NP-MRD: Showing NP-Card for 1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate (NP0226277)

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Record Information

Version

2.0

Created at

2022-09-06 05:15:38 UTC

Updated at

2022-09-06 05:15:38 UTC

NP-MRD ID

NP0226277

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate

Description

1-Ethyl 4-(17-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-5-yl)methyl butanedioate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate is found in Diospyros maritima. 1-Ethyl 4-(17-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosan-5-yl)methyl butanedioate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231521082D          

 52 57  0  0  0  0            999 V2000
    2.4110   -8.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1255   -8.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8400   -8.5261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5545   -8.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5545   -7.2886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2689   -8.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9834   -8.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6979   -8.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6979   -9.3511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4123   -8.1136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1268   -8.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8413   -8.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1738   -7.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4288   -6.8441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2538   -6.8441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5087   -7.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2624   -7.9643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9298   -7.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6835   -7.8149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7698   -8.6354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5234   -8.9709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4372   -8.1505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1909   -8.4860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9445   -8.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0308   -9.6421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7845   -9.9776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4519   -9.4927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3657   -8.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.2056   -9.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8730   -9.3433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6267   -9.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2941   -9.1940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0478   -9.5295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1340  -10.3500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8877  -10.6856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4666  -10.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7129  -10.4994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3633  -10.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9568  -10.7001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9020  -10.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6097   -9.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9422  -10.2763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1885   -9.9408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1023   -9.1203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4349   -9.6052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3486   -8.7847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9361   -9.4992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6812   -9.2697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9275   -8.9341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7387   -6.1766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5592   -6.2629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4032   -5.4230    0.0000 C   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 27  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 31 37  1  0  0  0  0
 25 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
 21 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 20 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 17 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 12 49  1  0  0  0  0
 15 50  1  0  0  0  0
 50 51  2  0  0  0  0
 50 52  1  0  0  0  0
M  END

     RDKit          3D

116121  0  0  0  0  0  0  0  0999 V2000
   -2.2556   -1.0842   -3.2996 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1921   -0.8139   -0.5076 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2528   -0.4095    0.5000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.5359   -2.0462    1.3672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5589   -1.5086    2.3728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9871   -0.1618    1.8955 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7915    0.4783    2.6016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5205    0.3781    0.7116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9361    1.6491    0.2750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5708    2.7138    1.2760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6803   -2.1461   -0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2792   -2.2864    0.3004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5856   -1.0522    0.7374 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1211   -0.6865    2.1020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7994   -0.0047   -0.2903 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1351    1.2834    0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1599    1.1997    1.2553 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5474   -0.0526    1.5481 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.7940   -1.1556    1.9124 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6827    1.1694    2.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
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   14.4097   -1.0932   -0.4913 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0874   -1.2198   -0.0053 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6530    1.0318   -1.9133 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2717    0.2253   -0.1195 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5295   -0.7089   -0.9957 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6108   -1.6866   -0.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1918    0.2564   -0.6776 C   0  0  1  0  0  0  0  0  0  0  0  0
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  -10.4542    2.8454    1.9434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4109    3.6732    0.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.4087   -2.7072    0.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8121   -2.7875   -1.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2918   -3.0778    1.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.3189   -0.2695    0.2777 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2323    2.3172   -0.9603 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5703    2.3312   -1.4097 H   0  0  0  0  0  0  0  0  0  0  0  0
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   14.6704   -1.6324   -1.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4516    2.1107   -1.6480 H   0  0  0  0  0  0  0  0  0  0  0  0
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  3 55  1  0
  3 56  1  0
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  1 53  1  0
  1 54  1  0
M  END


  Mrv1533004231521082D          

 52 57  0  0  0  0            999 V2000
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    3.1255   -8.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6979   -8.5261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   12.4372   -8.1505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1909   -8.4860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9445   -8.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0308   -9.6421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7845   -9.9776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4519   -9.4927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3657   -8.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.2056   -9.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8730   -9.3433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6267   -9.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2941   -9.1940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0478   -9.5295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1340  -10.3500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8877  -10.6856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4666  -10.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7129  -10.4994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3633  -10.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9568  -10.7001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9020  -10.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6097   -9.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9422  -10.2763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1885   -9.9408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1023   -9.1203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4349   -9.6052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3486   -8.7847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9361   -9.4992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6812   -9.2697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9275   -8.9341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7387   -6.1766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5592   -6.2629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4032   -5.4230    0.0000 C   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 27  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 31 37  1  0  0  0  0
 25 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
 21 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 20 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 17 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 12 49  1  0  0  0  0
 15 50  1  0  0  0  0
 50 51  2  0  0  0  0
 50 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0226277

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC(=O)CCC(=O)OCC12CCC(C1C1CCC3C4(C)CCC(OC(=O)C=CC5=CC=C(O)C=C5)C(C)(C)C4CCC3(C)C1(C)CC2)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C45H64O7/c1-9-50-37(47)18-19-38(48)51-28-45-25-20-32(29(2)3)40(45)33-15-16-35-42(6)23-22-36(52-39(49)17-12-30-10-13-31(46)14-11-30)41(4,5)34(42)21-24-44(35,8)43(33,7)26-27-45/h10-14,17,32-36,40,46H,2,9,15-16,18-28H2,1,3-8H3

> <INCHI_KEY>
JTYJREBXUVSAHQ-UHFFFAOYSA-N

> <FORMULA>
C45H64O7

> <MOLECULAR_WEIGHT>
717.0

> <EXACT_MASS>
716.465204401

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
116

> <JCHEM_AVERAGE_POLARIZABILITY>
84.83430158730647

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-ethyl 4-(17-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-5-yl)methyl butanedioate

> <ALOGPS_LOGP>
7.54

> <JCHEM_LOGP>
9.666290888666666

> <ALOGPS_LOGS>
-7.10

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.398614366561935

> <JCHEM_PKA_STRONGEST_BASIC>
-5.9547318749588785

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
203.79410000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.66e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-ethyl 4-(17-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-5-yl)methyl butanedioate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       4.501 -15.915   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.834 -15.145   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.168 -15.915   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.502 -15.145   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.502 -13.605   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.835 -15.915   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.169 -15.145   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.503 -15.915   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.503 -17.455   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      13.836 -15.145   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      15.170 -15.915   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.504 -15.145   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.258 -14.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.734 -12.776   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.274 -12.776   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.750 -14.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      19.156 -14.867   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.402 -13.961   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.809 -14.588   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.970 -16.119   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      23.377 -16.746   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      23.216 -15.214   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      24.623 -15.841   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      26.030 -16.467   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.191 -17.999   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      27.598 -18.625   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      28.844 -17.720   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      28.683 -16.188   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      30.250 -18.346   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      31.496 -17.441   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      32.903 -18.067   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      34.149 -17.162   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      35.556 -17.788   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      35.717 -19.320   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      37.124 -19.946   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      34.471 -20.225   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      33.064 -19.599   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      24.945 -18.904   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      26.053 -19.973   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      24.084 -20.180   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      23.538 -18.277   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      22.292 -19.183   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      20.885 -18.556   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      20.724 -17.025   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      19.478 -17.930   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      19.317 -16.398   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      18.547 -17.732   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      18.072 -17.303   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      16.665 -16.677   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      18.179 -11.530   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      19.710 -11.691   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      17.553 -10.123   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    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   16   49                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   50                                                  
CONECT   16   15   12   17                                                  
CONECT   17   16   18   46                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   44                                                  
CONECT   21   20   22   23   41                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   38                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   37                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   31                                                       
CONECT   38   25   39   40   41                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   38   21   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   20   45   46                                             
CONECT   45   44                                                            
CONECT   46   44   17   47   48                                             
CONECT   47   46                                                            
CONECT   48   46   49                                                       
CONECT   49   48   12                                                       
CONECT   50   15   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  114    0
END

View in JSmol

Synonyms

Value	Source
1-Ethyl 4-(17-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0,.0,.0,]henicosan-5-yl)methyl butanedioic acid	Generator
1-Ethyl 4-(17-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-5-yl)methyl butanedioic acid	Generator

Chemical Formula

C₄₅H₆₄O₇

Average Mass

717.0000 Da

Monoisotopic Mass

716.46520 Da

IUPAC Name

1-ethyl 4-(17-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-5-yl)methyl butanedioate

Traditional Name

1-ethyl 4-(17-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-1,2,14,18,18-pentamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-5-yl)methyl butanedioate

CAS Registry Number

Not Available

SMILES

CCOC(=O)CCC(=O)OCC12CCC(C1C1CCC3C4(C)CCC(OC(=O)C=CC5=CC=C(O)C=C5)C(C)(C)C4CCC3(C)C1(C)CC2)C(C)=C

InChI Identifier

InChI=1S/C45H64O7/c1-9-50-37(47)18-19-38(48)51-28-45-25-20-32(29(2)3)40(45)33-15-16-35-42(6)23-22-36(52-39(49)17-12-30-10-13-31(46)14-11-30)41(4,5)34(42)21-24-44(35,8)43(33,7)26-27-45/h10-14,17,32-36,40,46H,2,9,15-16,18-28H2,1,3-8H3

InChI Key

JTYJREBXUVSAHQ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Diospyros maritima	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 ester
Steroid
Coumaric acid ester
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Tricarboxylic acid or derivatives
Styrene
Fatty acid ester
Phenol
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Benzenoid
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Carboxylic acid derivative
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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
logP	7.54	ALOGPS
logP	9.67	ChemAxon
logS	-7.1	ALOGPS
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	203.79 m³·mol⁻¹	ChemAxon
Polarizability	84.83 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate (NP0226277)

MOL for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

3D MOL for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

3D SDF for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

3D-SDF for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

PDB for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

3D PDB for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

SMILES for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

INCHI for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

Structure for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)

3D Structure for NP0226277 (1-ethyl 4-(9-{[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-3a-yl)methyl butanedioate)