NP-MRD: Showing NP-Card for 2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid (NP0185961)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 01:36:15 UTC

Updated at

2022-09-04 01:36:15 UTC

NP-MRD ID

NP0185961

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid

Description

2-[(1S,2R,6S,7S,8S,10R,11S,13S,14Z,15R)-13-(acetyloxy)-8-hydroxy-2,6,10,11-tetramethyl-5,9-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-3-en-14-ylidene]-6-methylhept-5-enoic acid belongs to the class of organic compounds known as steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group. Based on a literature review very few articles have been published on 2-[(1S,2R,6S,7S,8S,10R,11S,13S,14Z,15R)-13-(acetyloxy)-8-hydroxy-2,6,10,11-tetramethyl-5,9-dioxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-3-en-14-ylidene]-6-methylhept-5-enoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042203362D          

 38 41  0  0  1  0            999 V2000
   -1.0015   -4.7841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2256   -4.5038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4051   -5.0356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0804   -3.6917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6955   -3.4114    0.0000 C   0  0  1  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
    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
    1.7494   -2.5921    0.0000 C   0  0  1  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  1  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  1  0  0  0  0  0  0  0  0  0
    5.5585   -4.7248    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  2  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
    2.5903   -4.9199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  1  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
    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
    0.7294   -1.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5466   -1.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8575   -0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6748   -0.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9857    0.5507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1811   -0.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3987   -2.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9051   -1.4291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7096   -2.8446    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 21 19  1  6  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 12 26  1  0  0  0  0
  7 26  1  0  0  0  0
 26 27  1  6  0  0  0
  9 28  1  6  0  0  0
  5 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 29 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
M  END

     RDKit          3D

 80 83  0  0  0  0  0  0  0  0999 V2000
    2.1455    6.1377   -0.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2128    4.9353    0.7483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7978    4.9017    1.8406 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6074    3.7831    0.3277 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5363    2.5571    0.9220 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0741    2.3929    1.4556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6185    2.0023    0.2165 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8359    3.2030   -0.6416 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3941    1.0004   -0.3754 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0642    0.9822   -1.8068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2824    0.2427   -1.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3191    0.6753   -0.9477 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2721   -0.5170   -0.7429 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5949   -0.0378   -0.1793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5527   -1.0815   -2.0706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9759   -2.3248   -2.1724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1817   -3.1799   -1.0032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6952   -4.3204   -1.0353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7475   -2.6511    0.3189 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2145   -3.8020    1.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6580   -1.5922    0.1009 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1722   -1.1031    1.4297 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0157   -1.5567    2.4561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0256    0.3657    1.4999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9679    0.8393    2.6149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9450    1.2952    0.3549 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9424    2.4199    0.6998 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7032    1.3490    0.1062 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8205    0.6864   -0.0825 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8645   -0.6008   -0.8679 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2908   -1.6884    0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3638   -3.0140   -0.5737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4913   -3.7013   -0.6288 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5340   -5.0122   -1.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7605   -3.2032   -0.0117 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1029    1.1558    0.4175 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1497    0.5032    0.2004 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2784    2.3224    1.1477 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0285    6.2895   -0.7393 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2140    6.1491   -0.7315 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0206    7.0209    0.5930 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1151    2.5932    1.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2504    3.3166    1.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1923    1.5419    2.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2477    4.0187    0.0266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6628    3.0599   -1.4003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0010    3.5909   -1.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0422    0.0038    0.0585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1800    1.9791   -2.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7331    0.5122   -2.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6186    0.3825   -2.9405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0099   -0.8278   -1.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9846    1.4127   -1.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6669   -0.1421    0.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8220    0.9547   -0.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3830   -0.7260   -0.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4226   -0.4960   -2.9478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1957   -2.7817   -3.1450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5818   -2.1618    0.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9054   -3.9604    1.9803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2251   -3.5707    1.5771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2011   -4.7332    0.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8582   -2.1182   -0.4490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1762   -1.5507    1.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5874   -1.3225    3.3244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7933    2.0336    1.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4552    3.1625    1.3994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2712    2.9803   -0.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5858   -0.4513   -1.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8578   -0.9295   -1.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4743   -1.7210    0.8959 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2011   -1.4436    0.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4825   -3.4283   -1.0386 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5666   -5.5513   -1.2637 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3134   -5.6711   -0.8624 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8111   -4.8229   -2.3764 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6290   -2.9334    1.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5639   -3.9443   -0.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0241   -2.2678   -0.5463 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4701    2.1888    2.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  1
 26 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9 28  1  0
 28  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  2  3
 33 34  1  0
 33 35  1  0
 29 36  1  0
 36 38  1  0
 36 37  2  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 13 21  1  0
  7 26  1  0
  7  9  1  0
 20 60  1  0
 20 61  1  0
 20 62  1  0
 19 59  1  1
 21 63  1  6
 22 64  1  1
 23 65  1  0
 27 66  1  0
 27 67  1  0
 27 68  1  0
 12 53  1  6
 11 51  1  0
 11 52  1  0
 10 49  1  0
 10 50  1  0
  9 48  1  1
  5 42  1  1
  6 43  1  0
  6 44  1  0
  8 45  1  0
  8 46  1  0
  8 47  1  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
 30 69  1  0
 30 70  1  0
 31 71  1  0
 31 72  1  0
 32 73  1  0
 34 74  1  0
 34 75  1  0
 34 76  1  0
 35 77  1  0
 35 78  1  0
 35 79  1  0
 38 80  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 15 57  1  0
 16 58  1  0
M  END


  Mrv1652309042203362D          

 38 41  0  0  1  0            999 V2000
   -1.0015   -4.7841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2256   -4.5038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4051   -5.0356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0804   -3.6917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6955   -3.4114    0.0000 C   0  0  1  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
    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
    1.7494   -2.5921    0.0000 C   0  0  1  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  1  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  1  0  0  0  0  0  0  0  0  0
    5.5585   -4.7248    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  2  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
    2.5903   -4.9199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  1  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
    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
    0.7294   -1.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5466   -1.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8575   -0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6748   -0.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9857    0.5507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1811   -0.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3987   -2.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9051   -1.4291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7096   -2.8446    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 21 19  1  6  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 12 26  1  0  0  0  0
  7 26  1  0  0  0  0
 26 27  1  6  0  0  0
  9 28  1  6  0  0  0
  5 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 29 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0185961

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@@H]2[C@H](O)C(=O)[C@]3(C)[C@@H](CC[C@H]4\C([C@H](C[C@]34C)OC(C)=O)=C(/CCC=C(C)C)C(O)=O)[C@@]2(C)C=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H42O7/c1-16(2)9-8-10-19(28(36)37)24-20-11-12-23-29(5)14-13-21(33)17(3)25(29)26(34)27(35)31(23,7)30(20,6)15-22(24)38-18(4)32/h9,13-14,17,20,22-23,25-26,34H,8,10-12,15H2,1-7H3,(H,36,37)/b24-19-/t17-,20+,22+,23+,25-,26+,29-,30+,31+/m1/s1

> <INCHI_KEY>
ZGQQEJUGWPCCHA-PQJOSAKVSA-N

> <FORMULA>
C31H42O7

> <MOLECULAR_WEIGHT>
526.67

> <EXACT_MASS>
526.293053692

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
58.09188912970697

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1S,2R,6S,7S,8S,10R,11S,13S,14Z,15R)-13-(acetyloxy)-8-hydroxy-2,6,10,11-tetramethyl-5,9-dioxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-14-ylidene]-6-methylhept-5-enoic acid

> <JCHEM_LOGP>
4.653620804666668

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.095870846102741

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.543670330033441

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6316336935053712

> <JCHEM_POLAR_SURFACE_AREA>
117.97000000000001

> <JCHEM_REFRACTIVITY>
144.80730000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1S,2R,6S,7S,8S,10R,11S,13S,14Z,15R)-13-(acetyloxy)-8-hydroxy-2,6,10,11-tetramethyl-5,9-dioxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-14-ylidene]-6-methylhept-5-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.869  -8.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.421  -8.407   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.756  -9.400   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.150  -6.891   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.158  -7.782   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.376  -8.820   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.867  -9.726   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.835  -9.184   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.724  -7.984   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.362  -2.246   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.887  -2.036   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.467  -0.609   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.993  -0.399   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.573   1.028   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.938  -1.614   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.744  -3.883   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.690  -2.668   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -1.325  -5.310   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   28                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   26                                             
CONECT    8    7                                                            
CONECT    9    7   10   28                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14   15   21                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   13   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   12    7   27                                             
CONECT   27   26                                                            
CONECT   28    9    5   29                                                  
CONECT   29   28   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   29   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Value	Source
2-[(1S,2R,6S,7S,8S,10R,11S,13S,14Z,15R)-13-(Acetyloxy)-8-hydroxy-2,6,10,11-tetramethyl-5,9-dioxotetracyclo[8.7.0.0,.0,]heptadec-3-en-14-ylidene]-6-methylhept-5-enoate	Generator

Chemical Formula

C₃₁H₄₂O₇

Average Mass

526.6700 Da

Monoisotopic Mass

526.29305 Da

IUPAC Name

2-[(1S,2R,6S,7S,8S,10R,11S,13S,14Z,15R)-13-(acetyloxy)-8-hydroxy-2,6,10,11-tetramethyl-5,9-dioxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-14-ylidene]-6-methylhept-5-enoic acid

Traditional Name

2-[(1S,2R,6S,7S,8S,10R,11S,13S,14Z,15R)-13-(acetyloxy)-8-hydroxy-2,6,10,11-tetramethyl-5,9-dioxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-14-ylidene]-6-methylhept-5-enoic acid

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@@H]2[C@H](O)C(=O)[C@]3(C)[C@@H](CC[C@H]4\C([C@H](C[C@]34C)OC(C)=O)=C(/CCC=C(C)C)C(O)=O)[C@@]2(C)C=CC1=O

InChI Identifier

InChI=1S/C31H42O7/c1-16(2)9-8-10-19(28(36)37)24-20-11-12-23-29(5)14-13-21(33)17(3)25(29)26(34)27(35)31(23,7)30(20,6)15-22(24)38-18(4)32/h9,13-14,17,20,22-23,25-26,34H,8,10-12,15H2,1-7H3,(H,36,37)/b24-19-/t17-,20+,22+,23+,25-,26+,29-,30+,31+/m1/s1

InChI Key

ZGQQEJUGWPCCHA-PQJOSAKVSA-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 steroid esters. Steroid esters are compounds containing a steroid moiety which bears a carboxylic acid ester group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid esters

Direct Parent

Steroid esters

Alternative Parents

Substituents

Steroid ester
3-oxo-delta-1-steroid
3-oxosteroid
6-hydroxysteroid
Hydroxysteroid
Oxosteroid
3-oxo-5-alpha-steroid
7-oxosteroid
Delta-1-steroid
Medium-chain fatty acid
Cyclohexenone
Hydroxy fatty acid
Branched fatty acid
Methyl-branched fatty acid
Fatty acid
Fatty acyl
Dicarboxylic acid or derivatives
Unsaturated fatty acid
Cyclic alcohol
Carboxylic acid ester
Ketone
Secondary alcohol
Cyclic ketone
Carboxylic acid derivative
Carboxylic acid
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Alcohol
Organooxygen compound
Organic oxide
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	4.65	ChemAxon
pKa (Strongest Acidic)	4.54	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	117.97 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	144.81 m³·mol⁻¹	ChemAxon
Polarizability	58.09 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162902632

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid (NP0185961)

MOL for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

3D MOL for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

3D SDF for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

3D-SDF for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

PDB for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

3D PDB for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

SMILES for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

INCHI for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

Structure for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)

3D Structure for NP0185961 (2-[(1z,2s,3as,3br,5s,5as,6s,9ar,9bs,11ar)-2-(acetyloxy)-5-hydroxy-3a,3b,6,9a-tetramethyl-4,7-dioxo-2h,3h,5h,5ah,6h,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-1-ylidene]-6-methylhept-5-enoic acid)