NP-MRD: Showing NP-Card for (+)-Tarecilioside E (NP0072432)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 17:46:48 UTC

Updated at

2022-04-28 17:46:48 UTC

NP-MRD ID

NP0072432

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Tarecilioside E

Description

(2R,3R,4S,5R,6R)-2-{[(1S,3R,6S,8R,10S,11S,12S,14S,15R,16R)-10,14-dihydroxy-15-[(2R,5R)-5-hydroxy-6-methyl-6-{[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}heptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-6-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus. (+)-Tarecilioside E is found in Tarenna gracilipes and Tarenna gracilipes (HAY.) OHWI. Based on a literature review very few articles have been published on (2R,3R,4S,5R,6R)-2-{[(1S,3R,6S,8R,10S,11S,12S,14S,15R,16R)-10,14-dihydroxy-15-[(2R,5R)-5-hydroxy-6-methyl-6-{[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}heptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-6-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219462D          

 55 61  0  0  1  0            999 V2000
   -0.5318   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2803   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318   -1.4557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8121   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2803   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -0.5346    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1561   -1.1653    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8758   -1.9412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0636   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4076   -2.5719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682   -1.0201    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2485   -0.2441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7167    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6083    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730   -0.2709    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3024   -1.0634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6195   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0783   -1.3437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5794    0.3804    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3966    0.2675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9030    0.9189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7202    0.8060    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2266    1.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8779    0.9510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7329    2.1087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5502    1.9958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.0565    2.6472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8738    2.5343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1847    1.7701    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.6783    1.1188    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8611    1.2316    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3547    0.5803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9892    0.3546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0019    1.6573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5753    1.9637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0311    0.0418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685    1.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705   -1.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0924    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8921   -2.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1635   -2.4176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9045   -1.8914    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3727   -2.5221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6530   -3.2980    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4651   -3.4432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9970   -2.8125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7167   -2.0366    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2485   -1.4059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8091   -2.9577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7454   -4.2191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1212   -3.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4015   -4.7046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  1  0  0  0
  9 11  1  1  0  0  0
  8 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
  7 15  1  0  0  0  0
 13 16  1  1  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 12 19  1  0  0  0  0
 18 20  1  1  0  0  0
 17 21  1  1  0  0  0
 21 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
 28 27  1  6  0  0  0
 28 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
 32 33  1  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  1  0  0  0
 32 35  1  1  0  0  0
 31 36  1  1  0  0  0
 25 37  1  0  0  0  0
 24 38  1  6  0  0  0
 21 39  1  6  0  0  0
 12 40  1  6  0  0  0
  7 41  1  1  0  0  0
  5 41  1  1  0  0  0
  3 42  1  0  0  0  0
  3 43  1  0  0  0  0
  2 44  1  1  0  0  0
 45 44  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 45 50  1  0  0  0  0
 50 51  1  1  0  0  0
 49 52  1  6  0  0  0
 48 53  1  6  0  0  0
 47 54  1  6  0  0  0
 54 55  1  0  0  0  0
M  END

     RDKit          3D

125131  0  0  0  0  0  0  0  0999 V2000
   -4.0149    3.4110    0.0584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2515    2.1201   -0.3487 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3207    1.0673   -0.3063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3736    1.4810   -1.3143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5263    0.5700   -1.4535 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0795   -0.6786   -1.8489 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5293    0.4842   -0.3770 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.9644    1.8193    0.1805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9200   -0.2897    0.8101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6634   -0.1563   -0.8291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6310   -1.4405   -1.2076 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.8592   -1.5376   -2.6188 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0357   -0.9165   -2.9532 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1504   -1.8486   -2.5213 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.1656   -3.0175   -3.2520 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0734   -2.0984   -1.0604 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.7375   -3.3199   -0.7988 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7100   -2.2161   -0.4750 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.3120   -3.5611   -0.2952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0695    1.9749    0.4945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2214    1.8212    1.9499 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3632    1.2082    2.4213 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0832    0.8934    2.4276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0821    1.1015    1.3266 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5255    2.4576    1.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9419    0.0162    1.1884 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6545   -0.2849    2.4640 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2722   -1.5433    3.0067 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109   -0.2317    2.5222 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8145    0.4167    1.3532 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3010    0.2744    1.4724 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6648   -0.8755    2.4334 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8858    1.5091    2.1936 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0904    0.0353    0.2583 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9449   -1.0713    0.3248 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2684   -0.7394    0.0258 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5290   -1.4027   -1.2011 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5941   -0.7825   -1.8545 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1755   -1.6646   -2.9342 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1575   -1.9327   -3.8512 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6742   -0.3964   -0.8593 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.8922   -0.5979   -1.4926 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6208   -1.2843    0.3638 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.9550   -2.6022    0.0533 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2635   -1.1965    1.0224 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.3989   -0.3211    2.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3121   -0.1261   -1.0216 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0614    0.7444   -1.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2126    0.0820    0.0489 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5348   -1.1265   -0.3585 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7581    0.1835   -0.0200 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1616    0.8810   -1.1742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1004    1.6276   -1.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9761    1.0584    0.1033 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3600   -0.2991   -0.3531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2851    4.0131   -0.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2990    4.0424    0.6469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8477    3.1749    0.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9675    2.2804   -1.4043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0403    0.0502   -0.5162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8227    1.2034    0.6846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8425    1.4567   -2.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6436    2.5562   -1.2117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0658    0.9518   -2.4045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9835   -0.8049   -2.8085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5140    2.6835   -0.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6794    1.9565    1.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0648    1.9740    0.1413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0038   -0.8343    0.5126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6180   -1.0796    1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7714    0.3600    1.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6959   -2.0116   -1.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1422   -0.0033   -2.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1017   -0.7324   -4.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1125   -1.3037   -2.7509 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7055   -3.6952   -2.8168 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7036   -1.3309   -0.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5653   -3.6052    0.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7758   -1.7832    0.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5089   -3.8901    0.6182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5466    3.0243    0.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1426    2.7909    2.4923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2222    0.7677    3.2752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7076    1.2600    3.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4152   -0.1446    2.4983 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2175    2.3288    2.4417 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657    2.8332    0.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2347    3.1711    1.9259 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3255   -0.9210    1.0119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2277    0.4417    3.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8469   -2.2700    2.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5742   -1.2602    2.6106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4698    0.3069    3.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5931    1.5242    1.5007 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4084   -1.8587    2.0272 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7723   -0.8617    2.4952 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3169   -0.6692    3.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3142    1.7007    3.1010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7153    2.3765    1.4947 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9607    1.4179    2.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7609    0.9198    0.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4232    0.3251   -0.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2132    0.1496   -2.3048 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0026   -1.0969   -3.4301 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5486   -2.5915   -2.4541 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4377   -1.2240   -3.8170 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6031    0.6716   -0.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6156   -0.0349   -1.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4030   -0.9284    1.0648 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8491   -3.1738    0.8528 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0631   -2.2115    1.4307 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2347   -0.7449    2.9795 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9568   -1.1742   -1.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9295    0.0738   -1.9169 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6142    0.5988   -2.0400 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2872    1.7799   -0.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5326   -1.4141   -1.4298 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5036   -1.9620    0.3278 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0784    0.1468   -2.0307 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9293    1.6244   -1.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0136    2.7213   -0.8968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7171    1.4932   -1.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9984   -0.8920    0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4440   -0.8467   -0.7464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9213   -0.1438   -1.3332 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
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  6
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
  2 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 30 49  1  0
 49 50  1  6
 51 50  1  6
 51 52  1  0
 52 53  1  0
 53 54  1  0
 54 55  1  6
 49 48  1  0
 48 47  1  0
 47 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 38 41  1  0
 41 42  1  0
 41 43  1  0
 43 44  1  0
 43 45  1  0
 45 46  1  0
 34 31  1  0
 31 32  1  1
 31 33  1  0
 18 11  1  0
 54 20  1  0
 45 36  1  0
 54 24  1  0
 51 26  1  0
 31 30  1  0
 51 49  1  0
  1 56  1  0
  1 57  1  0
  1 58  1  0
  2 59  1  6
  3 60  1  0
  3 61  1  0
  4 62  1  0
  4 63  1  0
  5 64  1  6
  6 65  1  0
  8 66  1  0
  8 67  1  0
  8 68  1  0
  9 69  1  0
  9 70  1  0
  9 71  1  0
 11 72  1  6
 13 73  1  0
 13 74  1  0
 14 75  1  1
 15 76  1  0
 16 77  1  1
 17 78  1  0
 18 79  1  1
 19 80  1  0
 20 81  1  1
 21 82  1  1
 22 83  1  0
 23 84  1  0
 23 85  1  0
 25 86  1  0
 25 87  1  0
 25 88  1  0
 26 89  1  6
 27 90  1  1
 28 91  1  0
 29 92  1  0
 29 93  1  0
 30 94  1  1
 50117  1  0
 50118  1  0
 52119  1  0
 52120  1  0
 53121  1  0
 53122  1  0
 55123  1  0
 55124  1  0
 55125  1  0
 48115  1  0
 48116  1  0
 47113  1  0
 47114  1  0
 34101  1  6
 36102  1  6
 38103  1  6
 39104  1  0
 39105  1  0
 40106  1  0
 41107  1  1
 42108  1  0
 43109  1  1
 44110  1  0
 45111  1  1
 46112  1  0
 32 95  1  0
 32 96  1  0
 32 97  1  0
 33 98  1  0
 33 99  1  0
 33100  1  0
M  END


  Mrv1652304282219462D          

 55 61  0  0  1  0            999 V2000
   -0.5318   -0.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8121   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2803   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5318   -1.4557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8121   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2803   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -0.5346    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1561   -1.1653    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8758   -1.9412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0636   -2.0864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4076   -2.5719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682   -1.0201    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2485   -0.2441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7167    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6083    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730   -0.2709    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3024   -1.0634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6195   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0783   -1.3437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5794    0.3804    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3966    0.2675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9030    0.9189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7202    0.8060    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2266    1.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8779    0.9510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7329    2.1087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5502    1.9958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.0565    2.6472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8738    2.5343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1847    1.7701    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.6783    1.1188    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8611    1.2316    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3547    0.5803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9892    0.3546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0019    1.6573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5753    1.9637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0311    0.0418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685    1.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7705   -1.8210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0924    0.0961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8921   -2.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1635   -2.4176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9045   -1.8914    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3727   -2.5221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6530   -3.2980    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4651   -3.4432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9970   -2.8125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7167   -2.0366    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2485   -1.4059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8091   -2.9577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7454   -4.2191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1212   -3.9287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4015   -4.7046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  1  0  0  0
  9 11  1  1  0  0  0
  8 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
  7 15  1  0  0  0  0
 13 16  1  1  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 12 19  1  0  0  0  0
 18 20  1  1  0  0  0
 17 21  1  1  0  0  0
 21 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
 28 27  1  6  0  0  0
 28 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
 32 33  1  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  1  0  0  0
 32 35  1  1  0  0  0
 31 36  1  1  0  0  0
 25 37  1  0  0  0  0
 24 38  1  6  0  0  0
 21 39  1  6  0  0  0
 12 40  1  6  0  0  0
  7 41  1  1  0  0  0
  5 41  1  1  0  0  0
  3 42  1  0  0  0  0
  3 43  1  0  0  0  0
  2 44  1  1  0  0  0
 45 44  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 45 50  1  0  0  0  0
 50 51  1  1  0  0  0
 49 52  1  6  0  0  0
 48 53  1  6  0  0  0
 47 54  1  6  0  0  0
 54 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0072432

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C41H70O14/c1-19(8-9-25(46)37(4,5)55-34-31(50)28(47)22(45)17-52-34)27-21(44)15-39(7)33-20(43)14-24-36(2,3)26(54-35-32(51)30(49)29(48)23(16-42)53-35)10-11-40(24)18-41(33,40)13-12-38(27,39)6/h19-35,42-51H,8-18H2,1-7H3/t19-,20+,21+,22-,23-,24+,25-,26+,27+,28-,29+,30+,31-,32-,33+,34+,35+,38-,39+,40-,41+/m1/s1

> <INCHI_KEY>
BHRNXASDOAEKSN-HGKWOHTCSA-N

> <FORMULA>
C41H70O14

> <MOLECULAR_WEIGHT>
786.997

> <EXACT_MASS>
786.476556934

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
125

> <JCHEM_AVERAGE_POLARIZABILITY>
87.02726198637738

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5R,6R)-2-{[(1S,3R,6S,8R,10S,11S,12S,14S,15R,16R)-10,14-dihydroxy-15-[(2R,5R)-5-hydroxy-6-methyl-6-{[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}heptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
0.65

> <JCHEM_LOGP>
-0.12164237466666636

> <ALOGPS_LOGS>
-3.63

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.450826492763905

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.923151340865196

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835440417778

> <JCHEM_POLAR_SURFACE_AREA>
239.21999999999994

> <JCHEM_REFRACTIVITY>
196.42990000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.84e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5R,6R)-2-{[(1S,3R,6S,8R,10S,11S,12S,14S,15R,16R)-10,14-dihydroxy-15-[(2R,5R)-5-hydroxy-6-methyl-6-{[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}heptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -0.993  -0.363   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.516  -1.811   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.523  -2.988   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.993  -2.717   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.516  -1.269   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.523  -0.092   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.032  -0.998   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.025  -2.175   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.501  -3.624   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.985  -3.895   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.494  -4.801   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.541  -1.904   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.064  -0.456   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.071   0.722   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.555   0.451   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.736   0.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.603  -0.506   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.031  -1.985   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.756  -2.849   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.479  -2.508   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.548   0.710   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.074   0.499   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.019   1.715   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.544   1.505   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.490   2.720   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.705   1.775   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      14.435   3.936   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      15.960   3.726   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      16.906   4.941   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      18.431   4.731   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      19.011   3.304   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      18.066   2.088   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.541   2.299   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      15.595   1.083   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      18.647   0.662   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      20.537   3.094   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      12.274   3.666   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      13.125   0.078   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       7.968   2.137   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.172  -3.399   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.039   0.179   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.665  -4.022   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -0.305  -4.513   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -3.032  -2.082   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      -3.555  -3.531   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -2.562  -4.708   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -3.086  -6.156   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -4.602  -6.427   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -5.594  -5.250   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -5.071  -3.802   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -6.064  -2.624   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0      -7.110  -5.521   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0      -5.125  -7.876   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      -2.093  -7.334   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      -2.616  -8.782   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   44                                                  
CONECT    3    2    4   42   43                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   41                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   15   41                                             
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    4                                                       
CONECT   11    9                                                            
CONECT   12    8   13   19   40                                             
CONECT   13   12   14   16   17                                             
CONECT   14   13   15                                                       
CONECT   15   14    7                                                       
CONECT   16   13                                                            
CONECT   17   13   18   21                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   12                                                       
CONECT   20   18                                                            
CONECT   21   17   22   39                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   38                                                  
CONECT   25   24   26   27   37                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33   35                                                  
CONECT   33   32   28   34                                                  
CONECT   34   33                                                            
CONECT   35   32                                                            
CONECT   36   31                                                            
CONECT   37   25                                                            
CONECT   38   24                                                            
CONECT   39   21                                                            
CONECT   40   12                                                            
CONECT   41    7    5                                                       
CONECT   42    3                                                            
CONECT   43    3                                                            
CONECT   44    2   45                                                       
CONECT   45   44   46   50                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48   54                                                  
CONECT   48   47   49   53                                                  
CONECT   49   48   50   52                                                  
CONECT   50   49   45   51                                                  
CONECT   51   50                                                            
CONECT   52   49                                                            
CONECT   53   48                                                            
CONECT   54   47   55                                                       
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  122    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₇₀O₁₄

Average Mass

786.9970 Da

Monoisotopic Mass

786.47656 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C41H70O14/c1-19(8-9-25(46)37(4,5)55-34-31(50)28(47)22(45)17-52-34)27-21(44)15-39(7)33-20(43)14-24-36(2,3)26(54-35-32(51)30(49)29(48)23(16-42)53-35)10-11-40(24)18-41(33,40)13-12-38(27,39)6/h19-35,42-51H,8-18H2,1-7H3/t19-,20+,21+,22-,23-,24+,25-,26+,27+,28-,29+,30+,31-,32-,33+,34+,35+,38-,39+,40-,41+/m1/s1

InChI Key

BHRNXASDOAEKSN-HGKWOHTCSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Tarenna gracilipes	LOTUS Database	35616633
Tarenna gracilipes (HAY.) OHWI	Plant	KNApSAcK

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Cucurbitacin glycosides

Alternative Parents

Substituents

Cucurbitacin glycoside skeleton
Triterpene saponin
Triterpene glycoside
Cycloartanol-skeleton
Triterpenoid
Cycloartane-skeleton
9b,19-cyclo-lanostane-skeleton
Trihydroxy bile acid, alcohol, or derivatives
24-hydroxysteroid
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
7-hydroxysteroid
7-alpha-hydroxysteroid
16-hydroxysteroid
16-beta-hydroxysteroid
Hydroxysteroid
O-glycosyl compound
Glycosyl compound
Oxane
Monosaccharide
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
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	0.65	ALOGPS
logP	-0.12	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	11.92	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	239.22 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	196.43 m³·mol⁻¹	ChemAxon
Polarizability	87.03 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

162857101

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Tarecilioside E (NP0072432)

MOL for NP0072432 ((+)-Tarecilioside E)

3D MOL for NP0072432 ((+)-Tarecilioside E)

3D SDF for NP0072432 ((+)-Tarecilioside E)

3D-SDF for NP0072432 ((+)-Tarecilioside E)

PDB for NP0072432 ((+)-Tarecilioside E)

3D PDB for NP0072432 ((+)-Tarecilioside E)

SMILES for NP0072432 ((+)-Tarecilioside E)

INCHI for NP0072432 ((+)-Tarecilioside E)

Structure for NP0072432 ((+)-Tarecilioside E)

3D Structure for NP0072432 ((+)-Tarecilioside E)