NP-MRD: Showing NP-Card for 3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate (NP0288403)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 18:05:13 UTC

Updated at

2022-09-09 18:05:13 UTC

NP-MRD ID

NP0288403

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate

Description

2,6,6,10,11-Pentamethyl-14-(2-methyl-5-oxo-2,5-dihydrofuran-2-yl)-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-3-en-16-yl acetate belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. 3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate is found in Cleome africana. Based on a literature review very few articles have been published on 2,6,6,10,11-pentamethyl-14-(2-methyl-5-oxo-2,5-dihydrofuran-2-yl)-5-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-3-en-16-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092220052D          

 34 38  0  0  0  0            999 V2000
    3.3449   -0.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5328   -0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2525    0.2212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0009   -1.1854    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
    4.1858   -3.0277    0.0000 C   0  0  0  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  0  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
    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  0  0  0  0  0  0  0  0  0  0
    2.3100   -4.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -3.3680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9702   -4.1909    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
    0.6955   -3.4114    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1192   -1.5321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1763   -2.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9038   -2.1502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7586   -1.3380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3303   -0.7432    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0586   -1.2252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -2.5921    0.0000 C   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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
  8 17  1  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
  7 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 27 33  1  0  0  0  0
 26 34  1  0  0  0  0
  5 34  1  0  0  0  0
 22 34  1  0  0  0  0
M  END

     RDKit          3D

 74 78  0  0  0  0  0  0  0  0999 V2000
   -1.6162   -2.4941    4.0265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6851   -2.5258    2.5676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2139   -3.5437    2.0101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2196   -1.5322    1.7195 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3135   -1.6153    0.2924 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1210   -1.8763   -0.2032 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7923   -0.5451   -0.1903 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2668   -0.6307    0.0007 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9423   -1.6811   -0.8226 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4577   -1.0640    1.4337 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6730   -0.9116    1.9210 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7159   -0.3523    1.0697 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8832   -0.8447    1.1551 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3680    0.7621    0.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2280    0.7211   -1.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7532    2.0349    0.9276 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8979    0.7423   -0.0679 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4102    1.5986   -1.1864 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8786    1.6664   -1.1164 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2934    0.2854   -1.3301 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8750   -0.1720   -2.6755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1755    0.2189   -1.4492 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5886   -0.5106   -2.7497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8808    1.5497   -1.5311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2613    1.9238   -0.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4912    0.5933    0.5859 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0099    0.4951    0.7821 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3798   -0.8101    1.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7542    0.6337   -0.4577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5506    1.6759   -0.3348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3652    2.2735    0.9998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9687    3.2806    1.4449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4238    1.5312    1.6492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9501   -0.4430   -0.3510 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6731   -1.4358    4.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4709   -3.0877    4.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6691   -2.9792    4.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8245   -2.5754    0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1395   -2.4244   -1.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6309   -2.5210    0.5623 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4206   -0.0066    0.7361 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1912   -2.3095   -1.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7508   -1.3091   -1.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4725   -2.4693   -0.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6768   -1.4737    2.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8888   -1.2076    2.9609 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0235    1.5273   -1.0562 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8457   -0.2256   -1.0886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7383    0.8018   -2.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7633    1.8497    1.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8716    2.8194    0.1293 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0045    2.2955    1.6746 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4663    1.2666    0.8509 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8072    1.4409   -2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7208    2.6558   -0.9101 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6020    2.4114   -1.8540 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7096    1.9816   -0.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9470   -0.3100   -2.6745 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6849    0.6944   -3.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4288   -1.1112   -3.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5067   -1.5930   -2.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1885   -0.0426   -3.6412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7066   -0.3249   -2.8009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3948    2.3234   -2.1033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729    1.3888   -2.0556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2060    2.5481   -0.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5456    2.5681    0.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0813    0.5735    1.5911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9330   -1.6782    0.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1091   -0.7749    2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4749   -0.9740    1.4380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6852    0.0119   -1.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2532    2.0905   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8974   -0.8487   -0.8368 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
  5  6  1  0
  6  7  1  0
  7 20  1  0
 20 21  1  6
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 14  1  0
 14 15  1  0
 14 16  1  0
 14 12  1  0
 12 13  2  0
 12 11  1  0
 11 10  2  0
 10  8  1  0
  8  9  1  6
 20 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 34  1  0
 26 27  1  0
 27 28  1  1
 27 33  1  0
 33 31  1  0
 31 32  2  0
 31 30  1  0
 30 29  2  0
 34  5  1  0
 29 27  1  0
  8  7  1  0
 34 22  1  0
  8 17  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  5 38  1  1
  6 39  1  0
  6 40  1  0
  7 41  1  1
 21 58  1  0
 21 59  1  0
 21 60  1  0
 19 56  1  0
 19 57  1  0
 18 54  1  0
 18 55  1  0
 17 53  1  1
 15 47  1  0
 15 48  1  0
 15 49  1  0
 16 50  1  0
 16 51  1  0
 16 52  1  0
 11 46  1  0
 10 45  1  0
  9 42  1  0
  9 43  1  0
  9 44  1  0
 23 61  1  0
 23 62  1  0
 23 63  1  0
 24 64  1  0
 24 65  1  0
 25 66  1  0
 25 67  1  0
 26 68  1  1
 34 74  1  6
 28 69  1  0
 28 70  1  0
 28 71  1  0
 30 73  1  0
 29 72  1  0
M  END


  Mrv1652309092220052D          

 34 38  0  0  0  0            999 V2000
    3.3449   -0.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5328   -0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2525    0.2212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0009   -1.1854    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
    4.1858   -3.0277    0.0000 C   0  0  0  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  0  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
    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  0  0  0  0  0  0  0  0  0  0
    2.3100   -4.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -3.3680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9702   -4.1909    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
    0.6955   -3.4114    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1192   -1.5321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1763   -2.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9038   -2.1502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7586   -1.3380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3303   -0.7432    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0586   -1.2252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -2.5921    0.0000 C   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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
  8 17  1  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
  7 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 27 33  1  0  0  0  0
 26 34  1  0  0  0  0
  5 34  1  0  0  0  0
 22 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0288403

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC2C(C)(CCC3C(C)(C)C(=O)C=CC23C)C2(C)CCC(C12)C1(C)OC(=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H40O5/c1-17(30)33-19-16-21-26(4)12-10-22(31)25(2,3)20(26)9-14-27(21,5)28(6)13-8-18(24(19)28)29(7)15-11-23(32)34-29/h10-12,15,18-21,24H,8-9,13-14,16H2,1-7H3

> <INCHI_KEY>
HHADFXKLJQYGKX-UHFFFAOYSA-N

> <FORMULA>
C29H40O5

> <MOLECULAR_WEIGHT>
468.634

> <EXACT_MASS>
468.287574388

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
51.7972346318149

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,6,6,10,11-pentamethyl-14-(2-methyl-5-oxo-2,5-dihydrofuran-2-yl)-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-16-yl acetate

> <JCHEM_LOGP>
5.495131108333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-5.038348929644585

> <JCHEM_POLAR_SURFACE_AREA>
69.67

> <JCHEM_REFRACTIVITY>
131.17029999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2,6,6,10,11-pentamethyl-14-(2-methyl-5-oxofuran-2-yl)-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-16-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       6.244  -1.307   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.728  -1.036   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.205   0.413   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.735  -2.213   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.184  -8.144   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.322  -8.817   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.312  -7.735   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.678  -7.823   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.089  -2.860   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.329  -4.740   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.687  -4.014   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.416  -2.498   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.483  -1.387   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       0.109  -2.287   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   20                                                  
CONECT    8    7    9   10   17                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14    8   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    7   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   23   24   34                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   34                                                  
CONECT   27   26   28   29   33                                             
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   27                                                       
CONECT   34   26    5   22                                                  
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Value	Source
2,6,6,10,11-Pentamethyl-14-(2-methyl-5-oxo-2,5-dihydrofuran-2-yl)-5-oxotetracyclo[8.7.0.0,.0,]heptadec-3-en-16-yl acetic acid	Generator

Chemical Formula

C₂₉H₄₀O₅

Average Mass

468.6340 Da

Monoisotopic Mass

468.28757 Da

IUPAC Name

2,6,6,10,11-pentamethyl-14-(2-methyl-5-oxo-2,5-dihydrofuran-2-yl)-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-16-yl acetate

Traditional Name

2,6,6,10,11-pentamethyl-14-(2-methyl-5-oxofuran-2-yl)-5-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-16-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC2C(C)(CCC3C(C)(C)C(=O)C=CC23C)C2(C)CCC(C12)C1(C)OC(=O)C=C1

InChI Identifier

InChI=1S/C29H40O5/c1-17(30)33-19-16-21-26(4)12-10-22(31)25(2,3)20(26)9-14-27(21,5)28(6)13-8-18(24(19)28)29(7)15-11-23(32)34-29/h10-12,15,18-21,24H,8-9,13-14,16H2,1-7H3

InChI Key

HHADFXKLJQYGKX-UHFFFAOYSA-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
Cleome africana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

Steroid lactone
Steroid ester
3-oxo-delta-1-steroid
3-oxosteroid
Oxosteroid
Delta-1-steroid
Cyclohexenone
2-furanone
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Carboxylic acid ester
Cyclic ketone
Ketone
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	5.5	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	69.67 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	131.17 m³·mol⁻¹	ChemAxon
Polarizability	51.8 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	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

85268853

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate (NP0288403)

MOL for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

3D MOL for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

3D SDF for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

3D-SDF for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

PDB for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

3D PDB for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

SMILES for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

INCHI for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

Structure for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)

3D Structure for NP0288403 (3a,3b,6,6,9a-pentamethyl-1-(2-methyl-5-oxofuran-2-yl)-7-oxo-1h,2h,3h,4h,5h,5ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-11-yl acetate)