NP-MRD: Showing NP-Card for 6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid (NP0208711)

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Record Information

Version

2.0

Created at

2022-09-05 05:49:12 UTC

Updated at

2022-09-05 05:49:12 UTC

NP-MRD ID

NP0208711

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid

Description

6-{[7,8-Dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton. 6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid is found in Eryngium campestre. 6-{[7,8-Dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191522282D          

 63 69  0  0  0  0            999 V2000
   11.4395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7895   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257    2.6619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907    1.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1058    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7766    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -3.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2645    0.4125    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
  6 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
 18 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
 23 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  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
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 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  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 35 43  1  0  0  0  0
 29 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 23 50  1  0  0  0  0
 28 50  1  0  0  0  0
 50 51  1  0  0  0  0
 20 52  1  0  0  0  0
 15 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
 11 55  1  0  0  0  0
 55 56  2  0  0  0  0
 55 57  1  0  0  0  0
  4 58  1  0  0  0  0
 58 59  1  0  0  0  0
 58 60  1  0  0  0  0
 60 61  1  0  0  0  0
 60 62  1  0  0  0  0
  2 62  1  0  0  0  0
 62 63  1  0  0  0  0
M  END

     RDKit          3D

137143  0  0  0  0  0  0  0  0999 V2000
   11.2145    3.2005    3.4027 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6923    1.9381    2.7940 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3729    0.6654    3.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6552    1.9394    1.9925 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1707    0.7043    1.4172 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6524   -0.4286    1.6044 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0631    0.7726    0.5733 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5000   -0.3818   -0.0480 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6824   -0.1922   -1.5293 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9347    0.9934   -2.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9852    2.1268   -2.1077 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6331    0.7395   -3.5168 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7395    1.4087   -1.3095 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2470    0.6676   -0.1327 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8028    0.2842   -0.2058 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9137    1.1271    0.2638 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4510    0.9235    0.2814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0661   -0.5232    0.2405 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4216   -0.7014    0.1390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9088   -1.9458    0.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0688    0.4227    0.9718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5551    0.3882    0.9658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2075    0.1823   -0.3561 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3741   -0.5671   -0.1203 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5265    0.1186   -0.3760 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2603   -0.5748   -1.3233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6018   -1.8518   -1.0259 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.8428   -2.2045   -1.7854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3428   -1.3285   -2.5268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4164   -3.4618   -1.6683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8742   -2.1891    0.4004 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3951   -3.5014    0.6241 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2410   -1.3090    1.4223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.0118   -1.3680    2.5949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4114    0.1226    0.8821 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.7404    0.1846    0.4690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4410    1.2324    1.0917 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.5110    0.6712    1.7300 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4735    1.5258    2.1846 C   0  0  2  0  0  0  0  0  0  0  0  0
  -11.8678    1.0167    1.8420 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3109    2.9526    1.7795 C   0  0  2  0  0  0  0  0  0  0  0  0
  -11.5708    3.5741    1.9407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9442    3.1021    0.3334 C   0  0  2  0  0  0  0  0  0  0  0  0
  -11.0281    2.8653   -0.5131 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8207    2.1890   -0.0182 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.0342    1.5084   -1.2299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4134   -0.5025   -1.3997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691    0.2750   -2.7209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9718   -1.8736   -1.6939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9356   -0.4336   -1.2390 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1615   -1.0646   -2.3259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3046   -0.7197   -2.1436 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8763   -1.1999   -0.8362 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6693   -2.7289   -0.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3442   -0.9996   -0.7814 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8452   -1.2083   -2.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0848   -2.0450    0.0399 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7259   -1.9881    1.3866 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5697   -1.8358    0.0061 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0802   -2.7847    0.9344 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0719   -0.4866    0.3867 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1357   -0.4447    1.9318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8692   -1.4674    2.4509 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0638    2.9951    4.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4312    3.7540    3.9545 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5730    3.8327    2.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7089   -0.0603    3.6253 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2014    0.8448    3.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7998    0.1861    2.2006 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1828    2.8829    1.7814 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0839   -1.2457    0.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4266   -1.1353   -2.0542 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8023   -0.1018   -1.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8538    1.7210   -2.6832 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2550    2.4666   -1.1097 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6009    2.9761   -2.7140 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5974    1.0444   -3.7765 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3867    1.1436   -4.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6478   -0.3705   -3.6886 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004191522282D          

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M  END
> <DATABASE_ID>
NP0208711

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(O)C(O)C(OC2OC2CCC3(C)C(CCC4(C)C3CC=C3C5CC(C)(C)CC(OC(=O)C=C(C)C)C5(CO)C(O)C(O)C43C)C2(C)C)C(O)=O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C47H74O16/c1-21(2)17-29(49)60-28-19-42(4,5)18-24-23-11-12-26-44(8)15-14-27(43(6,7)25(44)13-16-45(26,9)46(23,10)37(55)38(56)47(24,28)20-48)61-41-36(33(53)32(52)35(62-41)39(57)58)63-40-34(54)31(51)30(50)22(3)59-40/h11,17,22,24-28,30-38,40-41,48,50-56H,12-16,18-20H2,1-10H3,(H,57,58)

> <INCHI_KEY>
BDEJKSJKCUKQOE-UHFFFAOYSA-N

> <FORMULA>
C47H74O16

> <MOLECULAR_WEIGHT>
895.093

> <EXACT_MASS>
894.497686303

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
137

> <JCHEM_AVERAGE_POLARIZABILITY>
96.68510160614034

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid

> <ALOGPS_LOGP>
2.93

> <JCHEM_LOGP>
2.6280126269999986

> <ALOGPS_LOGS>
-4.12

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.097522716927632

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.4135826528854336

> <JCHEM_PKA_STRONGEST_BASIC>
-3.425520484684239

> <JCHEM_POLAR_SURFACE_AREA>
262.35999999999996

> <JCHEM_REFRACTIVITY>
224.82550000000012

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.73e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid

> <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      21.354  -1.897   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.584  -0.564   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      19.044  -0.564   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      18.274   0.770   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      16.734   0.770   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      15.964  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.734  -1.897   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      18.274  -1.897   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      15.964  -3.231   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      16.734  -4.565   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      14.424  -3.231   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      13.654  -1.897   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      14.424  -0.564   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      13.654   0.770   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.264  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.034   3.437   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.494   3.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -1.746   3.437   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -2.516   2.104   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -2.516   4.771   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -1.746   6.105   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.516   7.438   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.206   6.105   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.334   3.437   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       2.104   4.771   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       3.035   4.969   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       5.184   4.771   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       5.023   3.635   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      11.397   3.643   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      12.650   2.920   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      13.654  -4.565   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      12.114  -4.565   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      14.424  -5.898   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      19.044   2.104   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      18.274   3.437   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      20.584   2.104   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0      21.354   3.437   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      21.354   0.770   0.000  0.00  0.00           C+0
HETATM   63  O   UNK     0      22.894   0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   62                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   58                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   55                                                  
CONECT   12   11   13                                                       
CONECT   13   12    6   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   52                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   21   52                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   50                                             
CONECT   24   23                                                            
CONECT   25   23   18   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   50                                                  
CONECT   29   28   30   43                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31   35                                                       
CONECT   35   34   36   43                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   35   29   44   46                                             
CONECT   44   43   45                                                       
CONECT   45   44                                                            
CONECT   46   43   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   23   28   51                                             
CONECT   51   50                                                            
CONECT   52   20   15   53   54                                             
CONECT   53   52                                                            
CONECT   54   52                                                            
CONECT   55   11   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55                                                            
CONECT   58    4   59   60                                                  
CONECT   59   58                                                            
CONECT   60   58   61   62                                                  
CONECT   61   60                                                            
CONECT   62   60    2   63                                                  
CONECT   63   62                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  138    0
END

View in JSmol

Synonyms

Value	Source
6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylate	Generator

Chemical Formula

C₄₇H₇₄O₁₆

Average Mass

895.0930 Da

Monoisotopic Mass

894.49769 Da

IUPAC Name

6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(O)C(O)C(OC2OC2CCC3(C)C(CCC4(C)C3CC=C3C5CC(C)(C)CC(OC(=O)C=C(C)C)C5(CO)C(O)C(O)C43C)C2(C)C)C(O)=O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C47H74O16/c1-21(2)17-29(49)60-28-19-42(4,5)18-24-23-11-12-26-44(8)15-14-27(43(6,7)25(44)13-16-45(26,9)46(23,10)37(55)38(56)47(24,28)20-48)61-41-36(33(53)32(52)35(62-41)39(57)58)63-40-34(54)31(51)30(50)22(3)59-40/h11,17,22,24-28,30-38,40-41,48,50-56H,12-16,18-20H2,1-10H3,(H,57,58)

InChI Key

BDEJKSJKCUKQOE-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
Eryngium campestre	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Triterpene saponins

Alternative Parents

Substituents

Triterpene saponin
Triterpenoid
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Disaccharide
Glycosyl compound
O-glycosyl compound
Beta-hydroxy acid
Fatty acid ester
Fatty acyl
Pyran
Oxane
Dicarboxylic acid or derivatives
Hydroxy acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Acetal
Polyol
Carboxylic acid
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Alcohol
Organic oxygen compound
Organooxygen compound
Carbonyl group
Primary alcohol
Hydrocarbon derivative
Organic oxide
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	2.93	ALOGPS
logP	2.63	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	3.41	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	262.36 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	224.83 m³·mol⁻¹	ChemAxon
Polarizability	96.69 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73123268

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid (NP0208711)

MOL for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

3D MOL for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

3D SDF for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

3D-SDF for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

PDB for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

3D PDB for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

SMILES for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

INCHI for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

Structure for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)

3D Structure for NP0208711 (6-{[7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9-[(3-methylbut-2-enoyl)oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-3,4-dihydroxy-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxane-2-carboxylic acid)