NP-MRD: Showing NP-Card for (1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate (NP0310111)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 05:11:10 UTC

Updated at

2022-09-11 05:11:10 UTC

NP-MRD ID

NP0310111

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate

Description

24Beta-Methylcycloarta-25-ene-3beta-ol formate belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. (1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate is found in Tillandsia fasciculata. Based on a literature review very few articles have been published on 24beta-Methylcycloarta-25-ene-3beta-ol formate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112207112D          

 34 38  0  0  1  0            999 V2000
    9.4728    3.8195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6555    3.9323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3446    4.6965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1492    3.2810    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4601    2.5168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319    3.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8256    2.7425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0083    2.8554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6974    3.6196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5020    2.2041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7313    1.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971    1.4549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1995    0.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850    1.3097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3047    0.5338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926    0.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608    1.0193    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1486    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4327    0.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4352    0.4599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6168    1.5048    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1953    1.3596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7271    1.9903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5392    1.8451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    2.2807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092    2.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2411    1.7952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5214    2.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0532    1.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3335    2.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456    2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774    2.2309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0373    2.9732    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
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
 10  8  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  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  1  6  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  1  1  0  0  0
 30 29  1  1  0  0  0
 15 30  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 10 33  1  0  0  0  0
 13 33  1  0  0  0  0
 33 34  1  1  0  0  0
M  END

     RDKit          3D

 86 90  0  0  0  0  0  0  0  0999 V2000
   -6.7446    2.8677    3.9640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4538    3.1461    2.6999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1167    4.3140    2.0745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4843    2.2939    1.9769 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1806    1.6589    0.7967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9451    1.2472    2.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9356    0.3221    2.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7256    1.0781    1.7326 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0192    1.8294    2.8087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8122    0.0118    1.1677 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5849   -0.7750    0.0826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5945   -1.0779   -1.0144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2847   -0.7342   -0.3813 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0723   -1.7958    0.6029 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8241   -0.4972   -1.3644 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9418   -1.7285   -2.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2959   -1.8707   -2.8628 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3086   -1.9576   -1.7574 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6510   -2.3596   -2.2873 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9766   -3.7667   -1.8317 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6917   -2.3824   -3.8135 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7800   -1.4711   -1.8463 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9171   -0.3518   -2.6989 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0472   -0.1515   -3.4736 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9647   -1.0237   -3.3863 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7274   -1.0212   -0.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3384   -0.8024    0.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3159   -0.6779   -1.0071 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0703    0.6300   -1.5733 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0391   -0.0946   -0.6429 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8701    0.4601    0.7127 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5399    0.9748    1.1086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6493    0.5345    0.3615 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2162    1.5873   -0.5641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4585    3.4782    4.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3407    2.0370    4.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4240    5.1801    2.1863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0833    4.4750    2.6031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2933    4.1654    0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6614    2.9202    1.5282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8487    0.8225    1.1117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4188    1.2514    0.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7908    2.3797    0.2237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5197    1.6839    3.8401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7869    0.6022    3.2168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6570   -0.4391    3.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4513   -0.1784    1.4147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0792    1.7822    0.9745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5025    1.1594    3.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7136    2.4847    3.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3032    2.5345    2.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5055   -0.6116    1.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0100   -1.6970    0.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4120   -0.2007   -0.3302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6180   -2.1835   -1.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8014   -0.5302   -1.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0003   -2.3508    0.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7165   -2.6063    0.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2165   -1.4780    1.6386 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5370    0.3114   -2.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7447   -2.6606   -1.6492 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1897   -1.7214   -3.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2557   -2.8339   -3.4407 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4866   -1.0794   -3.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9256   -2.7507   -1.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0633   -3.8549   -1.5679 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3263   -4.0966   -0.9767 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8236   -4.4983   -2.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4253   -1.3907   -4.2332 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7676   -2.5456   -4.0855 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1208   -3.2086   -4.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7183   -2.0733   -1.9578 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1586    0.7096   -4.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2481   -1.7287    0.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3240   -0.0686   -0.3506 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0266   -1.6573    0.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3444    0.1334    0.7079 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7651    0.8742   -2.5833 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5920    1.4975   -1.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2385   -0.2836    1.4486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6135    1.3068    0.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5460    2.1101    1.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3800    0.7860    2.1847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3458    2.5297    0.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5565    1.8587   -1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643    1.2384   -1.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  4  1  0
  4  5  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 28  1  0
 28 29  1  6
 30 29  1  6
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  6
 28 27  1  0
 27 26  1  0
 26 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 22 19  1  0
 19 20  1  0
 19 21  1  0
 33 10  1  0
 33 13  1  0
 30 15  1  0
 19 18  1  0
 30 28  1  0
  9 49  1  0
  9 50  1  0
  9 51  1  0
  8 48  1  6
  7 46  1  0
  7 47  1  0
  6 44  1  0
  6 45  1  0
  4 40  1  6
  5 41  1  0
  5 42  1  0
  5 43  1  0
  3 37  1  0
  3 38  1  0
  3 39  1  0
  1 35  1  0
  1 36  1  0
 10 52  1  1
 11 53  1  0
 11 54  1  0
 12 55  1  0
 12 56  1  0
 14 57  1  0
 14 58  1  0
 14 59  1  0
 15 60  1  6
 16 61  1  0
 16 62  1  0
 17 63  1  0
 17 64  1  0
 18 65  1  1
 29 78  1  0
 29 79  1  0
 31 80  1  0
 31 81  1  0
 32 82  1  0
 32 83  1  0
 34 84  1  0
 34 85  1  0
 34 86  1  0
 27 76  1  0
 27 77  1  0
 26 74  1  0
 26 75  1  0
 22 72  1  1
 24 73  1  0
 20 66  1  0
 20 67  1  0
 20 68  1  0
 21 69  1  0
 21 70  1  0
 21 71  1  0
M  END


  Mrv1652309112207112D          

 34 38  0  0  1  0            999 V2000
    9.4728    3.8195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6555    3.9323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3446    4.6965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1492    3.2810    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4601    2.5168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319    3.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8256    2.7425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0083    2.8554    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6974    3.6196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5020    2.2041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7313    1.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971    1.4549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1995    0.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850    1.3097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3047    0.5338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926    0.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608    1.0193    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1486    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4327    0.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4352    0.4599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6168    1.5048    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1953    1.3596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7271    1.9903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5392    1.8451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    2.2807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092    2.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2411    1.7952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5214    2.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0532    1.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3335    2.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456    2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774    2.2309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0373    2.9732    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
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
 10  8  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  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  1  6  0  0  0
 16 17  1  0  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  1  1  0  0  0
 30 29  1  1  0  0  0
 15 30  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 10 33  1  0  0  0  0
 13 33  1  0  0  0  0
 33 34  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0310111

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CC[C@@H](C)C(C)=C)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@@H]4[C@]5(C[C@@]35CC[C@]12C)CC[C@H](OC=O)C4(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C32H52O2/c1-21(2)22(3)9-10-23(4)24-13-15-30(8)26-12-11-25-28(5,6)27(34-20-33)14-16-31(25)19-32(26,31)18-17-29(24,30)7/h20,22-27H,1,9-19H2,2-8H3/t22-,23-,24-,25+,26+,27+,29-,30+,31-,32+/m1/s1

> <INCHI_KEY>
FEOYVNADIQNWQG-JWOVXNMDSA-N

> <FORMULA>
C32H52O2

> <MOLECULAR_WEIGHT>
468.766

> <EXACT_MASS>
468.396730914

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
58.87868801599411

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-yl formate

> <JCHEM_LOGP>
8.285041848333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.826385983627846

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
140.17029999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-yl formate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      17.683   7.130   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.157   7.340   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.577   8.767   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.212   6.125   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.792   4.698   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.686   6.335   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.741   5.119   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.216   5.330   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.635   6.757   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.270   4.114   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.698   2.635   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.424   1.771   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.208   2.716   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.839   1.221   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.692   2.445   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.169   0.996   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.653   0.725   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.660   1.903   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.144   1.632   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.674   0.186   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.812   0.858   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.151   2.809   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.365   2.538   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -1.357   3.715   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.873   3.444   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.675   4.257   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.191   4.528   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.183   3.351   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.707   4.799   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.699   3.622   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.222   5.071   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.738   5.342   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.731   4.164   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.403   5.550   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   33                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   33                                             
CONECT   14   13                                                            
CONECT   15   13   16   30                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   28                                                  
CONECT   19   18   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   22   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   18   29   30                                             
CONECT   29   28   30                                                       
CONECT   30   29   15   28   31                                             
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   10   13   34                                             
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Value	Source
24b-Methylcycloarta-25-ene-3b-ol formate	Generator
24b-Methylcycloarta-25-ene-3b-ol formic acid	Generator
24beta-Methylcycloarta-25-ene-3beta-ol formic acid	Generator
24Β-methylcycloarta-25-ene-3β-ol formate	Generator
24Β-methylcycloarta-25-ene-3β-ol formic acid	Generator

Chemical Formula

C₃₂H₅₂O₂

Average Mass

468.7660 Da

Monoisotopic Mass

468.39673 Da

IUPAC Name

(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-yl formate

Traditional Name

(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-yl formate

CAS Registry Number

Not Available

SMILES

C[C@H](CC[C@@H](C)C(C)=C)[C@H]1CC[C@@]2(C)[C@@H]3CC[C@@H]4[C@]5(C[C@@]35CC[C@]12C)CC[C@H](OC=O)C4(C)C

InChI Identifier

InChI=1S/C32H52O2/c1-21(2)22(3)9-10-23(4)24-13-15-30(8)26-12-11-25-28(5,6)27(34-20-33)14-16-31(25)19-32(26,31)18-17-29(24,30)7/h20,22-27H,1,9-19H2,2-8H3/t22-,23-,24-,25+,26+,27+,29-,30+,31-,32+/m1/s1

InChI Key

FEOYVNADIQNWQG-JWOVXNMDSA-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
Tillandsia fasciculata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cycloartanols and derivatives

Direct Parent

Cycloartanols and derivatives

Alternative Parents

Substituents

Cycloartanol-skeleton
Triterpenoid
Cycloartane-skeleton
9b,19-cyclo-lanostane-skeleton
Steroid 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	8.29	ChemAxon
pKa (Strongest Basic)	-6.8	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	7	ChemAxon
Refractivity	140.17 m³·mol⁻¹	ChemAxon
Polarizability	58.88 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

101130233

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate (NP0310111)

MOL for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

3D MOL for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

3D SDF for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

3D-SDF for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

PDB for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

3D PDB for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

SMILES for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

INCHI for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

Structure for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)

3D Structure for NP0310111 ((1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r,5r)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl formate)