NP-MRD: Showing NP-Card for methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate (NP0300066)

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Record Information

Version

2.0

Created at

2022-09-10 12:15:40 UTC

Updated at

2022-09-10 12:15:40 UTC

NP-MRD ID

NP0300066

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate

Description

Methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-{[(2S,3R,4S,5R)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]propanoate belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate is found in Alnus pendula. Based on a literature review very few articles have been published on methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-{[(2S,3R,4S,5R)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]propanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102214152D          

 48 51  0  0  1  0            999 V2000
    5.1521    0.5181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7821   -0.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6358   -0.8265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8596   -1.1058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2295   -0.5732    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6969   -1.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7622    0.0568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0047    1.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8429   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529   -2.3925    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6283   -2.4182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -3.1452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6729   -3.8465    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2829   -4.5735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975   -3.8207    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9321   -4.5220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -3.0937    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7121   -3.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1467   -3.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7567   -4.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9713   -3.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4416   -0.6207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4930   -1.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1221   -1.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0465   -2.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8302   -2.7373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5686   -3.0293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4001   -3.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9347    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3247   -0.3660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6853    1.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5584    0.2648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7046    1.0767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1884   -0.2679    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  6  0  0  0
  8  5  1  6  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  1  0  0  0
 13 11  1  1  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 14 28  1  0  0  0  0
 29 28  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 30 38  1  0  0  0  0
 38 39  1  6  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 38 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 29 44  1  0  0  0  0
 11 44  1  0  0  0  0
 44 45  1  6  0  0  0
  2 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
M  END

     RDKit          3D

112115  0  0  0  0  0  0  0  0999 V2000
    7.5991   -0.3033    2.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8351   -1.0506    1.2524 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4122   -1.2784    1.5927 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5117   -0.7745    0.4567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0464   -1.0400    0.8315 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8366   -0.3074    2.1242 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8549   -2.3949    1.0897 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1945   -0.5323   -0.3145 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4624   -1.5148   -1.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1779   -2.3707   -1.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1816   -1.2469   -1.3888 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3447   -0.3418   -2.5603 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7382   -0.6019   -0.1033 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0249    0.6362    0.0286 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4459    1.6469    0.8073 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6065    2.8563    0.1243 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9459    3.2471    0.0933 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3389    3.2999    1.4456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7499    4.5801    1.9966 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7651    5.5400    1.9509 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6275    5.0957    1.1258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0807    6.0451    1.8565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2878    3.9538    0.6885 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1136    4.4410   -0.3625 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4790    4.4518   -0.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1816    5.0065   -1.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0840    4.0012    0.6360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4566    0.2236    0.4466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0226   -0.6016   -0.6562 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5551   -0.8819   -0.4706 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7564   -1.9316    0.5570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0766    0.4112    0.0791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4740    0.6177    0.4413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1293   -0.1749    1.4772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9116   -1.1063    1.1588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9507    0.0265    2.8429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5887   -0.7434    3.8377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0028   -1.1716   -1.8566 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3801   -1.2783   -2.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9191   -0.3502   -3.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2964   -2.3792   -1.8546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2725   -2.4156   -2.3595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7920   -2.1105   -2.5407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2408   -1.7156   -1.1554 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1251   -3.0114   -0.4601 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3655   -1.6981    0.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8121   -1.3849   -0.2135 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2180   -3.1894    0.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2800    0.2000    2.9106 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6349   -0.1563    1.7305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1778   -2.3299    1.8366 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1710   -0.6557    2.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6879    0.3330    0.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7972   -1.1561   -0.5149 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2215   -0.9875    2.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4601    0.6099    2.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7716   -0.1553    2.3862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4434   -2.5694    1.9725 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5849    0.4600   -0.5947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6336   -1.0255   -2.4156 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2662   -2.2173   -1.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1111   -2.9965   -2.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2782   -2.9359   -0.4998 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1750    0.3932   -2.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5811   -0.9834   -3.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5217    0.2652   -2.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5359   -1.3600    0.6995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1676    1.0811   -1.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3152    2.6731   -0.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4458    3.2892    1.4481 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8879    2.4020    1.9339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4088    4.3695    3.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6507    5.1665    2.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0541    5.5386    0.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1161    6.8740    1.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9191    3.5870    1.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5596    5.8048   -2.0452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2998    4.2167   -2.3301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1526    5.4518   -1.3222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9232    1.2595    0.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4698   -0.2300    1.4324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0618    0.1477   -1.5188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7406   -2.1157    1.0914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3521   -1.6683    1.4475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1536   -2.8971    0.2097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5482    0.4511    1.1113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6734    1.2856   -0.5210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1971    0.6183   -0.4163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5094    1.6910    0.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8773   -1.5664    4.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4928   -1.2432    3.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7736   -0.1514    4.7640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4932   -0.3501   -2.4836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3344    0.4900   -3.3911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9510   -0.4014   -3.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2055   -2.7644   -0.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3851   -2.0722   -1.9535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2099   -3.2004   -2.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4996   -3.3211   -1.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6653   -2.5605   -3.4092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3247   -3.0252   -2.9154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7128   -1.3195   -3.2760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4607   -3.6336   -1.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6110   -3.0304    0.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0345   -3.6798   -0.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8097   -1.3756   -0.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0789   -1.9058   -1.1806 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0264   -0.3144   -0.3160 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4736   -1.8251    0.5557 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1539   -3.4561    0.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7884   -3.5492    1.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6235   -3.6518   -0.7622 H   0  0  0  0  0  0  0  0  0  0  0  0
 37 36  1  0
 36 34  1  0
 34 35  2  0
 34 33  1  0
 33 32  1  0
 30 32  1  1
 30 31  1  0
 30 38  1  0
 38 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  1
 44 29  1  0
 29 28  1  0
 28 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  2  0
 14 13  1  0
 13  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
  8  5  1  0
  5  6  1  0
  5  7  1  1
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 46  1  0
 46 47  1  0
 46 48  1  0
 38 39  1  0
 39 41  1  0
 39 40  2  3
 29 30  1  0
 23 16  1  0
 11 13  1  0
 11 44  1  0
 37 90  1  0
 37 91  1  0
 37 92  1  0
 33 88  1  0
 33 89  1  0
 32 86  1  0
 32 87  1  0
 31 83  1  0
 31 84  1  0
 31 85  1  0
 38 93  1  6
 42 99  1  0
 42100  1  0
 43101  1  0
 43102  1  0
 45103  1  0
 45104  1  0
 45105  1  0
 29 82  1  6
 28 80  1  0
 28 81  1  0
 14 68  1  6
 16 69  1  6
 18 70  1  0
 18 71  1  0
 19 72  1  1
 20 73  1  0
 21 74  1  6
 22 75  1  0
 23 76  1  1
 26 77  1  0
 26 78  1  0
 26 79  1  0
 13 67  1  1
  8 59  1  6
  9 60  1  0
  9 61  1  0
 10 62  1  0
 10 63  1  0
 12 64  1  0
 12 65  1  0
 12 66  1  0
  6 55  1  0
  6 56  1  0
  6 57  1  0
  7 58  1  0
  4 53  1  0
  4 54  1  0
  3 51  1  0
  3 52  1  0
  1 49  1  0
  1 50  1  0
 46106  1  0
 47107  1  0
 47108  1  0
 47109  1  0
 48110  1  0
 48111  1  0
 48112  1  0
 41 96  1  0
 41 97  1  0
 41 98  1  0
 40 94  1  0
 40 95  1  0
M  END


  Mrv1652309102214152D          

 48 51  0  0  1  0            999 V2000
    5.1521    0.5181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7821   -0.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6358   -0.8265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8596   -1.1058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2295   -0.5732    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6969   -1.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7622    0.0568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0047    1.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8429   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529   -2.3925    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6283   -2.4182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -3.1452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6729   -3.8465    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2829   -4.5735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975   -3.8207    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9321   -4.5220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -3.0937    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7121   -3.0679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1467   -3.7692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7567   -4.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9713   -3.7434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4416   -0.6207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4930   -1.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1221   -1.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0465   -2.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8302   -2.7373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5686   -3.0293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4001   -3.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9347    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3247   -0.3660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6853    1.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5584    0.2648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7046    1.0767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1884   -0.2679    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  6  0  0  0
  8  5  1  6  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  1  0  0  0
 13 11  1  1  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 14 28  1  0  0  0  0
 29 28  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 30 38  1  0  0  0  0
 38 39  1  6  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 38 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 29 44  1  0  0  0  0
 11 44  1  0  0  0  0
 44 45  1  6  0  0  0
  2 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0300066

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CC[C@@]1(C)[C@@H](CC[C@]2(C)[C@@H]1C[C@@H](O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1OC(C)=O)[C@@H]1[C@H](CC[C@@]21C)[C@@](C)(O)CCC(=C)C(C)C)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C39H64O9/c1-22(2)24(5)12-19-39(10,44)27-14-18-38(9)32(27)29(48-35-34(47-25(6)40)33(43)28(41)21-46-35)20-30-36(7,16-15-31(42)45-11)26(23(3)4)13-17-37(30,38)8/h22,26-30,32-35,41,43-44H,3,5,12-21H2,1-2,4,6-11H3/t26-,27-,28+,29+,30+,32-,33-,34+,35-,36-,37+,38+,39-/m0/s1

> <INCHI_KEY>
JUVUYWNWPTYJBC-ZNROOEOWSA-N

> <FORMULA>
C39H64O9

> <MOLECULAR_WEIGHT>
676.932

> <EXACT_MASS>
676.455033641

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
77.229372457848

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-{[(2S,3R,4S,5R)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]propanoate

> <JCHEM_LOGP>
5.494580272999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.196121991184704

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.80795272965442

> <JCHEM_PKA_STRONGEST_BASIC>
-2.901318838233303

> <JCHEM_POLAR_SURFACE_AREA>
131.75

> <JCHEM_REFRACTIVITY>
182.93890000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-{[(2S,3R,4S,5R)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       9.617   0.967   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.793  -0.027   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.520  -1.543   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.071  -2.064   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.895  -1.070   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.901  -2.246   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.889   0.106   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.719  -0.076   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.832   1.460   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.406   2.042   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.412   0.866   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.742   2.253   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.223  -0.443   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.495  -1.800   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.307  -3.109   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.579  -4.466   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.040  -4.514   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.312  -5.871   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.123  -7.180   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.395  -8.537   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.662  -7.132   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.473  -8.441   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.390  -5.775   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.929  -5.727   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.741  -7.036   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.013  -8.393   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.280  -6.988   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.956  -1.848   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.145  -0.539   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.606  -0.587   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.824  -1.159   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.920  -2.095   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.228  -3.121   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.087  -4.628   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       1.550  -5.110   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -1.061  -5.655   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -0.747  -7.162   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -0.206   0.722   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.745   0.674   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.556   1.983   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -2.473  -0.683   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.522   2.079   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.062   2.127   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.873   0.818   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.146   2.334   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      12.242   0.494   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      12.515   2.010   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      13.418  -0.500   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   46                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7    8                                             
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    5    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   44                                             
CONECT   12   11                                                            
CONECT   13   11    8   14                                                  
CONECT   14   13   15   28                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   16   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   14   29                                                       
CONECT   29   28   30   44                                                  
CONECT   30   29   31   32   38                                             
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36                                                            
CONECT   38   30   39   42                                                  
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   38   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   29   11   45                                             
CONECT   45   44                                                            
CONECT   46    2   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

View in JSmol

Synonyms

Value	Source
Methyl 3-[(3S,3ar,4R,5ar,6S,7S,9ar,9BR)-4-{[(2S,3R,4S,5R)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]propanoic acid	Generator

Chemical Formula

C₃₉H₆₄O₉

Average Mass

676.9320 Da

Monoisotopic Mass

676.45503 Da

IUPAC Name

methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-{[(2S,3R,4S,5R)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]propanoate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)CC[C@@]1(C)[C@@H](CC[C@]2(C)[C@@H]1C[C@@H](O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1OC(C)=O)[C@@H]1[C@H](CC[C@@]21C)[C@@](C)(O)CCC(=C)C(C)C)C(C)=C

InChI Identifier

InChI=1S/C39H64O9/c1-22(2)24(5)12-19-39(10,44)27-14-18-38(9)32(27)29(48-35-34(47-25(6)40)33(43)28(41)21-46-35)20-30-36(7,16-15-31(42)45-11)26(23(3)4)13-17-37(30,38)8/h22,26-30,32-35,41,43-44H,3,5,12-21H2,1-2,4,6-11H3/t26-,27-,28+,29+,30+,32-,33-,34+,35-,36-,37+,38+,39-/m0/s1

InChI Key

JUVUYWNWPTYJBC-ZNROOEOWSA-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
Alnus pendula	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Glycosyl compound
O-glycosyl compound
Fatty acid ester
Dicarboxylic acid or derivatives
Monosaccharide
Fatty acyl
Oxane
Methyl ester
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
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	5.49	ChemAxon
pKa (Strongest Acidic)	12.81	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	131.75 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	182.94 m³·mol⁻¹	ChemAxon
Polarizability	77.23 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162956596

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate (NP0300066)

MOL for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

3D MOL for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

3D SDF for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

3D-SDF for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

PDB for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

3D PDB for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

SMILES for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

INCHI for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

Structure for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)

3D Structure for NP0300066 (methyl 3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-{[(2s,3r,4s,5r)-3-(acetyloxy)-4,5-dihydroxyoxan-2-yl]oxy}-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate)