NP-MRD: Showing NP-Card for 12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate (NP0207078)

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Record Information

Version

2.0

Created at

2022-09-05 03:33:05 UTC

Updated at

2022-09-05 03:33:05 UTC

NP-MRD ID

NP0207078

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate

Description

12-(Acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-8-yl pyridine-3-carboxylate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. 12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate is found in Tripterygium wilfordii. 12-(Acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-8-yl pyridine-3-carboxylate is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241513052D          

 56 62  0  0  0  0            999 V2000
    2.8972    2.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9588    1.5562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894    1.4798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1332    0.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8383    1.2558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6304    1.6200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4548    2.4538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3966    1.1845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9760    1.7719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7743    1.5638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9933    0.7684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4139    0.1810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6155    0.3891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6590    0.0462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5656   -0.1305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2212   -0.7717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0295   -0.9550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2596   -1.6916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0163   -2.0204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1098   -2.8401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4468   -3.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6901   -3.0022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5965   -2.1825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8281    0.1194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4852   -0.4756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4117   -0.6435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4842   -1.5233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2756   -2.4340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7959   -3.1547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7941   -3.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6118   -2.9512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1152   -3.6048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8009   -4.3676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9831   -4.4768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4797   -3.8232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574   -0.6042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -0.8385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2529   -1.2040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8469   -0.5954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2172   -2.1445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0242   -2.3161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2791   -3.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270   -3.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0800   -3.5422    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3349   -2.7576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8101    0.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727   -0.2290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8919   -1.1038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9693   -1.9276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1023   -1.1515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4154    0.8988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    1.4538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    1.0058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5158    1.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1071    0.8574    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 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  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 26 36  1  0  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
 36 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 47 52  1  0  0  0  0
  2 52  1  0  0  0  0
 24 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 46 54  1  0  0  0  0
 54 55  1  0  0  0  0
 54 56  1  0  0  0  0
M  END

     RDKit          3D

 99105  0  0  0  0  0  0  0  0999 V2000
    0.4478   -4.0544    2.7122 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0130   -4.0110    1.2928 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7553   -2.9150   -0.6831 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1803   -2.4007   -0.9581 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2656   -1.0257   -0.4065 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9000   -1.1242    0.8621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0690   -0.4301    1.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5867    0.2992    0.1988 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7718   -0.4845    2.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9362    0.2137    2.6110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5760    0.1387    3.8334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0358   -0.6469    4.8286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9095   -1.3186    4.5964 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2792   -1.2535    3.4128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9530   -0.3313   -0.1727 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2174    1.0634   -0.1570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9616    1.8653    0.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4731    1.3234    1.9618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2345    3.2981    0.9508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7679    3.9599   -0.1332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0103    5.3207   -0.0764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7350    6.0657    1.0458 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0520   -0.6009   -1.2984 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4883    0.2635   -2.4538 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3948   -0.0526   -0.9655 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.4016    5.0446   -4.5326 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1560    5.4531   -3.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7185    4.5233   -2.3002 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4790   -1.0156   -0.6075 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7574   -1.0131    0.7897 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9230   -0.5612    1.3435 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7999   -0.1210    0.5373 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2301   -0.5458    2.7568 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3318   -1.0011    3.6960 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6145   -0.9915    5.0550 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8369   -0.5104    5.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7561   -0.0474    4.5610 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4352   -0.0757    3.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3923   -2.3939   -1.1199 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2582   -2.6890   -2.0462 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6515   -2.4283   -3.4910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0338   -2.0240   -1.6644 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8250   -2.1257   -2.8328 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7033   -3.9552   -1.0697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9375   -3.1050   -0.5818 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.4918    0.6678    4.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5259   -0.5555    0.8290 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4291    5.7721   -0.9642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9477    7.1229    1.0241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9787    5.9842    3.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5380    3.5991    2.9687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5466    0.5316   -2.3175 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2614    0.5841   -0.0386 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8063   -4.1273   -3.7293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7155   -4.5322   -1.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2361   -4.4394   -2.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8841   -1.7555   -4.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0818   -2.4879   -3.2005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4478   -0.7838   -2.9145 H   0  0  0  0  0  0  0  0  0  0  0  0
 51 50  1  0
 50 49  1  0
 49 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  2  0
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 55 94  1  0
 55 95  1  0
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 56 97  1  0
 56 98  1  0
 56 99  1  0
M  END


  Mrv1533004241513052D          

 56 62  0  0  0  0            999 V2000
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    2.2756   -2.4340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7959   -3.1547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6118   -2.9512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1152   -3.6048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8009   -4.3676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9831   -4.4768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4797   -3.8232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5574   -0.6042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -0.8385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2529   -1.2040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8469   -0.5954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2172   -2.1445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0242   -2.3161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2791   -3.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270   -3.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0800   -3.5422    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3349   -2.7576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8101    0.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727   -0.2290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8919   -1.1038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9693   -1.9276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1023   -1.1515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4154    0.8988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    1.4538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    1.0058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5158    1.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1071    0.8574    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
  4 14  1  0  0  0  0
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 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
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 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 30 35  1  0  0  0  0
 26 36  1  0  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
 36 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 47 52  1  0  0  0  0
  2 52  1  0  0  0  0
 24 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 46 54  1  0  0  0  0
 54 55  1  0  0  0  0
 54 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207078

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(OC(=O)C2=CC=CC=C2)C(OC(=O)C2=CC=CC=C2)C2(C)C(OC(=O)C3=CC=CC=C3)C(OC(=O)C3=CC=CN=C3)C3C(OC(C)=O)C12OC3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C44H43NO11/c1-26-24-32(52-38(47)28-16-9-6-10-17-28)35(54-39(48)29-18-11-7-12-19-29)43(5)37(55-40(49)30-20-13-8-14-21-30)34(53-41(50)31-22-15-23-45-25-31)33-36(51-27(2)46)44(26,43)56-42(33,3)4/h6-23,25-26,32-37H,24H2,1-5H3

> <INCHI_KEY>
FMSHZBLGSXKBSB-UHFFFAOYSA-N

> <FORMULA>
C44H43NO11

> <MOLECULAR_WEIGHT>
761.824

> <EXACT_MASS>
761.283611209

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
77.39238987932384

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate

> <ALOGPS_LOGP>
5.43

> <JCHEM_LOGP>
7.780686567333335

> <ALOGPS_LOGS>
-6.12

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.23996234571409

> <JCHEM_POLAR_SURFACE_AREA>
153.62

> <JCHEM_REFRACTIVITY>
199.46350000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.75e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       5.408   4.518   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.523   2.905   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.074   2.762   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.715   1.354   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.032   2.344   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.510   3.024   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      10.182   4.580   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      11.940   2.211   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.022   3.307   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.512   2.919   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.921   1.434   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.839   0.338   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.349   0.726   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.830   0.086   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.522  -0.244   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.746  -1.441   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      11.255  -1.783   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.818  -3.158   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.230  -3.771   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.405  -5.302   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.167  -6.218   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.755  -5.604   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.580  -4.074   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.279   0.223   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.506  -0.888   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.502  -1.201   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.637  -2.843   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.248  -4.544   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.352  -5.889   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.216  -5.713   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.742  -5.509   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.682  -6.729   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.095  -8.153   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.568  -8.357   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.629  -7.137   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.907  -1.128   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       1.123  -1.565   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.472  -2.248   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -1.581  -1.111   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -0.405  -4.003   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -1.912  -4.323   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.388  -5.788   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -1.357  -6.932   0.000  0.00  0.00           C+0
HETATM   44  N   UNK     0       0.149  -6.612   0.000  0.00  0.00           N+0
HETATM   45  C   UNK     0       0.625  -5.147   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.148   0.303   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.379   0.935   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       3.869  -0.427   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       3.531  -2.060   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       3.676  -3.598   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       2.058  -2.149   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       4.509   1.678   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0       3.188   2.714   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0       1.787   1.878   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       0.963   3.282   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       0.200   1.600   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   52                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14    4   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24   14   25   26   52                                             
CONECT   25   24                                                            
CONECT   26   24   27   36                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   30                                                       
CONECT   36   26   37   46                                                  
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   36   47   54                                                  
CONECT   47   46   48   52                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
CONECT   52   47    2   24   53                                             
CONECT   53   52   54                                                       
CONECT   54   53   46   55   56                                             
CONECT   55   54                                                            
CONECT   56   54                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  124    0
END

View in JSmol

Synonyms

Value	Source
12-(Acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0,]dodecan-8-yl pyridine-3-carboxylic acid	Generator
12-(Acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylic acid	Generator

Chemical Formula

C₄₄H₄₃NO₁₁

Average Mass

761.8240 Da

Monoisotopic Mass

761.28361 Da

IUPAC Name

12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate

Traditional Name

12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate

CAS Registry Number

Not Available

SMILES

CC1CC(OC(=O)C2=CC=CC=C2)C(OC(=O)C2=CC=CC=C2)C2(C)C(OC(=O)C3=CC=CC=C3)C(OC(=O)C3=CC=CN=C3)C3C(OC(C)=O)C12OC3(C)C

InChI Identifier

InChI=1S/C44H43NO11/c1-26-24-32(52-38(47)28-16-9-6-10-17-28)35(54-39(48)29-18-11-7-12-19-29)43(5)37(55-40(49)30-20-13-8-14-21-30)34(53-41(50)31-22-15-23-45-25-31)33-36(51-27(2)46)44(26,43)56-42(33,3)4/h6-23,25-26,32-37H,24H2,1-5H3

InChI Key

FMSHZBLGSXKBSB-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
Tripterygium wilfordii	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Agarofuran
Sesquiterpenoid
Benzoate ester
Benzoic acid or derivatives
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
Benzoyl
Oxepane
Monocyclic benzene moiety
Benzenoid
Pyridine
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Azacycle
Oxacycle
Ether
Dialkyl ether
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen 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	5.43	ALOGPS
logP	7.78	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Basic)	3.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	153.62 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	199.46 m³·mol⁻¹	ChemAxon
Polarizability	77.39 Å³	ChemAxon
Number of Rings	7	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate (NP0207078)

MOL for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

3D MOL for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

3D SDF for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

3D-SDF for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

PDB for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

3D PDB for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

SMILES for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

INCHI for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

Structure for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)

3D Structure for NP0207078 (12-(acetyloxy)-4,5,7-tris(benzoyloxy)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-8-yl pyridine-3-carboxylate)