NP-MRD: Showing NP-Card for (2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate (NP0306706)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 23:21:16 UTC

Updated at

2022-09-10 23:21:16 UTC

NP-MRD ID

NP0306706

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate

Description

[(1'R,2R,2'R,3'R,5'R,7'R,8'R,10'S)-5'-(acetyloxy)-3',8'-dihydroxy-1',10'-dimethyl-9'-oxo-12'-oxaspiro[oxirane-2,6'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane]-11'(15'),13'-dien-7'-yl]methyl acetate belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate is found in Teucrium alyssifolium. Based on a literature review very few articles have been published on [(1'R,2R,2'R,3'R,5'R,7'R,8'R,10'S)-5'-(acetyloxy)-3',8'-dihydroxy-1',10'-dimethyl-9'-oxo-12'-oxaspiro[oxirane-2,6'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane]-11'(15'),13'-dien-7'-yl]methyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112201212D          

 33 37  0  0  1  0            999 V2000
    2.5088    0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2271   -0.3593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9377    0.0599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2350   -1.1843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9533   -1.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9611   -2.4150    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2895   -1.6582    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7983   -0.9953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1091   -1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4375   -0.8073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6004   -2.2270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9288   -1.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4200   -2.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8986   -1.4610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6856   -1.7085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6934   -2.5334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9112   -2.7958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5828   -3.5526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7632   -3.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2720   -2.9838    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9436   -3.7406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4523   -3.0778    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1239   -3.8346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6152   -4.4974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3043   -3.9286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8131   -3.2658    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9935   -3.3598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651   -4.1166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1563   -4.7795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8454   -4.2106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1415   -2.5090    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3847   -2.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0475   -1.6894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 13 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  1  0  0  0
 22 20  1  1  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 26 31  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 33  1  1  0  0  0
M  END

     RDKit          3D

 63 67  0  0  0  0  0  0  0  0999 V2000
    2.6090    4.6556   -0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8919    3.5086   -1.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6172    3.4249   -2.5693 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5065    2.4789   -0.5209 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8045    1.3275   -1.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5198    0.3810    0.0960 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3418    1.1730    1.0862 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2357    2.4129    1.3542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6031    1.4723    0.3590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0672    2.5920    0.2232 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3666    0.3545   -0.2507 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7554    0.8292   -1.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6750    0.3234    0.4579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4759    1.3404    0.6732 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5374    0.9721    1.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4533   -0.3994    1.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2632   -0.7810    1.0057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5700   -2.0802    0.9155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -1.7338    0.9461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6467   -0.9351   -0.2633 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2297   -1.7242   -1.4499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1650   -0.8893   -0.2714 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5233   -1.4180   -1.4996 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0206   -2.6455   -1.9239 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9877   -1.6477   -1.2096 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4332   -1.2451    0.1504 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8424   -1.1961    0.2411 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6262   -1.9793    1.0400 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0886   -1.8101    1.0248 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0150   -2.8149    1.7529 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8726    0.0289    0.6831 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4223    0.5734    1.8782 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8226    1.1722    0.6856 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9764    5.3795   -1.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4698    4.2106   -0.1673 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9980    5.1876   -0.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0384    1.7285   -1.5706 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4939    0.8753   -1.7990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4723    0.6639    2.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4739    3.0909    1.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9892    0.6332   -2.4083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8813    1.9473   -1.6229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7632    0.4458   -1.9436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3234    1.6604    1.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2137   -0.9545    2.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8736   -2.7077    0.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7353   -2.7079    1.8407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5436   -2.7010    0.8962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8915   -1.2581    1.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3384   -1.4882   -1.4587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8666   -1.3927   -2.4156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2015   -2.8147   -1.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1927   -1.6289    0.5220 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4521   -0.7530   -2.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7077   -3.1393   -2.4401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6225   -1.2115   -2.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2531   -2.7479   -1.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1558   -2.0561    0.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3885   -0.7653    1.3229 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5879   -2.4802    1.7546 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5318   -2.0430    0.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2457    0.0170    2.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9453    1.2888    2.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  6
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  6
 11 13  1  0
 13 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  6
 20 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  2  0
 26 31  1  0
 31 32  1  0
 32 33  1  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
 22  6  1  0
 31 33  1  6
 31  6  1  0
 20 11  1  0
 14 13  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  5 37  1  0
  5 38  1  0
  7 39  1  1
  8 40  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 21 50  1  0
 21 51  1  0
 21 52  1  0
 22 53  1  1
 23 54  1  6
 24 55  1  0
 25 56  1  0
 25 57  1  0
 26 58  1  1
 29 59  1  0
 29 60  1  0
 29 61  1  0
 32 62  1  0
 32 63  1  0
 16 45  1  0
 15 44  1  0
M  END


  Mrv1652309112201212D          

 33 37  0  0  1  0            999 V2000
    2.5088    0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2271   -0.3593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9377    0.0599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2350   -1.1843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9533   -1.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9611   -2.4150    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2895   -1.6582    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7983   -0.9953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1091   -1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4375   -0.8073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6004   -2.2270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9288   -1.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4200   -2.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8986   -1.4610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6856   -1.7085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6934   -2.5334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9112   -2.7958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5828   -3.5526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7632   -3.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2720   -2.9838    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9436   -3.7406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4523   -3.0778    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1239   -3.8346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6152   -4.4974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3043   -3.9286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8131   -3.2658    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9935   -3.3598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651   -4.1166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1563   -4.7795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8454   -4.2106    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1415   -2.5090    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3847   -2.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0475   -1.6894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 13 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  1  0  0  0
 22 20  1  1  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 26 31  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 33  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0306706

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@@]12[C@@H](O)C(=O)[C@]3(C)C4=C(CC[C@]3(C)[C@H]1[C@H](O)C[C@@H](OC(C)=O)[C@]21CO1)C=CO4

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O9/c1-12(25)31-10-23-17(15(27)9-16(33-13(2)26)24(23)11-32-24)21(3)7-5-14-6-8-30-20(14)22(21,4)18(28)19(23)29/h6,8,15-17,19,27,29H,5,7,9-11H2,1-4H3/t15-,16-,17-,19+,21-,22-,23+,24-/m1/s1

> <INCHI_KEY>
ITKHSXRKRUBYAB-FAEWSUHZSA-N

> <FORMULA>
C24H30O9

> <MOLECULAR_WEIGHT>
462.495

> <EXACT_MASS>
462.188982546

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
47.09532690319938

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1'R,2R,2'R,3'R,5'R,7'R,8'R,10'S)-5'-(acetyloxy)-3',8'-dihydroxy-1',10'-dimethyl-9'-oxo-12'-oxaspiro[oxirane-2,6'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-11'(15'),13'-dien-7'-yl]methyl acetate

> <JCHEM_LOGP>
0.3119219050000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.939928299420107

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.50452663673444

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8057537805450106

> <JCHEM_POLAR_SURFACE_AREA>
135.8

> <JCHEM_REFRACTIVITY>
111.55720000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,2R,2'R,3'R,5'R,7'R,8'R,10'S)-5'-(acetyloxy)-3',8'-dihydroxy-1',10'-dimethyl-9'-oxo-12'-oxaspiro[oxirane-2,6'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-11'(15'),13'-dien-7'-ylmethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       4.683   0.087   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.024  -0.671   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.350   0.112   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.039  -2.211   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.379  -2.968   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.394  -4.508   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.007  -3.095   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.090  -1.858   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.537  -2.920   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.150  -1.507   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.454  -4.157   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.067  -2.744   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.984  -3.982   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.877  -2.727   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      14.346  -3.189   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.361  -4.729   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.901  -5.219   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.288  -6.632   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.758  -6.807   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.841  -5.570   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.228  -6.982   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.311  -5.745   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.698  -7.158   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.615  -8.395   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.168  -7.333   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.251  -6.096   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.721  -6.272   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.108  -7.684   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.025  -8.922   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.578  -7.860   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.864  -4.683   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.451  -4.070   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.689  -3.153   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22   31                                             
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   20                                             
CONECT   12   11                                                            
CONECT   13   11   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   11   21   22                                             
CONECT   21   20                                                            
CONECT   22   20    6   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   26    6   32   33                                             
CONECT   32   31   33                                                       
CONECT   33   32   31                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Value	Source
[(1'r,2R,2'r,3'r,5'r,7'r,8'r,10's)-5'-(Acetyloxy)-3',8'-dihydroxy-1',10'-dimethyl-9'-oxo-12'-oxaspiro[oxirane-2,6'-tetracyclo[8.7.0.0,.0,]heptadecane]-11'(15'),13'-dien-7'-yl]methyl acetic acid	Generator

Chemical Formula

C₂₄H₃₀O₉

Average Mass

462.4950 Da

Monoisotopic Mass

462.18898 Da

IUPAC Name

[(1'R,2R,2'R,3'R,5'R,7'R,8'R,10'S)-5'-(acetyloxy)-3',8'-dihydroxy-1',10'-dimethyl-9'-oxo-12'-oxaspiro[oxirane-2,6'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-11'(15'),13'-dien-7'-yl]methyl acetate

Traditional Name

(1'R,2R,2'R,3'R,5'R,7'R,8'R,10'S)-5'-(acetyloxy)-3',8'-dihydroxy-1',10'-dimethyl-9'-oxo-12'-oxaspiro[oxirane-2,6'-tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane]-11'(15'),13'-dien-7'-ylmethyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@@]12[C@@H](O)C(=O)[C@]3(C)C4=C(CC[C@]3(C)[C@H]1[C@H](O)C[C@@H](OC(C)=O)[C@]21CO1)C=CO4

InChI Identifier

InChI=1S/C24H30O9/c1-12(25)31-10-23-17(15(27)9-16(33-13(2)26)24(23)11-32-24)21(3)7-5-14-6-8-30-20(14)22(21,4)18(28)19(23)29/h6,8,15-17,19,27,29H,5,7,9-11H2,1-4H3/t15-,16-,17-,19+,21-,22-,23+,24-/m1/s1

InChI Key

ITKHSXRKRUBYAB-FAEWSUHZSA-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
Teucrium alyssifolium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Benzofuran
Dicarboxylic acid or derivatives
Cyclic alcohol
Heteroaromatic compound
Furan
Carboxylic acid ester
Ketone
Secondary alcohol
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	0.31	ChemAxon
pKa (Strongest Acidic)	12.5	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	135.8 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	111.56 m³·mol⁻¹	ChemAxon
Polarizability	47.1 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Not Available

Chemspider ID

8823090

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10647732

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate (NP0306706)

MOL for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

3D MOL for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

3D SDF for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

3D-SDF for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

PDB for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

3D PDB for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

SMILES for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

INCHI for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

Structure for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)

3D Structure for NP0306706 ((2r,3'bs,5'r,5'ar,7'r,9'r,9'ar,9'br)-7'-(acetyloxy)-5',9'-dihydroxy-3'b,9'b-dimethyl-4'-oxo-7',8',9',9'a,10',11'-hexahydro-5'h-spiro[oxirane-2,6'-phenanthro[1,2-b]furan]-5'a-ylmethyl acetate)