NP-MRD: Showing NP-Card for 5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one (NP0065902)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 10:05:30 UTC

Updated at

2022-04-28 10:05:30 UTC

NP-MRD ID

NP0065902

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one

Description

1-[(5R)-2-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(3aS,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-3a,4,5,6,7,7a-hexahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaen-1-yl]-5-methoxy-3,3-dimethylcyclopent-1-en-1-yl]ethan-1-one belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one is found in Pittosporum tobira . Based on a literature review very few articles have been published on 1-[(5R)-2-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(3aS,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-3a,4,5,6,7,7a-hexahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaen-1-yl]-5-methoxy-3,3-dimethylcyclopent-1-en-1-yl]ethan-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282212052D          

 45 47  0  0  1  0            999 V2000
   -9.2462    5.0178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8337    4.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0087    4.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5962    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7712    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3587    2.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5337    2.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2962    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8837    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8371   -1.9309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2505    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0251    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5962    5.0178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0712    5.0178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5561    4.3504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3407    4.6053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.3407    5.4303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5561    5.6853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7192    6.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9488    6.2437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0082    4.1204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9219    3.2999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3012    3.5658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8532    2.9527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4942    3.3942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 17 26  1  0  0  0  0
 22 27  1  6  0  0  0
 20 28  1  0  0  0  0
 20 29  1  0  0  0  0
 16 30  1  0  0  0  0
 12 31  1  0  0  0  0
  7 32  1  0  0  0  0
  3 33  1  0  0  0  0
  1 34  1  0  0  0  0
 34 35  2  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
 34 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 36 41  1  6  0  0  0
 41 42  1  0  0  0  0
 35 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
M  END

     RDKit          3D

101103  0  0  0  0  0  0  0  0999 V2000
   14.9922   -2.0121    0.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7291   -1.4988    0.7207 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3071   -0.8150   -0.4169 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.9101    0.5857   -0.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5072    0.3528    0.4819 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.5858   -0.0846    1.9089 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8070    1.6790    0.2964 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0028   -0.7252   -0.4182 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6001   -1.0450   -0.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5584   -0.4289   -0.2004 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1579   -0.7370   -0.4918 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7940   -1.7836   -1.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1782   -0.0650    0.0870 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8053   -0.3846   -0.2112 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7793    0.2434    0.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3762   -0.1243   -0.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1064   -1.1845   -0.9990 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3691    0.5082    0.5562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0226    0.2244    0.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9889    0.9210    0.9152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3590    0.5761    0.6000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3859    1.2003    1.1577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1176    2.2731    2.1236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7082    0.7568    0.7557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8500    1.2727    1.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1373    0.7430    0.7395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2452    1.2709    1.2136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1994    2.3778    2.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5274    0.7483    0.7343 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7595    1.1450    1.0903 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7850    0.3353    0.3493 C   0  0  1  0  0  0  0  0  0  0  0  0
  -12.2699    1.1005   -0.8532 C   0  0  1  0  0  0  0  0  0  0  0  0
  -13.1687    2.2108   -0.3464 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1156    1.7881   -1.5709 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0516    0.2199   -1.7610 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8640   -1.2486   -1.5606 C   0  0  2  0  0  0  0  0  0  0  0  0
  -13.7307   -1.7629   -0.5683 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4434   -1.6233   -1.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9542   -0.8806   -0.0036 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.8710   -1.7358    1.2448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6719   -0.2813   -0.2005 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0207   -1.4088   -0.9537 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9773   -2.5243   -1.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2351   -3.1420   -2.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9174   -3.0082   -2.3186 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3034   -2.5477    1.5523 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.0214   -2.7754   -0.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.7140   -1.2163    0.3515 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.0489   -0.8195   -1.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5015    1.0646    0.6805 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.8505    1.2269   -1.0221 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1071    0.7211    2.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6176   -0.1600    2.2729 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0054   -1.0058    2.0644 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2866    1.6830   -0.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6266    2.4605    0.1707 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2244    2.0048    1.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3988   -1.8507   -1.4038 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7725    0.3679    0.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3798   -2.7027   -0.9767 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0567   -1.4045   -2.2045 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6520   -2.1162   -2.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4214    0.7147    0.7752 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5766   -1.2002   -0.9174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9784    1.0320    1.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3680   -2.1817   -0.5888 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1422   -1.1339   -1.5060 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8559   -0.9970   -1.8387 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6100    1.3071    1.2774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2894   -0.5618   -0.4004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6637    1.6821    1.5996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5385   -0.2245   -0.1202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2898    2.9385    1.7412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9722    2.9465    2.3096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7594    1.9090    3.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8295   -0.0521    0.0258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7669    2.0673    1.9371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1798   -0.0578    0.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1971    2.6252    2.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7822    3.3020    1.7745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5363    2.1174    3.0664 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9246    1.9298    1.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6110    0.1479    1.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6714    1.9195    0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9234    2.4802   -1.1395 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5595    3.1065   -0.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4829    2.4919   -2.3414 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4852    2.3586   -0.8723 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5143    0.9864   -2.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8866    0.4841   -2.8466 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.1444    0.4368   -1.6101 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1189   -1.8112   -2.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.6323   -1.3704   -0.6937 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7707   -1.5867   -2.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5018   -2.7131   -0.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8925   -1.9772    1.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3714   -1.1105    2.0201 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3159   -2.6643    1.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.0976   -2.4620   -2.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0700   -3.4408   -3.4388 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.4348   -4.0413   -1.7364 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  1
  5  7  1  0
  5  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31 39  1  0
 39 40  1  1
 39 38  1  0
 38 36  1  0
 36 37  1  0
 36 35  1  0
 35 32  1  0
 32 33  1  1
 32 34  1  0
 39 41  1  0
  8 42  2  0
 42 43  1  0
 43 44  1  0
 43 45  2  0
 42  3  1  0
 41 29  1  0
 32 31  1  0
  1 46  1  0
  1 47  1  0
  1 48  1  0
  3 49  1  6
  4 50  1  0
  4 51  1  0
  6 52  1  0
  6 53  1  0
  6 54  1  0
  7 55  1  0
  7 56  1  0
  7 57  1  0
  9 58  1  0
 10 59  1  0
 12 60  1  0
 12 61  1  0
 12 62  1  0
 13 63  1  0
 14 64  1  0
 15 65  1  0
 17 66  1  0
 17 67  1  0
 17 68  1  0
 18 69  1  0
 19 70  1  0
 20 71  1  0
 21 72  1  0
 23 73  1  0
 23 74  1  0
 23 75  1  0
 24 76  1  0
 25 77  1  0
 26 78  1  0
 28 79  1  0
 28 80  1  0
 28 81  1  0
 30 82  1  0
 31 83  1  1
 40 96  1  0
 40 97  1  0
 40 98  1  0
 38 94  1  0
 38 95  1  0
 36 92  1  6
 37 93  1  0
 35 90  1  0
 35 91  1  0
 33 84  1  0
 33 85  1  0
 33 86  1  0
 34 87  1  0
 34 88  1  0
 34 89  1  0
 44 99  1  0
 44100  1  0
 44101  1  0
M  END


  Mrv1652304282212052D          

 45 47  0  0  1  0            999 V2000
   -9.2462    5.0178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8337    4.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0087    4.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5962    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7712    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3587    2.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5337    2.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2962    2.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8837    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587    1.4455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8371   -1.9309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2505    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0251    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    3.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5962    5.0178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0712    5.0178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5561    4.3504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3407    4.6053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.3407    5.4303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5561    5.6853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7192    6.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9488    6.2437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0082    4.1204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9219    3.2999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3012    3.5658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8532    2.9527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4942    3.3942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 17 26  1  0  0  0  0
 22 27  1  6  0  0  0
 20 28  1  0  0  0  0
 20 29  1  0  0  0  0
 16 30  1  0  0  0  0
 12 31  1  0  0  0  0
  7 32  1  0  0  0  0
  3 33  1  0  0  0  0
  1 34  1  0  0  0  0
 34 35  2  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
 34 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 36 41  1  6  0  0  0
 41 42  1  0  0  0  0
 35 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0065902

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1CC(C)(C)C(\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)C2=C[C@@H]3[C@@](C)(C[C@@H](O)CC3(C)C)O2)=C1C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C41H56O4/c1-28(18-14-19-30(3)22-23-34-38(32(5)42)36(44-11)27-39(34,6)7)16-12-13-17-29(2)20-15-21-31(4)35-24-37-40(8,9)25-33(43)26-41(37,10)45-35/h12-24,33,36-37,43H,25-27H2,1-11H3/b13-12+,18-14+,20-15+,23-22+,28-16+,29-17+,30-19+,31-21+/t33-,36+,37-,41+/m0/s1

> <INCHI_KEY>
GAJFEAZNYLBZJM-OVMDFUJESA-N

> <FORMULA>
C41H56O4

> <MOLECULAR_WEIGHT>
612.895

> <EXACT_MASS>
612.417860283

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
76.57173917508104

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[(5R)-2-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(3aS,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-3a,4,5,6,7,7a-hexahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaen-1-yl]-5-methoxy-3,3-dimethylcyclopent-1-en-1-yl]ethan-1-one

> <ALOGPS_LOGP>
8.30

> <JCHEM_LOGP>
7.248221100333334

> <ALOGPS_LOGS>
-6.13

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.391514433912448

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.14846653588069

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7338498816411017

> <JCHEM_POLAR_SURFACE_AREA>
55.76

> <JCHEM_REFRACTIVITY>
199.65260000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.51e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[(5R)-2-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(3aS,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-3a,5,6,7-tetrahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaen-1-yl]-5-methoxy-3,3-dimethylcyclopent-1-en-1-yl]ethanone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0     -17.260   9.367   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -16.490   8.033   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -14.950   8.033   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -14.180   6.699   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -12.640   6.699   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -11.870   5.366   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.330   5.366   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.560   4.032   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.020   4.032   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -7.250   2.698   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.710   2.698   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.940   1.365   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.400   1.365   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.630   0.031   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.090   0.031   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.320  -1.303   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.429  -3.604   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.126  -2.549   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       7.591  -2.843   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.201   1.597   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.647   1.597   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.090  -2.637   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -5.710   0.031   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -9.560   6.699   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -14.180   9.367   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -18.800   9.367   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -19.705   8.121   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -21.169   8.597   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -21.169  10.137   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -19.705  10.612   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -20.009  12.122   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -18.571  11.655   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0     -22.415   7.691   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0     -22.254   6.160   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0     -19.229   6.656   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0     -20.259   5.512   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0     -17.723   6.336   0.000  0.00  0.00           C+0
CONECT    1    2   34                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   33                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   32                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   31                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   30                                                  
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21   28   29                                             
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   19   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   17                                                       
CONECT   27   22                                                            
CONECT   28   20                                                            
CONECT   29   20                                                            
CONECT   30   16                                                            
CONECT   31   12                                                            
CONECT   32    7                                                            
CONECT   33    3                                                            
CONECT   34    1   35   38                                                  
CONECT   35   34   36   43                                                  
CONECT   36   35   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   34   39   40                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   36   42                                                       
CONECT   42   41                                                            
CONECT   43   35   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₅₆O₄

Average Mass

612.8950 Da

Monoisotopic Mass

612.41786 Da

IUPAC Name

Traditional Name

1-[(5R)-2-[(1E,3E,5E,7E,9E,11E,13E,15E)-16-[(3aS,6S,7aR)-6-hydroxy-4,4,7a-trimethyl-3a,5,6,7-tetrahydro-1-benzofuran-2-yl]-3,7,12-trimethylheptadeca-1,3,5,7,9,11,13,15-octaen-1-yl]-5-methoxy-3,3-dimethylcyclopent-1-en-1-yl]ethanone

CAS Registry Number

Not Available

SMILES

CO[C@@H]1CC(C)(C)C(\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)C2=C[C@@H]3[C@@](C)(C[C@@H](O)CC3(C)C)O2)=C1C(C)=O

InChI Identifier

InChI=1S/C41H56O4/c1-28(18-14-19-30(3)22-23-34-38(32(5)42)36(44-11)27-39(34,6)7)16-12-13-17-29(2)20-15-21-31(4)35-24-37-40(8,9)25-33(43)26-41(37,10)45-35/h12-24,33,36-37,43H,25-27H2,1-11H3/b13-12+,18-14+,20-15+,23-22+,28-16+,29-17+,30-19+,31-21+/t33-,36+,37-,41+/m0/s1

InChI Key

GAJFEAZNYLBZJM-OVMDFUJESA-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
Pittosporum tobira	Plant	KNApSAcK

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
Benzofuran
Dihydrofuran
Cyclic alcohol
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	8.3	ALOGPS
logP	7.25	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	15.15	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	199.65 m³·mol⁻¹	ChemAxon
Polarizability	76.57 Å³	ChemAxon
Number of Rings	3	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

163057365

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one (NP0065902)

MOL for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

3D MOL for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

3D SDF for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

3D-SDF for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

PDB for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

3D PDB for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

SMILES for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

INCHI for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

Structure for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)

3D Structure for NP0065902 (5',8'-Epoxy-3'-hydroxy-3-methoxy-4,6-didehydro-5',8'-dihydro-4,6-cyclo-5,6-seco-beta,beta-caroten-5-one)