NP-MRD: Showing NP-Card for methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate (NP0267050)

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Record Information

Version

2.0

Created at

2022-09-08 11:42:07 UTC

Updated at

2022-09-08 11:42:07 UTC

NP-MRD ID

NP0267050

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate

Description

Aperterpene N belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. Based on a literature review very few articles have been published on Aperterpene N.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082213422D          

 33 36  0  0  1  0            999 V2000
    2.0009   -1.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2812   -1.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0934   -2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3737   -2.8825    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1858   -3.0277    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9055   -2.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7176   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5297   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8100   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2782   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9917   -4.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9942   -4.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -3.8037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9343   -4.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2146   -5.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -4.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5309   -4.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -3.3680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2274   -4.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7337   -4.8203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6325   -4.7406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8302   -5.5416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784   -3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -4.6668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6955   -3.4114    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3065   -4.1389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0686   -3.1005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9249   -2.6189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4185   -1.9676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -2.5921    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3895   -1.8497    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  6  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  2 32  1  0  0  0  0
 20 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END

     RDKit          3D

 67 70  0  0  0  0  0  0  0  0999 V2000
   -2.1072   -2.1405   -2.5718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6046   -1.4740   -1.5440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2640   -1.7864   -0.9696 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2981   -0.4601   -0.5001 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7765   -0.4727   -0.3745 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3242   -1.7073    0.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3197   -0.4600   -1.8186 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8071   -0.3318   -1.8663 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3666    0.6244   -0.8896 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4162    1.1855   -1.1566 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7186    0.9446    0.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0082    2.4296    0.6797 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3191    0.1682    1.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2494    0.8245    0.2201 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4336    1.2800    1.3793 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9299    1.5297    2.4642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0269    1.4036    1.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4818    0.0106    0.6742 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2029   -0.8401    1.9217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9439    0.0769    0.3983 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7175   -0.7333    1.4089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6174   -0.2312    2.1322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4694   -2.0867    1.5901 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2035   -2.8307    2.5415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5162    1.4491    0.4551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6095    2.1797    1.4235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0028    1.8756   -0.8936 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6408    3.2771   -1.2513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4043    1.8026   -0.8813 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4114    0.8486   -1.7776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0482    1.0269   -2.9204 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3782   -0.3980   -0.9464 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8331   -0.8756   -0.8729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5063   -2.9372   -2.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0795   -1.9078   -2.9817 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3255   -2.2618   -1.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4189   -2.5242   -0.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0601    0.2637   -1.3367 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5009   -1.6912    1.3157 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6075   -2.5459   -0.0012 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2801   -2.0446   -0.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8923    0.4621   -2.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0324   -1.3485   -2.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3361   -1.3278   -1.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0598    0.0711   -2.8914 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1385    3.0603    0.4790 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8562    2.7876    0.0788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2750    2.5855    1.7581 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2419    0.7263    1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7458   -0.8275    1.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7124    0.0457    2.4254 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0023    1.5940   -0.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2516    2.1519    0.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4805    1.6389    2.1067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493   -1.9034    1.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9853   -0.6661    2.6885 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7485   -0.4804    2.4149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6432   -3.7137    2.9157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1947   -3.0895    2.1213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3888   -2.1736    3.4280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7117    3.6476   -0.8168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6603    3.3794   -2.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4590    3.9640   -0.8924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7661    2.0085    0.0207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3943   -0.3824   -0.0615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3642   -0.6736   -1.8303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8452   -1.9960   -0.7678 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 21  1  0
 21 22  2  0
 20 21  1  1
 20 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 27 29  1  1
 27 30  1  0
 30 31  2  0
 30 32  1  0
 32 33  1  1
 32  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  1
 32 20  1  0
 18  4  1  0
 18 20  1  0
 14  5  1  0
 24 58  1  0
 24 59  1  0
 24 60  1  0
 28 61  1  0
 28 62  1  0
 28 63  1  0
 29 64  1  0
 33 65  1  0
 33 66  1  0
 33 67  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  6
  6 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
 12 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  6
 17 53  1  0
 17 54  1  0
 19 55  1  0
 19 56  1  0
 19 57  1  0
M  END


  Mrv1652309082213422D          

 33 36  0  0  1  0            999 V2000
    2.0009   -1.1854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2812   -1.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0934   -2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3737   -2.8825    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1858   -3.0277    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9055   -2.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7176   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5297   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8100   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2782   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9917   -4.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9942   -4.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -3.8037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9343   -4.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2146   -5.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -4.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5309   -4.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -3.3680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2274   -4.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7337   -4.8203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6325   -4.7406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8302   -5.5416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784   -3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -4.6668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6955   -3.4114    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3065   -4.1389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0686   -3.1005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9249   -2.6189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4185   -1.9676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -2.5921    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3895   -1.8497    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  6  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  2 32  1  0  0  0  0
 20 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0267050

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]12C(=O)[C@](C)(O)C(=O)[C@@]1(C)C(=C)C[C@@H]1[C@@]3(C)CCC(=O)C(C)(C)[C@@H]3C(=O)C[C@@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C26H34O7/c1-13-11-15-22(4)10-9-16(28)21(2,3)17(22)14(27)12-23(15,5)26(20(31)33-8)19(30)25(7,32)18(29)24(13,26)6/h15,17,32H,1,9-12H2,2-8H3/t15-,17+,22-,23-,24-,25-,26+/m1/s1

> <INCHI_KEY>
AAEFHLQEFDWSRN-LTUMHGGBSA-N

> <FORMULA>
C26H34O7

> <MOLECULAR_WEIGHT>
458.551

> <EXACT_MASS>
458.230453435

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
47.92071353883304

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,2R,7R,10R,11S,13R,15S)-13-hydroxy-2,6,6,10,13,15-hexamethyl-16-methylidene-5,8,12,14-tetraoxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-11-carboxylate

> <JCHEM_LOGP>
3.5898479836666697

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.51836451677802

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.488399375586404

> <JCHEM_PKA_STRONGEST_BASIC>
-4.334774093483316

> <JCHEM_POLAR_SURFACE_AREA>
114.81

> <JCHEM_REFRACTIVITY>
119.0826999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,2R,7R,10R,11S,13R,15S)-13-hydroxy-2,6,6,10,13,15-hexamethyl-16-methylidene-5,8,12,14-tetraoxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-11-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       3.735  -2.213   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.184  -8.144   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.322  -8.817   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.867  -9.726   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.724  -7.984   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.158  -7.782   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.103  -8.998   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       3.047  -8.849   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.416 -10.344   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.145  -8.711   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.572  -7.726   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -0.128  -5.788   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.781  -3.673   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.594  -3.453   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   18                                                  
CONECT    5    4    6    7   14                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11    5   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    4   19   20                                             
CONECT   19   18                                                            
CONECT   20   18   21   25   32                                             
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23                                                            
CONECT   25   20   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    2   20   33                                             
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₄O₇

Average Mass

458.5510 Da

Monoisotopic Mass

458.23045 Da

IUPAC Name

methyl (1R,2R,7R,10R,11S,13R,15S)-13-hydroxy-2,6,6,10,13,15-hexamethyl-16-methylidene-5,8,12,14-tetraoxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-11-carboxylate

Traditional Name

methyl (1R,2R,7R,10R,11S,13R,15S)-13-hydroxy-2,6,6,10,13,15-hexamethyl-16-methylidene-5,8,12,14-tetraoxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-11-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]12C(=O)[C@](C)(O)C(=O)[C@@]1(C)C(=C)C[C@@H]1[C@@]3(C)CCC(=O)C(C)(C)[C@@H]3C(=O)C[C@@]21C

InChI Identifier

InChI=1S/C26H34O7/c1-13-11-15-22(4)10-9-16(28)21(2,3)17(22)14(27)12-23(15,5)26(20(31)33-8)19(30)25(7,32)18(29)24(13,26)6/h15,17,32H,1,9-12H2,2-8H3/t15-,17+,22-,23-,24-,25-,26+/m1/s1

InChI Key

AAEFHLQEFDWSRN-LTUMHGGBSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

Oxosteroids

Alternative Parents

Substituents

6-oxosteroid
3-oxo-5-alpha-steroid
16-hydroxysteroid
16-beta-hydroxysteroid
Oxosteroid
17-oxosteroid
15-oxosteroid
Hydroxysteroid
3-oxosteroid
Acyloin
Methyl ester
Tertiary alcohol
Cyclic alcohol
Cyclic ketone
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	3.59	ChemAxon
pKa (Strongest Acidic)	11.49	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	114.81 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	119.08 m³·mol⁻¹	ChemAxon
Polarizability	47.92 Å³	ChemAxon
Number of Rings	4	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

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

146682520

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate (NP0267050)

MOL for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

3D MOL for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

3D SDF for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

3D-SDF for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

PDB for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

3D PDB for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

SMILES for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

INCHI for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

Structure for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)

3D Structure for NP0267050 (methyl (2r,3as,3br,5ar,9ar,9br,11as)-2-hydroxy-2,3b,6,6,9a,11a-hexamethyl-11-methylidene-1,3,5,7-tetraoxo-hexahydrocyclopenta[a]phenanthrene-3a-carboxylate)