  1  0
 26 76  1  0
 26 77  1  0
 26 78  1  0
 27 79  1  6
 34 83  1  0
 34 84  1  0
 35 85  1  0
 35 86  1  0
 37 87  1  0
 38 88  1  1
 39 89  1  0
 39 90  1  0
 40 91  1  0
 40 92  1  0
 42 93  1  0
 43 94  1  0
 43 95  1  0
 29 80  1  0
 33 81  1  0
 33 82  1  0
 44 96  1  1
 45 97  1  0
 46 98  1  1
 47 99  1  0
 48100  1  6
 49101  1  0
M  END


  Mrv1652309032206242D          

 49 55  0  0  0  0            999 V2000
   -3.9355   -6.5230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4673   -5.8923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2794   -6.0375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8113   -5.4068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6234   -5.5520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5310   -4.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7188   -4.4856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4385   -3.7097    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1870   -5.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3749   -4.9711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0946   -4.1952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2825   -4.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0022   -3.2741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901   -3.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098   -2.3529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -2.2077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -1.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069   -1.1414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -0.5107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -1.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -1.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -0.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -1.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0646   -0.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7474    0.3984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7742    1.2229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3987   -0.1080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1184   -0.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -2.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -2.7639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -2.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4850   -3.0585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705   -2.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -3.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -3.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -2.6932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9660   -3.4691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -2.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6582   -3.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1539   -3.6143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9385   -4.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4067   -5.1662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7507   -4.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0310   -5.4566    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 28 33  1  0  0  0  0
 27 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 22 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 19 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 16 43  1  0  0  0  0
 14 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 12 48  1  0  0  0  0
 48 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0168573

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(O)CC(O)C1OCC1OC(OC2CCC3(C=O)C4CCC5(C)C(CCC5(O)C4CCC3(O)C2)C2=CC(=O)OC2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C35H52O14/c1-17-30(23(37)12-26(39)47-17)46-15-24-27(40)28(41)29(42)31(49-24)48-19-3-8-33(16-36)21-4-7-32(2)20(18-11-25(38)45-14-18)6-10-35(32,44)22(21)5-9-34(33,43)13-19/h11,16-17,19-24,26-31,37,39-44H,3-10,12-15H2,1-2H3

> <INCHI_KEY>
YKGXWWGUIXUCTH-UHFFFAOYSA-N

> <FORMULA>
C35H52O14

> <MOLECULAR_WEIGHT>
696.787

> <EXACT_MASS>
696.335706354

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
73.39048524093312

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

> <ALOGPS_LOGP>
-1.36

> <JCHEM_LOGP>
-0.7257860990000005

> <ALOGPS_LOGS>
-3.05

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.9781201793324

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.182629233069253

> <JCHEM_PKA_STRONGEST_BASIC>
0.26896009723728354

> <JCHEM_POLAR_SURFACE_AREA>
221.89999999999998

> <JCHEM_REFRACTIVITY>
167.6891

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.21e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2H-furan-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.346 -12.176   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.339 -10.999   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -9.855 -11.270   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0     -10.848 -10.093   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0     -12.364 -10.364   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0     -10.324  -8.644   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.809  -8.373   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -8.285  -6.925   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -7.816  -9.551   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -6.300  -9.279   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -5.777  -7.831   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.261  -7.560   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.737  -6.112   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.221  -5.841   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.698  -4.392   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.182  -4.121   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.341  -2.673   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.857  -2.402   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.850  -3.579   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.373  -2.131   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.380  -0.953   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.366  -3.308   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.889  -1.859   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.405  -1.588   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.398  -2.766   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.069  -1.380   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.937  -2.816   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.882  -1.600   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.454  -0.121   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.728   0.744   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      10.779   2.283   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      11.944  -0.202   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      11.421  -1.650   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.365  -4.295   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.090  -5.159   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.874  -4.214   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       6.505  -5.709   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       5.358  -4.485   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.835  -5.934   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.319  -6.205   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.326  -5.027   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       1.803  -6.476   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       0.810  -5.298   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -1.229  -7.018   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       0.287  -6.747   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -1.752  -8.466   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -0.759  -9.644   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -3.268  -8.737   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -3.791 -10.186   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    2   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   48                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   44                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   43                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   22   41                                             
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   38                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   36                                             
CONECT   26   25                                                            
CONECT   27   25   28   34                                                  
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   28                                                       
CONECT   34   27   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   25   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   22   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   19   42   43                                             
CONECT   42   41                                                            
CONECT   43   41   16                                                       
CONECT   44   14   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   12   49                                                  
CONECT   49   48                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₂O₁₄

Average Mass

696.7870 Da

Monoisotopic Mass

696.33571 Da

IUPAC Name

5-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

Traditional Name

5-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-7,11-dihydroxy-15-methyl-14-(5-oxo-2H-furan-3-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-2-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC1OC(O)CC(O)C1OCC1OC(OC2CCC3(C=O)C4CCC5(C)C(CCC5(O)C4CCC3(O)C2)C2=CC(=O)OC2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C35H52O14/c1-17-30(23(37)12-26(39)47-17)46-15-24-27(40)28(41)29(42)31(49-24)48-19-3-8-33(16-36)21-4-7-32(2)20(18-11-25(38)45-14-18)6-10-35(32,44)22(21)5-9-34(33,43)13-19/h11,16-17,19-24,26-31,37,39-44H,3-10,12-15H2,1-2H3

InChI Key

YKGXWWGUIXUCTH-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
Draba nemorosa	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
Steroidal glycoside
19-oxosteroid
14-hydroxysteroid
5-hydroxysteroid
Hydroxysteroid
Oxosteroid
Glycosyl compound
O-glycosyl compound
2-furanone
Monosaccharide
Oxane
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Hemiacetal
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Dialkyl ether
Ether
Organoheterocyclic compound
Oxacycle
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Aldehyde
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	-1.4	ALOGPS
logP	-0.73	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	7.18	ChemAxon
pKa (Strongest Basic)	0.27	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	221.9 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	167.69 m³·mol⁻¹	ChemAxon
Polarizability	73.39 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

78168871

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde (NP0168573)

MOL for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D MOL for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D SDF for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D-SDF for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

PDB for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D PDB for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

SMILES for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

INCHI for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

Structure for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

3D Structure for NP0168573 (7-[(6-{[(4,6-dihydroxy-2-methyloxan-3-yl)oxy]methyl}-3,4,5-trihydroxyoxan-2-yl)oxy]-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)