NP-MRD: Showing NP-Card for 10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one (NP0197705)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 16:00:55 UTC

Updated at

2022-09-04 16:00:55 UTC

NP-MRD ID

NP0197705

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one

Description

Latisxanthone B belongs to the class of organic compounds known as 2-prenylated xanthones. These are organic compounds containing a C5-isoprenoid group linked to a xanthone moiety at the 2-position. Xanthone is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring that carries a ketone group. 10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one is found in Garcinia latissima. Based on a literature review very few articles have been published on Latisxanthone B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042218002D          

 36 40  0  0  0  0            999 V2000
   -3.0924   -2.2494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2997   -2.0205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1016   -1.2197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7053   -2.5926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9126   -2.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3182   -2.9358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5163   -3.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0782   -4.3087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8708   -4.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4653   -4.6519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2579   -4.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8524   -4.9951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6542   -5.7960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6450   -4.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8432   -3.9655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2487   -3.3934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4561   -3.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8616   -3.0502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0597   -2.2494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0690   -3.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4745   -2.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6726   -1.9061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6358   -3.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2303   -4.3087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0321   -5.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8552   -5.1656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1198   -5.9299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2395   -5.3383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1200   -5.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9126   -5.3383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5071   -4.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9672   -5.4511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2614   -4.4321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3089   -3.9655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9034   -3.3934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6961   -3.6222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 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
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  2  0  0  0  0
  6 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 14 28  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
  7 34  1  0  0  0  0
  4 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END

     RDKit          3D

 64 68  0  0  0  0  0  0  0  0999 V2000
   -3.4704    1.4478    1.6442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6142    1.8842    0.8122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7753    2.4487    1.6523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7047    1.8298   -0.4596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7830    1.3534   -1.4730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4973    0.8074   -1.0953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4294   -0.4725   -0.5819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2236   -1.0281   -0.2353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0590   -0.2723   -0.4111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -0.8550   -0.0641 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1997   -0.2065   -0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3801   -0.8221    0.1707 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3167   -2.1299    0.6811 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6174   -0.2148    0.0617 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6224    1.0735   -0.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4635    1.7109   -0.8222 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2457    1.0701   -0.6979 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    1.7178   -1.0791 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1307    2.8759   -1.5303 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1047    1.0198   -0.9269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3235    1.5581   -1.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4612    2.8163   -1.7809 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9161    1.7053   -0.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0021    1.0883   -0.2048 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0411   -0.2758    0.3382 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8156   -1.1127   -0.6837 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7766   -0.2925    1.6754 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7795   -0.8540    0.4381 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1887   -2.3685    0.2859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2772   -3.0921    0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5869   -2.5424    0.0862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2472   -3.4104   -0.9724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5433   -2.5437    1.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5747   -1.2333   -0.4008 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9400    2.3281   -0.9994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7125    1.3793   -1.5497 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6217    0.3561    1.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5143    1.9102    2.6730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4868    1.7171    1.2685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1610    1.6503    2.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3335    3.2475    2.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5104    2.8971    0.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3114    0.6175   -2.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5509    2.1946   -2.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4271   -2.5935    0.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4678    2.7280   -1.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8192    3.4962   -1.9822 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9156    2.7292   -0.9668 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9517    1.6425   -0.3246 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9775   -2.1251   -0.2560 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1997   -1.1313   -1.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7927   -0.6812   -0.9224 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7736    0.7490    2.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2633   -0.9321    2.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8483   -0.5713    1.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2288   -2.7844    0.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2251   -4.0864    0.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4046   -3.8528   -1.5614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8355   -2.8084   -1.6770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8005   -4.2324   -0.4908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4362   -1.9786    0.9529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1169   -2.0146    2.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8541   -3.5710    1.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3039    1.0396   -2.3904 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7 34  1  0
 34 31  1  0
 31 32  1  0
 31 33  1  0
 31 30  1  0
 30 29  2  0
 29  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
  4 35  1  0
 35 36  1  0
 21  6  1  0
  8  7  1  0
 20  9  1  0
 17 11  1  0
 28 14  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  3 40  1  0
  3 41  1  0
  3 42  1  0
  5 43  1  0
  5 44  1  0
 32 58  1  0
 32 59  1  0
 32 60  1  0
 33 61  1  0
 33 62  1  0
 33 63  1  0
 30 57  1  0
 29 56  1  0
 13 45  1  0
 23 48  1  0
 24 49  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
 27 53  1  0
 27 54  1  0
 27 55  1  0
 16 46  1  0
 22 47  1  0
 36 64  1  0
M  END


  Mrv1652309042218002D          

 36 40  0  0  0  0            999 V2000
   -3.0924   -2.2494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2997   -2.0205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1016   -1.2197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7053   -2.5926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9126   -2.3638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3182   -2.9358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5163   -3.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0782   -4.3087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8708   -4.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4653   -4.6519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2579   -4.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8524   -4.9951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6542   -5.7960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6450   -4.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8432   -3.9655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2487   -3.3934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4561   -3.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8616   -3.0502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0597   -2.2494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0690   -3.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4745   -2.7070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6726   -1.9061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6358   -3.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2303   -4.3087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0321   -5.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8552   -5.1656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1198   -5.9299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2395   -5.3383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1200   -5.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9126   -5.3383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5071   -4.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9672   -5.4511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2614   -4.4321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3089   -3.9655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9034   -3.3934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6961   -3.6222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 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
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  2  0  0  0  0
  6 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 14 28  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
  7 34  1  0  0  0  0
  4 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0197705

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=C(CC1=C2OC(C)(C)C=CC2=C2OC3=C(O)C4=C(C=CC(C)(C)O4)C=C3C(=O)C2=C1O)OO

> <INCHI_IDENTIFIER>
InChI=1S/C28H28O8/c1-13(2)18(36-32)12-17-21(30)19-20(29)16-11-14-7-9-27(3,4)34-23(14)22(31)26(16)33-25(19)15-8-10-28(5,6)35-24(15)17/h7-11,30-32H,12H2,1-6H3

> <INCHI_KEY>
AYNRFDZREQAQQD-UHFFFAOYSA-N

> <FORMULA>
C28H28O8

> <MOLECULAR_WEIGHT>
492.524

> <EXACT_MASS>
492.178417862

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
52.967797244775774

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0^{3,12}.0^{4,9}.0^{16,21}]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one

> <JCHEM_LOGP>
5.624605284333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.675207976857957

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.061900306646029

> <JCHEM_PKA_STRONGEST_BASIC>
-3.754808069388115

> <JCHEM_POLAR_SURFACE_AREA>
114.68000000000002

> <JCHEM_REFRACTIVITY>
137.20420000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0^{3,12}.0^{4,9}.0^{16,21}]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.772  -4.199   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.293  -3.772   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.923  -2.277   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.183  -4.839   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.704  -4.412   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.594  -5.480   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.964  -6.975   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.146  -8.043   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.625  -7.616   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.735  -8.684   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.215  -8.256   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.324  -9.324   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.955 -10.819   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.804  -8.897   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.174  -7.402   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.064  -6.334   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.585  -6.762   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.475  -5.694   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.845  -4.199   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.995  -6.121   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.886  -5.053   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.256  -3.558   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.654  -6.975   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.763  -8.043   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.393  -9.538   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.930  -9.642   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.557 -11.069   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.914  -9.965   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.224  -9.538   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.704  -9.965   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.813  -8.897   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.672 -10.175   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.221  -8.273   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -2.443  -7.402   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -3.553  -6.334   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -5.033  -6.762   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   35                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   21                                                  
CONECT    7    6    8   34                                                  
CONECT    8    7    9   29                                                  
CONECT    9    8   10   20                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   28                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    9   21                                                  
CONECT   21   20    6   22                                                  
CONECT   22   21                                                            
CONECT   23   15   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   14                                                       
CONECT   29    8   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31    7                                                       
CONECT   35    4   36                                                       
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₂₈O₈

Average Mass

492.5240 Da

Monoisotopic Mass

492.17842 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)=C(CC1=C2OC(C)(C)C=CC2=C2OC3=C(O)C4=C(C=CC(C)(C)O4)C=C3C(=O)C2=C1O)OO

InChI Identifier

InChI=1S/C28H28O8/c1-13(2)18(36-32)12-17-21(30)19-20(29)16-11-14-7-9-27(3,4)34-23(14)22(31)26(16)33-25(19)15-8-10-28(5,6)35-24(15)17/h7-11,30-32H,12H2,1-6H3

InChI Key

AYNRFDZREQAQQD-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
Garcinia latissima	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-prenylated xanthones. These are organic compounds containing a C5-isoprenoid group linked to a xanthone moiety at the 2-position. Xanthone is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring that carries a ketone group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2-prenylated xanthones

Alternative Parents

Substituents

2-prenylated xanthone
Pyranoxanthone
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Alkyl aryl ether
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Hydroperoxide
Oxacycle
Peroxol
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00053418

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

102505133

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one (NP0197705)

MOL for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

3D MOL for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

3D SDF for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

3D-SDF for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

PDB for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

3D PDB for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

SMILES for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

INCHI for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

Structure for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)

3D Structure for NP0197705 (10-(2-hydroperoxy-3-methylbut-2-en-1-yl)-11,22-dihydroxy-7,7,19,19-tetramethyl-2,8,20-trioxapentacyclo[12.8.0.0³,¹².0⁴,⁹.0¹⁶,²¹]docosa-1(22),3,5,9,11,14,16(21),17-octaen-13-one)