NP-MRD: Showing NP-Card for 4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate (NP0316330)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 15:27:27 UTC

Updated at

2022-09-11 15:27:28 UTC

NP-MRD ID

NP0316330

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate

Description

4,5,12-Tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl furan-3-carboxylate belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. 4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate is found in Celastrus angulatus. 4,5,12-Tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl furan-3-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191522002D          

 50 53  0  0  0  0            999 V2000
    4.2399   -1.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9282   -1.6515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8220   -1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6535   -2.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5999   -1.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2697   -0.2982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5437   -1.3367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4955   -1.6515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3965   -2.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1336   -1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3959   -0.6913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6563   -0.1429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8736   -0.4817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4867    0.7236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6774   -0.8008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4952   -0.9482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7773   -1.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4754   -1.1703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6343   -1.9627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2675   -2.3973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0182   -2.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8282   -3.7347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6654   -4.0224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9372   -4.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9688   -3.8164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1139   -3.6851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2228   -4.6802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4700   -5.5984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1290   -6.1534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9451   -6.3547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0425   -7.2021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1081   -6.6109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8058   -2.8818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9261   -3.2285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3887   -4.0380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2655   -4.8846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6199   -3.9452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1205   -4.6019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3417   -4.3299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3597   -3.5051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1497   -3.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0631   -3.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2908   -3.0297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5886   -3.6016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5950   -4.4334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9234   -3.9969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8842    0.1022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3192    0.8848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0831    1.7167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1450    1.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 26 33  1  0  0  0  0
  9 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 37 41  1  0  0  0  0
 25 42  1  0  0  0  0
 20 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 15 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
M  END

     RDKit          3D

 98101  0  0  0  0  0  0  0  0999 V2000
    2.7670    5.6378    0.2672 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0967    4.2594    0.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9758    4.2057    1.2700 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0426    5.2701    0.9145 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4376    2.8781    1.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5821    2.3603    2.6497 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2324    2.0755    0.5606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6713    0.7783    1.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3716    0.0175   -0.0352 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6027    0.7753   -0.4423 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8938    1.7648    0.5728 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0596    3.0920    0.2914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3655    4.0726    1.3927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9441    3.4317   -0.9119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8637   -0.0431   -0.5004 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0497   -0.8267   -1.6193 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0372   -0.6728   -2.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1821   -1.5498   -3.7398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8561    0.2600   -2.4000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0748   -0.7809    0.7706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8635   -1.5595    1.2097 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5585   -1.1577    2.6473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2910   -2.9074    1.3035 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6790   -1.4255    0.3204 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9577   -2.0926   -0.8873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9396   -2.9140   -1.2431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6520   -2.9292   -2.7429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1086   -4.3713   -0.8565 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2639   -2.3660   -0.4634 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6862   -1.0099   -0.9680 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4840   -0.4333    0.0169 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7827   -0.0215   -0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3299   -0.1711   -1.2322 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5239    0.5775    1.0497 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9060    0.9979    0.6748 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6503   -0.4275    2.1819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4965   -0.1388   -1.2665 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2289    1.0186   -1.9781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7740    1.2879   -3.2487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5478    0.3744   -3.7053 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5305    2.4655   -4.0294 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2807    3.5460   -3.7807 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1486    4.3823   -4.8658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7035    3.8245   -5.7228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1304    2.6951   -5.2752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4980   -2.1216    0.8538 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9174   -3.3342    1.4329 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5173   -3.7978    2.6594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0329   -5.0844    3.1497 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2736   -3.1305    3.3439 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4802    6.2369   -0.6355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6100    6.1565    1.2160 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8886    5.5351    0.1521 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8941    3.5398    0.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6908    4.0930   -0.7624 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4533    4.5838    2.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5302    6.1090    0.4088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8481    4.9201    0.2675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4137    5.7510    1.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0966    0.3467    1.6066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4801    1.0795    1.7640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5390    1.3371   -1.3728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4590    4.0596    1.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1095    5.1071    1.1055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8938    3.7710    2.3473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7030    0.7383   -0.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5873   -0.9961   -4.6115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8585   -2.3759   -3.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1681   -1.9573   -3.9891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4581   -0.1264    1.5977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9622   -1.4626    0.5814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9394   -1.9224    3.3845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000   -1.0389    2.8621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0896   -0.2243    2.9369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7367   -3.0859    2.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5688   -2.6485   -3.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4082   -3.9522   -3.1129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2181   -2.3075   -3.0241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0434   -4.6224   -0.3721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1989   -4.7175   -0.2822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0751   -5.0537   -1.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0715   -3.0749   -0.3581 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3103   -1.0719   -1.8860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9314    1.4120    1.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0421    2.0853    0.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1587    0.7405   -0.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6991    0.4948    1.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6868   -0.4954    2.7063 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0511   -1.3960    1.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4118   -0.0120    2.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2255   -0.7149   -1.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8796    3.6782   -2.9140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6585    5.3164   -4.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8365    2.0455   -5.7921 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1725   -1.6444    1.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9191   -5.8301    2.3475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1430   -5.0139    3.3444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5791   -5.3989    4.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  9  8  1  1
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 10 15  1  0
 15 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  1
 21 24  1  0
 24 25  1  6
 25 26  1  0
 26 27  1  0
 26 28  1  0
 26 29  1  0
 29 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 48 50  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  2  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 30 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  2  0
 39 41  1  0
 41 45  2  0
 45 44  1  0
 44 43  1  0
 43 42  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 24  9  1  0
 46 24  1  0
 42 41  1  0
 37  9  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  2 54  1  0
  2 55  1  0
  3 56  1  1
  4 57  1  0
  4 58  1  0
  4 59  1  0
  8 60  1  0
  8 61  1  0
 10 62  1  6
 13 63  1  0
 13 64  1  0
 13 65  1  0
 15 66  1  6
 20 70  1  0
 20 71  1  0
 22 72  1  0
 22 73  1  0
 22 74  1  0
 23 75  1  0
 27 76  1  0
 27 77  1  0
 27 78  1  0
 28 79  1  0
 28 80  1  0
 28 81  1  0
 29 82  1  1
 46 95  1  1
 49 96  1  0
 49 97  1  0
 49 98  1  0
 30 83  1  6
 34 84  1  0
 35 85  1  0
 35 86  1  0
 35 87  1  0
 36 88  1  0
 36 89  1  0
 36 90  1  0
 37 91  1  6
 45 94  1  0
 43 93  1  0
 42 92  1  0
 18 67  1  0
 18 68  1  0
 18 69  1  0
M  END


  Mrv1533004191522002D          

 50 53  0  0  0  0            999 V2000
    4.2399   -1.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9282   -1.6515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8220   -1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6535   -2.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5999   -1.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2697   -0.2982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5437   -1.3367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4955   -1.6515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3965   -2.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1336   -1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3959   -0.6913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6563   -0.1429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8736   -0.4817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4867    0.7236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6774   -0.8008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4952   -0.9482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7773   -1.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4754   -1.1703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6343   -1.9627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2675   -2.3973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0182   -2.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8282   -3.7347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6654   -4.0224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9372   -4.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9688   -3.8164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1139   -3.6851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2228   -4.6802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4700   -5.5984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1290   -6.1534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9451   -6.3547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0425   -7.2021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1081   -6.6109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8058   -2.8818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9261   -3.2285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3887   -4.0380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2655   -4.8846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6199   -3.9452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1205   -4.6019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3417   -4.3299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3597   -3.5051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1497   -3.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0631   -3.0816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2908   -3.0297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5886   -3.6016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5950   -4.4334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9234   -3.9969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8842    0.1022    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3192    0.8848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0831    1.7167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1450    1.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 26 33  1  0  0  0  0
  9 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 37 41  1  0  0  0  0
 25 42  1  0  0  0  0
 20 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 15 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0316330

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)OCC12C(OC(C)=O)C(CC(C)(O)C11OC(C)(C)C(C1OC(C)=O)C(OC(=O)C(C)C)C2OC(=O)C1=COC=C1)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H48O15/c1-11-18(4)30(40)44-16-34-26(46-20(6)37)23(45-19(5)36)14-33(10,42)35(34)27(47-21(7)38)24(32(8,9)50-35)25(48-29(39)17(2)3)28(34)49-31(41)22-12-13-43-15-22/h12-13,15,17-18,23-28,42H,11,14,16H2,1-10H3

> <INCHI_KEY>
QDQMEZHVPUKELZ-UHFFFAOYSA-N

> <FORMULA>
C35H48O15

> <MOLECULAR_WEIGHT>
708.754

> <EXACT_MASS>
708.299320846

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
71.23884981681414

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate

> <ALOGPS_LOGP>
3.04

> <JCHEM_LOGP>
2.8359545980000007

> <ALOGPS_LOGS>
-3.72

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.668642508283767

> <JCHEM_PKA_STRONGEST_BASIC>
-3.05255608748

> <JCHEM_POLAR_SURFACE_AREA>
200.39999999999998

> <JCHEM_REFRACTIVITY>
167.53679999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.35e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       7.914  -2.091   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.199  -3.083   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.868  -3.267   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.553  -4.945   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.320  -2.270   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.703  -0.557   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      14.082  -2.495   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      15.858  -3.083   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.540  -4.163   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.049  -2.669   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      15.672  -1.290   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      14.292  -0.267   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.831  -0.899   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      13.975   1.351   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.064  -1.495   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      19.591  -1.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      20.118  -3.220   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      21.421  -2.185   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      21.717  -3.664   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      19.166  -4.475   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      20.567  -5.388   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      20.213  -6.972   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.775  -7.509   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      20.416  -8.595   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.608  -7.124   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      17.013  -6.879   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      17.216  -8.736   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      17.677 -10.450   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      18.907 -11.486   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      16.698 -11.862   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      16.879 -13.444   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      15.135 -12.340   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.437  -5.379   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      14.795  -6.027   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      13.792  -7.538   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      13.562  -9.118   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      12.357  -7.364   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.425  -8.590   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.971  -8.082   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      10.005  -6.543   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      11.479  -6.099   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      18.784  -5.752   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      17.343  -5.655   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      16.032  -6.723   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      16.044  -8.276   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      14.790  -7.461   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      18.450   0.191   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      19.263   1.652   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      18.822   3.204   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      20.804   2.092   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   20   33                                             
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   47                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17    9   21   42                                             
CONECT   21   20   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26   42                                                  
CONECT   26   25   27   33                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   26    9   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   41                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   37                                                       
CONECT   42   25   20   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   15   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  106    0
END

View in JSmol

Synonyms

Value	Source
4,5,12-Tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0,]dodecan-7-yl furan-3-carboxylic acid	Generator
4,5,12-Tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylic acid	Generator

Chemical Formula

C₃₅H₄₈O₁₅

Average Mass

708.7540 Da

Monoisotopic Mass

708.29932 Da

IUPAC Name

4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate

Traditional Name

4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)OCC12C(OC(C)=O)C(CC(C)(O)C11OC(C)(C)C(C1OC(C)=O)C(OC(=O)C(C)C)C2OC(=O)C1=COC=C1)OC(C)=O

InChI Identifier

InChI=1S/C35H48O15/c1-11-18(4)30(40)44-16-34-26(46-20(6)37)23(45-19(5)36)14-33(10,42)35(34)27(47-21(7)38)24(32(8,9)50-35)25(48-29(39)17(2)3)28(34)49-31(41)22-12-13-43-15-22/h12-13,15,17-18,23-28,42H,11,14,16H2,1-10H3

InChI Key

QDQMEZHVPUKELZ-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
Celastrus angulatus	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
Agarofuran
Sesquiterpenoid
Furoic acid ester
Furoic acid or derivatives
Furan-3-carboxylic acid ester
Furan-3-carboxylic acid or derivatives
Oxepane
Fatty acid ester
Cyclitol or derivatives
Fatty acyl
Furan
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Heteroaromatic compound
Carboxylic acid ester
Oxacycle
Dialkyl ether
Ether
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic oxide
Organooxygen compound
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	3.04	ALOGPS
logP	2.84	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	13.67	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	200.4 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	167.54 m³·mol⁻¹	ChemAxon
Polarizability	71.24 Å³	ChemAxon
Number of Rings	4	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

85193681

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate (NP0316330)

MOL for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

3D MOL for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

3D SDF for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

3D-SDF for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

PDB for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

3D PDB for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

SMILES for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

INCHI for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

Structure for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)

3D Structure for NP0316330 (4,5,12-tris(acetyloxy)-2-hydroxy-2,10,10-trimethyl-6-{[(2-methylbutanoyl)oxy]methyl}-8-[(2-methylpropanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl furan-3-carboxylate)