NP-MRD: Showing NP-Card for (1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate (NP0144384)

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Record Information

Version

2.0

Created at

2022-09-01 23:20:45 UTC

Updated at

2022-09-01 23:20:46 UTC

NP-MRD ID

NP0144384

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate

Description

[(1R,2S,4S,5S,6S,7R,8S,9S,12R)-4,5,12-tris(acetyloxy)-7,8-bis(benzoyloxy)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-6-yl]methyl benzoate belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. (1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate is found in Microtropis japonica. Based on a literature review very few articles have been published on [(1R,2S,4S,5S,6S,7R,8S,9S,12R)-4,5,12-tris(acetyloxy)-7,8-bis(benzoyloxy)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-6-yl]methyl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022201202D          

 55 60  0  0  1  0            999 V2000
    6.2915    1.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2964    1.3218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0717    2.1898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5913    0.5377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351    0.5561    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6653    1.4212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.1234    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6531    0.4578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934    0.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0348   -0.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4905    0.8110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0588   -0.8122    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4269   -1.5948    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4772   -1.7784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4351   -1.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0604   -1.3991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5639   -2.8887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -3.5886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5148   -4.3168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3393   -4.3452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7761   -3.6453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3884   -2.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2845   -1.6626    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3444   -2.5984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0633   -3.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5831   -4.2138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5634   -4.0541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3837   -3.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8700   -4.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5360   -5.3870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7157   -5.4749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2294   -4.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -0.9114    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5429   -1.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5084   -1.6030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4169   -1.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2587   -1.9022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5062   -0.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8999   -0.2023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0811    0.6025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8688    0.8480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4751    0.2886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2939   -0.5162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5838   -0.9369    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0525   -1.9004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7715   -2.5635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5937   -2.7928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0422   -3.3845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7368   -0.5133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9981   -1.2269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7723   -2.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5046   -2.8527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9571   -2.2107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 14 11  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 25 35  1  0  0  0  0
  9 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 40 45  1  0  0  0  0
 35 46  1  0  0  0  0
  5 46  1  0  0  0  0
 46 47  1  1  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
 14 51  1  0  0  0  0
  9 51  1  0  0  0  0
 51 52  1  6  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 53 55  2  0  0  0  0
M  END

     RDKit          3D

 99104  0  0  0  0  0  0  0  0999 V2000
    3.4704    4.8770   -2.0133 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4044    3.7182   -1.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4589    3.1214   -0.6923 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2146    3.2072   -0.5834 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0874    2.1278    0.2863 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4868    2.4802    1.5655 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1103    2.0439    1.8854 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1091    1.6938    3.3780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5994    1.0858    1.0249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8696    1.6729    0.7599 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8604    0.7900    0.9776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0256    0.8478    0.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4270    0.9459    2.3658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1906   -0.5986    0.9181 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8985   -0.8310   -0.5101 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0271   -2.2390   -0.7681 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9952   -2.7540   -1.6279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7545   -1.8901   -2.1656 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1340   -4.1715   -1.8961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1184   -4.5963   -2.7574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2878   -5.9526   -3.0451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4619   -6.8797   -2.4619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4776   -6.4613   -1.6013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3193   -5.1133   -1.3237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5207   -0.4065   -0.9873 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3237   -1.5252   -1.0756 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995   -2.1080   -2.2812 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2430   -1.5315   -3.3234 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5272   -3.2680   -2.4605 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8678   -3.6579   -3.7528 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175   -4.7501   -4.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0820   -5.5412   -3.0177 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7563   -5.1744   -1.7208 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9954   -4.0620   -1.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0011    0.8552   -0.3698 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4972    1.9865   -1.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1836    3.2743   -0.9292 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6091    4.3480   -1.7304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2688    4.1093   -2.7644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2812    5.6963   -1.3508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4262    6.0417   -0.2274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7256    7.3620    0.1041 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3071    8.3927   -0.7114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4043    8.0586   -1.8425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6944    6.7521   -2.1606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4746    0.8776   -0.3602 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1193   -0.2077    0.2913 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1391   -0.8542   -0.3597 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9077   -1.9841    0.2251 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4546   -0.4768   -1.5141 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9290   -0.1752    1.7093 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0218   -1.1995    1.6907 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2916   -1.8742    2.8695 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3092   -2.9873    2.9224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3392   -1.5317    3.9008 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4739    5.3014   -2.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2359    5.5983   -1.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1775    1.7986    0.4624 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1587    2.0215    2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6583    3.5840    1.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4809    3.0333    1.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8028    0.8990    3.6196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8653    1.6182    3.8282 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5726    2.6214    3.8501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8259    1.3323   -0.9359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4419   -0.1827   -0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8309    1.4402    0.5021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5398    1.1218    2.3295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0195    1.8207    2.9091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3079    0.0632    3.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7659   -1.3584    1.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6908   -0.3501   -1.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8000   -3.8974   -3.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0669   -6.2513   -3.7227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6305   -7.9255   -2.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8450   -7.2222   -1.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5216   -4.8409   -0.6334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7379   -0.1644   -2.0908 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5203   -3.0593   -4.6015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8711   -5.0350   -5.0775 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -6.3988   -3.2711 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1205   -5.7947   -0.9082 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7297   -3.7624   -0.4434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6005    1.9289   -1.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.8277   -2.3235 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7706    5.2880    0.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2821    7.5946    0.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5363    9.4269   -0.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7555    8.8294   -2.5155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2552    6.4771   -3.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8655    0.9263   -1.3938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3454   -2.6102   -0.5785 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3451   -2.6152    0.9080 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7716   -1.5542    0.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3395    0.0268    2.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0524   -3.5948    3.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3195   -2.5555    3.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2717   -3.5791    1.9909 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 46  1  0
 46 47  1  0
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 46 35  1  0
 35 36  1  6
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 37 38  1  0
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 41 42  1  0
 42 43  2  0
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 44 45  2  0
 35 25  1  0
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 27 29  1  0
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 33 34  2  0
 25 15  1  0
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 17 19  1  0
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 15 14  1  0
 14 51  1  0
 51 52  1  0
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 53 54  1  0
 53 55  2  0
 51  9  1  0
  9 10  1  6
 10 11  1  0
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  9  7  1  0
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 45 40  1  0
 34 29  1  0
 24 19  1  0
 11 14  1  0
  8 63  1  0
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  7 62  1  1
  6 60  1  0
  6 61  1  0
  5 59  1  1
  1 56  1  0
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  1 58  1  0
 46 92  1  6
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 49 94  1  0
 49 95  1  0
 36 85  1  0
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 41 87  1  0
 42 88  1  0
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 44 90  1  0
 45 91  1  0
 25 79  1  6
 30 80  1  0
 31 81  1  0
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 15 73  1  6
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 14 72  1  1
 51 96  1  1
 54 97  1  0
 54 98  1  0
 54 99  1  0
 12 66  1  0
 12 67  1  0
 12 68  1  0
 13 69  1  0
 13 70  1  0
 13 71  1  0
M  END


  Mrv1652309022201202D          

 55 60  0  0  1  0            999 V2000
    6.2915    1.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2964    1.3218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0717    2.1898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5913    0.5377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351    0.5561    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6653    1.4212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.1234    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6531    0.4578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934    0.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0348   -0.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4905    0.8110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0588   -0.8122    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4269   -1.5948    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4772   -1.7784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4351   -1.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0604   -1.3991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5639   -2.8887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -3.5886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5148   -4.3168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3393   -4.3452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7761   -3.6453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3884   -2.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2845   -1.6626    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3444   -2.5984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0633   -3.4739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5831   -4.2138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5634   -4.0541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3837   -3.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8700   -4.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5360   -5.3870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7157   -5.4749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2294   -4.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -0.9114    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5429   -1.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5084   -1.6030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4169   -1.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2587   -1.9022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5062   -0.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8999   -0.2023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0811    0.6025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8688    0.8480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4751    0.2886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2939   -0.5162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5838   -0.9369    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0525   -1.9004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7715   -2.5635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5937   -2.7928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0422   -3.3845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7368   -0.5133    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9981   -1.2269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7723   -2.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5046   -2.8527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9571   -2.2107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 14 11  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 25 35  1  0  0  0  0
  9 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 40 45  1  0  0  0  0
 35 46  1  0  0  0  0
  5 46  1  0  0  0  0
 46 47  1  1  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
 14 51  1  0  0  0  0
  9 51  1  0  0  0  0
 51 52  1  6  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 53 55  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0144384

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@]2(COC(=O)C3=CC=CC=C3)[C@@H](OC(=O)C3=CC=CC=C3)[C@@H](OC(=O)C3=CC=CC=C3)[C@H]3[C@@H](OC(C)=O)[C@@]12OC3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C42H44O13/c1-24-22-31(50-25(2)43)34(51-26(3)44)41(23-49-37(46)28-16-10-7-11-17-28)36(54-39(48)30-20-14-9-15-21-30)33(53-38(47)29-18-12-8-13-19-29)32-35(52-27(4)45)42(24,41)55-40(32,5)6/h7-21,24,31-36H,22-23H2,1-6H3/t24-,31-,32-,33-,34+,35+,36-,41-,42-/m0/s1

> <INCHI_KEY>
BFFBXPBHYOLSOD-BEWIUAKOSA-N

> <FORMULA>
C42H44O13

> <MOLECULAR_WEIGHT>
756.801

> <EXACT_MASS>
756.278191477

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
76.88614015783494

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,4S,5S,6S,7R,8S,9S,12R)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-8-yl benzoate

> <ALOGPS_LOGP>
4.63

> <JCHEM_LOGP>
6.104538809666665

> <ALOGPS_LOGS>
-5.62

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.230592746161827

> <JCHEM_POLAR_SURFACE_AREA>
167.03

> <JCHEM_REFRACTIVITY>
191.87609999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.80e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4S,5S,6S,7R,8S,9S,12R)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-8-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      11.744   2.574   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.887   2.467   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.467   4.088   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.570   1.004   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.528  -0.443   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.832   0.943   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.292   1.038   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.975   2.653   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.358  -0.230   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.086   0.855   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.668   0.065   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.065  -0.107   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.916   1.514   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.976  -1.516   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.664  -2.977   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.891  -3.320   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.812  -3.693   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.979  -2.612   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.053  -5.392   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.237  -6.699   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.961  -8.058   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.500  -8.111   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.315  -6.804   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.592  -5.445   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.264  -3.104   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.376  -4.850   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.852  -6.485   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.955  -7.866   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.785  -7.568   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.316  -7.404   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.224  -8.648   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.601 -10.056   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.069 -10.220   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.162  -8.976   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.118  -1.701   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.613  -2.784   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       8.416  -2.992   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      10.112  -3.058   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      11.683  -3.551   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      10.278  -1.422   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.146  -0.378   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       9.485   1.125   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      10.955   1.583   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      12.087   0.539   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      11.749  -0.964   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       6.690  -1.749   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       7.565  -3.547   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       8.907  -4.785   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      10.442  -5.213   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       9.412  -6.318   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       3.242  -0.958   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       3.730  -2.290   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       3.308  -3.922   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       2.809  -5.325   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       1.786  -4.127   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   46                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   35   51                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15   51                                                  
CONECT   15   14   16   25                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   15   26   35                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   29                                                       
CONECT   35   25    9   36   46                                             
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   45                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   40                                                       
CONECT   46   35    5   47                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
CONECT   51   14    9   52                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  120    0
END

View in JSmol

Synonyms

Value	Source
[(1R,2S,4S,5S,6S,7R,8S,9S,12R)-4,5,12-Tris(acetyloxy)-7,8-bis(benzoyloxy)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0,]dodecan-6-yl]methyl benzoic acid	Generator

Chemical Formula

C₄₂H₄₄O₁₃

Average Mass

756.8010 Da

Monoisotopic Mass

756.27819 Da

IUPAC Name

(1R,2S,4S,5S,6S,7R,8S,9S,12R)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-8-yl benzoate

Traditional Name

(1R,2S,4S,5S,6S,7R,8S,9S,12R)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-8-yl benzoate

CAS Registry Number

Not Available

SMILES

C[C@H]1C[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@]2(COC(=O)C3=CC=CC=C3)[C@@H](OC(=O)C3=CC=CC=C3)[C@@H](OC(=O)C3=CC=CC=C3)[C@H]3[C@@H](OC(C)=O)[C@@]12OC3(C)C

InChI Identifier

InChI=1S/C42H44O13/c1-24-22-31(50-25(2)43)34(51-26(3)44)41(23-49-37(46)28-16-10-7-11-17-28)36(54-39(48)30-20-14-9-15-21-30)33(53-38(47)29-18-12-8-13-19-29)32-35(52-27(4)45)42(24,41)55-40(32,5)6/h7-21,24,31-36H,22-23H2,1-6H3/t24-,31-,32-,33-,34+,35+,36-,41-,42-/m0/s1

InChI Key

BFFBXPBHYOLSOD-BEWIUAKOSA-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
Microtropis japonica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
Sesquiterpenoid
Agarofuran
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Oxepane
Benzenoid
Monocyclic benzene moiety
Tetrahydrofuran
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	4.63	ALOGPS
logP	6.1	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	167.03 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	191.88 m³·mol⁻¹	ChemAxon
Polarizability	76.89 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	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

162982658

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,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate (NP0144384)

MOL for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

3D MOL for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

3D SDF for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

3D-SDF for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

PDB for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

3D PDB for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

SMILES for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

INCHI for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

Structure for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)

3D Structure for NP0144384 ((1r,2s,4s,5s,6s,7r,8s,9s,12r)-4,5,12-tris(acetyloxy)-7-(benzoyloxy)-6-[(benzoyloxy)methyl]-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl benzoate)