NP-MRD: Showing NP-Card for 7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate (NP0226837)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 05:59:57 UTC

Updated at

2022-09-06 05:59:57 UTC

NP-MRD ID

NP0226837

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate

Description

7,12-Bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-5-yl benzoate belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene). 7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate is found in Orthosphenia mexicana and Rzedowskia tolantonguensis. 7,12-Bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-5-yl benzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231521532D          

 38 41  0  0  0  0            999 V2000
    3.8360    2.3248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0904    2.0582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9117    1.1389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3703    2.6311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6290    2.2237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881    1.5419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8298    1.5673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    0.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9060    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0812    0.0746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4054   -0.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5921   -0.6663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5808    0.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1007    0.1726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8607    0.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4547   -0.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6909    0.8749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6954    1.4426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3272    2.2252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5304    2.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4859    3.3177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0834    4.1794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9136    4.4482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0527    5.0538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0175    1.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1394    1.9384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3758    2.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1434    3.5614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2757    2.4649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5932    1.9927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0382    2.8677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9957    3.7607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8907    2.9455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2054    3.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0232    3.8171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5263    3.1633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2117    2.4006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3939    2.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
  6 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
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 18 25  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
  7 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
M  END

     RDKit          3D

 74 77  0  0  0  0  0  0  0  0999 V2000
   -1.2047    4.2599   -3.1063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0138    3.8685   -1.6918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1332    4.6811   -0.7324 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6947    2.5798   -1.3885 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4816    2.0421   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1352    0.5396   -0.1428 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1721    0.2475    1.3160 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7728    1.4086    1.8994 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9189    1.3396    2.6521 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5255    2.5728    3.2322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4937    0.2490    2.8786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0453    0.0047    2.1792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1483   -0.7542    1.5432 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5129   -1.4276    0.3146 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3770   -2.3950   -0.1353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0887   -3.7324   -0.2894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1541   -4.6317   -0.7902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9374   -4.1394   -0.0007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3919   -0.1805   -0.5621 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5305    0.5937   -0.2931 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1446    0.1499    0.8374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3419   -0.7187    0.4659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7030    1.2166    1.7409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5105   -0.5982   -1.9737 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0090    0.4179   -2.9506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4728   -1.6488   -2.0351 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2330   -1.2826   -2.3821 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8553   -0.2943   -2.3103 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0887    0.2806   -0.9309 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1755   -0.3393   -0.2885 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4434    0.1942   -0.1498 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850    1.3192   -0.6458 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5394   -0.5201    0.5325 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3481   -1.7643    1.0701 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4442   -2.3503    1.6909 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6714   -1.7449    1.7808 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8028   -0.4812    1.2153 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7509    0.1294    0.5964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9198    5.1053   -3.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2215    4.4902   -3.6050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6399    3.4213   -3.7025 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3473    2.6174    0.3372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3662    2.2703    0.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8722   -0.5836    1.4804 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6808    2.4448    4.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5299    2.7229    2.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8693    3.4590    3.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3975    0.9370    2.6570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6872   -0.6165    3.0549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6299   -1.5161    2.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4928   -1.7889    0.5627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1132   -4.3052   -0.3056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3244   -4.5270   -1.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0002   -5.6924   -0.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2936   -0.2990    0.9268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5585   -0.7601   -0.5973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2817   -1.7363    0.9423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2622    0.6993    2.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4778    1.7552    1.1194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0257    1.9647    2.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6710   -0.1152   -3.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6986    1.1012   -2.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2423    1.0074   -3.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8607   -1.7050   -2.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1223   -2.1751   -1.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2844   -1.6619   -3.4322 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8232   -0.7627   -2.6414 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6517    0.4840   -3.0676 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5342    1.2933   -1.1966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3909   -2.2461    1.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3516   -3.3383    2.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5324   -2.1822    2.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7561    0.0333    1.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9081    1.1136    0.1729 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  1
  6 29  1  0
 29 28  1  0
 28 27  1  0
 27 24  1  0
 24 25  1  0
 24 26  1  1
 24 19  1  0
 19 20  1  1
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21 13  1  0
 13 12  1  0
 12  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 29 30  1  0
 30 31  1  0
 31 32  2  0
 31 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  2  0
 19  6  1  0
 14 19  1  0
 38 33  1  0
  7  6  1  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  5 42  1  0
  5 43  1  0
 29 69  1  6
 28 67  1  0
 28 68  1  0
 27 65  1  0
 27 66  1  0
 25 61  1  0
 25 62  1  0
 25 63  1  0
 26 64  1  0
 22 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  0
 23 59  1  0
 23 60  1  0
 13 50  1  1
 12 48  1  0
 12 49  1  0
  7 44  1  6
 10 45  1  0
 10 46  1  0
 10 47  1  0
 14 51  1  1
 17 52  1  0
 17 53  1  0
 17 54  1  0
 34 70  1  0
 35 71  1  0
 36 72  1  0
 37 73  1  0
 38 74  1  0
M  END


  Mrv1533004231521532D          

 38 41  0  0  0  0            999 V2000
    3.8360    2.3248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0904    2.0582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9117    1.1389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3703    2.6311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6290    2.2237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881    1.5419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8298    1.5673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    0.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9060    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0812    0.0746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4054   -0.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5921   -0.6663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5808    0.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1007    0.1726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8607    0.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4547   -0.0477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6909    0.8749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6954    1.4426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3272    2.2252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5304    2.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4859    3.3177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0834    4.1794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9136    4.4482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0527    5.0538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0175    1.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1394    1.9384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3758    2.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1434    3.5614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2757    2.4649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5932    1.9927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0382    2.8677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9957    3.7607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8907    2.9455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2054    3.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0232    3.8171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5263    3.1633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2117    2.4006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3939    2.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
  6 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
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 18 25  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
  7 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0226837

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC12C(CCC(C)(O)C11OC(C)(C)C(CC2OC(C)=O)C1OC(C)=O)OC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H36O10/c1-16(29)34-15-27-21(37-24(32)19-10-8-7-9-11-19)12-13-26(6,33)28(27)23(36-18(3)31)20(25(4,5)38-28)14-22(27)35-17(2)30/h7-11,20-23,33H,12-15H2,1-6H3

> <INCHI_KEY>
AJNVKAMSVDVVDH-UHFFFAOYSA-N

> <FORMULA>
C28H36O10

> <MOLECULAR_WEIGHT>
532.586

> <EXACT_MASS>
532.230847359

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
54.46006656446288

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate

> <ALOGPS_LOGP>
2.83

> <JCHEM_LOGP>
1.8433674103333337

> <ALOGPS_LOGS>
-4.36

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.754781679288836

> <JCHEM_PKA_STRONGEST_BASIC>
-3.343458493479063

> <JCHEM_POLAR_SURFACE_AREA>
134.66000000000003

> <JCHEM_REFRACTIVITY>
131.398

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.35e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       7.161   4.340   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.769   3.842   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.435   2.126   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       4.424   4.911   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.041   4.151   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.844   2.878   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.416   2.926   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.254   1.619   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.558   0.233   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.018   0.139   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.623  -1.413   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.105  -1.244   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.084   1.407   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.188   0.322   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.607   1.111   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.715  -0.089   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.156   1.633   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.298   2.693   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.611   4.154   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.990   4.280   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.907   6.193   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.156   7.802   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.705   8.303   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.098   9.434   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.033   2.135   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.260   3.618   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.702   5.111   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.268   6.648   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -2.381   4.601   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.841   3.720   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.671   5.353   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.592   7.020   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       7.263   5.498   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.850   6.922   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.377   7.125   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.316   5.905   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.729   4.481   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.202   4.278   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   13   20                                             
CONECT    7    6    8   30                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10    6   14   25                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19   25                                                  
CONECT   19   18   20                                                       
CONECT   20   19    6   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   18   13   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30    7   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   33                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Value	Source
7,12-Bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0,]dodecan-5-yl benzoic acid	Generator
7,12-Bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoic acid	Generator

Chemical Formula

C₂₈H₃₆O₁₀

Average Mass

532.5860 Da

Monoisotopic Mass

532.23085 Da

IUPAC Name

7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate

Traditional Name

7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC12C(CCC(C)(O)C11OC(C)(C)C(CC2OC(C)=O)C1OC(C)=O)OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C28H36O10/c1-16(29)34-15-27-21(37-24(32)19-10-8-7-9-11-19)12-13-26(6,33)28(27)23(36-18(3)31)20(25(4,5)38-28)14-22(27)35-17(2)30/h7-11,20-23,33H,12-15H2,1-6H3

InChI Key

AJNVKAMSVDVVDH-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
Orthosphenia mexicana	LOTUS Database	35616633
Rzedowskia tolantonguensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Agarofurans

Alternative Parents

Substituents

Agarofuran
Tetracarboxylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Oxepane
Monocyclic benzene moiety
Benzenoid
Tertiary alcohol
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.83	ALOGPS
logP	1.84	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	13.75	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	134.66 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	131.4 m³·mol⁻¹	ChemAxon
Polarizability	54.46 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

13995952

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate (NP0226837)

MOL for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

3D MOL for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

3D SDF for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

3D-SDF for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

PDB for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

3D PDB for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

SMILES for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

INCHI for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

Structure for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)

3D Structure for NP0226837 (7,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl benzoate)