NP-MRD: Showing NP-Card for 9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one (NP0146497)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 01:54:39 UTC

Updated at

2022-09-02 01:54:39 UTC

NP-MRD ID

NP0146497

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one

Description

9-[(5-{[4,5-Dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]Pentacosan-25-one belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one is found in Thalictrum minus. 9-[(5-{[4,5-Dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]Pentacosan-25-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191518152D          

 64 73  0  0  0  0            999 V2000
    7.9440   -7.4647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3744   -6.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9801   -6.0362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4104   -5.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0161   -4.6077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1913   -4.5869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7610   -5.2908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1553   -6.0154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9362   -5.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5058   -5.9738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5419   -4.5453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7171   -4.5245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -3.7999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9722   -3.8415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7970   -3.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2273   -3.1584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8330   -2.4338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0082   -2.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6139   -1.6884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0442   -0.9845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6499   -0.2599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8251   -0.2391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3948   -0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5700   -0.9221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1757   -0.1975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7453   -0.9014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6060    0.5063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2117    1.2310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3869    1.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9566    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5684    1.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3509   -0.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9282   -0.8961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5077   -1.6059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1033   -0.8868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6520   -0.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0698   -0.7035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7971   -0.2269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5684   -0.5197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5710    0.6062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2701    0.1681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2403   -0.6563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5114   -1.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0185   -1.6935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0414   -1.6552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1877   -0.6047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1579    0.2198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1472    1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7131    1.3658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1152    0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0664    1.4070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4308    0.4856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4803    1.3091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1412    0.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8690   -1.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2994   -0.3015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2633   -1.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0881   -1.7507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2352   -5.3531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6655   -4.6493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6295   -6.0778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4543   -6.0986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1992   -6.7816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5935   -7.5063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 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
 20 21  1  0  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
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 25 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
 33 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
 38 39  2  0  0  0  0
 38 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
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
 36 47  1  0  0  0  0
 40 47  1  0  0  0  0
 40 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 30 50  1  0  0  0  0
 36 50  1  0  0  0  0
 50 51  1  0  0  0  0
 27 52  1  0  0  0  0
 22 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
 20 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  1  0  0  0  0
 17 57  1  0  0  0  0
 57 58  1  0  0  0  0
  4 59  1  0  0  0  0
 59 60  1  0  0  0  0
 59 61  1  0  0  0  0
 61 62  1  0  0  0  0
 61 63  1  0  0  0  0
  2 63  1  0  0  0  0
 63 64  1  0  0  0  0
M  END

     RDKit          3D

138147  0  0  0  0  0  0  0  0999 V2000
    7.5714    1.3244    2.5722 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4237    2.2211    1.7116 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3216    1.7631    0.3923 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0187    0.5525    0.2626 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.7021   -0.0709   -0.9384 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2077   -1.3611   -0.7829 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2455   -2.2900   -1.3765 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1195   -3.5981   -0.8821 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2963   -2.2785   -2.8676 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1698   -1.2855   -3.3396 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9345   -2.1293   -3.4956 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2690   -3.4624   -3.6821 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1285   -4.3655   -4.3397 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1531   -1.1883   -2.8670 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9009   -1.4780   -1.5181 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9985   -0.4985   -1.0930 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7904   -1.0347   -0.6433 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6477   -0.6663   -1.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9062    0.4175   -1.1128 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1926    0.1228    0.0463 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9733   -0.4407   -0.1898 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1276    0.3198    0.2451 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8569   -0.4724    1.2481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3428   -0.4802    1.2291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8992    0.8023    0.5968 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1667    1.9204    1.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3674    0.9859    0.7249 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9367    0.4040    1.9861 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.1529    1.1702    2.4608 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1645   -0.1721    2.0827 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9867   -0.4644    0.8861 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.4024   -1.8494    1.0129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4804   -2.0892    0.2100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9529   -3.1855   -0.1637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0235   -0.7581   -0.1629 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.5008   -0.6832   -0.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8923    0.5674    0.6446 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3819    0.5432    2.0826 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1745    1.9853    2.4896 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4107   -0.0890    2.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0314   -0.1507    2.1785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3383    0.1417    0.8390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.4794   -0.4410   -1.5288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0031   -0.5072   -1.6323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1935   -0.3894   -0.3880 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3715   -1.6955   -0.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2595    0.8237   -0.4583 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2306    2.0275   -0.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5735    0.8586   -1.7820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2000    1.5547   -1.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3908    0.6836   -0.8090 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9106    0.7833   -0.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    2.1517   -1.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756   -0.1190   -2.1114 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9837   -0.7731    0.9743 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6274   -0.6095    2.3003 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4690   -0.5878    0.7452 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1753   -1.3459    1.6957 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4967    0.8975    0.2516 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9016    1.1160   -1.0652 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7441    2.2119    0.9833 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.0748    2.3504    1.3447 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8422    2.2059    2.2071 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0644    3.2930    3.0227 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0943    1.9169    3.3994 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2342    0.5415    2.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8015    0.8536    1.9569 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0503    3.2693    1.7856 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8360   -0.0811    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1429   -1.6488    0.2955 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2447   -1.9380   -1.0009 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8626   -3.6217    0.0576 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6841   -3.2832   -3.2019 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6219   -0.5693   -3.7376 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1199   -1.7341   -4.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3687   -3.3698   -4.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0231   -3.9600   -2.7024 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6476   -5.1385   -4.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5066   -2.4900   -1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8915   -2.1504   -0.7424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9736   -1.5027   -1.7956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1066   -0.3529   -2.5333 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0522    1.0936    0.5619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3870    1.2345    0.6886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5331   -1.5593    1.2068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4439   -0.1757    2.2647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6538   -1.3114    0.5564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7256   -0.6729    2.2182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8086    2.6981    0.6913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4825    1.5618    2.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9603    2.4611    1.9792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4491    2.1108    0.9561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2488    0.5103    2.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3760   -0.8127    2.9959 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9963   -1.5670    0.3475 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8914   -0.5690   -1.1348 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4938    1.4535    0.1309 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9996    0.6461    0.6764 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4671    2.7040    1.6948 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7568    2.2096    3.4071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1102    2.1874    2.7227 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1879    0.2515    4.0316 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4015    0.2306    2.6371 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2606   -1.1798    2.9294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4564    0.2478    3.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2381   -1.2371    2.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4557    1.1876    0.6671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9906   -1.1799   -2.2224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9396    0.5311   -1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7681   -1.4367   -2.2413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7053    0.2934   -2.3764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5652   -1.7384   -1.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0991   -2.5152   -0.5197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9675   -1.8427    0.6998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6428    2.8712   -1.0086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0816    1.8671   -1.1617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4199    2.4162    0.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0898    1.4846   -2.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3913   -0.1123   -2.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4149    2.5245   -1.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8413    1.6576   -2.7135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6309   -0.3802   -1.1226 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1826    2.0575   -2.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3336    2.7658   -1.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1616    2.6750   -0.6433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2557   -0.0739   -2.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5199   -1.1632   -1.7400 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5281    0.1294   -2.4883 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7741   -1.8562    0.7320 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9380   -1.2689    2.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7162    0.4873    0.8302 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3694   -2.2573    1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1393    0.1305    0.6895 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8726    1.1466   -1.1404 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4293    3.0772    0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6300    2.7190    0.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0716    1.2890    2.7923 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3699    4.0686    2.5213 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
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  1
 25 51  1  0
 51 50  1  0
 50 49  1  0
 49 47  1  0
 47 48  1  6
 47 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  1
 32 33  1  0
 33 34  2  0
 35 33  1  1
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 38 40  1  0
 38 41  1  0
 41 42  1  0
 35 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  1
 51 52  1  0
 52 53  1  0
 52 54  1  0
 20 55  1  0
 55 56  1  0
 55 57  1  0
 57 58  1  0
  4 59  1  0
 59 60  1  0
 59 61  1  0
 61 62  1  0
 61 63  1  0
 63 64  1  0
 63  2  1  0
 15  6  1  0
 57 17  1  0
 52 22  1  0
 27 25  1  0
 30 28  1  0
 42 31  1  0
 45 47  1  0
 45 31  1  0
 42 35  1  0
  1 65  1  0
  1 66  1  0
  1 67  1  0
  2 68  1  6
  4 69  1  1
  6 70  1  1
  7 71  1  1
  8 72  1  0
  9 73  1  6
 10 74  1  0
 11 75  1  6
 12 76  1  0
 12 77  1  0
 13 78  1  0
 15 79  1  6
 17 80  1  1
 18 81  1  0
 18 82  1  0
 20 83  1  1
 22 84  1  1
 23 85  1  0
 23 86  1  0
 24 87  1  0
 24 88  1  0
 26 89  1  0
 26 90  1  0
 26 91  1  0
 51122  1  6
 50120  1  0
 50121  1  0
 49118  1  0
 49119  1  0
 48115  1  0
 48116  1  0
 48117  1  0
 27 92  1  1
 28 93  1  1
 30 94  1  1
 36 95  1  0
 36 96  1  0
 37 97  1  0
 37 98  1  0
 39 99  1  0
 39100  1  0
 39101  1  0
 40102  1  0
 40103  1  0
 40104  1  0
 41105  1  0
 41106  1  0
 42107  1  6
 43108  1  0
 43109  1  0
 44110  1  0
 44111  1  0
 46112  1  0
 46113  1  0
 46114  1  0
 53123  1  0
 53124  1  0
 53125  1  0
 54126  1  0
 54127  1  0
 54128  1  0
 55129  1  6
 56130  1  0
 57131  1  6
 58132  1  0
 59133  1  1
 60134  1  0
 61135  1  6
 62136  1  0
 63137  1  1
 64138  1  0
M  END


  Mrv1533004191518152D          

 64 73  0  0  0  0            999 V2000
    7.9440   -7.4647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3744   -6.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9801   -6.0362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4104   -5.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0161   -4.6077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1913   -4.5869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7610   -5.2908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1553   -6.0154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9362   -5.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5058   -5.9738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5419   -4.5453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7171   -4.5245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -3.7999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9722   -3.8415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7970   -3.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2273   -3.1584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8330   -2.4338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0082   -2.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6139   -1.6884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0442   -0.9845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6499   -0.2599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8251   -0.2391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3948   -0.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5700   -0.9221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1757   -0.1975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7453   -0.9014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6060    0.5063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2117    1.2310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3869    1.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9566    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5684    1.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3509   -0.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9282   -0.8961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5077   -1.6059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1033   -0.8868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6520   -0.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0698   -0.7035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7971   -0.2269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5684   -0.5197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5710    0.6062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2701    0.1681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2403   -0.6563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5114   -1.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0185   -1.6935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0414   -1.6552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1877   -0.6047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1579    0.2198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1472    1.3601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7131    1.3658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1152    0.5834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0664    1.4070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4308    0.4856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4803    1.3091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1412    0.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8690   -1.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2994   -0.3015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2633   -1.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0881   -1.7507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2352   -5.3531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6655   -4.6493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6295   -6.0778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4543   -6.0986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1992   -6.7816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5935   -7.5063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 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
 20 21  1  0  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
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 25 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
 33 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
 38 39  2  0  0  0  0
 38 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
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
 36 47  1  0  0  0  0
 40 47  1  0  0  0  0
 40 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 30 50  1  0  0  0  0
 36 50  1  0  0  0  0
 50 51  1  0  0  0  0
 27 52  1  0  0  0  0
 22 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
 20 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  1  0  0  0  0
 17 57  1  0  0  0  0
 57 58  1  0  0  0  0
  4 59  1  0  0  0  0
 59 60  1  0  0  0  0
 59 61  1  0  0  0  0
 61 62  1  0  0  0  0
 61 63  1  0  0  0  0
  2 63  1  0  0  0  0
 63 64  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0146497

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(O)C(O)C(CO)OC2OC2COC(OC3CCC4(C)C(CCC5(C)C4C4OC4C46OC(=O)C7(CCC(C)(C)CC47)CCC56C)C3(C)C)C(O)C2O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C47H74O17/c1-20-26(49)29(52)32(55)38(58-20)63-33-30(53)27(50)21(18-48)59-39(33)60-22-19-57-37(31(54)28(22)51)61-25-10-11-43(6)23(42(25,4)5)9-12-44(7)35(43)34-36(62-34)47-24-17-41(2,3)13-15-46(24,40(56)64-47)16-14-45(44,47)8/h20-39,48-55H,9-19H2,1-8H3

> <INCHI_KEY>
CLQALJAEJWNGNT-UHFFFAOYSA-N

> <FORMULA>
C47H74O17

> <MOLECULAR_WEIGHT>
911.092

> <EXACT_MASS>
910.492600923

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
138

> <JCHEM_AVERAGE_POLARIZABILITY>
98.76998269752073

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one

> <ALOGPS_LOGP>
2.34

> <JCHEM_LOGP>
2.0381260643333343

> <ALOGPS_LOGS>
-3.85

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
10

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.360782723479602

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.879676552078612

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810837892566813

> <JCHEM_POLAR_SURFACE_AREA>
256.04999999999995

> <JCHEM_REFRACTIVITY>
219.60300000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.28e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      14.829 -13.934   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      15.632 -12.620   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      14.896 -11.268   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      15.699  -9.954   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      14.963  -8.601   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      13.424  -8.562   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.620  -9.876   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      13.357 -11.229   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      11.081  -9.837   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.278 -11.151   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.345  -8.485   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.805  -8.446   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.069  -7.093   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      11.148  -7.171   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.688  -7.210   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.491  -5.896   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      12.755  -4.543   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.215  -4.504   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.479  -3.152   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      11.283  -1.838   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.546  -0.485   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.007  -0.446   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.204  -1.760   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.664  -1.721   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.928  -0.369   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.125  -1.683   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.731   0.945   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.995   2.298   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.456   2.337   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.652   1.023   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.928   2.382   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.388  -0.330   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.599  -1.673   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.814  -2.998   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       2.059  -1.655   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.217  -0.323   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.130  -1.313   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.488  -0.424   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -2.928  -0.970   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -1.066   1.132   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.371   0.314   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.315  -1.225   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -0.955  -1.946   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -1.901  -3.161   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       0.077  -3.090   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       0.350  -1.129   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       0.295   0.410   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -0.275   2.539   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       1.331   2.549   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       2.082   1.089   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       1.991   2.626   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       8.271   0.906   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       8.363   2.444   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       9.597   1.689   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      12.822  -1.877   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      13.625  -0.563   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0      13.558  -3.229   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0      15.098  -3.268   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0      17.239  -9.993   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      18.042  -8.679   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      17.975 -11.345   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      19.515 -11.384   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0      17.172 -12.659   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0      17.908 -14.012   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   63                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   59                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14    6   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   57                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   55                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   52                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   32                                             
CONECT   26   25                                                            
CONECT   27   25   28   52                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32   50                                             
CONECT   31   30                                                            
CONECT   32   30   25   33                                                  
CONECT   33   32   34   35                                                  
CONECT   34   33   35                                                       
CONECT   35   34   33   36                                                  
CONECT   36   35   37   47   50                                             
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   47   48                                             
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   45   46                                             
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   43   47                                                       
CONECT   47   46   36   40                                                  
CONECT   48   40   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   30   36   51                                             
CONECT   51   50                                                            
CONECT   52   27   22   53   54                                             
CONECT   53   52                                                            
CONECT   54   52                                                            
CONECT   55   20   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   17   58                                                  
CONECT   58   57                                                            
CONECT   59    4   60   61                                                  
CONECT   60   59                                                            
CONECT   61   59   62   63                                                  
CONECT   62   61                                                            
CONECT   63   61    2   64                                                  
CONECT   64   63                                                            
MASTER        0    0    0    0    0    0    0    0   64    0  146    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₇H₇₄O₁₇

Average Mass

911.0920 Da

Monoisotopic Mass

910.49260 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(O)C(O)C(CO)OC2OC2COC(OC3CCC4(C)C(CCC5(C)C4C4OC4C46OC(=O)C7(CCC(C)(C)CC47)CCC56C)C3(C)C)C(O)C2O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C47H74O17/c1-20-26(49)29(52)32(55)38(58-20)63-33-30(53)27(50)21(18-48)59-39(33)60-22-19-57-37(31(54)28(22)51)61-25-10-11-43(6)23(42(25,4)5)9-12-44(7)35(43)34-36(62-34)47-24-17-41(2,3)13-15-46(24,40(56)64-47)16-14-45(44,47)8/h20-39,48-55H,9-19H2,1-8H3

InChI Key

CLQALJAEJWNGNT-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
Thalictrum minus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Oligosaccharide
Glycosyl compound
O-glycosyl compound
Caprolactone
Oxepane
Gamma butyrolactone
Oxane
Tetrahydrofuran
Carboxylic acid ester
Lactone
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Dialkyl ether
Ether
Oxirane
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxygen compound
Primary 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	2.34	ALOGPS
logP	2.04	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	11.88	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	256.05 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	219.6 m³·mol⁻¹	ChemAxon
Polarizability	98.77 Å³	ChemAxon
Number of Rings	10	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one (NP0146497)

MOL for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

3D MOL for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

3D SDF for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

3D-SDF for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

PDB for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

3D PDB for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

SMILES for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

INCHI for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

Structure for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)

3D Structure for NP0146497 (9-[(5-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-3,4-dihydroxyoxan-2-yl)oxy]-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.0¹,¹⁵.0²,⁴.0⁵,¹⁴.0⁶,¹¹.0¹⁸,²³]pentacosan-25-one)