NP-MRD: Showing NP-Card for (1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid (NP0314325)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 12:22:00 UTC

Updated at

2022-09-11 12:22:00 UTC

NP-MRD ID

NP0314325

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid

Description

(1R,2S,4S,5R,9S,10S,12S,14R)-14-(acetyloxy)-5,9-dimethyl-2-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]Hexadecane-5-carboxylic acid belongs to the class of organic compounds known as atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12. Based on a literature review very few articles have been published on (1R,2S,4S,5R,9S,10S,12S,14R)-14-(acetyloxy)-5,9-dimethyl-2-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]Hexadecane-5-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112214222D          

 33 36  0  0  1  0            999 V2000
   -1.1601    0.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3438    0.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3340    0.9474    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6176    0.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4032   -0.7550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1032   -0.4486    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6689   -1.1367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2184   -1.8279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5918   -2.5636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1414   -3.2548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4156   -2.6081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8660   -1.9169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7890   -3.3438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3385   -4.0349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -1.3653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9240   -0.6486    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5811    0.1017    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2412    0.8535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0595    0.7739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8808    0.6956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2236   -0.0547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7453   -0.7269    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6957   -1.5504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4003   -1.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2935   -2.0465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1622   -0.9119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7076    0.1920    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1816    0.8931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1640   -0.2063    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2916   -0.8941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1150   -0.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4829   -0.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5706   -1.5314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
  7 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 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
 16 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 17 27  1  0  0  0  0
  6 27  1  0  0  0  0
 27 28  1  1  0  0  0
  3 28  1  0  0  0  0
  6 29  1  0  0  0  0
  2 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
M  END

     RDKit          3D

 71 74  0  0  0  0  0  0  0  0999 V2000
    2.5322   -3.3480   -1.7959 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4966   -2.9995   -1.0799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1487   -3.5911   -1.0921 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2133   -3.8810    0.3472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1658   -2.6698    1.2024 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2935   -1.4606    0.3481 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3415   -0.3000    1.2600 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0769    0.8268    0.8294 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0755    1.3922    1.6065 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2661    0.8152    2.7207 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8440    2.5310    1.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9396    3.0754    2.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6681    3.1555    0.0742 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6496    2.7502   -0.8903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0660    0.2531    1.5595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6717    0.6223    0.2558 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9073   -0.5694   -0.5874 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9885   -1.4829   -0.0976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3275   -0.0865   -1.9749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3531    0.9818   -1.9901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8835    1.4215   -0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8425    1.5599    0.3844 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3579    3.0191    0.3586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4818    1.3780    1.7068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6975    0.9649    1.7683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9021    1.6103    2.9277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5917   -1.2765   -0.8403 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7476   -2.5040   -1.6659 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6709   -1.8458   -0.0964 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4483   -0.8481   -0.6921 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7930   -0.6635   -0.3040 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6449    0.3857   -0.9157 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2504   -1.4160    0.5786 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4927   -2.8574   -1.7277 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4465   -4.1767   -2.4857 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0779   -4.5256   -1.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5551   -4.6353    0.6942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1795   -4.4391    0.4213 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6278   -2.7750    1.9738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0964   -2.4395    1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7331   -0.6305    2.2676 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5941    3.9680    2.6449 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2965    2.2564    2.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8183    3.3517    1.4834 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2954    4.0257   -0.1965 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6472    3.0269   -0.4440 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6901    3.4061   -1.8086 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6571    1.7099   -1.2070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8454    1.2123    2.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6447   -0.3876    2.2110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8843    1.2248   -0.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9258   -1.4106   -0.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7378   -2.5468   -0.0545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2997   -1.2352    0.9616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7684   -0.9689   -2.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4226    0.1866   -2.5734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8831    1.8723   -2.5152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2181    0.7393   -2.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7643    0.7992   -0.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3541    2.4291   -0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4998    3.1700    1.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1902    3.7106    0.5495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9801    3.2741   -0.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0483    1.0933    3.7659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0202   -0.5391   -1.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3707   -2.3701   -2.7252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7590   -2.9010   -1.7853 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2740   -2.3494    0.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5834   -0.0981   -1.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0227    1.1133   -0.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1391    0.9157   -1.7285 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 11  2  0
 11 12  1  0
 11  9  1  0
  9 10  2  0
  9  8  1  0
  8  7  1  0
  7 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  1
 24 26  1  0
 24 25  2  0
 17 27  1  0
 27 28  1  0
 28  3  1  0
  3  4  1  0
  4  5  1  0
  6  5  1  1
  6 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 31 33  2  0
 29  2  1  0
  2  1  2  3
  6  7  1  0
 22 16  1  0
  6 27  1  0
  2  3  1  0
 14 46  1  0
 14 47  1  0
 14 48  1  0
 13 45  1  0
 12 42  1  0
 12 43  1  0
 12 44  1  0
  7 41  1  1
 15 49  1  0
 15 50  1  0
 16 51  1  6
 18 52  1  0
 18 53  1  0
 18 54  1  0
 19 55  1  0
 19 56  1  0
 20 57  1  0
 20 58  1  0
 21 59  1  0
 21 60  1  0
 23 61  1  0
 23 62  1  0
 23 63  1  0
 26 64  1  0
 27 65  1  6
 28 66  1  0
 28 67  1  0
  3 36  1  6
  4 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
 29 68  1  1
 32 69  1  0
 32 70  1  0
 32 71  1  0
  1 34  1  0
  1 35  1  0
M  END


  Mrv1652309112214222D          

 33 36  0  0  1  0            999 V2000
   -1.1601    0.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3438    0.4570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3340    0.9474    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6176    0.1465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4032   -0.7550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1032   -0.4486    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6689   -1.1367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2184   -1.8279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5918   -2.5636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1414   -3.2548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4156   -2.6081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8660   -1.9169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7890   -3.3438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3385   -4.0349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4870   -1.3653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9240   -0.6486    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5811    0.1017    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2412    0.8535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0595    0.7739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8808    0.6956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2236   -0.0547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7453   -0.7269    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6957   -1.5504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4003   -1.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2935   -2.0465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1622   -0.9119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7076    0.1920    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1816    0.8931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1640   -0.2063    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2916   -0.8941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1150   -0.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4829   -0.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5706   -1.5314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
  7 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 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
 16 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 17 27  1  0  0  0  0
  6 27  1  0  0  0  0
 27 28  1  1  0  0  0
  3 28  1  0  0  0  0
  6 29  1  0  0  0  0
  2 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0314325

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@H]1C[C@H]2[C@@](C)(CCC[C@@]2(C)C(O)=O)[C@@H]2C[C@@H]3CC[C@]12[C@H](OC(C)=O)C3=C

> <INCHI_IDENTIFIER>
InChI=1S/C27H38O6/c1-7-15(2)23(29)33-21-14-19-25(5,10-8-11-26(19,6)24(30)31)20-13-18-9-12-27(20,21)22(16(18)3)32-17(4)28/h7,18-22H,3,8-14H2,1-2,4-6H3,(H,30,31)/b15-7-/t18-,19-,20-,21-,22+,25+,26+,27+/m0/s1

> <INCHI_KEY>
OVQZREXPGSSAST-IWXRWPOCSA-N

> <FORMULA>
C27H38O6

> <MOLECULAR_WEIGHT>
458.595

> <EXACT_MASS>
458.266838944

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
49.884189358939274

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,4S,5R,9S,10S,12S,14R)-14-(acetyloxy)-5,9-dimethyl-2-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0^{1,10}.0^{4,9}]hexadecane-5-carboxylic acid

> <JCHEM_LOGP>
5.156178735333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.257041120573369

> <JCHEM_PKA_STRONGEST_BASIC>
-6.624633680219053

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
123.22189999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4S,5R,9S,10S,12S,14R)-14-(acetyloxy)-5,9-dimethyl-2-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0^{1,10}.0^{4,9}]hexadecane-5-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

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      -2.165   1.076   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.642   0.853   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.623   1.769   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.153   0.274   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.753  -1.409   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.059  -0.837   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.115  -2.122   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.274  -3.412   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.971  -4.785   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.131  -6.076   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.509  -4.868   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.350  -3.578   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.206  -6.242   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.365  -7.532   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.642  -2.549   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.458  -1.211   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.818   0.190   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.184   1.593   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.711   1.445   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.244   1.299   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.884  -0.102   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.991  -1.357   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.899  -2.894   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.214  -2.293   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.014  -3.820   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       9.636  -1.702   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.187   0.358   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.206   1.667   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.306  -0.385   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.544  -1.669   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -2.081  -1.575   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.768  -0.196   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -2.932  -2.859   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   27   29                                             
CONECT    7    6    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15    7   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18   19   27                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   17    6   28                                                  
CONECT   28   27    3                                                       
CONECT   29    6    2   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   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
(1R,2S,4S,5R,9S,10S,12S,14R)-14-(Acetyloxy)-5,9-dimethyl-2-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0,.0,]hexadecane-5-carboxylate	Generator

Chemical Formula

C₂₇H₃₈O₆

Average Mass

458.5950 Da

Monoisotopic Mass

458.26684 Da

IUPAC Name

(1R,2S,4S,5R,9S,10S,12S,14R)-14-(acetyloxy)-5,9-dimethyl-2-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0^{1,10}.0^{4,9}]hexadecane-5-carboxylic acid

Traditional Name

(1R,2S,4S,5R,9S,10S,12S,14R)-14-(acetyloxy)-5,9-dimethyl-2-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0^{1,10}.0^{4,9}]hexadecane-5-carboxylic acid

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@H]1C[C@H]2[C@@](C)(CCC[C@@]2(C)C(O)=O)[C@@H]2C[C@@H]3CC[C@]12[C@H](OC(C)=O)C3=C

InChI Identifier

InChI=1S/C27H38O6/c1-7-15(2)23(29)33-21-14-19-25(5,10-8-11-26(19,6)24(30)31)20-13-18-9-12-27(20,21)22(16(18)3)32-17(4)28/h7,18-22H,3,8-14H2,1-2,4-6H3,(H,30,31)/b15-7-/t18-,19-,20-,21-,22+,25+,26+,27+/m0/s1

InChI Key

OVQZREXPGSSAST-IWXRWPOCSA-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 atisane diterpenoids. These are diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Atisane diterpenoids

Alternative Parents

Substituents

Atisane diterpenoid
Tricarboxylic acid or derivatives
Alkaloid or derivatives
Fatty acid ester
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
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	5.16	ChemAxon
pKa (Strongest Acidic)	4.26	ChemAxon
pKa (Strongest Basic)	-6.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	123.22 m³·mol⁻¹	ChemAxon
Polarizability	49.88 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

162857743

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid (NP0314325)

MOL for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D MOL for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D SDF for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D-SDF for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

PDB for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D PDB for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

SMILES for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

INCHI for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

Structure for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)

3D Structure for NP0314325 ((1r,2s,4s,5r,9s,10s,12s,14r)-14-(acetyloxy)-5,9-dimethyl-2-{[(2z)-2-methylbut-2-enoyl]oxy}-13-methylidenetetracyclo[10.2.2.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylic acid)