NP-MRD: Showing NP-Card for (1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate (NP0149145)

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Record Information

Version

2.0

Created at

2022-09-02 04:59:37 UTC

Updated at

2022-09-02 04:59:37 UTC

NP-MRD ID

NP0149145

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate

Description

Lupa-20(29)-ene-3beta,16beta-diol 3-hexadecanoate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on Lupa-20(29)-ene-3beta,16beta-diol 3-hexadecanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022206592D          

 49 53  0  0  1  0            999 V2000
   -6.1334    1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3264    1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7744    1.6527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0714    0.2549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5564   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0714   -1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3731   -1.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8125    1.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2822    0.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6585   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 22 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 41 44  1  0  0  0  0
 18 44  1  0  0  0  0
 44 45  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 17 47  1  0  0  0  0
 12 47  1  0  0  0  0
 47 48  1  6  0  0  0
 14 49  1  0  0  0  0
 49  4  1  6  0  0  0
  7 49  1  0  0  0  0
M  END

     RDKit          3D

129133  0  0  0  0  0  0  0  0999 V2000
   -9.9275    1.6821    2.9509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9950    1.8436    2.0325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8250    2.6777    2.4628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1308    1.3517    0.6962 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.5487    0.7199    0.4685 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4083    0.0155   -0.8773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9566    0.1796   -1.2168 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.8249    1.4881   -1.9295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4161   -0.8865   -2.1068 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.9423   -0.6365   -3.3848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9233   -0.6022   -2.2168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2739   -0.7478   -0.8608 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.5167   -2.1787   -0.5037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9149    0.1418    0.2090 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.3567   -0.4185    1.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8734   -0.2822    1.5688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1681   -0.7401    0.3552 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6653   -0.5089    0.3769 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2299    0.8805    0.5705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1775   -1.3293    1.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7229   -1.5752    1.6188 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0575   -1.5814    0.3657 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0068   -0.5058    0.4782 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3621   -0.7432    0.5388 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7699   -1.9258    0.4867 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3044    0.4330    0.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7296    0.4291    2.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6483    1.5466    2.4596 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9368    1.6066    1.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7645    0.3728    1.9167 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1109    0.4353    1.2011 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9901    0.6104   -0.2601 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2578    0.6528   -1.0059 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2419    1.7182   -0.7963 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.6197    0.8967    1.2076 C   0  0  0  0  0  0  0  0  0  0  0  0
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   13.7567   -1.9305   -2.2757 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1294   -1.2293   -0.8293 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7008   -0.7535   -2.1392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1744   -0.9900   -2.1268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8236   -0.3399   -0.9156 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7335    1.1499   -1.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3526    0.1736    0.1962 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.8075    2.0551    3.9393 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8389    1.1722    2.7129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0280    2.7529    1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3881    2.1972    3.3652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1720    3.7113    2.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0153    2.1757   -0.0685 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6849   -0.0499    1.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3114    1.4936    0.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0663    0.5164   -1.6281 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6417   -1.0627   -0.7788 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2094   -1.8780    0.3778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1576    1.5037   -0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7163   -2.3126    1.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2128   -0.9313    2.4123 H   0  0  0  0  0  0  0  0  0  0  0  0
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   13.2553   -0.4322    1.3997 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.6279    1.0209    0.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
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   14.3346   -1.7861   -0.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.6914   -0.3263   -1.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.4087   -2.8332   -2.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.7044   -2.3008   -2.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.8922   -1.3029   -3.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0613   -0.6031   -2.8826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3924    0.6647   -1.6903 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1076   -0.4029   -1.5653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2667   -3.4075   -1.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4887   -2.4780   -2.8070 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5177   -3.1504   -1.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5534   -2.2785   -0.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3614    0.2290   -2.4454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2812   -1.4643   -2.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6816   -0.5261   -3.0236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3630   -2.0634   -2.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6350    1.5749   -1.6645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5452    1.7552   -0.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9212    1.4016   -1.9272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8203   -0.7659    0.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
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 39 38  1  0
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 18 44  1  0
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 47 17  1  0
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 16 15  1  0
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 49  4  1  0
  4  5  1  0
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  6  7  1  0
  7  8  1  6
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  9 10  1  0
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  4  2  1  0
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  2  1  2  3
 44 41  1  0
 41 42  1  0
 41 43  1  0
 41 22  1  0
 17 18  1  0
 12 14  1  0
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 40112  1  0
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 39110  1  0
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 44121  1  1
 45122  1  0
 45123  1  0
 46124  1  0
 46125  1  0
 48126  1  0
 48127  1  0
 48128  1  0
 17 75  1  1
 16 73  1  0
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 15 71  1  0
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 14 70  1  6
 49129  1  1
  4 55  1  6
  5 56  1  0
  5 57  1  0
  6 58  1  0
  6 59  1  0
  8 60  1  0
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 11 66  1  0
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 13 68  1  0
 13 69  1  0
  3 52  1  0
  3 53  1  0
  3 54  1  0
  1 50  1  0
  1 51  1  0
 42115  1  0
 42116  1  0
 42117  1  0
 43118  1  0
 43119  1  0
 43120  1  0
M  END


  Mrv1652309022206592D          

 49 53  0  0  1  0            999 V2000
   -6.1334    1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3264    1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7744    1.6527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0714    0.2549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5564   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0714   -1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3731   -1.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8125    1.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2822    0.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6585   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 22 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 41 44  1  0  0  0  0
 18 44  1  0  0  0  0
 44 45  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 17 47  1  0  0  0  0
 12 47  1  0  0  0  0
 47 48  1  6  0  0  0
 14 49  1  0  0  0  0
 49  4  1  6  0  0  0
  7 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0149145

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC[C@@H]2[C@H]4[C@@H](CC[C@]4(C)[C@@H](O)C[C@@]32C)C(C)=C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C46H80O3/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-40(48)49-39-28-30-43(6)36(42(39,4)5)27-31-45(8)37(43)25-24-35-41-34(33(2)3)26-29-44(41,7)38(47)32-46(35,45)9/h34-39,41,47H,2,10-32H2,1,3-9H3/t34-,35+,36-,37+,38-,39-,41+,43-,44+,45+,46+/m0/s1

> <INCHI_KEY>
DSAMWSFCGLZQHC-RBMVAVJMSA-N

> <FORMULA>
C46H80O3

> <MOLECULAR_WEIGHT>
681.143

> <EXACT_MASS>
680.610746436

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
129

> <JCHEM_AVERAGE_POLARIZABILITY>
88.25458530714505

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,4S,5S,8R,9R,10R,13R,14R,17S,19R)-4-hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-17-yl hexadecanoate

> <ALOGPS_LOGP>
9.66

> <JCHEM_LOGP>
13.138289316333331

> <ALOGPS_LOGS>
-7.74

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3903221726765621

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
206.01520000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.25e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4S,5S,8R,9R,10R,13R,14R,17S,19R)-4-hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-17-yl hexadecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0     -11.449   2.261   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.943   1.941   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.912   3.085   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.467   0.476   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.372  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.467  -2.016   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.163  -3.072   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -6.668  -3.850   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.668   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.335   3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.334   5.390   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.667   3.080   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.668   5.390   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.336   5.390   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.003   5.390   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.337   4.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.670   5.390   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      16.004   4.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      17.338   5.390   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      18.672   4.620   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      20.005   5.390   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      21.339   4.620   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      22.673   5.390   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.517   3.347   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.527   1.633   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -4.001   0.770   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -3.096  -0.476   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -8.002  -0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   49                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   49                                             
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14   47                                             
CONECT   13   12                                                            
CONECT   14   12   15   49                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   47                                                  
CONECT   18   17   19   20   44                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   41                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   22   42   43   44                                             
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44   41   18   45                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   17   12   48                                             
CONECT   48   47                                                            
CONECT   49   14    4    7                                                  
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Value	Source
Lupa-20(29)-ene-3b,16b-diol 3-hexadecanoate	Generator
Lupa-20(29)-ene-3b,16b-diol 3-hexadecanoic acid	Generator
Lupa-20(29)-ene-3beta,16beta-diol 3-hexadecanoic acid	Generator
Lupa-20(29)-ene-3β,16β-diol 3-hexadecanoate	Generator
Lupa-20(29)-ene-3β,16β-diol 3-hexadecanoic acid	Generator

Chemical Formula

C₄₆H₈₀O₃

Average Mass

681.1430 Da

Monoisotopic Mass

680.61075 Da

IUPAC Name

(1R,2R,4S,5S,8R,9R,10R,13R,14R,17S,19R)-4-hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-17-yl hexadecanoate

Traditional Name

(1R,2R,4S,5S,8R,9R,10R,13R,14R,17S,19R)-4-hydroxy-1,2,5,14,18,18-hexamethyl-8-(prop-1-en-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosan-17-yl hexadecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC[C@@H]2[C@H]4[C@@H](CC[C@]4(C)[C@@H](O)C[C@@]32C)C(C)=C)C1(C)C

InChI Identifier

InChI=1S/C46H80O3/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-40(48)49-39-28-30-43(6)36(42(39,4)5)27-31-45(8)37(43)25-24-35-41-34(33(2)3)26-29-44(41,7)38(47)32-46(35,45)9/h34-39,41,47H,2,10-32H2,1,3-9H3/t34-,35+,36-,37+,38-,39-,41+,43-,44+,45+,46+/m0/s1

InChI Key

DSAMWSFCGLZQHC-RBMVAVJMSA-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

Not Available

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
12-alpha-hydroxysteroid
Hydroxysteroid
Steroid
Fatty acid ester
Fatty acyl
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic 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	9.66	ALOGPS
logP	13.14	ChemAxon
logS	-7.7	ALOGPS
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	206.02 m³·mol⁻¹	ChemAxon
Polarizability	88.25 Å³	ChemAxon
Number of Rings	5	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

114811069

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101634610

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate (NP0149145)

MOL for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

3D MOL for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

3D SDF for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

3D-SDF for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

PDB for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

3D PDB for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

SMILES for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

INCHI for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

Structure for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)

3D Structure for NP0149145 ((1r,3as,4s,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-4-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl hexadecanoate)