NP-MRD: Showing NP-Card for (5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one (NP0221434)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-05 23:00:40 UTC

Updated at

2022-09-05 23:00:41 UTC

NP-MRD ID

NP0221434

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one

Description

Montalicin b belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain. Thus, montalicin b is considered to be an annonaceae acetogenin. (5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one is found in Annona montana. It was first documented in 2022 (PMID: 36075636). Based on a literature review a significant number of articles have been published on Montalicin b (PMID: 36075614) (PMID: 36075610) (PMID: 36075538) (PMID: 36075481).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062201002D          

 41 42  0  0  1  0            999 V2000
   16.3351   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0495   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7640   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4785   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1930   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9074   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6219   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3364   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0508   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7653   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4798   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1942   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.9087   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.6232   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.3377   -6.4129    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.3377   -7.2379    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.0521   -6.0004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   27.1384   -5.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.9453   -5.0084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3578   -5.7229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.1783   -5.8091    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.6632   -5.1417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.5139   -6.5628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3344   -6.6490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.6699   -7.4027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4904   -7.4890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.8260   -8.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.6464   -8.3289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.9820   -9.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.8025   -9.1688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.1380   -9.9224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   33.6531  -10.5899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.9585  -10.0087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.2941  -10.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.1010  -10.9339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.1873  -11.7544    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   36.9017  -12.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.4336  -12.0899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.8816  -11.4768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.0611  -11.5631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8058   -6.3360    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 17 15  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 34 39  1  0  0  0  0
 39 40  2  0  0  0  0
 20 41  1  0  0  0  0
 17 41  1  0  0  0  0
M  END

     RDKit          3D

105106  0  0  0  0  0  0  0  0999 V2000
  -11.7262   -3.4236    0.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4627   -2.5237    0.8340 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8388   -1.2625    0.1796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8191   -0.2218    0.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2208    0.4223    1.1921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4522   -0.3362    2.1950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2811   -1.1010    1.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2324   -0.2269    0.9820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6697    0.7900    1.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6388    1.6954    1.3400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9098    2.6190    0.2515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3172    2.2929   -1.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6359    1.5309   -2.1135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2192    0.1493   -2.1006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1973   -0.3797   -1.2051 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1250   -1.8129   -1.5554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7479    0.0357   -1.5262 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4857    1.4172   -1.0753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5367    1.2243    0.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0787   -0.0967   -0.2324 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0899    0.0759   -1.3194 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6022   -1.1703   -1.7497 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2436    0.9119   -0.8670 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9187    0.2617    0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0901    1.0821    0.8055 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0915    1.2438   -0.2701 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6238   -0.1080   -0.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6672    0.0428   -1.7843 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2710   -1.2310   -2.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0031   -2.0229   -1.2058 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1562   -1.3037   -0.5774 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6880   -0.1550    0.0519 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7731   -2.1699    0.5001 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9142   -1.4129    1.1129 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3586   -0.2054    0.8168 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5106    0.1912    1.6561 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.6996    0.6757    0.8603 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7437   -0.9077    2.4635 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8016   -1.8778    2.1782 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6729   -3.0261    2.7257 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9679   -0.8504   -0.7773 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5185   -2.8492    1.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0556   -3.5517   -0.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5213   -4.3667    1.3342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7026   -3.0347    0.1715 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1304   -2.5243    1.8572 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1910   -1.5492   -0.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8154   -0.8440    0.6059 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2481    0.6356   -0.6171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9668   -0.5580   -0.6510 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0734    0.9198    1.7683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6342    1.3344    0.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0091    0.4512    2.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0592   -0.9626    2.8445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5684   -1.9135    0.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7929   -1.6110    2.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4006   -0.9115    0.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6496    0.1831    0.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4754    1.4783    2.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2054    0.3002    2.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6136    1.2359    1.2447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3788    2.4232    2.2511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6697    3.4516    0.6550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0092    3.3647    0.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4788    3.4019   -1.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4404    1.9799   -1.1353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7769    2.2208   -2.5294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3545    1.6759   -3.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0492   -0.2426   -3.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1851   -0.4739   -1.8761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3130   -0.3747   -0.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3374   -2.1509   -1.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5428   -0.1602   -2.5993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8404    1.9136   -1.8483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3347    2.0294   -0.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113    1.1163    1.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624    2.0445    0.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4760   -0.5802    0.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6400    0.5671   -2.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7207   -1.7815   -0.9691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9474    0.9460   -1.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9080    1.9440   -0.6311 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1734    0.2724    1.1543 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1499   -0.7739    0.0871 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7786    2.0065    1.3046 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5685    0.4571    1.6170 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9810    1.7727    0.1861 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7387    1.8370   -1.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0112   -0.5939    0.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8006   -0.7996   -1.0388 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3451    0.8579   -1.5415 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0659    0.4306   -2.6673 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4192   -1.8808   -2.5994 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9114   -1.0973   -3.1314 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3306   -2.3545   -0.3886 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4023   -2.9507   -1.6714 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9728   -1.0821   -1.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2977   -0.4670    0.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1246   -3.1428    0.0876 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0501   -2.4195    1.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9309    0.4261    0.0446 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1120    1.0462    2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.1824    1.4655    1.5112 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.4658   -0.0783    0.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3728    1.2367   -0.0373 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  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 41  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 34 35  2  0
 35 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 39 40  2  0
 41 17  1  0
 39 34  1  0
  1 42  1  0
  1 43  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  3 47  1  0
  3 48  1  0
  4 49  1  0
  4 50  1  0
  5 51  1  0
  5 52  1  0
  6 53  1  0
  6 54  1  0
  7 55  1  0
  7 56  1  0
  8 57  1  0
  8 58  1  0
  9 59  1  0
  9 60  1  0
 10 61  1  0
 10 62  1  0
 11 63  1  0
 11 64  1  0
 12 65  1  0
 12 66  1  0
 13 67  1  0
 13 68  1  0
 14 69  1  0
 14 70  1  0
 15 71  1  1
 16 72  1  0
 17 73  1  6
 18 74  1  0
 18 75  1  0
 19 76  1  0
 19 77  1  0
 20 78  1  1
 21 79  1  6
 22 80  1  0
 23 81  1  0
 23 82  1  0
 24 83  1  0
 24 84  1  0
 25 85  1  0
 25 86  1  0
 26 87  1  0
 26 88  1  0
 27 89  1  0
 27 90  1  0
 28 91  1  0
 28 92  1  0
 29 93  1  0
 29 94  1  0
 30 95  1  0
 30 96  1  0
 31 97  1  6
 32 98  1  0
 33 99  1  0
 33100  1  0
 35101  1  0
 36102  1  1
 37103  1  0
 37104  1  0
 37105  1  0
M  END


  Mrv1652309062201002D          

 41 42  0  0  1  0            999 V2000
   16.3351   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0495   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7640   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4785   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1930   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9074   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6219   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3364   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0508   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7653   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4798   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1942   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.9087   -6.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.6232   -6.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.3377   -6.4129    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   26.3377   -7.2379    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.0521   -6.0004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   27.1384   -5.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.9453   -5.0084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3578   -5.7229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.1783   -5.8091    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.6632   -5.1417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.5139   -6.5628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3344   -6.6490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.6699   -7.4027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4904   -7.4890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.8260   -8.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.6464   -8.3289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.9820   -9.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.8025   -9.1688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.1380   -9.9224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   33.6531  -10.5899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.9585  -10.0087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.2941  -10.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.1010  -10.9339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.1873  -11.7544    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   36.9017  -12.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.4336  -12.0899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.8816  -11.4768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.0611  -11.5631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8058   -6.3360    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 17 15  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 34 39  1  0  0  0  0
 39 40  2  0  0  0  0
 20 41  1  0  0  0  0
 17 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0221434

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCC[C@@H](O)[C@H]1CC[C@@H](O1)[C@H](O)CCCCCCCC[C@@H](O)CC1=C[C@H](C)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H64O6/c1-3-4-5-6-7-8-9-10-11-12-16-19-22-31(37)33-24-25-34(41-33)32(38)23-20-17-14-13-15-18-21-30(36)27-29-26-28(2)40-35(29)39/h26,28,30-34,36-38H,3-25,27H2,1-2H3/t28-,30+,31+,32+,33+,34+/m0/s1

> <INCHI_KEY>
CUSWJPKBSDURBG-YZDQYAEISA-N

> <FORMULA>
C35H64O6

> <MOLECULAR_WEIGHT>
580.891

> <EXACT_MASS>
580.470289781

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
74.82305318861657

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5S)-3-[(2R,11R)-2,11-dihydroxy-11-[(2R,5R)-5-[(1R)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
9.092973164999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.972784244576374

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.312197120980954

> <JCHEM_PKA_STRONGEST_BASIC>
-2.722022871174217

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
167.6737

> <JCHEM_ROTATABLE_BOND_COUNT>
26

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(5S)-3-[(2R,11R)-2,11-dihydroxy-11-[(2R,5R)-5-[(1R)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      30.492 -11.971   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      31.826 -11.201   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      33.159 -11.971   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      34.493 -11.201   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      35.827 -11.971   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      37.161 -11.201   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      38.494 -11.971   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      39.828 -11.201   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      41.162 -11.971   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      42.495 -11.201   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      43.829 -11.971   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      45.163 -11.201   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      46.496 -11.971   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      47.830 -11.201   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      49.164 -11.971   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      49.164 -13.511   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      50.497 -11.201   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      50.658  -9.669   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      52.165  -9.349   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      52.935 -10.683   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      54.466 -10.844   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      55.371  -9.598   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      55.093 -12.251   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      56.624 -12.412   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      57.251 -13.818   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      58.782 -13.979   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      59.408 -15.386   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      60.940 -15.547   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      61.566 -16.954   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      63.098 -17.115   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      63.724 -18.522   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      62.819 -19.768   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      65.256 -18.683   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      65.882 -20.090   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      67.389 -20.410   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      67.550 -21.941   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      68.883 -22.711   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      66.143 -22.568   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      65.112 -21.423   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      63.581 -21.584   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      51.904 -11.827   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   41                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   41                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   34   40                                                  
CONECT   40   39                                                            
CONECT   41   20   17                                                       
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₆₄O₆

Average Mass

580.8910 Da

Monoisotopic Mass

580.47029 Da

IUPAC Name

(5S)-3-[(2R,11R)-2,11-dihydroxy-11-[(2R,5R)-5-[(1R)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-2,5-dihydrofuran-2-one

Traditional Name

(5S)-3-[(2R,11R)-2,11-dihydroxy-11-[(2R,5R)-5-[(1R)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCC[C@@H](O)[C@H]1CC[C@@H](O1)[C@H](O)CCCCCCCC[C@@H](O)CC1=C[C@H](C)OC1=O

InChI Identifier

InChI=1S/C35H64O6/c1-3-4-5-6-7-8-9-10-11-12-16-19-22-31(37)33-24-25-34(41-33)32(38)23-20-17-14-13-15-18-21-30(36)27-29-26-28(2)40-35(29)39/h26,28,30-34,36-38H,3-25,27H2,1-2H3/t28-,30+,31+,32+,33+,34+/m0/s1

InChI Key

CUSWJPKBSDURBG-YZDQYAEISA-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
Annona montana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Annonaceous acetogenins

Alternative Parents

Substituents

Annonaceae acetogenin skeleton
Long chain fatty alcohol
2-furanone
Dihydrofuran
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxygen compound
Organic oxide
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	9.09	ChemAxon
pKa (Strongest Acidic)	13.31	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	26	ChemAxon
Refractivity	167.67 m³·mol⁻¹	ChemAxon
Polarizability	74.82 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00051631

Chemspider ID

113386000

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162922687

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pugliese NR, Balletti A, Armenia S, De Biase N, Faita F, Mengozzi A, Paneni F, Ruschitzka F, Virdis A, Ghiadoni L, Taddei S, Williams B, Antonini-Canterin F, Masi S: Ventricular-Arterial Coupling Derived From Proximal Aortic Stiffness and Aerobic Capacity Across the Heart Failure Spectrum. JACC Cardiovasc Imaging. 2022 Sep;15(9):1545-1559. doi: 10.1016/j.jcmg.2022.03.024. Epub 2022 May 11. [PubMed:36075614 ]
Cerutti A, Filipska M, Fa XM, Tacho-Pinot R: Impact of the mucosal milieu on antibody responses to allergens. J Allergy Clin Immunol. 2022 Sep;150(3):503-512. doi: 10.1016/j.jaci.2022.07.007. [PubMed:36075636 ]
Qi B, Hariri A, Nezhad R, Fu L, Li Y, Jin Z, Yim W, He T, Cheng Y, Zhou J, Jokerst JV: A miniaturized ultrasound transducer for monitoring full-mouth oral health: a preliminary study. Dentomaxillofac Radiol. 2022 Sep 8:20220220. doi: 10.1259/dmfr.20220220. [PubMed:36075610 ]
Gronbeck C, Grant-Kels JM, Lu J, Feng H: Increased Utilization of Teledermatology Among Medicare Part B Beneficiaries During the Covid-19 Pandemic. Clin Dermatol. 2022 Sep 5. pii: S0738-081X(22)00120-1. doi: 10.1016/j.clindermatol.2022.09.004. [PubMed:36075538 ]
Murray J, Bauer A, Loret de Mola C, Martins RC, Blumenberg C, Esposti MD, Stein A, Barros FC, Hallal PC, Silveira MF, Bertoldi AD, Domingues MR: Child and Maternal Mental Health Before and During the COVID-19 Pandemic: Longitudinal Social Inequalities in a Brazilian Birth Cohort. J Am Acad Child Adolesc Psychiatry. 2022 Sep 1. pii: S0890-8567(22)01323-5. doi: 10.1016/j.jaac.2022.07.832. [PubMed:36075481 ]
LOTUS database [Link]

Showing NP-Card for (5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one (NP0221434)

MOL for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

3D MOL for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

3D SDF for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

3D-SDF for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

PDB for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

3D PDB for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

SMILES for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

INCHI for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

Structure for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)

3D Structure for NP0221434 ((5s)-3-[(2r,11r)-2,11-dihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5-methyl-5h-furan-2-one)