NP-MRD: Showing NP-Card for (+)-Sampsonione L (NP0077097)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 22:15:50 UTC

Updated at

2022-04-28 22:15:50 UTC

NP-MRD ID

NP0077097

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Sampsonione L

Description

(1S,3S,8R,10S)-8-benzoyl-3-(2-hydroxypropan-2-yl)-9,9-dimethyl-6,10-bis(3-methylbut-2-en-1-yl)-4-oxatricyclo[6.3.1.0¹,⁵]Dodec-5-ene-7,12-dione belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. (+)-Sampsonione L is found in Hypericum sampsonii. Based on a literature review very few articles have been published on (1S,3S,8R,10S)-8-benzoyl-3-(2-hydroxypropan-2-yl)-9,9-dimethyl-6,10-bis(3-methylbut-2-en-1-yl)-4-oxatricyclo[6.3.1.0¹,⁵]Dodec-5-ene-7,12-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292200152D          

 38 41  0  0  1  0            999 V2000
    3.5422    0.4268    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0637    1.1222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7827    1.9324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9301    2.0183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3592    1.3445    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8584    0.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1651   -0.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0135   -0.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8360   -1.0658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6657   -0.8385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9848   -1.5994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4854   -2.2561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8044   -3.0169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6670   -2.1519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0593    0.8391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0103    1.6668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7820    1.9698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3152    2.1111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3799    2.5554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7595    2.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1291    1.4160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9583    0.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4640    1.5438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2942    2.5797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9893    3.3463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5007    3.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1959    4.7602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3171    3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7277    0.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8453    1.3862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1991   -0.0723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9598    0.2471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -0.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7523   -1.3898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6485   -2.2083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8878   -2.5276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2309   -2.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3347   -1.2101    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  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
  1  8  1  0  0  0  0
  8  9  2  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 16 18  1  6  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
  5 22  1  6  0  0  0
  1 22  1  0  0  0  0
 22 23  2  0  0  0  0
  3 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  2 29  1  0  0  0  0
  2 30  1  0  0  0  0
  1 31  1  6  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
M  END

     RDKit          3D

 80 83  0  0  0  0  0  0  0  0999 V2000
    5.6260   -0.2595    1.9980 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5409   -0.7280    2.8941 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7340   -0.6190    4.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4417   -1.2255    2.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2442   -1.3365    0.9110 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0110   -0.5982    0.4563 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0795   -1.3170   -0.1510 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8877   -2.6700   -0.3326 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0870   -2.9167   -1.4778 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7898   -3.8285   -2.4574 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1527   -3.9806   -3.6588 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9844   -5.2019   -1.8733 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9840   -3.2378   -2.8625 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1743   -1.5488   -2.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0838   -0.6788   -0.8379 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3157   -0.7325    0.0034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4715    0.3371    1.0115 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9382    0.8109    1.0841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8299   -0.3192    1.4439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8416   -0.7644    0.7189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1740   -0.1284   -0.5767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6956   -1.9119    1.1590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4717    1.4094    1.1201 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2990    1.1580    2.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0283    2.7905    1.3736 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6103    1.5078    0.0972 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0380    2.8539   -0.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2189    3.2480    0.0587 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3195    3.8383   -1.0811 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8670    5.0940   -1.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1919    6.0204   -2.1353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0565    5.7752   -2.6495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6214    4.5520   -2.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9249    3.6179   -1.6033 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8745    0.8264    0.6919 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6898    1.4778    1.3170 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3165    0.7034   -1.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4036    1.1421   -2.2071 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9928   -1.0867    1.3375 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2775    0.6065    1.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5197    0.0594    2.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4377    0.2080    4.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1726   -1.5414    4.7986 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7797   -0.3409    4.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6489   -1.5695    3.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2239   -2.3824    0.6160 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1298   -0.8661    0.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8571   -3.3778   -1.1258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2969   -3.4406   -4.5062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2790   -5.0341   -3.9552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1464   -3.5732   -3.4552 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1696   -5.9112   -2.1611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0306   -5.2087   -0.7629 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9152   -5.6483   -2.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8001   -2.7375   -3.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1747   -1.5266   -2.5380 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6416   -1.2831   -2.7577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1824   -0.6619   -0.7223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3932   -1.7804    0.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4465   -0.2528    1.9972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0446    1.6679    1.7676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1901    1.1605    0.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6394   -0.8269    2.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2253    0.9892   -0.4247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4672   -0.4116   -1.3635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1929   -0.4107   -0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0333   -2.5438    0.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5538   -1.5338    1.7906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0721   -2.4945    1.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9514    1.9786    2.7131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5608    1.0507    3.2007 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7794    0.1874    2.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3048    2.9261    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9665    3.0208    0.8494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3144    3.6106    1.2019 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8559    5.2915   -0.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6497    6.9736   -2.3387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5957    6.5071   -3.2521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6083    4.3465   -2.7787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4840    2.7000   -1.4440 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  1  0
 20 19  2  3
 19 18  1  0
 18 17  1  0
 17 16  1  0
 15 16  1  1
 15 14  1  0
 14  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
  6 35  1  0
 35 36  2  0
 35 26  1  0
 26 27  1  6
 27 28  2  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  2  0
 26 37  1  0
 37 38  2  0
 26 23  1  0
 23 24  1  1
 23 25  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 10 13  1  6
 23 17  1  0
  7 15  1  0
 34 29  1  0
 37 15  1  0
 21 64  1  0
 21 65  1  0
 21 66  1  0
 22 67  1  0
 22 68  1  0
 22 69  1  0
 19 63  1  0
 18 61  1  0
 18 62  1  0
 17 60  1  1
 16 58  1  0
 16 59  1  0
 14 56  1  0
 14 57  1  0
  9 48  1  1
  5 46  1  0
  5 47  1  0
  4 45  1  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  3 42  1  0
  3 43  1  0
  3 44  1  0
 30 76  1  0
 31 77  1  0
 32 78  1  0
 33 79  1  0
 34 80  1  0
 24 70  1  0
 24 71  1  0
 24 72  1  0
 25 73  1  0
 25 74  1  0
 25 75  1  0
 11 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 12 54  1  0
 13 55  1  0
M  END


  Mrv1652304292200152D          

 38 41  0  0  1  0            999 V2000
    3.5422    0.4268    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0637    1.1222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7827    1.9324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9301    2.0183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3592    1.3445    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8584    0.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1651   -0.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0135   -0.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8360   -1.0658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6657   -0.8385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9848   -1.5994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4854   -2.2561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8044   -3.0169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6670   -2.1519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0593    0.8391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0103    1.6668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7820    1.9698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3152    2.1111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3799    2.5554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7595    2.8062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1291    1.4160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9583    0.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4640    1.5438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2942    2.5797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9893    3.3463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5007    3.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1959    4.7602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3171    3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7277    0.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8453    1.3862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1991   -0.0723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9598    0.2471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -0.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7523   -1.3898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6485   -2.2083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8878   -2.5276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2309   -2.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3347   -1.2101    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  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
  1  8  1  0  0  0  0
  8  9  2  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 16 18  1  6  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
  5 22  1  6  0  0  0
  1 22  1  0  0  0  0
 22 23  2  0  0  0  0
  3 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  2 29  1  0  0  0  0
  2 30  1  0  0  0  0
  1 31  1  6  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0077097

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC[C@H]1C[C@]23C[C@H](OC2=C(CC=C(C)C)C(=O)[C@@](C(=O)C2=CC=CC=C2)(C3=O)C1(C)C)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C33H42O5/c1-20(2)14-16-23-18-32-19-25(31(7,8)37)38-28(32)24(17-15-21(3)4)27(35)33(29(32)36,30(23,5)6)26(34)22-12-10-9-11-13-22/h9-15,23,25,37H,16-19H2,1-8H3/t23-,25-,32-,33-/m0/s1

> <INCHI_KEY>
HDUWARMIHZANDI-AQCLMGBYSA-N

> <FORMULA>
C33H42O5

> <MOLECULAR_WEIGHT>
518.694

> <EXACT_MASS>
518.303224452

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
58.45391904702997

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3S,8R,10S)-8-benzoyl-3-(2-hydroxypropan-2-yl)-9,9-dimethyl-6,10-bis(3-methylbut-2-en-1-yl)-4-oxatricyclo[6.3.1.0^{1,5}]dodec-5-ene-7,12-dione

> <ALOGPS_LOGP>
5.32

> <JCHEM_LOGP>
6.6787013443333345

> <ALOGPS_LOGS>
-5.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.306630178205651

> <JCHEM_PKA_STRONGEST_BASIC>
-3.102079960052847

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
152.78199999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.09e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3S,8R,10S)-8-benzoyl-3-(2-hydroxypropan-2-yl)-9,9-dimethyl-6,10-bis(3-methylbut-2-en-1-yl)-4-oxatricyclo[6.3.1.0^{1,5}]dodec-5-ene-7,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       6.612   0.797   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.586   2.095   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.061   3.607   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.470   3.767   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.404   2.510   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.469   1.170   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.042  -0.339   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.625  -0.486   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.294  -1.990   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.109  -1.565   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.705  -2.985   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.773  -4.211   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.368  -5.631   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.245  -4.017   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.977   1.566   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.886   3.111   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.326   3.677   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.588   3.941   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.709   4.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.418   5.238   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.241   2.643   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.522   1.665   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.466   2.882   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.016   4.815   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.447   6.246   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.401   7.455   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.832   8.886   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.925   7.232   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.825   1.181   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.045   2.588   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.838  -0.135   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.258   0.461   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       7.645  -1.663   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.871  -2.594   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.677  -4.122   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.257  -4.718   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.031  -3.787   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.225  -2.259   0.000  0.00  0.00           C+0
CONECT    1    2    8   22   31                                             
CONECT    2    1    3   29   30                                             
CONECT    3    2    4   24                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   17   22                                             
CONECT    6    5    7   15                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    1    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    6   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16    5                                                       
CONECT   18   16   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22    5    1   23                                                  
CONECT   23   22                                                            
CONECT   24    3   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29    2                                                            
CONECT   30    2                                                            
CONECT   31    1   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   33                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₂O₅

Average Mass

518.6940 Da

Monoisotopic Mass

518.30322 Da

IUPAC Name

(1S,3S,8R,10S)-8-benzoyl-3-(2-hydroxypropan-2-yl)-9,9-dimethyl-6,10-bis(3-methylbut-2-en-1-yl)-4-oxatricyclo[6.3.1.0^{1,5}]dodec-5-ene-7,12-dione

Traditional Name

(1S,3S,8R,10S)-8-benzoyl-3-(2-hydroxypropan-2-yl)-9,9-dimethyl-6,10-bis(3-methylbut-2-en-1-yl)-4-oxatricyclo[6.3.1.0^{1,5}]dodec-5-ene-7,12-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CC[C@H]1C[C@]23C[C@H](OC2=C(CC=C(C)C)C(=O)[C@@](C(=O)C2=CC=CC=C2)(C3=O)C1(C)C)C(C)(C)O

InChI Identifier

InChI=1S/C33H42O5/c1-20(2)14-16-23-18-32-19-25(31(7,8)37)38-28(32)24(17-15-21(3)4)27(35)33(29(32)36,30(23,5)6)26(34)22-12-10-9-11-13-22/h9-15,23,25,37H,16-19H2,1-8H3/t23-,25-,32-,33-/m0/s1

InChI Key

HDUWARMIHZANDI-AQCLMGBYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Hypericum sampsonii	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Aromatic monoterpenoid
Monoterpenoid
Benzoyl
Aryl alkyl ketone
Cyclohexenone
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Tertiary alcohol
Vinylogous ester
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Alcohol
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.32	ALOGPS
logP	6.68	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	14.31	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	80.67 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	152.78 m³·mol⁻¹	ChemAxon
Polarizability	58.45 Å³	ChemAxon
Number of Rings	4	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

162896627

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Sampsonione L (NP0077097)

MOL for NP0077097 ((+)-Sampsonione L)

3D MOL for NP0077097 ((+)-Sampsonione L)

3D SDF for NP0077097 ((+)-Sampsonione L)

3D-SDF for NP0077097 ((+)-Sampsonione L)

PDB for NP0077097 ((+)-Sampsonione L)

3D PDB for NP0077097 ((+)-Sampsonione L)

SMILES for NP0077097 ((+)-Sampsonione L)

INCHI for NP0077097 ((+)-Sampsonione L)

Structure for NP0077097 ((+)-Sampsonione L)

3D Structure for NP0077097 ((+)-Sampsonione L)