NP-MRD: Showing NP-Card for Turrillianoside (NP0073964)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 19:10:50 UTC

Updated at

2022-04-28 19:10:50 UTC

NP-MRD ID

NP0073964

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Turrillianoside

Description

(2S,3R,4R,5R,6S)-2-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1'R,2S,2'S,3S,4'S,5S,7'S,8'S,9'S,10'R,12'S,13'R,16'S)-5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosan]-18'-ene-3,10'-dioloxy]oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative. Turrillianoside is found in Veronica turrilliana. Based on a literature review very few articles have been published on (2S,3R,4R,5R,6S)-2-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1'R,2S,2'S,3S,4'S,5S,7'S,8'S,9'S,10'R,12'S,13'R,16'S)-5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosan]-18'-ene-3,10'-dioloxy]oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282221102D          

 53 60  0  0  1  0            999 V2000
   10.8476    1.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2179    2.0253    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7645    2.7146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9409    2.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4876    3.3559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6640    3.3080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2937    2.5708    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.7470    1.8815    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.5707    1.9294    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0240    1.2401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2004    1.1922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3768    1.1442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5532    1.0963    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0998    1.7856    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4701    2.5228    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8834    3.1028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1505    2.7240    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2843    1.9099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5514    1.5312    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9646    2.1111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3349    2.8484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734    1.3392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8594    1.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3365    1.8436    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6277    2.6155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4417    2.7493    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7329    3.5212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5224    1.7098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4270    0.7156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6545    1.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1829    0.3591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0415    2.0732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4948    1.3840    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3184    1.4319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7717    0.7426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.4014    0.0054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5778   -0.0426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1245    0.6467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3009    0.5988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2075   -0.7798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8548   -0.6839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4845   -1.4212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.9378   -2.1105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.5675   -2.8477    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.7439   -2.8956    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.2906   -2.2063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6609   -1.4691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4670   -2.2543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3736   -3.6329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0208   -3.5370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7614   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.5953    0.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0486    0.1012    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  2  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  9 11  1  1  0  0  0
  8 12  1  1  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
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 17 21  1  1  0  0  0
 20 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
 20 26  1  0  0  0  0
 26 27  1  6  0  0  0
 24 28  1  1  0  0  0
 19 29  1  6  0  0  0
 14 30  1  1  0  0  0
 13 31  1  1  0  0  0
  2 32  1  1  0  0  0
 33 32  1  6  0  0  0
 33 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
 37 38  1  0  0  0  0
 33 38  1  0  0  0  0
 38 39  1  1  0  0  0
 37 40  1  6  0  0  0
 36 41  1  1  0  0  0
 42 41  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 42 47  1  0  0  0  0
 46 48  1  6  0  0  0
 45 49  1  1  0  0  0
 44 50  1  6  0  0  0
 43 51  1  6  0  0  0
 35 52  1  6  0  0  0
 52 53  1  0  0  0  0
M  END

     RDKit          3D

115122  0  0  0  0  0  0  0  0999 V2000
  -11.0941    0.8106   -2.1672 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0921    0.1914   -0.7632 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.2991    1.0375    0.1781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6089    0.3126    1.1413 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5340   -0.2725    0.5338 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.8471   -1.1922    1.3710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5951   -0.7697    1.5607 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4427   -1.7498    1.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3913   -0.6961    1.2356 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0325   -1.0696    0.9341 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4906   -1.8837    2.1267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1058   -2.2568    1.7546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3605   -1.4689    1.0170 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0194   -1.9379    0.6989 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9777   -0.8838    1.1902 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7205   -0.4574    0.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0881   -0.6729    0.3122 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6795    0.5853    0.2284 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0268    0.4354    0.5530 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6105    1.7635    0.9085 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8768    2.2410    2.0123 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7286   -0.2445   -0.6030 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0763   -0.2411   -0.3594 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8124    0.4301   -1.3305 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.6147   -0.5535   -1.9516 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5638   -0.9108   -0.9711 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0653   -2.3109   -1.1658 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6671    0.1238   -1.0344 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1427    0.3134    0.2824 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0390    1.4289   -1.4850 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.8638    1.3335   -2.8805 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6875    1.5185   -0.8076 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1627    2.7699   -1.1258 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1553   -1.6414   -0.7313 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5639   -2.1958   -1.9468 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6513   -1.6328   -0.7158 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1294   -2.8975   -0.5959 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2531    0.2625    1.8661 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1937    0.8606    1.0022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8105   -0.1660    0.4918 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6637   -0.1204   -1.0363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2095    0.1965    0.9070 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8125    1.3358    0.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3070    1.4253    0.2098 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7513    2.3183   -0.7355 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9402    0.1002    0.0568 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4451   -0.4856   -1.2776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3345   -0.1251    0.1700 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.4534    0.7807    0.1527 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.5517    1.8530    1.1585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9409   -1.0704   -0.6864 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.4936   -2.3909   -0.6489 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4423   -1.1459   -0.8681 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1739    1.4481   -2.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0876    0.0120   -2.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0159    1.3979   -2.3038 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1502    0.0715   -0.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0040    1.7580    0.6685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6065    1.6594   -0.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3968   -0.0749    2.3680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2724   -2.2230    2.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5851   -2.4269    0.6449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3960   -0.0558    2.1647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8396   -1.6851    0.0606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4157   -1.1755    2.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1329   -2.7415    2.3344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7330   -3.2244    2.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2484   -2.9000    1.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1520   -2.1590   -0.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6772   -1.2924    1.9476 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2511   -1.1378    1.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0809   -0.2315    1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6545    1.5908    1.2482 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5122    2.4779    0.0877 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1425    1.7442    2.8144 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4361    0.2894   -1.5266 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1705    0.8403   -2.1254 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0317   -0.8941    0.0168 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3511   -2.8541   -1.8226 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0810   -2.8918   -0.2055 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0849   -2.3059   -1.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.4779   -0.2159   -1.7074 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0185    1.2624    0.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6681    2.3041   -1.2299 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4103    0.6191   -3.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8894    1.4354    0.2994 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0539    3.3541   -0.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5111   -2.3167    0.0740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8772   -2.0275   -2.6498 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3114   -1.2406   -1.7192 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0650   -3.1051    0.3807 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8761   -0.1028    2.8401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0028    1.0379    2.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6786    1.4344    0.1902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3581    1.6068    1.6142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6240    0.9306   -1.3802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3667   -0.7706   -1.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3549   -0.5256   -1.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1133    0.4879    2.0007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4850    1.4879   -0.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4388    2.2817    0.6900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5650    1.8102    1.2407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9588    3.2154   -0.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5944    0.0242   -1.6946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3047   -0.2836   -1.9914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4085   -1.5773   -1.2055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6312   -1.0001   -0.5033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6576    1.1611   -0.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4647    2.8468    0.6292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8322    1.8717    1.9665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5580    1.9188    1.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4445   -0.6005   -1.5747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3558   -2.7117    0.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5934   -1.5957   -1.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8251   -1.9003   -0.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
 50 49  1  0
 49 48  1  0
 48  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  6
 40 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 44 46  1  0
 46 47  1  6
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  1  0
 32 33  1  0
 22 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
  7  6  1  0
  5  6  1  1
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  2 53  1  0
 53 51  1  0
 51 52  1  0
  5 49  1  0
 51  5  1  0
 46 48  1  0
 36 17  1  0
 46  9  1  0
 32 24  1  0
 42 10  1  0
 40 13  1  0
 50109  1  0
 50110  1  0
 50111  1  0
 49108  1  6
 48107  1  6
  7 60  1  1
  8 61  1  0
  8 62  1  0
  9 63  1  1
 10 64  1  6
 11 65  1  0
 11 66  1  0
 12 67  1  0
 14 68  1  0
 14 69  1  0
 15 70  1  1
 38 92  1  0
 38 93  1  0
 39 94  1  0
 39 95  1  0
 41 96  1  0
 41 97  1  0
 41 98  1  0
 42 99  1  1
 43100  1  0
 43101  1  0
 44102  1  1
 45103  1  0
 47104  1  0
 47105  1  0
 47106  1  0
 17 71  1  1
 19 72  1  1
 20 73  1  0
 20 74  1  0
 21 75  1  0
 22 76  1  6
 24 77  1  6
 26 78  1  1
 27 79  1  0
 27 80  1  0
 27 81  1  0
 28 82  1  6
 29 83  1  0
 30 84  1  6
 31 85  1  0
 32 86  1  1
 33 87  1  0
 34 88  1  1
 35 89  1  0
 36 90  1  6
 37 91  1  0
  3 58  1  0
  3 59  1  0
  2 57  1  1
  1 54  1  0
  1 55  1  0
  1 56  1  0
 53114  1  0
 53115  1  0
 51112  1  6
 52113  1  0
M  END


  Mrv1652304282221102D          

 53 60  0  0  1  0            999 V2000
   10.8476    1.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2179    2.0253    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7645    2.7146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9409    2.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4876    3.3559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6640    3.3080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2937    2.5708    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.7470    1.8815    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.5707    1.9294    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0240    1.2401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2004    1.1922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3768    1.1442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5532    1.0963    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0998    1.7856    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4701    2.5228    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8834    3.1028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1505    2.7240    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2843    1.9099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5514    1.5312    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9646    2.1111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3349    2.8484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6734    1.3392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8594    1.2055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3365    1.8436    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6277    2.6155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4417    2.7493    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7329    3.5212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5224    1.7098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4270    0.7156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6545    1.0911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1829    0.3591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0415    2.0732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4948    1.3840    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3184    1.4319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7717    0.7426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.4014    0.0054    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5778   -0.0426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1245    0.6467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3009    0.5988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2075   -0.7798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8548   -0.6839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4845   -1.4212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.9378   -2.1105    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.5675   -2.8477    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.7439   -2.8956    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.2906   -2.2063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6609   -1.4691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4670   -2.2543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3736   -3.6329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0208   -3.5370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7614   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.5953    0.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0486    0.1012    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  2  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  9 11  1  1  0  0  0
  8 12  1  1  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
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 17 21  1  1  0  0  0
 20 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
 20 26  1  0  0  0  0
 26 27  1  6  0  0  0
 24 28  1  1  0  0  0
 19 29  1  6  0  0  0
 14 30  1  1  0  0  0
 13 31  1  1  0  0  0
  2 32  1  1  0  0  0
 33 32  1  6  0  0  0
 33 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
 37 38  1  0  0  0  0
 33 38  1  0  0  0  0
 38 39  1  1  0  0  0
 37 40  1  6  0  0  0
 36 41  1  1  0  0  0
 42 41  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 42 47  1  0  0  0  0
 46 48  1  6  0  0  0
 45 49  1  1  0  0  0
 44 50  1  6  0  0  0
 43 51  1  6  0  0  0
 35 52  1  6  0  0  0
 52 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0073964

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@@H]2[C@H](C[C@H]3[C@@H]4CC=C5C[C@H](CC[C@]5(C)[C@H]4C[C@@H](O)[C@]23C)O[C@@H]2O[C@H](CO)[C@@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)[C@H](O)[C@H]2O)O[C@@]11OC[C@@H](C)C[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C39H62O14/c1-16-10-27(42)39(48-15-16)17(2)28-24(53-39)12-23-21-7-6-19-11-20(8-9-37(19,4)22(21)13-26(41)38(23,28)5)50-36-33(47)31(45)34(25(14-40)51-36)52-35-32(46)30(44)29(43)18(3)49-35/h6,16-18,20-36,40-47H,7-15H2,1-5H3/t16-,17-,18-,20-,21+,22-,23-,24-,25+,26+,27-,28+,29-,30+,31+,32+,33+,34+,35-,36+,37-,38+,39-/m0/s1

> <INCHI_KEY>
GLANCWZQIQVJID-NJLQRSTASA-N

> <FORMULA>
C39H62O14

> <MOLECULAR_WEIGHT>
754.911

> <EXACT_MASS>
754.413956676

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
115

> <JCHEM_AVERAGE_POLARIZABILITY>
82.58261764767619

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4R,5R,6S)-2-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1'R,2S,2'S,3S,4'S,5S,7'S,8'S,9'S,10'R,12'S,13'R,16'S)-5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosan]-18'-ene-3,10'-dioloxy]oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

> <ALOGPS_LOGP>
0.57

> <JCHEM_LOGP>
0.3555309213333301

> <ALOGPS_LOGS>
-3.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.445320778155399

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.924232314471215

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9395336353627277

> <JCHEM_POLAR_SURFACE_AREA>
217.21999999999997

> <JCHEM_REFRACTIVITY>
186.31540000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.57e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R,5R,6S)-2-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1'R,2S,2'S,3S,4'S,5S,7'S,8'S,9'S,10'R,12'S,13'R,16'S)-5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosan]-18'-ene-3,10'-dioloxy]oxan-3-yl]oxy}-6-methyloxane-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      20.249   2.404   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.940   3.781   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.094   5.067   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.556   4.978   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.710   6.264   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.173   6.175   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.482   4.799   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.328   3.512   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.865   3.602   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.711   2.315   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.174   2.225   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.637   2.136   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.099   2.046   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.253   3.333   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.944   4.709   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.849   5.792   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.481   5.085   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.731   3.565   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.363   2.858   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.267   3.941   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.959   5.317   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       8.724   2.500   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.204   2.250   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.228   3.441   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.772   4.882   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.291   5.132   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.835   6.573   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.708   3.192   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.130   1.336   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.422   2.037   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      13.408   0.670   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      22.477   3.870   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      23.324   2.583   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      24.861   2.673   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      25.707   1.386   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      25.016   0.010   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      23.479  -0.079   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      22.632   1.207   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      21.095   1.118   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      22.787  -1.456   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      25.862  -1.277   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      25.171  -2.653   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      26.017  -3.940   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      25.326  -5.316   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      23.789  -5.405   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      22.942  -4.118   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      23.634  -2.742   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      21.405  -4.208   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      23.097  -6.781   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      26.172  -6.602   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      27.555  -3.850   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      27.245   1.476   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      28.091   0.189   0.000  0.00  0.00           O+0
CONECT    1    2   10                                                       
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   15                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8    4   10   11                                             
CONECT   10    9    1                                                       
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14   31                                                  
CONECT   14   13   15   18   30                                             
CONECT   15   14    7   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17   14   19                                                  
CONECT   19   18   20   29                                                  
CONECT   20   19   21   22   26                                             
CONECT   21   20   17                                                       
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25   20   27                                                  
CONECT   27   26                                                            
CONECT   28   24                                                            
CONECT   29   19                                                            
CONECT   30   14                                                            
CONECT   31   13                                                            
CONECT   32    2   33                                                       
CONECT   33   32   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   52                                                  
CONECT   36   35   37   41                                                  
CONECT   37   36   38   40                                                  
CONECT   38   37   33   39                                                  
CONECT   39   38                                                            
CONECT   40   37                                                            
CONECT   41   36   42                                                       
CONECT   42   41   43   47                                                  
CONECT   43   42   44   51                                                  
CONECT   44   43   45   50                                                  
CONECT   45   44   46   49                                                  
CONECT   46   45   47   48                                                  
CONECT   47   46   42                                                       
CONECT   48   46                                                            
CONECT   49   45                                                            
CONECT   50   44                                                            
CONECT   51   43                                                            
CONECT   52   35   53                                                       
CONECT   53   52                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  120    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₆₂O₁₄

Average Mass

754.9110 Da

Monoisotopic Mass

754.41396 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@@H]2[C@H](C[C@H]3[C@@H]4CC=C5C[C@H](CC[C@]5(C)[C@H]4C[C@@H](O)[C@]23C)O[C@@H]2O[C@H](CO)[C@@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)[C@H](O)[C@H]2O)O[C@@]11OC[C@@H](C)C[C@@H]1O

InChI Identifier

InChI=1S/C39H62O14/c1-16-10-27(42)39(48-15-16)17(2)28-24(53-39)12-23-21-7-6-19-11-20(8-9-37(19,4)22(21)13-26(41)38(23,28)5)50-36-33(47)31(45)34(25(14-40)51-36)52-35-32(46)30(44)29(43)18(3)49-35/h6,16-18,20-36,40-47H,7-15H2,1-5H3/t16-,17-,18-,20-,21+,22-,23-,24-,25+,26+,27-,28+,29-,30+,31+,32+,33+,34+,35-,36+,37-,38+,39-/m0/s1

InChI Key

GLANCWZQIQVJID-NJLQRSTASA-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
Veronica turrilliana	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal saponins

Alternative Parents

Substituents

Steroidal saponin
Triterpenoid
Spirostane skeleton
23-hydroxysteroid
Hydroxysteroid
12-hydroxysteroid
Delta-5-steroid
O-glycosyl compound
Glycosyl compound
Disaccharide
Ketal
Oxane
Tetrahydrofuran
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	0.57	ALOGPS
logP	0.36	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	11.92	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	217.22 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	186.32 m³·mol⁻¹	ChemAxon
Polarizability	82.58 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

163013151

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Turrillianoside (NP0073964)

MOL for NP0073964 (Turrillianoside)

3D MOL for NP0073964 (Turrillianoside)

3D SDF for NP0073964 (Turrillianoside)

3D-SDF for NP0073964 (Turrillianoside)

PDB for NP0073964 (Turrillianoside)

3D PDB for NP0073964 (Turrillianoside)

SMILES for NP0073964 (Turrillianoside)

INCHI for NP0073964 (Turrillianoside)

Structure for NP0073964 (Turrillianoside)

3D Structure for NP0073964 (Turrillianoside)