NP-MRD: Showing NP-Card for methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate (NP0330553)

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Record Information

Version

2.0

Created at

2022-09-12 16:00:46 UTC

Updated at

2022-09-12 16:00:46 UTC

NP-MRD ID

NP0330553

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate

Description

Methyl 2,6,6,10,11,15-hexamethyl-3,14-bis(prop-1-en-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-5-carboxylate belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate is found in Euphorbia drupifera. Methyl 2,6,6,10,11,15-hexamethyl-3,14-bis(prop-1-en-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecane-5-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171517512D          

 33 36  0  0  0  0            999 V2000
    7.5148   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7951    0.0722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5435    1.4789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0784   -1.1393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2663   -1.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6102   -1.7701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    1.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0307   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6113    1.4304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3705   -1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2424   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8025    2.0051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5311    1.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  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  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  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  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 16 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 13 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
M  END

     RDKit          3D

 83 86  0  0  0  0  0  0  0  0999 V2000
    1.5863    2.8125    1.8371 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6968    1.5072    1.9951 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5049    0.9619    3.3618 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0005    0.6620    0.8568 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6352    1.4410   -0.3106 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6631    0.5488   -1.0338 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0153    0.7673   -0.5420 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7250   -0.1067    0.0015 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6390    2.0294   -0.6501 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9540    2.2399   -0.1712 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1759   -0.8701   -1.0629 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3341   -1.2997   -2.5578 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9457   -1.8783   -0.3466 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6847   -0.8725   -0.9303 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0498   -2.1106   -1.4476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3971   -2.2660   -1.0832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0158   -0.8955   -0.9223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9226   -0.2324   -2.2411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3356   -0.2602    0.2513 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9452    1.0711    0.5071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3617    1.3014    0.2360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2049    0.2991   -0.4554 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7262    0.8750   -1.7310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4819   -0.1039    0.3358 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8587    0.9110    1.3109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8731    0.7010    2.5967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3318    2.2789    0.8726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2294   -1.4689    0.8580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7092   -1.4376    0.8911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4980   -1.0163   -0.5677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1985   -2.0054   -1.4349 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1204   -0.4213    0.4247 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4403   -1.6231    1.3644 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3599    3.4510    2.6827 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7114    3.3130    0.8618 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3313    1.7546    4.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5844    0.3441    3.3478 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3854    0.3887    3.7156 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9650    0.1607    1.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2651    2.2309    0.1706 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9180    1.9061   -0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6353    1.0068   -2.0777 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0825    1.5584    0.6979 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0717    3.2747    0.2405 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7132    1.9720   -0.9057 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6218   -0.7584   -3.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2280   -2.3855   -2.6479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3603   -0.9572   -2.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4434   -2.8651   -0.4701 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2489   -1.7287    0.6820 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9208   -2.0540   -0.9065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4162    0.0312   -1.5634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5637   -3.0187   -1.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2098   -2.0983   -2.5704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6155   -2.9475   -0.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8732   -2.7316   -1.9967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7318    0.8482   -2.2302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2655   -0.7809   -2.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8898   -0.3432   -2.8230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7531   -0.9145    1.0915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3090    1.8019   -0.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7689    1.2782    1.6038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4502    2.3036   -0.2721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9064    1.5057    1.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1580    0.1425   -2.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0532    1.6318   -2.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6307    1.5121   -1.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3610   -0.2078   -0.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1652    1.4984    3.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6005   -0.2214    3.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5907    2.9117    0.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7440    2.8250    1.7520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1969    2.1812    0.1699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6789   -1.6228    1.8462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6105   -2.2901    0.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6015   -0.5563    1.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2279   -2.3372    1.1811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2591   -1.7603   -1.6680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1930   -3.0223   -0.9942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7427   -2.1317   -2.4431 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5224   -1.6575    2.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2723   -1.4129    2.0313 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4650   -2.5674    0.8446 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  7  1  0
  7  8  2  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
  4 32  1  0
 32 33  1  1
 32 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  6
 24 25  1  0
 25 27  1  0
 25 26  2  3
 14 11  1  0
 11 12  1  0
 11 13  1  0
 11  6  1  0
 19 32  1  0
 30 22  1  0
 30 17  1  0
 10 43  1  0
 10 44  1  0
 10 45  1  0
  6 42  1  6
  5 40  1  0
  5 41  1  0
  4 39  1  1
  3 36  1  0
  3 37  1  0
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  1 34  1  0
  1 35  1  0
 33 81  1  0
 33 82  1  0
 33 83  1  0
 14 52  1  6
 15 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 18 57  1  0
 18 58  1  0
 18 59  1  0
 19 60  1  1
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 20 62  1  0
 21 63  1  0
 21 64  1  0
 23 65  1  0
 23 66  1  0
 23 67  1  0
 24 68  1  6
 28 74  1  0
 28 75  1  0
 29 76  1  0
 29 77  1  0
 31 78  1  0
 31 79  1  0
 31 80  1  0
 27 71  1  0
 27 72  1  0
 27 73  1  0
 26 69  1  0
 26 70  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
M  END


  Mrv1533004171517512D          

 33 36  0  0  0  0            999 V2000
    7.5148   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7951    0.0722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5435    1.4789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0784   -1.1393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2663   -1.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6102   -1.7701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    1.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0307   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6113    1.4304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3705   -1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2424   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8025    2.0051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5311    1.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  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  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  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  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 16 26  1  0  0  0  0
 21 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 13 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0330553

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1CC(C(C)=C)C2(C)C(CCC3(C)C2CCC2(C)C(CCC32C)C(C)=C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C31H50O2/c1-19(2)21-12-17-30(9)28(21,7)15-14-25-29(30,8)16-13-24-27(5,6)23(26(32)33-11)18-22(20(3)4)31(24,25)10/h21-25H,1,3,12-18H2,2,4-11H3

> <INCHI_KEY>
DLUHNQYRSRXMIN-UHFFFAOYSA-N

> <FORMULA>
C31H50O2

> <MOLECULAR_WEIGHT>
454.739

> <EXACT_MASS>
454.38108085

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
55.994097594781785

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2,6,6,10,11,15-hexamethyl-3,14-bis(prop-1-en-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5-carboxylate

> <ALOGPS_LOGP>
7.48

> <JCHEM_LOGP>
7.719007544000002

> <ALOGPS_LOGS>
-6.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.069168746858083

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
137.38049999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.23e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2,6,6,10,11,15-hexamethyl-3,14-bis(prop-1-en-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5-carboxylate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      14.028  -1.314   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      14.551   0.135   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      13.558   1.312   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      14.081   2.761   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      12.042   1.041   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.519  -0.407   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.003  -0.678   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.480  -2.127   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.964  -2.398   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.472  -3.304   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.010   0.499   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.487  -0.949   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.533   1.947   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.541   3.125   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.025   2.854   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.502   1.405   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.509   2.583   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.494   0.228   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.971  -1.221   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.455  -1.492   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.462  -0.314   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.791  -1.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.923  -0.264   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.495   1.215   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.770   2.079   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.986   1.134   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.874   2.670   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.978  -1.480   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.558  -2.907   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.452  -1.269   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.049   2.218   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.831   3.743   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.191   3.252   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12   13   18                                             
CONECT   12   11                                                            
CONECT   13   11   14   31                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   26                                             
CONECT   17   16                                                            
CONECT   18   16   11   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   26                                             
CONECT   22   21                                                            
CONECT   23   21   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   16   21   27                                             
CONECT   27   26                                                            
CONECT   28   23   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   13    5   32   33                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2,6,6,10,11,15-hexamethyl-3,14-bis(prop-1-en-2-yl)tetracyclo[8.7.0.0,.0,]heptadecane-5-carboxylic acid	Generator
Methyl 2,6,6,10,11,15-hexamethyl-3,14-bis(prop-1-en-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5-carboxylic acid	Generator

Chemical Formula

C₃₁H₅₀O₂

Average Mass

454.7390 Da

Monoisotopic Mass

454.38108 Da

IUPAC Name

methyl 2,6,6,10,11,15-hexamethyl-3,14-bis(prop-1-en-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5-carboxylate

Traditional Name

methyl 2,6,6,10,11,15-hexamethyl-3,14-bis(prop-1-en-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1CC(C(C)=C)C2(C)C(CCC3(C)C2CCC2(C)C(CCC32C)C(C)=C)C1(C)C

InChI Identifier

InChI=1S/C31H50O2/c1-19(2)21-12-17-30(9)28(21,7)15-14-25-29(30,8)16-13-24-27(5,6)23(26(32)33-11)18-22(20(3)4)31(24,25)10/h21-25H,1,3,12-18H2,2,4-11H3

InChI Key

DLUHNQYRSRXMIN-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
Euphorbia drupifera	LOTUS Database	35616633

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

Oxosteroid
17-oxosteroid
Pinguisane sesquiterpenoid
Sesquiterpenoid
Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoid
Methyl ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	7.48	ALOGPS
logP	7.72	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	137.38 m³·mol⁻¹	ChemAxon
Polarizability	55.99 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate (NP0330553)

MOL for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

3D MOL for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

3D SDF for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

3D-SDF for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

PDB for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

3D PDB for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

SMILES for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

INCHI for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

Structure for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)

3D Structure for NP0330553 (methyl 3a,3b,6,6,9a,11a-hexamethyl-1,9-bis(prop-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthrene-7-carboxylate)