NP-MRD: Showing NP-Card for (1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde (NP0299500)

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Record Information

Version

2.0

Created at

2022-09-10 11:21:39 UTC

Updated at

2022-09-10 11:21:39 UTC

NP-MRD ID

NP0299500

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(2S,5S,7S,11S,14R,15R)-5-{[(2R,5R)-6-({[(3R,6S)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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. (1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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 Maquira coriacea. Based on a literature review very few articles have been published on (2S,5S,7S,11S,14R,15R)-5-{[(2R,5R)-6-({[(3R,6S)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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


  Mrv1652309102213212D          

 50 56  0  0  1  0            999 V2000
   -1.9446    1.0910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4128    0.4603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6931   -0.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1613   -0.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492   -0.8011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4416   -1.7222    0.0000 C   0  0  2  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  1  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  2  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  2  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  1  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  1  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  1  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
   -2.2537   -1.8674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7855   -1.2367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5976   -1.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8779   -2.1579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6901   -2.3031    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9704   -3.0790    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
   -5.7825   -3.2242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3143   -2.5935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.1264   -2.7387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0340   -1.8176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2219   -1.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9416   -0.8965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5052   -0.4608    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0370    0.1699    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  6  0  0  0
  8  7  1  1  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  1  0  0  0
 12 13  2  0  0  0  0
 11 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  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 14 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 11 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
  8 35  1  0  0  0  0
  6 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 40 39  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  1  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 40 47  1  0  0  0  0
 47 48  1  0  0  0  0
 37 49  1  0  0  0  0
  3 49  1  0  0  0  0
 49 50  1  1  0  0  0
M  END

     RDKit          3D

104110  0  0  0  0  0  0  0  0999 V2000
    3.8440    0.7989    4.7732 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6024    0.3840    3.4908 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2704    1.0959    2.4996 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2301    0.1937    1.7797 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4083    0.8822    1.4852 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6853   -0.3895    0.4923 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3734    0.1960   -0.7178 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7226    0.0598   -0.7532 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1814   -1.2501   -0.8313 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2244   -1.4676    0.2189 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6549   -1.9248    1.4363 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2189   -2.5145   -0.2453 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9821   -1.9431   -1.4116 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.5540   -2.9523   -2.1869 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1869   -1.0843   -2.1700 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8691   -1.4701   -2.1933 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1786   -0.5367   -3.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3244   -0.2849    0.4054 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7665    0.9868    0.4801 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4466    0.7452    0.6191 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5755    1.0475   -0.3832 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0461   -0.1676   -1.0979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3653    0.1406   -1.5238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1855    0.2758   -0.2535 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6334   -0.7977    0.6349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1161   -0.6093    1.6999 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6179    0.0527   -0.4746 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9274   -0.6820   -1.7902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3880   -0.9077   -1.9699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2462   -0.6098   -0.7731 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1883   -1.8287    0.1254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6637   -0.4439   -1.3316 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.6914   -1.1186   -0.4783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4628   -2.1052   -0.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3302   -2.5213    0.1666 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2229   -3.4433    0.1746 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0526   -1.7365    1.2524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0565   -0.8283    0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8973    1.0287   -1.4798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0281    1.6547   -0.4411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9543    0.6682   -0.0757 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9265    0.4358    1.3198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5706    1.1750   -0.4038 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1587    2.2737    0.5508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7752    2.6849    0.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7730    1.5719    0.3790 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6552    1.5110    1.7643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4415    2.0793   -0.1457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3229    1.8228    1.5833 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8859    2.9982    1.0823 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3146    0.2297    5.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9240    0.6828    4.9878 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5676    1.8709    4.8518 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8623    1.8606    3.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5035   -0.6148    2.4840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4292    1.7840    1.8762 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9318   -1.4613    0.4958 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9535   -0.3796   -1.5991 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1003    1.2597   -0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3880   -2.0119   -0.8176 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7556   -0.5233    0.4414 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0912   -1.5387    2.2220 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6796   -3.4535   -0.5024 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8751   -2.7619    0.6170 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8125   -1.3353   -1.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4347   -2.7624   -3.1334 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8054   -2.5228   -2.5200 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8775   -0.2328   -4.0160 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3107   -1.0334   -3.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9551    0.4017   -2.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9975    1.4570   -0.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2786    1.4982   -1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6364   -0.3790   -2.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0299   -1.0685   -0.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3758    1.0622   -2.1408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7634   -0.6551   -2.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7094   -1.8419    0.2799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9663   -0.7022    0.2996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6023   -0.0712   -2.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4010   -1.6764   -1.7443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5694   -1.9771   -2.2213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8102   -0.3163   -2.8340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3922   -2.5548   -0.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1340   -2.3932   -0.0332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9627   -1.6200    1.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7511   -0.8728   -2.3602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4498   -2.5545   -1.8935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3969    0.2277    1.0542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2065   -1.0423    1.6403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5850    1.3611   -2.4973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9750    1.2104   -1.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6544    1.8998    0.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6347    2.6059   -0.8595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3150    1.2070    1.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6469    1.6621   -1.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8197    3.1426    0.4065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2175    1.9698    1.6076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4312    3.6133    0.5997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8194    2.8602   -0.9781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9746    2.1342    2.0840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1218    2.8851    0.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7153    2.6634   -1.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4869    2.1522    2.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1739    3.5102    0.6262 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
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
  6 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  1
 25 26  2  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  1
 30 32  1  0
 32 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  1
 41 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  1  1
 46 48  1  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
 35 37  1  0
 37 38  1  0
 19 49  1  0
 49 50  1  0
 49  3  1  0
 16  9  1  0
 48 21  1  0
 38 33  1  0
 46 24  1  0
 43 27  1  0
 41 30  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  3 54  1  1
  4 55  1  1
  5 56  1  0
  6 57  1  1
  7 58  1  0
  7 59  1  0
  9 60  1  1
 10 61  1  1
 11 62  1  0
 12 63  1  0
 12 64  1  0
 13 65  1  1
 14 66  1  0
 16 67  1  6
 17 68  1  0
 17 69  1  0
 17 70  1  0
 19 71  1  6
 21 72  1  6
 22 73  1  0
 22 74  1  0
 23 75  1  0
 23 76  1  0
 25 77  1  0
 27 78  1  1
 28 79  1  0
 28 80  1  0
 29 81  1  0
 29 82  1  0
 31 83  1  0
 31 84  1  0
 31 85  1  0
 32 86  1  6
 39 90  1  0
 39 91  1  0
 40 92  1  0
 40 93  1  0
 42 94  1  0
 43 95  1  6
 44 96  1  0
 44 97  1  0
 45 98  1  0
 45 99  1  0
 47100  1  0
 48101  1  0
 48102  1  0
 34 87  1  0
 38 88  1  0
 38 89  1  0
 49103  1  1
 50104  1  0
M  END


  Mrv1652309102213212D          

 50 56  0  0  1  0            999 V2000
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   -1.4128    0.4603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6931   -0.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1613   -0.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492   -0.8011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4416   -1.7222    0.0000 C   0  0  2  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  1  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  2  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  2  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  1  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  1  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  1  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
   -2.2537   -1.8674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7855   -1.2367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5976   -1.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8779   -2.1579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6901   -2.3031    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9704   -3.0790    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
   -5.7825   -3.2242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3143   -2.5935    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.1264   -2.7387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0340   -1.8176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2219   -1.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9416   -0.8965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5052   -0.4608    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0370    0.1699    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  6  0  0  0
  8  7  1  1  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  1  0  0  0
 12 13  2  0  0  0  0
 11 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  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 14 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 11 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
  8 35  1  0  0  0  0
  6 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 40 39  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  1  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 40 47  1  0  0  0  0
 47 48  1  0  0  0  0
 37 49  1  0  0  0  0
  3 49  1  0  0  0  0
 49 50  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0299500

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1[C@H](O)C(CO[C@@H]2C(O)C[C@@H](O)OC2C)O[C@@H](O[C@H]2CC[C@]3(C=O)C4CC[C@]5(C)[C@H](CC[C@]5(O)C4CC[C@]3(O)C2)C2=CC(=O)OC2)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C36H54O14/c1-18-30(24(38)13-27(40)48-18)47-16-25-28(41)31(45-3)29(42)32(50-25)49-20-4-9-34(17-37)22-5-8-33(2)21(19-12-26(39)46-15-19)7-11-36(33,44)23(22)6-10-35(34,43)14-20/h12,17-18,20-25,27-32,38,40-44H,4-11,13-16H2,1-3H3/t18?,20-,21+,22?,23?,24?,25?,27-,28+,29?,30-,31?,32+,33+,34-,35-,36-/m0/s1

> <INCHI_KEY>
WEDKAKRDVPRQSU-AWRXHTBRSA-N

> <FORMULA>
C36H54O14

> <MOLECULAR_WEIGHT>
710.814

> <EXACT_MASS>
710.351356419

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
74.79055238290329

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S,7S,11S,14R,15R)-5-{[(2R,5R)-6-({[(3R,6S)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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

> <JCHEM_LOGP>
-0.08265959533333353

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.017912062775574

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.182629841979494

> <JCHEM_PKA_STRONGEST_BASIC>
0.2689600972373577

> <JCHEM_POLAR_SURFACE_AREA>
210.89999999999995

> <JCHEM_REFRACTIVITY>
172.44029999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5S,7S,11S,14R,15R)-5-{[(2R,5R)-6-({[(3R,6S)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.630   2.037   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.637   0.859   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.160  -0.589   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.168  -1.766   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.652  -1.495   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.691  -3.215   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.698  -4.392   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.182  -4.121   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.341  -2.673   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.857  -2.402   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.850  -3.579   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.373  -2.131   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.380  -0.953   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.366  -3.308   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.889  -1.859   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.405  -1.588   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.398  -2.766   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.069  -1.380   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.937  -2.816   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.882  -1.600   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.454  -0.121   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.728   0.744   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.779   2.283   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      11.944  -0.202   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.421  -1.650   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.365  -4.295   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.090  -5.159   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.874  -4.214   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.505  -5.709   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.358  -4.485   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.835  -5.934   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.319  -6.205   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.326  -5.027   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       1.803  -6.476   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       0.810  -5.298   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -4.207  -3.486   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -5.200  -2.309   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -6.716  -2.580   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -7.239  -4.028   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -8.755  -4.299   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -9.278  -5.747   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -8.285  -6.925   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0     -10.794  -6.019   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -11.787  -4.841   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0     -13.303  -5.112   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0     -11.263  -3.393   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -9.748  -3.122   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -9.224  -1.673   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -4.676  -0.860   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -5.669   0.317   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   49                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   36                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   35                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   14   33                                             
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   30                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   28                                             
CONECT   18   17                                                            
CONECT   19   17   20   26                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   20                                                       
CONECT   26   19   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   17   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   14   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   11   34   35                                             
CONECT   34   33                                                            
CONECT   35   33    8                                                       
CONECT   36    6   37                                                       
CONECT   37   36   38   49                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   47                                                  
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   40   48                                                  
CONECT   48   47                                                            
CONECT   49   37    3   50                                                  
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₅₄O₁₄

Average Mass

710.8140 Da

Monoisotopic Mass

710.35136 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1[C@H](O)C(CO[C@@H]2C(O)C[C@@H](O)OC2C)O[C@@H](O[C@H]2CC[C@]3(C=O)C4CC[C@]5(C)[C@H](CC[C@]5(O)C4CC[C@]3(O)C2)C2=CC(=O)OC2)C1O

InChI Identifier

InChI=1S/C36H54O14/c1-18-30(24(38)13-27(40)48-18)47-16-25-28(41)31(45-3)29(42)32(50-25)49-20-4-9-34(17-37)22-5-8-33(2)21(19-12-26(39)46-15-19)7-11-36(33,44)23(22)6-10-35(34,43)14-20/h12,17-18,20-25,27-32,38,40-44H,4-11,13-16H2,1-3H3/t18?,20-,21+,22?,23?,24?,25?,27-,28+,29?,30-,31?,32+,33+,34-,35-,36-/m0/s1

InChI Key

WEDKAKRDVPRQSU-AWRXHTBRSA-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
Maquira coriacea	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
Lactone
Secondary alcohol
Carboxylic acid ester
Hemiacetal
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Acetal
Dialkyl ether
Ether
Oxacycle
Organic oxygen compound
Organic oxide
Aldehyde
Alcohol
Carbonyl group
Hydrocarbon derivative
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
logP	-0.083	ChemAxon
pKa (Strongest Acidic)	7.18	ChemAxon
pKa (Strongest Basic)	0.27	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	210.9 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	172.44 m³·mol⁻¹	ChemAxon
Polarizability	74.79 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

10745

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11218

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde (NP0299500)

MOL for NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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 NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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 NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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 NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

PDB for NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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 NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

SMILES for NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

INCHI for NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)

Structure for NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-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 NP0299500 ((1r,3as,5as,7s,9as,11ar)-7-{[(2r,5r)-6-({[(3r,6s)-4,6-dihydroxy-2-methyloxan-3-yl]oxy}methyl)-3,5-dihydroxy-4-methoxyoxan-2-yl]oxy}-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthrene-9a-carbaldehyde)