NP-MRD: Showing NP-Card for 6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate (NP0149634)

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Record Information

Version

2.0

Created at

2022-09-02 05:32:53 UTC

Updated at

2022-09-02 05:32:54 UTC

NP-MRD ID

NP0149634

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate

Description

6-{[2-Formyl-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-5-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate 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. 6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate is found in Erysimum cheiranthoides. 6-{[2-Formyl-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-5-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161521212D          

 51 57  0  0  0  0            999 V2000
    0.6569   -6.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1552   -6.5728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6870   -5.9421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991   -6.0873    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
   -1.7507   -4.6807    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
   -3.0946   -4.1952    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
   -0.6582   -3.7596    0.0000 C   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
    0.4054   -5.0210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6857   -4.2451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9372   -5.6517    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
    5.0168   -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
    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
   -1.7794   -6.8633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5916   -7.0085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2476   -7.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5279   -8.2699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4355   -7.3487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0963   -7.9795    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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  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
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 10 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  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 24 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 21 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 18 39  1  0  0  0  0
 29 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 40 45  1  0  0  0  0
  4 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  2 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END

     RDKit          3D

105111  0  0  0  0  0  0  0  0999 V2000
    7.2556   -2.5272    3.1179 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2358   -2.4207    2.0415 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9842   -3.4335    1.3445 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5410   -1.2706    1.7557 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5894   -1.2513    0.7184 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2095   -0.9814    1.1783 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2954   -0.6677    0.0403 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0617   -1.2700    0.1361 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0290   -0.4127    0.2742 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7670   -0.5815    1.5548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1592   -1.0534    1.5246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8483   -1.1278    0.2166 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8490   -2.5517   -0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6380   -2.8646   -1.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3108   -0.7779    0.3926 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1696   -1.1517   -0.7866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6215   -1.1813   -0.2884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9520   -0.0603    0.6223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9874   -0.5364    2.0832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2204    0.6725    0.3986 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.9424    0.4708   -0.8449 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1194   -0.1150   -0.9670 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5411   -0.1423   -2.3470 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5981   -0.6202   -2.8118 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5534    0.4656   -3.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5346    0.8952   -2.2000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9256    2.1624    0.6650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5339    2.1052    1.3197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9169    1.0267    0.4559 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8817    1.5187   -0.8146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5387    0.6286    0.8560 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5164    1.5974    0.3263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7078    1.1499   -0.8224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2921   -0.2781   -0.8634 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8288   -0.7988   -2.0774 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8258   -0.5187   -0.9762 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230   -0.8500   -1.1462 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0190   -0.0503   -1.3844 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5198    1.3698   -1.4427 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0782   -0.2083   -0.3123 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2605   -0.6975   -0.7467 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4028    0.0033   -0.4985 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3062   -0.6189    0.3710 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1515    0.3573    0.9396 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3914    1.4635    1.5981 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0174    0.9684   -0.1472 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.9580    2.3493   -0.1492 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5953    0.4474   -1.5164 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9988   -0.8885   -1.6544 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0825    0.5566   -1.7133 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7861   -0.1086   -2.8870 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0945   -3.1272    2.7627 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5317   -1.5241    3.5157 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7720   -3.0664    3.9575 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5784   -2.2600    0.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8207   -1.9441    1.6117 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354   -0.1611    1.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0897    0.4409    0.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4368    0.6096    0.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1947   -1.3056    2.2188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7005    0.3715    2.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7778   -0.4029    2.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2999   -2.0725    2.0078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587   -3.3025    0.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6551   -1.4516    1.2353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1044   -0.4992   -1.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8533   -2.1578   -1.1051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2639   -1.3368   -1.1528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6588   -2.1436    0.3224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1502   -0.1691    2.6782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9173   -0.2229    2.6012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0386   -1.6637    2.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9664    0.4428    1.2391 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7072   -0.5290   -0.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6060    0.4625   -2.5779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5400    2.0169   -2.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6617    2.6403    1.3038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8267    2.6270   -0.3486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0495    3.0864    1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.8740    2.4971   -0.9083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4730    0.6990    1.9670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8174    1.9626    1.1380 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.2281    1.4966   -1.7643 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6963   -1.5458   -1.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4190    0.1539   -1.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4722   -0.3130   -2.3520 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4185    1.4422   -1.6219 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6714    1.9056   -0.4600 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9816    1.9439   -2.2763 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0944    0.7470    0.2411 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0700    0.9131    0.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7954   -0.1422    1.6829 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2420    2.3549    0.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0320    1.8382    2.4483 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4603    1.1173    2.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0694    0.6789   -0.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8554    2.7664   -0.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1349    1.0535   -2.2722 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1244   -1.0664   -2.6343 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8707    1.6269   -1.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9698    0.5006   -3.6714 H   0  0  0  0  0  0  0  0  0  0  0  0
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 44 43  1  0
 43 42  1  0
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 37  7  1  0
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  7  8  1  0
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 12 13  1  6
 13 14  2  0
 12 15  1  0
 15 16  1  0
 16 17  1  0
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 27 28  1  0
 28 29  1  0
 29 30  1  6
 29 31  1  0
 31 32  1  0
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 36  9  1  0
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 39 93  1  0
  7 58  1  1
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  5 55  1  6
  1 52  1  0
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  1 54  1  0
  9 59  1  1
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 16 66  1  0
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 32 84  1  0
 33 85  1  0
 33 86  1  0
 35 87  1  0
 36 88  1  0
 36 89  1  0
 22 74  1  0
 26 75  1  0
 26 76  1  0
 50104  1  6
 51105  1  0
 48102  1  6
 49103  1  0
 46100  1  1
 47101  1  0
M  END


  Mrv1533004161521212D          

 51 57  0  0  0  0            999 V2000
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   -2.2825   -4.0500    0.0000 C   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
   -2.0022   -3.2741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6582   -3.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6857   -4.2451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    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
    5.0168   -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
    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
   -1.7794   -6.8633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5916   -7.0085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2476   -7.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5279   -8.2699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4355   -7.3487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0963   -7.9795    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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  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
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 10 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  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 24 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 21 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 18 39  1  0  0  0  0
 29 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 40 45  1  0  0  0  0
  4 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  2 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0149634

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(C)OC(CC2OC(C)=O)OC2CCC3(C=O)C4CCC5(C)C(CCC5(O)C4CCC3(O)C2)C2=CC(=O)OC2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C37H54O14/c1-18-29(41)30(42)31(43)33(48-18)51-32-19(2)47-28(14-26(32)49-20(3)39)50-22-5-10-35(17-38)24-6-9-34(4)23(21-13-27(40)46-16-21)8-12-37(34,45)25(24)7-11-36(35,44)15-22/h13,17-19,22-26,28-33,41-45H,5-12,14-16H2,1-4H3

> <INCHI_KEY>
JPDBUGXWRYMUSG-UHFFFAOYSA-N

> <FORMULA>
C37H54O14

> <MOLECULAR_WEIGHT>
722.825

> <EXACT_MASS>
722.351356419

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
77.31684192731124

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-{[2-formyl-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate

> <ALOGPS_LOGP>
-0.20

> <JCHEM_LOGP>
0.7622492780000003

> <ALOGPS_LOGS>
-3.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.218375776686942

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.182632188248246

> <JCHEM_PKA_STRONGEST_BASIC>
0.2689707751947149

> <JCHEM_POLAR_SURFACE_AREA>
207.73999999999995

> <JCHEM_REFRACTIVITY>
175.29690000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.32e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-{[2-formyl-7,11-dihydroxy-15-methyl-14-(5-oxo-2H-furan-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       1.226 -11.998   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.290 -12.269   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.282 -11.092   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -2.798 -11.363   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -3.791 -10.186   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.268  -8.737   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.261  -7.560   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.777  -7.831   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.737  -6.112   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -2.221  -5.841   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.229  -7.018   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.752  -8.466   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.759  -9.644   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.757  -9.372   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.280  -7.924   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.749 -10.550   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.698  -4.392   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.182  -4.121   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.341  -2.673   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.857  -2.402   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.850  -3.579   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.373  -2.131   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.380  -0.953   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.366  -3.308   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.889  -1.859   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.405  -1.588   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.398  -2.766   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.069  -1.380   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.937  -2.816   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.365  -4.295   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.090  -5.159   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.874  -4.214   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.505  -5.709   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.358  -4.485   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.835  -5.934   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.319  -6.205   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.326  -5.027   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       1.803  -6.476   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       0.810  -5.298   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       9.882  -1.600   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.454  -0.121   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.728   0.744   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      10.779   2.283   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      11.944  -0.202   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      11.421  -1.650   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -3.322 -12.811   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -4.838 -13.082   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -2.329 -13.989   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -2.852 -15.437   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      -0.813 -13.718   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       0.180 -14.895   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   50                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   46                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11    6   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   10   18                                                       
CONECT   18   17   19   39                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   24   37                                             
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   34                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   32                                             
CONECT   28   27                                                            
CONECT   29   27   30   40                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27   33   34                                             
CONECT   33   32                                                            
CONECT   34   32   24   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   21   38   39                                             
CONECT   38   37                                                            
CONECT   39   37   18                                                       
CONECT   40   29   41   45                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   40                                                       
CONECT   46    4   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48    2   51                                                  
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  114    0
END

View in JSmol

Synonyms

Value	Source
6-{[2-formyl-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0,.0,]heptadecan-5-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetic acid	Generator
6-{[2-formyl-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetic acid	Generator

Chemical Formula

C₃₇H₅₄O₁₄

Average Mass

722.8250 Da

Monoisotopic Mass

722.35136 Da

IUPAC Name

6-{[2-formyl-7,11-dihydroxy-15-methyl-14-(5-oxo-2,5-dihydrofuran-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate

Traditional Name

6-{[2-formyl-7,11-dihydroxy-15-methyl-14-(5-oxo-2H-furan-3-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-5-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(C)OC(CC2OC(C)=O)OC2CCC3(C=O)C4CCC5(C)C(CCC5(O)C4CCC3(O)C2)C2=CC(=O)OC2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C37H54O14/c1-18-29(41)30(42)31(43)33(48-18)51-32-19(2)47-28(14-26(32)49-20(3)39)50-22-5-10-35(17-38)24-6-9-34(4)23(21-13-27(40)46-16-21)8-12-37(34,45)25(24)7-11-36(35,44)15-22/h13,17-19,22-26,28-33,41-45H,5-12,14-16H2,1-4H3

InChI Key

JPDBUGXWRYMUSG-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
Erysimum cheiranthoides	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
Disaccharide
Glycosyl compound
O-glycosyl compound
2-furanone
Dicarboxylic acid or derivatives
Oxane
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Polyol
Aldehyde
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
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	-0.2	ALOGPS
logP	0.76	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	7.18	ChemAxon
pKa (Strongest Basic)	0.27	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	207.74 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	175.3 m³·mol⁻¹	ChemAxon
Polarizability	77.32 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate (NP0149634)

MOL for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

3D MOL for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

3D SDF for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

3D-SDF for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

PDB for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

3D PDB for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

SMILES for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

INCHI for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

Structure for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)

3D Structure for NP0149634 (6-{[9a-formyl-3a,5a-dihydroxy-11a-methyl-1-(5-oxo-2h-furan-3-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]oxy}-2-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-4-yl acetate)