NP-MRD: Showing NP-Card for (1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid (NP0285328)

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Record Information

Version

2.0

Created at

2022-09-09 13:27:42 UTC

Updated at

2022-09-09 13:27:43 UTC

NP-MRD ID

NP0285328

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid

Description

2Alpha,3alpha-Dihydroxy-24-[(3-methoxy-4-hydroxy-trans-cinnamoyl)oxy]urs-12-en-28-oic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid is found in Prunus africana. Based on a literature review very few articles have been published on 2alpha,3alpha-Dihydroxy-24-[(3-methoxy-4-hydroxy-trans-cinnamoyl)oxy]urs-12-en-28-oic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092215272D          

 48 53  0  0  1  0            999 V2000
   10.6695    6.6001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5262    5.7877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7510    5.5055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6077    4.6930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8325    4.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6892    3.5984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9140    3.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7707    2.5038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4027    1.9735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9955    2.2216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8522    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9337    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  2  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
    6.0770   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 O   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  1  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  1  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  2  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  2  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  2  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
    0.3020   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    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  1  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
   -0.1105    1.8414    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
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  1  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
    8.2005    4.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3438    5.7536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1190    6.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2623    6.8483    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 30 29  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 30 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 37 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 29 43  1  0  0  0  0
 24 43  1  0  0  0  0
 43 44  1  6  0  0  0
  5 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
  3 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END

     RDKit          3D

104109  0  0  0  0  0  0  0  0999 V2000
   11.1428    3.3231    2.2859 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6545    2.2647    1.5007 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8042    1.3700    0.8608 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4176    1.5161    0.9970 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5640    0.6562    0.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1107    0.7375    0.4793 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4475    1.6407    1.1616 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9983    1.7279    1.2619 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5014    2.6498    1.9504 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1327    0.8464    0.6362 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259    1.0296    0.8014 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0279   -0.0598    0.0205 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4829    0.1473   -1.4315 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6306   -1.3737    0.4510 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9332   -1.3975   -0.1089 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8689   -2.4849   -0.1595 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2648   -2.5796   -1.5159 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3869   -2.3708   -0.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1266   -1.2067    0.7276 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1869   -1.6093    2.1113 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5570    0.0029    0.1772 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0388    1.2046    0.8794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4142    1.3524    0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2642    0.1645    0.9660 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2416    0.3490    2.4572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5945   -1.0211    0.4005 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3638   -2.2978    0.3960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6564   -1.9934   -0.2742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2438   -0.8368   -0.2359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5359   -0.6471   -0.9411 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4554   -0.0305   -2.2832 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5248   -0.9382   -3.1147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7958   -0.1138   -2.9641 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.7148    0.8226   -4.1804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9565    0.2333   -2.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5521    0.7425   -0.7668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5858   -0.1146   -0.0019 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.4246   -1.2591    0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5682   -1.5040    1.7297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0510   -2.0546   -0.4116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0839    0.6084    1.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7003    0.3471    1.6836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6755    0.2810    0.5278 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8591    1.6371   -0.1151 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1371   -0.3595   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4929   -0.5287   -0.5264 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3527    0.3608    0.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7234    0.2006   -0.0377 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6588    2.8318    3.1731 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9540    3.9720    2.6541 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3364    3.8923    1.7858 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0453    2.3307    1.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5013   -0.0008   -0.0516 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0729    2.3775    1.6907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4470    1.0681    1.8579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5302    2.0037    0.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6219   -0.1397   -2.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3254   -0.5066   -1.6999 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6922    1.2223   -1.6147 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8000   -1.4417    1.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3690   -2.2316    0.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2655   -3.4409    0.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1432   -3.5263   -1.7954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0580   -2.3160   -1.1662 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0334   -3.2961    0.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7695   -1.9526    2.6092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7709   -0.9034    2.7170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7978   -2.5674    2.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1450    0.0875   -0.8822 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5279    2.1125    0.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2283    1.2988    1.9352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7096    2.3107    0.8344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3804    1.2329   -0.6544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5006    1.4493    2.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9824   -0.2144    3.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5448   -0.7746   -0.7199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8404   -3.0306   -0.2500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4866   -2.7704    1.3841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1241   -2.8391   -0.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9223   -1.6884   -1.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0762    0.9586   -2.4160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2327   -0.3840   -4.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.4225    1.8246   -3.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.5137    1.0718   -2.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.6212   -2.7916   -0.9291 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2746    1.7020    1.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7309   -0.6681    2.1609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4616    1.0677    2.4468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9372    1.8966   -0.3040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6586    2.3680    0.7272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2107    1.8786   -0.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4862   -1.0602   -0.8746 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9091   -1.3456   -1.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0898   -0.5509   -0.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 12 11  1  1
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 36 37  1  0
 37 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  6
 37 38  1  1
 38 40  1  0
 38 39  2  0
  5 45  2  0
 45 46  1  0
 46 47  2  0
 47 48  1  0
 47  3  1  0
 21 12  1  0
 43 24  1  0
 26 19  1  0
 43 29  1  0
 37 30  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  4 52  1  0
  6 53  1  0
  7 54  1  0
 11 55  1  0
 11 56  1  0
 13 57  1  0
 13 58  1  0
 13 59  1  0
 14 60  1  1
 15 61  1  0
 16 62  1  1
 17 63  1  0
 18 64  1  0
 18 65  1  0
 20 66  1  0
 20 67  1  0
 20 68  1  0
 21 69  1  6
 22 70  1  0
 22 71  1  0
 23 72  1  0
 23 73  1  0
 25 74  1  0
 25 75  1  0
 25 76  1  0
 26 77  1  6
 27 78  1  0
 27 79  1  0
 28 80  1  0
 30 81  1  6
 31 82  1  1
 32 83  1  0
 32 84  1  0
 32 85  1  0
 33 86  1  6
 34 87  1  0
 34 88  1  0
 34 89  1  0
 35 90  1  0
 35 91  1  0
 36 92  1  0
 36 93  1  0
 41 95  1  0
 41 96  1  0
 42 97  1  0
 42 98  1  0
 44 99  1  0
 44100  1  0
 44101  1  0
 40 94  1  0
 45102  1  0
 46103  1  0
 48104  1  0
M  END


  Mrv1652309092215272D          

 48 53  0  0  1  0            999 V2000
   10.6695    6.6001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5262    5.7877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7510    5.5055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6077    4.6930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8325    4.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6892    3.5984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9140    3.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7707    2.5038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4027    1.9735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9955    2.2216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8522    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9337    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  2  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
    6.0770   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 O   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  1  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  1  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  2  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  2  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  2  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
    0.3020   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    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  1  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
   -0.1105    1.8414    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
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  1  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
    8.2005    4.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3438    5.7536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1190    6.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2623    6.8483    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 30 29  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 30 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 37 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 29 43  1  0  0  0  0
 24 43  1  0  0  0  0
 43 44  1  6  0  0  0
  5 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
  3 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0285328

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)OC[C@@]2(C)[C@H](O)[C@H](O)C[C@@]3(C)[C@H]2CC[C@]2(C)[C@@H]3CC=C3[C@@H]4[C@@H](C)[C@H](C)CC[C@@]4(CC[C@@]23C)C(O)=O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H56O8/c1-23-14-17-40(35(45)46)19-18-38(5)26(33(40)24(23)2)10-12-31-36(3)21-28(42)34(44)37(4,30(36)15-16-39(31,38)6)22-48-32(43)13-9-25-8-11-27(41)29(20-25)47-7/h8-11,13,20,23-24,28,30-31,33-34,41-42,44H,12,14-19,21-22H2,1-7H3,(H,45,46)/b13-9+/t23-,24+,28-,30-,31-,33+,34-,36+,37-,38-,39-,40+/m1/s1

> <INCHI_KEY>
YFHPZWBRSMIKOC-SWUWCAIHSA-N

> <FORMULA>
C40H56O8

> <MOLECULAR_WEIGHT>
664.88

> <EXACT_MASS>
664.397518763

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
76.06096071470495

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,4aS,6aS,6bR,8aR,9S,10S,11R,12aR,12bR,14bS)-10,11-dihydroxy-9-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-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>
6.7987847766666665

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.867719581422131

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.7441221547229295

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1618678772294704

> <JCHEM_POLAR_SURFACE_AREA>
133.52

> <JCHEM_REFRACTIVITY>
184.84599999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4aS,6aS,6bR,8aR,9S,10S,11R,12aR,12bR,14bS)-10,11-dihydroxy-9-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      19.916  12.320   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      19.649  10.804   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      18.202  10.277   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.934   8.760   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.487   8.234   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.220   6.717   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.773   6.190   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.505   4.674   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      15.685   3.684   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      13.058   4.147   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      12.791   2.630   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.076   3.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.654   0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      12.114  -1.897   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.264  -0.564   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.034   3.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.494   3.437   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.206  -1.897   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       1.334   3.437   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       2.104   4.771   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.023   3.635   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      15.308   9.224   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      15.575  10.740   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      17.022  11.267   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      17.290  12.783   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   47                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   45                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   21                                             
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21   26                                             
CONECT   20   19                                                            
CONECT   21   19   12   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   43                                             
CONECT   25   24                                                            
CONECT   26   24   19   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   43                                                  
CONECT   30   29   31   37                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   30   38   41                                             
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   37   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   29   24   44                                             
CONECT   44   43                                                            
CONECT   45    5   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46    3   48                                                  
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  106    0
END

View in JSmol

Synonyms

Value	Source
2a,3a-Dihydroxy-24-[(3-methoxy-4-hydroxy-trans-cinnamoyl)oxy]urs-12-en-28-Oate	Generator
2a,3a-Dihydroxy-24-[(3-methoxy-4-hydroxy-trans-cinnamoyl)oxy]urs-12-en-28-Oic acid	Generator
2alpha,3alpha-Dihydroxy-24-[(3-methoxy-4-hydroxy-trans-cinnamoyl)oxy]urs-12-en-28-Oate	Generator
2Α,3α-dihydroxy-24-[(3-methoxy-4-hydroxy-trans-cinnamoyl)oxy]urs-12-en-28-Oate	Generator
2Α,3α-dihydroxy-24-[(3-methoxy-4-hydroxy-trans-cinnamoyl)oxy]urs-12-en-28-Oic acid	Generator

Chemical Formula

C₄₀H₅₆O₈

Average Mass

664.8800 Da

Monoisotopic Mass

664.39752 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)OC[C@@]2(C)[C@H](O)[C@H](O)C[C@@]3(C)[C@H]2CC[C@]2(C)[C@@H]3CC=C3[C@@H]4[C@@H](C)[C@H](C)CC[C@@]4(CC[C@@]23C)C(O)=O)=CC=C1O

InChI Identifier

InChI=1S/C40H56O8/c1-23-14-17-40(35(45)46)19-18-38(5)26(33(40)24(23)2)10-12-31-36(3)21-28(42)34(44)37(4,30(36)15-16-39(31,38)6)22-48-32(43)13-9-25-8-11-27(41)29(20-25)47-7/h8-11,13,20,23-24,28,30-31,33-34,41-42,44H,12,14-19,21-22H2,1-7H3,(H,45,46)/b13-9+/t23-,24+,28-,30-,31-,33+,34-,36+,37-,38-,39-,40+/m1/s1

InChI Key

YFHPZWBRSMIKOC-SWUWCAIHSA-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
Prunus africana	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
12-hydroxysteroid
Hydroxysteroid
12-beta-hydroxysteroid
Steroid
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Methoxyphenol
Styrene
Methoxybenzene
Phenoxy compound
Phenol ether
Anisole
Phenol
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Fatty acid ester
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic alcohol
Carboxylic acid ester
1,2-diol
Secondary alcohol
Carboxylic acid derivative
Ether
Carboxylic acid
Carbonyl group
Organic oxygen compound
Organic oxide
Organooxygen compound
Alcohol
Hydrocarbon derivative
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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

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

101995318

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid (NP0285328)

MOL for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

3D MOL for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

3D SDF for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

3D-SDF for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

PDB for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

3D PDB for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

SMILES for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

INCHI for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

Structure for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)

3D Structure for NP0285328 ((1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-({[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid)