NP-MRD: Showing NP-Card for (1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid (NP0271276)

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Record Information

Version

2.0

Created at

2022-09-08 17:31:13 UTC

Updated at

2022-09-08 17:31:14 UTC

NP-MRD ID

NP0271276

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid

Description

Brevicuspisaponin 2 belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid is found in Ilex brevicuspis. (1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid was first documented in 2000 (PMID: 10820800). Based on a literature review very few articles have been published on Brevicuspisaponin 2.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082219312D          

 45 50  0  0  1  0            999 V2000
   -0.1105   -3.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -3.8230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1105   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -5.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -5.2520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -6.6809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -5.9664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -5.2520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1895   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8395   -4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4270   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3145   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -3.8230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3145   -3.1086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -2.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -2.3941    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.9645   -1.6796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645   -3.1086    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.7895   -3.1086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -3.8230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9645   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -5.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8522   -5.5341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9955   -6.3466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9337   -6.0644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5657   -6.5947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -5.2520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8395   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -5.2520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6882   -6.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -3.8230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8266   -3.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1558   -2.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  6  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  1  0  0  0
 21 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 37  1  0  0  0  0
 17 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 16 40  1  0  0  0  0
 11 40  1  0  0  0  0
 40 41  1  6  0  0  0
 42 13  1  1  0  0  0
  5 42  1  0  0  0  0
 42 43  1  0  0  0  0
  2 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  1  0  0  0
M  END

     RDKit          3D

101106  0  0  0  0  0  0  0  0999 V2000
   -6.1415    2.3855    1.8712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0037    0.8864    1.8037 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.0152    0.3807    0.8184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5306   -0.9029    0.2395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3983   -0.5377   -0.7331 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1086    0.1853   -1.8354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7974    1.3756   -2.0944 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1000   -0.3965   -2.5905 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8154   -1.7562   -1.3313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4813   -1.5201   -1.9697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4518   -0.9773   -0.9812 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3551   -2.0172    0.0801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0740    0.3024   -0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4300    1.4274   -0.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0855    1.5759   -1.3495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3580    0.3156   -0.9676 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1173    0.4576   -1.1474 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5558    1.1063   -2.4121 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6004    1.3608   -0.0072 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1597    0.6066    1.1399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3807   -0.2590    0.7904 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5430    0.4422    0.9909 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2356    0.0409    2.1280 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0419    1.0641    3.0796 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1814    1.7215    3.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9186    2.1547    2.1965 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9866    2.6184    1.2837 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5423    0.8740    1.6398 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8353    1.0001    0.2987 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6566   -0.3138    1.9590 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1212   -0.9632    3.1336 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -0.8946   -0.5614 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1120   -0.2750   -1.5480 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4326   -0.4925   -1.0734 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5914   -2.3853   -0.5484 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9330   -2.4560   -0.1573 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7501   -0.8727   -0.8548 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2055   -1.9298   -1.7577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2487   -2.0632   -1.3618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0755   -0.8211   -1.5730 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2763   -0.7252   -3.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4428    0.3830   -0.0009 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5806    0.4434    1.4590 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6933    1.5708    1.9700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3253   -0.6187    2.2480 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9991   -2.9620   -0.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7357   -1.7899    0.9411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3206   -2.3691    0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9440    2.3586   -0.4267 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0163    2.5664    1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  9  1  0
  9 10  1  0
 10 11  1  0
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 13 14  2  0
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 42 43  1  0
 43 44  1  0
 43 45  1  1
  5  6  1  6
  6  8  1  0
  6  7  2  0
 43  2  1  0
 42  5  1  0
 40 11  1  0
 40 16  1  0
 37 17  1  0
 30 23  1  0
  1 46  1  0
  1 47  1  0
  1 48  1  0
  2 49  1  1
  3 50  1  0
  3 51  1  0
  4 52  1  0
  4 53  1  0
  9 55  1  0
  9 56  1  0
 10 57  1  0
 10 58  1  0
 12 59  1  0
 12 60  1  0
 12 61  1  0
 14 62  1  0
 15 63  1  0
 15 64  1  0
 16 65  1  1
 18 66  1  0
 18 67  1  0
 18 68  1  0
 19 69  1  0
 19 70  1  0
 20 71  1  0
 20 72  1  0
 21 73  1  1
 23 74  1  1
 25 75  1  0
 25 76  1  0
 26 77  1  1
 27 78  1  0
 28 79  1  1
 29 80  1  0
 30 81  1  6
 31 82  1  0
 33 83  1  0
 33 84  1  0
 34 85  1  0
 35 86  1  0
 35 87  1  0
 36 88  1  0
 37 89  1  1
 38 90  1  0
 38 91  1  0
 39 92  1  0
 39 93  1  0
 41 94  1  0
 41 95  1  0
 41 96  1  0
 42 97  1  6
 44 98  1  0
 44 99  1  0
 44100  1  0
 45101  1  0
  8 54  1  0
M  END


  Mrv1652309082219312D          

 45 50  0  0  1  0            999 V2000
   -0.1105   -3.1086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -3.8230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1105   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -5.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -5.2520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -6.6809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -5.9664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -5.2520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1895   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8395   -4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4270   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -3.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3145   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -3.8230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3145   -3.1086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -2.3941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -2.3941    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.9645   -1.6796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645   -3.1086    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.7895   -3.1086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -3.8230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9645   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -5.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8522   -5.5341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9955   -6.3466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9337   -6.0644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5657   -6.5947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -5.2520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8395   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -5.2520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6882   -6.0725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -3.8230    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8266   -3.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1558   -2.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  6  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  1  0  0  0
 21 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 37  1  0  0  0  0
 17 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 16 40  1  0  0  0  0
 11 40  1  0  0  0  0
 40 41  1  6  0  0  0
 42 13  1  1  0  0  0
  5 42  1  0  0  0  0
 42 43  1  0  0  0  0
  2 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0271276

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[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@H](O)[C@H]6O)C(CO)(CO)[C@@H]5CC[C@@]34C)[C@@H]2[C@]1(C)O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H56O10/c1-19-8-13-34(29(41)42)15-14-31(3)20(27(34)33(19,5)43)6-7-22-30(2)11-10-24(45-28-26(40)25(39)21(38)16-44-28)35(17-36,18-37)23(30)9-12-32(22,31)4/h6,19,21-28,36-40,43H,7-18H2,1-5H3,(H,41,42)/t19-,21-,22+,23+,24-,25-,26+,27+,28-,30+,31+,32+,33+,34-/m0/s1

> <INCHI_KEY>
NNZRYRAKIFSXJY-RNXSOLSLSA-N

> <FORMULA>
C35H56O10

> <MOLECULAR_WEIGHT>
636.823

> <EXACT_MASS>
636.387348003

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
70.20011034010277

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
1.6425088976666662

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.242064415414772

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.643417366544616

> <JCHEM_PKA_STRONGEST_BASIC>
-2.820173478409008

> <JCHEM_POLAR_SURFACE_AREA>
177.14

> <JCHEM_REFRACTIVITY>
165.30330000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.206  -5.803   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.564  -7.136   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.206  -8.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.564  -9.804   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.104  -9.804   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334 -11.137   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.104 -12.471   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -0.206 -11.137   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.874 -11.137   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.414 -11.137   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.184  -9.804   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.954 -11.137   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.414  -8.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.184  -7.136   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.724  -7.136   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.494  -8.470   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.034  -8.470   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.264  -7.136   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.804  -7.136   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.344  -7.136   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.114  -8.470   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      13.654  -8.470   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      14.424  -7.136   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      13.654  -5.803   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.424  -4.469   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.964  -4.469   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      16.734  -3.135   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      16.734  -5.803   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      18.274  -5.803   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      15.964  -7.136   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      16.734  -8.470   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      11.344  -9.804   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.791 -10.330   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      13.058 -11.847   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      11.076 -11.320   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      12.256 -12.310   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       9.804  -9.804   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.034 -11.137   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.494 -11.137   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.724  -9.804   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.885 -11.335   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.874  -8.470   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.104  -7.136   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.410  -6.320   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       2.157  -5.597   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   43                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    9   42                                             
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    5   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   40                                             
CONECT   12   11                                                            
CONECT   13   11   14   42                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   40                                                  
CONECT   17   16   18   19   37                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   32                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   30                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   23   31                                                  
CONECT   31   30                                                            
CONECT   32   21   33   35   37                                             
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   32   36                                                       
CONECT   36   35                                                            
CONECT   37   32   17   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   16   11   41                                             
CONECT   41   40                                                            
CONECT   42   13    5   43                                                  
CONECT   43   42    2   44   45                                             
CONECT   44   43                                                            
CONECT   45   43                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₆O₁₀

Average Mass

636.8230 Da

Monoisotopic Mass

636.38735 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[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@H](O)[C@H]6O)C(CO)(CO)[C@@H]5CC[C@@]34C)[C@@H]2[C@]1(C)O)C(O)=O

InChI Identifier

InChI=1S/C35H56O10/c1-19-8-13-34(29(41)42)15-14-31(3)20(27(34)33(19,5)43)6-7-22-30(2)11-10-24(45-28-26(40)25(39)21(38)16-44-28)35(17-36,18-37)23(30)9-12-32(22,31)4/h6,19,21-28,36-40,43H,7-18H2,1-5H3,(H,41,42)/t19-,21-,22+,23+,24-,25-,26+,27+,28-,30+,31+,32+,33+,34-/m0/s1

InChI Key

NNZRYRAKIFSXJY-RNXSOLSLSA-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
Ilex brevicuspis	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
Steroid
Glycosyl compound
O-glycosyl compound
Monosaccharide
Oxane
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Acetal
Polyol
Organic oxygen compound
Carbonyl group
Organic oxide
Organooxygen compound
Alcohol
Hydrocarbon derivative
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

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

24711717

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44575753

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Taketa AT, Schmittmann-Schlager T, Guillaume D, Gosmann G, Schenkel EP: Triterpenoid glycosides and a triterpene from Ilex brevicuspis. Phytochemistry. 2000 Apr;53(8):901-4. doi: 10.1016/s0031-9422(99)00517-8. [PubMed:10820800 ]
LOTUS database [Link]

Showing NP-Card for (1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid (NP0271276)

MOL for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

3D MOL for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

3D SDF for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

3D-SDF for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

PDB for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

3D PDB for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

SMILES for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

INCHI for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

Structure for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)

3D Structure for NP0271276 ((1r,2s,4as,6as,6br,8ar,10s,12ar,12br,14bs)-1-hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid)