NP-MRD: Showing NP-Card for (-)-Lanceocrepidiaside F (NP0073608)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 18:49:53 UTC

Updated at

2022-04-28 18:49:53 UTC

NP-MRD ID

NP0073608

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Lanceocrepidiaside F

Description

[(2R,3S,4S,5R,6S)-6-{[(3aS,6S,6aS,9aR,9bS)-6a-hydroxy-6-methyl-3-methylidene-2,7-dioxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-3,4,5-trihydroxyoxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative. (-)-Lanceocrepidiaside F is found in Crepidiastrum lanceolatum NAKAI. Based on a literature review very few articles have been published on [(2R,3S,4S,5R,6S)-6-{[(3aS,6S,6aS,9aR,9bS)-6a-hydroxy-6-methyl-3-methylidene-2,7-dioxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-3,4,5-trihydroxyoxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220492D          

 41 45  0  0  1  0            999 V2000
    3.6659   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1803   -0.8820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9967   -1.6863    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2534   -2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101   -1.6863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3265   -0.8820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8409   -0.2370    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3864    0.4515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9461    0.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5541   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8656   -1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6417   -2.2007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6412   -1.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9157    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204    0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8305    1.2239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3545    1.8612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0646    2.6336    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2508    2.7687    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9609    3.5411    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4848    4.1784    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2987    4.0432    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5886    3.2708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8227    4.6805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5328    5.4529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0568    6.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8706    5.9549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7669    6.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2908    7.4997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0010    8.2721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5249    8.9094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3388    8.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6287    8.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1047    7.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8627    9.4115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1950    4.9508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1470    3.6763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7268    2.1315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8016   -1.4248    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
  1  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  6 11  1  1  0  0  0
 11 12  2  0  0  0  0
  3 13  1  1  0  0  0
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
  1 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  6  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
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 24 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 34 37  1  0  0  0  0
 23 38  1  6  0  0  0
 22 39  1  1  0  0  0
 21 40  1  6  0  0  0
  2 41  1  1  0  0  0
M  END

     RDKit          3D

 75 79  0  0  0  0  0  0  0  0999 V2000
   -6.4346   -1.7781    1.7665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4430   -1.3998    1.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6465   -2.3069    0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8194   -3.5641    0.0955 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7151   -1.5254   -0.5242 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2916   -0.2602   -0.6377 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8439   -0.0687    0.7824 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7609    1.0720    0.9300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0960    1.8389   -0.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9464    2.7149   -0.7825 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5427    3.9383   -1.4520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1495    1.8936   -1.7355 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9431    1.1388   -2.6002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0593    2.5815   -2.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0086    3.7640   -2.7912 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9992    1.5986   -2.5719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1827    0.6038   -1.6893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2909   -0.5691   -1.5676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7184   -0.6756   -0.3027 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1049   -1.7907   -0.2579 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4399   -1.4489   -0.0521 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7481   -1.0688    1.2273 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2551   -0.9927    1.3411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8223   -0.0535    0.4438 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2110    0.0644    0.4966 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8961   -0.6430    1.3102 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8870    1.0389   -0.4211 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3469    0.9690   -0.1707 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0824    0.0821   -0.9341 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4380    0.0029   -0.7141 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0594    0.7856    0.2436 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4397    0.6665    0.4274 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3073    1.6562    0.9863 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9464    1.7488    0.7789 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2626   -2.0100    2.2956 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2947   -1.4031    3.1147 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6632   -3.2724    1.6954 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6722   -4.0175    1.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3927   -2.8289    0.7239 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4334   -2.2558    1.4737 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3701    0.8665   -0.8951 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9588   -1.0162    2.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7465   -2.8015    1.8185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1310   -0.3426   -1.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9304    0.0063    1.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7312    0.7744    1.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3037    1.7968    1.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9319    2.5330   -0.0538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4472    1.2011   -1.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2804    3.0088    0.0549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4047    4.2507   -0.7957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9167    3.6574   -2.4419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8476    4.7972   -1.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6899    1.2591   -3.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1686    1.6297   -3.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8199   -1.5127   -1.8735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4061   -0.4799   -2.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0691   -2.2773   -1.2529 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3660   -0.0589    1.4928 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7277   -1.9782    1.1198 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5960   -0.6993    2.3543 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6667    0.7340   -1.4711 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5087    2.0610   -0.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6236   -0.5512   -1.6992 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0678   -0.6711   -1.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0291    1.2794   -0.1317 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7838    2.2652    1.7301 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3123    2.4292    1.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0819   -2.3366    2.9673 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3864   -0.4027    3.0148 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1685   -3.8224    2.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9765   -4.6877    1.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8068   -3.7319    0.2277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5505   -2.8244    2.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0814    1.4192    0.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  6 41  1  0
 41 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 31 33  1  0
 33 34  2  0
 22 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 17 16  2  0
 16 14  1  0
 14 15  2  0
 14 12  1  0
 12 13  1  6
 12 10  1  0
  2  7  1  0
 12 41  1  0
 39 20  1  0
 34 28  1  0
 11 51  1  0
 11 52  1  0
 11 53  1  0
 10 50  1  1
  9 48  1  0
  9 49  1  0
  8 46  1  0
  8 47  1  0
  7 45  1  1
  6 44  1  6
  1 42  1  0
  1 43  1  0
 41 75  1  1
 18 56  1  0
 18 57  1  0
 20 58  1  6
 22 59  1  1
 23 60  1  0
 23 61  1  0
 27 62  1  0
 27 63  1  0
 29 64  1  0
 30 65  1  0
 32 66  1  0
 33 67  1  0
 34 68  1  0
 35 69  1  1
 36 70  1  0
 37 71  1  1
 38 72  1  0
 39 73  1  6
 40 74  1  0
 16 55  1  0
 13 54  1  0
M  END


  Mrv1652304282220492D          

 41 45  0  0  1  0            999 V2000
    3.6659   -0.2370    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1803   -0.8820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9967   -1.6863    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2534   -2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5101   -1.6863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3265   -0.8820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8409   -0.2370    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3864    0.4515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5912    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9461    0.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5541   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8656   -1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6417   -2.2007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9527   -0.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6412   -1.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9157    0.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204    0.4515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8305    1.2239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3545    1.8612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0646    2.6336    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2508    2.7687    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9609    3.5411    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4848    4.1784    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2987    4.0432    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5886    3.2708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8227    4.6805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5328    5.4529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0568    6.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8706    5.9549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7669    6.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2908    7.4997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0010    8.2721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5249    8.9094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3388    8.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6287    8.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1047    7.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8627    9.4115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1950    4.9508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1470    3.6763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7268    2.1315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8016   -1.4248    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
  1  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  6 11  1  1  0  0  0
 11 12  2  0  0  0  0
  3 13  1  1  0  0  0
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
  1 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  6  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
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 24 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 34 37  1  0  0  0  0
 23 38  1  6  0  0  0
 22 39  1  1  0  0  0
 21 40  1  6  0  0  0
  2 41  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0073608

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@@H]2[C@H](OC(=O)C2=C)[C@H]2C(CO[C@H]3O[C@H](COC(=O)CC4=CC=C(O)C=C4)[C@@H](O)[C@H](O)[C@H]3O)=CC(=O)[C@]12O

> <INCHI_IDENTIFIER>
InChI=1S/C29H34O12/c1-13-3-8-18-14(2)27(36)41-26(18)22-16(10-20(31)29(13,22)37)11-39-28-25(35)24(34)23(33)19(40-28)12-38-21(32)9-15-4-6-17(30)7-5-15/h4-7,10,13,18-19,22-26,28,30,33-35,37H,2-3,8-9,11-12H2,1H3/t13-,18-,19+,22+,23+,24-,25+,26-,28-,29+/m0/s1

> <INCHI_KEY>
CVJWQIVIVIAFKM-RKNISOCASA-N

> <FORMULA>
C29H34O12

> <MOLECULAR_WEIGHT>
574.579

> <EXACT_MASS>
574.205026535

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
57.5699875260248

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3S,4S,5R,6S)-6-{[(3aS,6S,6aS,9aR,9bS)-6a-hydroxy-6-methyl-3-methylidene-2,7-dioxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-3,4,5-trihydroxyoxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate

> <ALOGPS_LOGP>
0.98

> <JCHEM_LOGP>
0.9379329410000006

> <ALOGPS_LOGS>
-3.05

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.39908898226644

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.4909724710793

> <JCHEM_PKA_STRONGEST_BASIC>
-3.649085218110849

> <JCHEM_POLAR_SURFACE_AREA>
189.28

> <JCHEM_REFRACTIVITY>
139.3309

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.15e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4S,5R,6S)-6-{[(3aS,6S,6aS,9aR,9bS)-6a-hydroxy-6-methyl-3-methylidene-2,7-dioxo-3aH,4H,5H,6H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-3,4,5-trihydroxyoxan-2-yl]methyl (4-hydroxyphenyl)acetate

> <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       6.843  -0.442   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.803  -1.646   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.461  -3.148   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.073  -3.816   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.686  -3.148   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.343  -1.646   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.303  -0.442   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.455   0.843   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.970   0.433   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.766   1.393   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.901  -1.105   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.616  -1.954   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.665  -4.108   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.245  -1.105   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.530  -1.954   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.176   0.433   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.691   0.843   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.150   2.285   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.128   3.474   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.587   4.916   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.068   5.168   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.527   6.610   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.505   7.800   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.024   7.547   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.565   6.106   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.002   8.737   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.461  10.179   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.439  11.368   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.958  11.116   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       8.898  12.810   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.876  14.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.335  15.441   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.313  16.631   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.832  16.379   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.374  14.937   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      11.395  13.747   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.810  17.568   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       5.964   9.241   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       4.008   6.862   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       5.090   3.979   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       8.963  -2.660   0.000  0.00  0.00           O+0
CONECT    1    2    7   17                                                  
CONECT    2    1    3   14   41                                             
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    1    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    6   12                                                  
CONECT   12   11                                                            
CONECT   13    3                                                            
CONECT   14    2   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    1   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22   40                                                  
CONECT   22   21   23   39                                                  
CONECT   23   22   24   38                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24   20                                                       
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   34                                                            
CONECT   38   23                                                            
CONECT   39   22                                                            
CONECT   40   21                                                            
CONECT   41    2                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Value	Source
[(2R,3S,4S,5R,6S)-6-{[(3as,6S,6as,9ar,9BS)-6a-hydroxy-6-methyl-3-methylidene-2,7-dioxo-2H,3H,3ah,4H,5H,6H,6ah,7H,9ah,9BH-azuleno[4,5-b]furan-9-yl]methoxy}-3,4,5-trihydroxyoxan-2-yl]methyl 2-(4-hydroxyphenyl)acetic acid	Generator

Chemical Formula

C₂₉H₃₄O₁₂

Average Mass

574.5790 Da

Monoisotopic Mass

574.20503 Da

IUPAC Name

Traditional Name

[(2R,3S,4S,5R,6S)-6-{[(3aS,6S,6aS,9aR,9bS)-6a-hydroxy-6-methyl-3-methylidene-2,7-dioxo-3aH,4H,5H,6H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-3,4,5-trihydroxyoxan-2-yl]methyl (4-hydroxyphenyl)acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@@H]2[C@H](OC(=O)C2=C)[C@H]2C(CO[C@H]3O[C@H](COC(=O)CC4=CC=C(O)C=C4)[C@@H](O)[C@H](O)[C@H]3O)=CC(=O)[C@]12O

InChI Identifier

InChI=1S/C29H34O12/c1-13-3-8-18-14(2)27(36)41-26(18)22-16(10-20(31)29(13,22)37)11-39-28-25(35)24(34)23(33)19(40-28)12-38-21(32)9-15-4-6-17(30)7-5-15/h4-7,10,13,18-19,22-26,28,30,33-35,37H,2-3,8-9,11-12H2,1H3/t13-,18-,19+,22+,23+,24-,25+,26-,28-,29+/m0/s1

InChI Key

CVJWQIVIVIAFKM-RKNISOCASA-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
Crepidiastrum lanceolatum NAKAI	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Guaianolides and derivatives

Alternative Parents

Substituents

Terpene glycoside
Guaianolide-skeleton
Sesquiterpenoid
Guaiane sesquiterpenoid
O-glycosyl compound
Glycosyl compound
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Oxane
Monosaccharide
Gamma butyrolactone
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	0.98	ALOGPS
logP	0.94	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	9.49	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	189.28 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	139.33 m³·mol⁻¹	ChemAxon
Polarizability	57.57 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

163050165

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Lanceocrepidiaside F (NP0073608)

MOL for NP0073608 ((-)-Lanceocrepidiaside F)

3D MOL for NP0073608 ((-)-Lanceocrepidiaside F)

3D SDF for NP0073608 ((-)-Lanceocrepidiaside F)

3D-SDF for NP0073608 ((-)-Lanceocrepidiaside F)

PDB for NP0073608 ((-)-Lanceocrepidiaside F)

3D PDB for NP0073608 ((-)-Lanceocrepidiaside F)

SMILES for NP0073608 ((-)-Lanceocrepidiaside F)

INCHI for NP0073608 ((-)-Lanceocrepidiaside F)

Structure for NP0073608 ((-)-Lanceocrepidiaside F)

3D Structure for NP0073608 ((-)-Lanceocrepidiaside F)