NP-MRD: Showing NP-Card for 2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol (NP0328963)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 12:53:11 UTC

Updated at

2022-09-12 12:53:11 UTC

NP-MRD ID

NP0328963

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol

Description

2-{[4-Hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosane]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-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. 2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol is found in Asparagus acutifolius. 2-{[4-Hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosane]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171513252D          

 60 68  0  0  0  0            999 V2000
    4.3030   -3.2858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1170   -3.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4082   -2.3802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2223   -2.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7452   -2.8845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4540   -3.6564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6399   -3.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1155   -2.1473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9311   -2.2716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6640   -1.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2507   -2.4728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0743   -2.4249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4446   -1.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2682   -1.6397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7215   -2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5451   -2.2811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9984   -2.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6282   -3.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8046   -3.7555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3512   -3.0662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9810   -3.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5276   -3.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1573   -3.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3337   -3.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8804   -3.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4351   -3.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0648   -3.0857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9405   -3.9013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319   -3.4645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076   -4.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8221   -2.9224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2754   -3.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0990   -3.5638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5523   -4.2531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3759   -4.2051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8292   -4.8944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1820   -4.9903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6353   -5.6796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2651   -6.4168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4415   -6.4648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0712   -7.2020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5245   -7.8913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1542   -8.6285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3481   -7.8433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8014   -8.5326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -7.1061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5420   -7.0582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3584   -5.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9881   -5.7755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9051   -4.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0815   -4.3969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7112   -5.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1645   -5.8234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7942   -6.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9706   -6.6086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6003   -7.3458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5173   -5.9193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6937   -5.9672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8876   -5.1821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4343   -4.4928    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
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 12 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
 11 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  9 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 17 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 39 46  1  0  0  0  0
 46 47  1  0  0  0  0
 37 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 32 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  1  0  0  0  0
 57 58  1  0  0  0  0
 57 59  1  0  0  0  0
 52 59  1  0  0  0  0
 59 60  1  0  0  0  0
M  END

     RDKit          3D

130138  0  0  0  0  0  0  0  0999 V2000
   11.5192    1.9143   -1.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4242    1.6258   -2.2360 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3631    0.1482   -2.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7973   -0.5729   -1.3633 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3934   -0.1068   -1.1426 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.1103    1.0395   -1.8816 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0603    2.0286   -1.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274   -1.1181   -1.5660 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2899   -1.9499   -0.5054 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8559   -2.5100   -0.5752 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0954   -1.2745   -0.4038 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6515   -1.3153   -0.1224 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8252   -2.2355   -0.9425 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3803   -2.0861   -0.6372 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0607   -0.8837    0.2657 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3769   -0.8226    0.5841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0442    0.4980    0.6191 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3018    0.3934    0.0876 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3433    0.6759    0.9090 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0529    1.7188    0.4177 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9597    1.4843   -0.5630 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4071    2.2094   -1.8056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1406    1.6419   -2.0759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2689    0.1076   -0.9596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6706   -0.1081   -0.9030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2186   -0.4601   -2.1050 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.7844   -1.7319   -2.1110 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8331   -1.8996   -1.2494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9287   -0.9019   -1.3926 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.7781   -1.0580   -0.2780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4279    0.4971   -1.5225 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.4706    1.2409   -2.1174 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2818    0.5300   -2.4958 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.7631    1.8164   -2.6292 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6640   -1.0069   -0.1842 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5165   -2.0946   -0.0158 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2839   -0.4650    1.1628 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4214    0.0579    1.7580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6726   -0.4838    3.0024 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5932    0.5148    3.9729 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6317    1.4090    3.9580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4511    1.3880    2.7036 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.5544    2.2420    2.9461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0056    0.0156    2.4719 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.2719   -0.1376    3.0584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0692   -1.0424    3.0111 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.4738   -1.4135    4.2955 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2686    1.6210   -0.0175 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2140    1.5415    0.3422 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7166    0.2980   -0.3351 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3292    0.4330   -1.8175 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1993    0.1446   -0.2681 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8472    0.9381    0.8420 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3433    0.7940    0.7999 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7427   -0.6416    0.8408 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2514   -1.3221    2.1096 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1658   -0.9584    0.6627 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6823   -1.6726    1.7723 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0596    0.1781    0.2933 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2755    0.1401    1.2011 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9465    1.0198   -0.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1647    2.5762   -0.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3500    2.4103   -1.7852 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6457    2.1375   -3.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3993   -0.1805   -2.7781 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6991    0.0437   -3.4520 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8248   -1.6688   -1.6289 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4794   -0.3679   -0.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1274    2.4026   -0.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7272    2.9019   -2.3157 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0270   -2.7261   -0.3258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6976   -3.3005    0.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7153   -2.9834   -1.5912 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3154   -0.5835   -1.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5410   -1.6488    0.9529 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0592   -2.1941   -2.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1220   -3.2845   -0.6446 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9583   -2.9763   -0.0869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8116   -2.0229   -1.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6047   -1.1133    1.2308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6070   -1.3487    1.5615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9061   -1.4896   -0.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1794    0.8264    1.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9227    0.9575    1.9118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8938    2.0545   -0.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3086    3.2907   -1.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0302    1.9374   -2.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2799    0.7936   -2.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0348   -0.0957   -2.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4512   -0.4970   -2.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2233   -2.9267   -1.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4442   -1.8856   -0.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5511   -1.1173   -2.3010 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6792   -1.9563    0.1210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1736    0.8978   -0.5391 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1639    0.6776   -2.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6846    0.1903   -3.4757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2982    2.4397   -2.0452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7898   -1.3980   -0.7501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4953   -2.6540   -0.8103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8830   -1.2154    1.8655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9235   -1.2509    3.2896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1932    2.4425    4.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3155    1.3035    4.8327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9344    1.8283    1.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3381    3.1639    2.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1725   -0.1076    1.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6738    0.7181    3.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1669   -1.9304    2.3422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8337   -1.0746    4.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4484    1.5869   -1.0959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6015    2.6195    0.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7043    2.4163   -0.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2978    1.5193    1.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3969   -0.0781   -2.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1195   -0.0180   -2.4575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3275    1.5242   -2.0960 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6632    0.5073   -1.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6413    2.0222    0.5942 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3943    0.7702    1.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8108    1.3716    1.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6635    1.1925   -0.2071 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4183   -0.8132    2.5871 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1228   -2.4095    1.9903 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1151   -1.2158    2.8338 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2784   -2.5790    1.8205 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5968    1.1741    0.4386 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8747    0.3580    2.2345 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6992   -0.8909    1.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0098    0.9151    0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
 60 59  1  0
 59  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  2  7  1  0
  7  6  1  0
  5  8  1  6
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 48  1  0
 48 49  1  0
 49 50  1  0
 50 51  1  6
 50 52  1  0
 52 53  1  0
 53 54  1  0
 54 55  1  0
 55 56  1  1
 55 57  1  0
 57 58  1  1
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 24 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 42 44  1  0
 44 45  1  0
 44 46  1  0
 46 47  1  0
 57 59  1  0
 37 19  1  0
 46 39  1  0
  6  5  1  0
 57  9  1  0
 33 26  1  0
 55 11  1  0
 52 12  1  0
 50 15  1  0
 60128  1  0
 60129  1  0
 60130  1  0
 59127  1  6
  4 67  1  0
  4 68  1  0
  3 65  1  0
  3 66  1  0
  2 64  1  6
  1 61  1  0
  1 62  1  0
  1 63  1  0
  7 69  1  0
  7 70  1  0
  9 71  1  1
 10 72  1  0
 10 73  1  0
 11 74  1  6
 12 75  1  1
 13 76  1  0
 13 77  1  0
 14 78  1  0
 14 79  1  0
 15 80  1  1
 16 81  1  0
 16 82  1  0
 17 83  1  1
 48111  1  0
 48112  1  0
 49113  1  0
 49114  1  0
 51115  1  0
 51116  1  0
 51117  1  0
 52118  1  6
 53119  1  0
 53120  1  0
 54121  1  0
 54122  1  0
 56123  1  0
 56124  1  0
 56125  1  0
 58126  1  0
 19 84  1  1
 21 85  1  1
 22 86  1  0
 22 87  1  0
 23 88  1  0
 24 89  1  6
 26 90  1  6
 28 91  1  0
 28 92  1  0
 29 93  1  6
 30 94  1  0
 31 95  1  1
 32 96  1  0
 33 97  1  6
 34 98  1  0
 35 99  1  6
 36100  1  0
 37101  1  1
 39102  1  1
 41103  1  0
 41104  1  0
 42105  1  6
 43106  1  0
 44107  1  6
 45108  1  0
 46109  1  6
 47110  1  0
M  END


  Mrv1533004171513252D          

 60 68  0  0  0  0            999 V2000
    4.3030   -3.2858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1170   -3.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4082   -2.3802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2223   -2.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7452   -2.8845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4540   -3.6564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6399   -3.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1155   -2.1473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9311   -2.2716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6640   -1.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2507   -2.4728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0743   -2.4249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4446   -1.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2682   -1.6397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7215   -2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5451   -2.2811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9984   -2.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6282   -3.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8046   -3.7555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3512   -3.0662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9810   -3.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5276   -3.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1573   -3.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3337   -3.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8804   -3.2101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4351   -3.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0648   -3.0857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9405   -3.9013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319   -3.4645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076   -4.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8221   -2.9224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2754   -3.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0990   -3.5638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5523   -4.2531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3759   -4.2051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8292   -4.8944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1820   -4.9903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6353   -5.6796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2651   -6.4168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4415   -6.4648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0712   -7.2020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5245   -7.8913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1542   -8.6285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3481   -7.8433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8014   -8.5326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -7.1061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5420   -7.0582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3584   -5.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9881   -5.7755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9051   -4.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0815   -4.3969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7112   -5.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1645   -5.8234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7942   -6.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9706   -6.6086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6003   -7.3458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5173   -5.9193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6937   -5.9672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8876   -5.1821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4343   -4.4928    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
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 12 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
 11 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  9 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 17 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 39 46  1  0  0  0  0
 46 47  1  0  0  0  0
 37 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 32 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  1  0  0  0  0
 57 58  1  0  0  0  0
 57 59  1  0  0  0  0
 52 59  1  0  0  0  0
 59 60  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0328963

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2(CCC(C)CO2)OC2CC3C4CCC5CC(CCC5(C)C4CCC3(C)C12O)OC1OC(CO)C(OC2OCC(O)C(O)C2O)C(O)C1OC1OCC(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C43H70O17/c1-19-7-12-42(55-16-19)20(2)43(52)29(60-42)14-25-23-6-5-21-13-22(8-10-40(21,3)24(23)9-11-41(25,43)4)56-39-36(59-38-33(50)31(48)27(46)18-54-38)34(51)35(28(15-44)57-39)58-37-32(49)30(47)26(45)17-53-37/h19-39,44-52H,5-18H2,1-4H3

> <INCHI_KEY>
TZNBDVDMJWNYEW-UHFFFAOYSA-N

> <FORMULA>
C43H70O17

> <MOLECULAR_WEIGHT>
859.016

> <EXACT_MASS>
858.461300794

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
130

> <JCHEM_AVERAGE_POLARIZABILITY>
93.2589403468447

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol

> <ALOGPS_LOGP>
0.50

> <JCHEM_LOGP>
0.6166884583333343

> <ALOGPS_LOGS>
-3.06

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.355495687961884

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.880555043015638

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5265806620519013

> <JCHEM_POLAR_SURFACE_AREA>
255.90999999999994

> <JCHEM_REFRACTIVITY>
205.66710000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.50e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       8.032  -6.134   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.552  -5.884   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.095  -4.443   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.615  -4.193   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.591  -5.384   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      12.048  -6.825   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      10.528  -7.075   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      13.282  -4.008   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      14.805  -4.240   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.173  -3.533   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.268  -4.616   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.805  -4.526   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      19.497  -3.150   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.034  -3.061   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.880  -4.347   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      23.418  -4.258   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      24.264  -5.545   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.573  -6.921   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      22.035  -7.010   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.189  -5.724   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      20.498  -7.100   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.652  -5.813   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      18.960  -7.189   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.423  -7.279   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      16.577  -5.992   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.746  -7.289   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.054  -5.760   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      14.822  -7.282   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.686  -6.467   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.454  -7.989   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      25.801  -5.455   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      26.647  -6.742   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      28.185  -6.652   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      29.031  -7.939   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      30.568  -7.850   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      31.415  -9.136   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      28.340  -9.315   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      29.186 -10.602   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      28.495 -11.978   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      26.957 -12.068   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      26.266 -13.444   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      27.112 -14.730   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      26.421 -16.107   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      28.650 -14.641   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      29.496 -15.928   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      29.341 -13.265   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      30.878 -13.175   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      26.802  -9.405   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      26.111 -10.781   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      25.956  -8.118   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      24.419  -8.208   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      23.728  -9.584   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      24.574 -10.870   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      23.883 -12.247   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      22.345 -12.336   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      21.654 -13.712   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0      21.499 -11.049   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0      19.962 -11.139   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0      22.190  -9.673   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      21.344  -8.386   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    8   29                                             
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    5    9                                                       
CONECT    9    8   10   27                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   31                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   12   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   11   26   27                                             
CONECT   26   25                                                            
CONECT   27   25    9   28   29                                             
CONECT   28   27                                                            
CONECT   29   27    5   30                                                  
CONECT   30   29                                                            
CONECT   31   17   32                                                       
CONECT   32   31   33   50                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35                                                            
CONECT   37   34   38   48                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   46                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   39   47                                                  
CONECT   47   46                                                            
CONECT   48   37   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   32   51                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53   59                                                  
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   58   59                                                  
CONECT   58   57                                                            
CONECT   59   57   52   60                                                  
CONECT   60   59                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  136    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₃H₇₀O₁₇

Average Mass

859.0160 Da

Monoisotopic Mass

858.46130 Da

IUPAC Name

2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosane]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1C2(CCC(C)CO2)OC2CC3C4CCC5CC(CCC5(C)C4CCC3(C)C12O)OC1OC(CO)C(OC2OCC(O)C(O)C2O)C(O)C1OC1OCC(O)C(O)C1O

InChI Identifier

InChI=1S/C43H70O17/c1-19-7-12-42(55-16-19)20(2)43(52)29(60-42)14-25-23-6-5-21-13-22(8-10-40(21,3)24(23)9-11-41(25,43)4)56-39-36(59-38-33(50)31(48)27(46)18-54-38)34(51)35(28(15-44)57-39)58-37-32(49)30(47)26(45)17-53-37/h19-39,44-52H,5-18H2,1-4H3

InChI Key

TZNBDVDMJWNYEW-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
Asparagus acutifolius	LOTUS Database	35616633

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
Oligosaccharide
Hydroxysteroid
17-hydroxysteroid
Glycosyl compound
O-glycosyl compound
Ketal
Oxane
Tertiary alcohol
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Oxacycle
Polyol
Acetal
Organoheterocyclic compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Organic oxygen 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	0.5	ALOGPS
logP	0.62	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	11.88	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	255.91 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	205.67 m³·mol⁻¹	ChemAxon
Polarizability	93.26 Å³	ChemAxon
Number of Rings	9	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

74218488

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol (NP0328963)

MOL for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

3D MOL for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

3D SDF for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

3D-SDF for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

PDB for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

3D PDB for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

SMILES for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

INCHI for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

Structure for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)

3D Structure for NP0328963 (2-{[4-hydroxy-2-(hydroxymethyl)-6-{5,7',9',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-8'-oloxy}-5-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl]oxy}oxane-3,4,5-triol)