NP-MRD: Showing NP-Card for Flaccidin B (NP0052076)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-27 23:14:56 UTC

Updated at

2022-04-27 23:14:56 UTC

NP-MRD ID

NP0052076

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Flaccidin B

Description

(4AS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-{[(2S,3R,5R)-5-hydroxy-4-oxo-3-{[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Flaccidin B is found in Anemone flaccida. Based on a literature review very few articles have been published on (4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-{[(2S,3R,5R)-5-hydroxy-4-oxo-3-{[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282201142D          

 53 59  0  0  1  0            999 V2000
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  1  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  1  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  2  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
    4.0145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  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
    2.7770    1.1270    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
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    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
   -0.1105    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
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6882   -1.1225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7766   -0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1058   -1.1265    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
    7.7270    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3145    1.8414    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.7270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520    2.5559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    2.5559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2520    2.5559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8395    3.2704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2520    3.9849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0770    3.9849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4895    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    4.6993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  6  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  6  0  0  0
 15 12  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 16 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
 15 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 16 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 11 28  1  1  0  0  0
  8 29  1  6  0  0  0
  5 30  1  6  0  0  0
  3 31  1  0  0  0  0
  3 32  1  0  0  0  0
  2 33  1  6  0  0  0
 34 33  1  1  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 34 40  1  0  0  0  0
 38 41  1  6  0  0  0
 35 42  1  1  0  0  0
 43 42  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 43 48  1  0  0  0  0
 47 49  1  6  0  0  0
 49 50  1  0  0  0  0
 46 51  1  6  0  0  0
 45 52  1  1  0  0  0
 44 53  1  6  0  0  0
M  END

     RDKit          3D

117123  0  0  0  0  0  0  0  0999 V2000
   -8.2245    2.5632   -1.6993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9177    1.1018   -1.4484 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.3619    0.3261   -2.6591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7523    0.6993   -0.2330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0202    1.1895    0.9792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8409    0.2769    1.2488 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.3882   -0.9056    1.9857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2273   -2.0447    1.4292 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0295   -0.7908    3.1920 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9200    0.9946    2.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5704    0.3651    2.3597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8807    0.2651    1.0542 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5259    1.6914    0.6628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7626   -0.3751    0.0341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3316   -1.2292   -0.8963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9277   -1.6759   -1.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0979   -0.7728   -0.2324 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6008   -1.0664   -0.3056 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2278   -2.2761    0.5006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1989   -1.2619   -1.7222 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2947   -1.4686   -1.7912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0654   -0.2934   -1.2580 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4136   -0.5304   -1.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2815    0.0313   -1.9575 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0172   -0.8864   -2.7167 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5006   -0.3391   -3.9016 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6000    0.6398   -3.5048 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1688    1.2533   -4.5866 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0221    1.5551   -2.5010 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0970    2.7344   -2.6195 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3444    0.9260   -1.3391 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3349    0.1942   -0.7011 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5499    0.5355    0.6119 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8623    0.9577    0.8144 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7921    0.0414    0.3296 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1665    0.6331    0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1318   -0.2537    0.0654 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6949   -1.2829    1.0493 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8646   -1.4589    1.7838 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5543   -1.2877    2.0444 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2759   -2.6148    2.3658 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3124   -0.6779    1.4671 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4094   -0.3080    2.4910 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4347    0.4674   -0.1412 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3718    0.2484    1.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5916    1.9654   -0.4156 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0373    0.1961    0.2212 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2380    0.1690    1.7149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6446   -0.0037    2.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5991   -0.5997    1.1567 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1312   -1.9562    1.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2362   -0.1079   -0.0515 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4594    0.9414   -1.1436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3273    2.7143   -1.5537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8903    2.8868   -2.7078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7401    3.1893   -0.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5373   -0.4050   -2.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5385    1.0024   -3.5343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3134   -0.1913   -2.4540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8540   -0.3955   -0.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7504    1.1822   -0.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6710    1.1285    1.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7116    2.2520    0.8890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4928   -1.6031    3.5739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9402    2.0539    1.9473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3929    0.9377    3.2195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7512   -0.5901    2.8828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9892    1.0769    3.0227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1694    2.4527    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5089    1.9971    0.8988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6584    1.8604   -0.4251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0375   -1.6724   -1.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6862   -1.4616   -2.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7689   -2.7442   -0.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1828    0.2270   -0.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6817   -3.1621   -0.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8793   -2.3521    0.5059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5083   -2.2258    1.5619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5330   -0.4696   -2.4102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6559   -2.2115   -2.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4963   -1.6147   -2.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5964   -2.4491   -1.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0929    0.4107   -2.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7042    0.6405   -2.7128 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0073   -1.1896   -4.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7351    0.1087   -4.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3515    0.0103   -2.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9684    0.7062   -5.3962 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8855    1.6892   -0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9072    1.3335    0.9879 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6667   -0.1412   -0.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2581    1.5801   -0.0715 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3255    0.8303    1.6151 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.2209   -0.1256   -0.9260 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6049   -2.1061    0.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6779   -1.8266    2.6842 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7975   -0.7452    2.9805 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8006   -2.6145    3.2502 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7242   -1.4354    0.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1588    0.6439    2.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4127    0.5044    0.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3447   -0.7532    1.4648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1145    0.9462    1.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7437    2.1372   -1.5062 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3550    2.4501    0.1938 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6324    2.4821   -0.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5848    1.0852   -0.1103 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4766   -0.5309    2.2367 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1045    1.1883    2.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6275   -0.6873    3.0208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0669    0.9279    2.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7606   -2.8077    1.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2342   -2.0361    1.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8236   -2.1219    2.7087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7702   -1.0093   -0.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0598    1.9267   -0.8404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8992    0.6213   -2.0364 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  1
 18 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  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 35 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 22 44  1  0
 44 45  1  1
 44 46  1  0
 44 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  1  0
 50 51  1  1
 14 52  1  0
 52 53  1  0
  6  7  1  1
  7  9  1  0
  7  8  2  0
 53  2  1  0
 52  6  1  0
 50 12  1  0
 50 17  1  0
 47 18  1  0
 31 24  1  0
 42 33  1  0
  1 54  1  0
  1 55  1  0
  1 56  1  0
  3 57  1  0
  3 58  1  0
  3 59  1  0
  4 60  1  0
  4 61  1  0
  5 62  1  0
  5 63  1  0
 10 65  1  0
 10 66  1  0
 11 67  1  0
 11 68  1  0
 13 69  1  0
 13 70  1  0
 13 71  1  0
 15 72  1  0
 16 73  1  0
 16 74  1  0
 17 75  1  6
 19 76  1  0
 19 77  1  0
 19 78  1  0
 20 79  1  0
 20 80  1  0
 21 81  1  0
 21 82  1  0
 22 83  1  6
 24 84  1  6
 26 85  1  0
 26 86  1  0
 27 87  1  1
 28 88  1  0
 31 89  1  1
 33 90  1  1
 35 91  1  6
 36 92  1  0
 36 93  1  0
 37 94  1  0
 38 95  1  6
 39 96  1  0
 40 97  1  1
 41 98  1  0
 42 99  1  6
 43100  1  0
 45101  1  0
 45102  1  0
 45103  1  0
 46104  1  0
 46105  1  0
 46106  1  0
 47107  1  6
 48108  1  0
 48109  1  0
 49110  1  0
 49111  1  0
 51112  1  0
 51113  1  0
 51114  1  0
 52115  1  6
 53116  1  0
 53117  1  0
  9 64  1  0
M  END


  Mrv1652304282201142D          

 53 59  0  0  1  0            999 V2000
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  1  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  1  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  2  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
    4.0145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  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
    2.7770    1.1270    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
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    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
   -0.1105    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
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6882   -1.1225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7766   -0.7392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1058   -1.1265    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
    7.7270    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3145    1.8414    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.7270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520    2.5559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    2.5559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2520    2.5559    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8395    3.2704    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2520    3.9849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0770    3.9849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4895    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    4.6993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  6  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  6  0  0  0
 15 12  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 16 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
 15 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
 16 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 11 28  1  1  0  0  0
  8 29  1  6  0  0  0
  5 30  1  6  0  0  0
  3 31  1  0  0  0  0
  3 32  1  0  0  0  0
  2 33  1  6  0  0  0
 34 33  1  1  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 34 40  1  0  0  0  0
 38 41  1  6  0  0  0
 35 42  1  1  0  0  0
 43 42  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 43 48  1  0  0  0  0
 47 49  1  6  0  0  0
 49 50  1  0  0  0  0
 46 51  1  6  0  0  0
 45 52  1  1  0  0  0
 44 53  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0052076

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6OC[C@@H](O)C(=O)[C@@H]6O[C@@H]6O[C@@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C41H64O12/c1-36(2)14-16-41(35(48)49)17-15-39(6)21(22(41)18-36)8-9-26-38(5)12-11-27(37(3,4)25(38)10-13-40(26,39)7)52-34-32(28(44)23(43)20-50-34)53-33-31(47)30(46)29(45)24(19-42)51-33/h8,22-27,29-34,42-43,45-47H,9-20H2,1-7H3,(H,48,49)/t22-,23+,24-,25-,26+,27-,29+,30-,31+,32-,33-,34-,38-,39+,40+,41-/m0/s1

> <INCHI_KEY>
OPTUUKHEYUERDZ-FOGUJVPSSA-N

> <FORMULA>
C41H64O12

> <MOLECULAR_WEIGHT>
748.951

> <EXACT_MASS>
748.439777501

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
117

> <JCHEM_AVERAGE_POLARIZABILITY>
82.56000460292945

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-{[(2S,3R,5R)-5-hydroxy-4-oxo-3-{[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid

> <ALOGPS_LOGP>
3.69

> <JCHEM_LOGP>
4.298673258333335

> <ALOGPS_LOGS>
-4.46

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.041120123929348

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.744259170656001

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810837218223547

> <JCHEM_POLAR_SURFACE_AREA>
192.43999999999997

> <JCHEM_REFRACTIVITY>
191.72190000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.57e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-{[(2S,3R,5R)-5-hydroxy-4-oxo-3-{[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.494  -1.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.034  -1.897   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.742   2.920   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.510   3.643   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334  -1.897   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.206  -1.897   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.954  -1.897   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.885  -2.095   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.264   2.104   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.650  -1.380   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      11.397  -2.103   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      13.654   0.770   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      14.424   2.104   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      13.654   3.437   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      14.424   4.771   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      13.654   6.105   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      15.964   4.771   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      16.734   3.437   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      15.964   2.104   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      16.734   6.105   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      12.114   3.437   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      11.344   4.771   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       9.804   4.771   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.034   6.105   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       9.804   7.438   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      11.344   7.438   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      12.114   6.105   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      12.114   8.772   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      11.344  10.106   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0       9.034   8.772   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0       7.494   6.105   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       9.034   3.437   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   33                                                  
CONECT    3    2    4   31   32                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   30                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   14                                                  
CONECT    8    7    9   11   29                                             
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12   18   28                                             
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    7                                                       
CONECT   15   12   16   22                                                  
CONECT   16   15   17   19   25                                             
CONECT   17   16   18                                                       
CONECT   18   17   11                                                       
CONECT   19   16   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21   15                                                       
CONECT   23   21                                                            
CONECT   24   21                                                            
CONECT   25   16   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   11                                                            
CONECT   29    8                                                            
CONECT   30    5                                                            
CONECT   31    3                                                            
CONECT   32    3                                                            
CONECT   33    2   34                                                       
CONECT   34   33   35   40                                                  
CONECT   35   34   36   42                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   41                                                  
CONECT   39   38   40                                                       
CONECT   40   39   34                                                       
CONECT   41   38                                                            
CONECT   42   35   43                                                       
CONECT   43   42   44   48                                                  
CONECT   44   43   45   53                                                  
CONECT   45   44   46   52                                                  
CONECT   46   45   47   51                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47   43                                                       
CONECT   49   47   50                                                       
CONECT   50   49                                                            
CONECT   51   46                                                            
CONECT   52   45                                                            
CONECT   53   44                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  118    0
END

View in JSmol

Synonyms

Value	Source
(4AS,6as,6BR,8ar,10S,12ar,12BR,14BS)-10-{[(2S,3R,5R)-5-hydroxy-4-oxo-3-{[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate	Generator

Chemical Formula

C₄₁H₆₄O₁₂

Average Mass

748.9510 Da

Monoisotopic Mass

748.43978 Da

IUPAC Name

(4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-{[(2S,3R,5R)-5-hydroxy-4-oxo-3-{[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid

Traditional Name

(4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-{[(2S,3R,5R)-5-hydroxy-4-oxo-3-{[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6OC[C@@H](O)C(=O)[C@@H]6O[C@@H]6O[C@@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1)C(O)=O

InChI Identifier

InChI=1S/C41H64O12/c1-36(2)14-16-41(35(48)49)17-15-39(6)21(22(41)18-36)8-9-26-38(5)12-11-27(37(3,4)25(38)10-13-40(26,39)7)52-34-32(28(44)23(43)20-50-34)53-33-31(47)30(46)29(45)24(19-42)51-33/h8,22-27,29-34,42-43,45-47H,9-20H2,1-7H3,(H,48,49)/t22-,23+,24-,25-,26+,27-,29+,30-,31+,32-,33-,34-,38-,39+,40+,41-/m0/s1

InChI Key

OPTUUKHEYUERDZ-FOGUJVPSSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anemone flaccida	Plant	KNApSAcK

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
O-glycosyl compound
Glycosyl compound
Oxane
Monosaccharide
Cyclic ketone
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
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	3.69	ALOGPS
logP	4.3	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	4.74	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	192.44 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	191.72 m³·mol⁻¹	ChemAxon
Polarizability	82.56 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

163067493

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Flaccidin B (NP0052076)

MOL for NP0052076 (Flaccidin B)

3D MOL for NP0052076 (Flaccidin B)

3D SDF for NP0052076 (Flaccidin B)

3D-SDF for NP0052076 (Flaccidin B)

PDB for NP0052076 (Flaccidin B)

3D PDB for NP0052076 (Flaccidin B)

SMILES for NP0052076 (Flaccidin B)

INCHI for NP0052076 (Flaccidin B)

Structure for NP0052076 (Flaccidin B)

3D Structure for NP0052076 (Flaccidin B)