NP-MRD: Showing NP-Card for [(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate (NP0149233)

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Record Information

Version

2.0

Created at

2022-09-02 05:05:58 UTC

Updated at

2022-09-02 05:05:58 UTC

NP-MRD ID

NP0149233

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate

Description

Euphorbialoid D belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. [(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate is found in Euphorbia prolifera. Based on a literature review very few articles have been published on euphorbialoid D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022207052D          

 54 59  0  0  1  0            999 V2000
   -1.2856   -4.4415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0622   -3.6473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2628   -3.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0394   -2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6155   -2.0589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7601   -2.4459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9835   -1.6517    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4723   -1.0041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3521   -1.0371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9302   -0.3179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7243   -0.5413    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5447    0.2639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3483   -0.0015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1327    0.7948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1593   -0.1528    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9556    0.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1263    0.6715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8237    1.1122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7908    1.9366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5541    0.7286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5466   -0.8812    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3662   -0.7868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8578   -1.4493    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5298   -2.2063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7103   -2.3008    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3823   -3.0578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5852   -3.9182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5459   -4.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6935   -3.6258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2187   -1.6382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2023   -2.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4797   -2.8613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4633   -3.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3608   -4.5047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1695   -4.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8920   -3.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5981   -4.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5817   -4.9660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8592   -5.3642    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1531   -4.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4223   -1.8538    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2710   -2.6648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4930   -2.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6707   -2.8736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3417   -3.7503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9684   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8171   -5.0978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0391   -5.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4124   -4.8358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5637   -4.0248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7573   -1.3656    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1858   -0.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0105   -0.6696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4465    0.0904    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  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 11 10  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 13  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 21 15  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 30 25  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 35 40  1  0  0  0  0
 30 41  1  0  0  0  0
 41 42  1  6  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 45 50  1  0  0  0  0
 41 51  1  0  0  0  0
 51  7  1  1  0  0  0
 51 11  1  0  0  0  0
 23 52  1  0  0  0  0
 22 52  1  1  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
M  END

     RDKit          3D

103108  0  0  0  0  0  0  0  0999 V2000
    5.5211   -2.8999    3.0800 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1857   -3.5751    2.7944 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6935   -3.0939    1.4729 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4869   -1.6330    1.4148 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6485   -0.8635    2.4150 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1048   -1.0499    0.2394 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8695    0.3212    0.0168 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9229    0.6822   -1.0707 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2258    0.0028   -0.7693 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3275    0.0133   -2.3205 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9328   -0.4447   -1.9058 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0479   -1.7582   -1.5108 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8899   -0.1766   -2.8886 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0477    0.7505   -3.6183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3434   -1.0476   -2.9728 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1508   -0.4433   -4.0886 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2834   -2.2383   -3.3270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1169   -3.4738   -3.5932 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9256   -4.5051   -3.9315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3171   -3.7175   -3.5515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0540   -1.1167   -1.6567 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5027   -1.3911   -1.9410 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5003   -1.2308   -0.9057 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0485   -0.8518    0.4414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5886   -0.6336    0.6108 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9592   -1.7963    1.0760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4130   -1.8632    2.3242 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2724   -3.1055    2.8304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4626   -0.8831    3.1039 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8919   -0.0573   -0.6579 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8510    1.0924   -1.0089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2085    1.8408    0.1321 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0501    2.9213    0.1070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5071    3.2571   -1.0175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3874    3.6298    1.3314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2018    4.7394    1.3189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5270    5.3926    2.5131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0260    4.9213    3.7261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2436    3.8500    3.7076 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9212    3.2075    2.5525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3321    0.5049   -0.1398 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1392    1.9212    0.1360 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3658    2.5324    1.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7722    1.8007    2.2807 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1729    3.9589    1.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2601    4.7991    0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4369    6.1616    0.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1775    6.6730    2.0557 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2570    5.8406    3.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4330    4.4719    2.8093 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6353    0.5179   -0.8303 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2563   -2.5591   -1.4476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3771   -3.0774   -2.3808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7212   -3.6251   -0.5935 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2237   -3.6071    3.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3987   -2.0388    3.7432 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9529   -2.6001    2.1213 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4086   -4.6772    2.7038 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4814   -3.4674    3.6160 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6894   -3.5799    1.3045 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3413   -3.4721    0.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9758    0.9678    0.8728 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0060    1.7624   -1.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0303    0.5245   -1.3392 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5228    0.0670    0.2988 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2277   -1.0612   -1.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9306   -0.8689   -2.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2095    0.7426   -3.1399 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8268   -2.2096   -1.9224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4293   -0.0434   -4.8430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6675    0.4337   -3.7012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7495   -1.1582   -4.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4684   -5.4851   -4.1094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5675   -4.1583   -4.7784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6131   -4.6146   -3.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6845   -2.0756   -1.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8380   -1.0324   -2.9648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4803   -0.7145   -1.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3673   -1.6332    1.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5872    0.0692    0.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4414    0.1484    1.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3476   -3.8289    2.0030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2530   -2.7602    3.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3589   -3.4805    3.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7089    0.8541   -1.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2807    1.8447   -1.6549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5906    5.1060    0.3839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1691    6.2671    2.4999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2994    5.4552    4.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2800    2.3482    2.6351 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6310    0.1410    0.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4786    4.4559   -0.4271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7771    6.8334    0.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3038    7.7285    2.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4591    6.2436    4.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7740    3.8327    3.6093 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8363    1.5234   -1.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3213   -3.1909   -1.8444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9952   -4.0118   -2.8405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5485   -2.3740   -3.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0080   -3.4857    0.4613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1669   -4.6192   -0.9001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6349   -3.7939   -0.6327 H   0  0  0  0  0  0  0  0  0  0  0  0
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 51  7  1  0
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  3 60  1  0
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 12 69  1  0
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 41 91  1  1
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 31 85  1  0
 31 86  1  0
 36 87  1  0
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 25 81  1  1
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 16 70  1  0
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 16 72  1  0
 19 73  1  0
 19 74  1  0
 19 75  1  0
 53 98  1  0
 53 99  1  0
 53100  1  0
 54101  1  0
 54102  1  0
 54103  1  0
 28 82  1  0
 28 83  1  0
 28 84  1  0
M  END


  Mrv1652309022207052D          

 54 59  0  0  1  0            999 V2000
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   -1.0622   -3.6473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2628   -3.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0394   -2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6155   -2.0589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9835   -1.6517    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4723   -1.0041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.7243   -0.5413    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.1327    0.7948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9556    0.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1263    0.6715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5541    0.7286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3662   -0.7868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.7103   -2.3008    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3823   -3.0578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5852   -3.9182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5459   -4.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6935   -3.6258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2187   -1.6382    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2023   -2.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4797   -2.8613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4633   -3.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3608   -4.5047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1695   -4.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8920   -3.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5981   -4.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5817   -4.9660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8592   -5.3642    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1531   -4.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4223   -1.8538    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2710   -2.6648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4930   -2.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6707   -2.8736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3417   -3.7503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9684   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8171   -5.0978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0391   -5.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4124   -4.8358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5637   -4.0248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7573   -1.3656    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1858   -0.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0105   -0.6696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4465    0.0904    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  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 11 10  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 13  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 21 15  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 30 25  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 35 40  1  0  0  0  0
 30 41  1  0  0  0  0
 41 42  1  6  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 45 50  1  0  0  0  0
 41 51  1  0  0  0  0
 51  7  1  1  0  0  0
 51 11  1  0  0  0  0
 23 52  1  0  0  0  0
 22 52  1  1  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0149233

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)O[C@H]1[C@@H](C)C[C@@]2(O)[C@H]1[C@@H](OC(=O)C1=CC=CC=C1)[C@]1(COC(=O)C3=CC=CN=C3)[C@@H](C[C@H]3[C@@H]([C@H]1[C@](C)(OC(C)=O)C2=O)C3(C)C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C41H49NO12/c1-8-13-29(45)52-32-22(2)19-41(49)31(32)34(53-36(47)25-14-10-9-11-15-25)40(21-50-35(46)26-16-12-17-42-20-26)28(51-23(3)43)18-27-30(38(27,5)6)33(40)39(7,37(41)48)54-24(4)44/h9-12,14-17,20,22,27-28,30-34,49H,8,13,18-19,21H2,1-7H3/t22-,27-,28+,30-,31+,32-,33-,34+,39-,40+,41+/m0/s1

> <INCHI_KEY>
ZBBKIZHIJNBDOS-HUCZTCEXSA-N

> <FORMULA>
C41H49NO12

> <MOLECULAR_WEIGHT>
747.838

> <EXACT_MASS>
747.325476022

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
77.09395359660972

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1R,2R,3R,4S,5S,7R,9S,10R,11S,13S,15R)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0^{3,7}.0^{11,13}]pentadecan-1-yl]methyl pyridine-3-carboxylate

> <ALOGPS_LOGP>
4.16

> <JCHEM_LOGP>
4.890097390333333

> <ALOGPS_LOGS>
-5.17

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.584731108180687

> <JCHEM_PKA_STRONGEST_BASIC>
3.242774482341211

> <JCHEM_POLAR_SURFACE_AREA>
181.69000000000003

> <JCHEM_REFRACTIVITY>
189.72229999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.05e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,2R,3R,4S,5S,7R,9S,10R,11S,13S,15R)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0^{3,7}.0^{11,13}]pentadecan-1-yl]methyl pyridine-3-carboxylate

> <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      -2.400  -8.291   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.983  -6.808   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.491  -6.428   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.074  -4.946   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.149  -3.843   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       1.419  -4.566   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.836  -3.083   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.882  -1.874   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.657  -1.936   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.736  -0.593   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.219  -1.010   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.883   0.493   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.383  -0.003   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.981   1.484   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.897  -0.285   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.384   0.117   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.836   1.254   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.138   2.076   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.076   3.615   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.501   1.360   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.620  -1.645   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.150  -1.469   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.068  -2.705   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.456  -4.118   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.926  -4.295   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.314  -5.708   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.692  -7.314   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.619  -8.358   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.761  -6.768   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.008  -3.058   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.978  -4.598   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.629  -5.341   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.598  -6.881   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.407  -8.409   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       5.916  -7.677   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.265  -6.934   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.583  -7.730   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.553  -9.270   0.000  0.00  0.00           C+0
HETATM   39  N   UNK     0       7.204 -10.013   0.000  0.00  0.00           N+0
HETATM   40  C   UNK     0       5.886  -9.217   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.522  -3.460   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       4.239  -4.974   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       2.787  -5.487   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       1.252  -5.364   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       2.505  -7.001   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       3.674  -8.002   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.392  -9.516   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       1.940 -10.028   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       0.770  -9.027   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       1.052  -7.513   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       3.280  -2.549   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       9.680  -1.292   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      11.220  -1.250   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      10.167   0.169   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   51                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13   51                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   21                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   15   22   30                                                  
CONECT   22   21   23   52                                                  
CONECT   23   22   24   52                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   21   31   41                                             
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   35                                                       
CONECT   41   30   42   51                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   50                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   45                                                       
CONECT   51   41    7   11                                                  
CONECT   52   23   22   53   54                                             
CONECT   53   52                                                            
CONECT   54   52                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  118    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₄₉NO₁₂

Average Mass

747.8380 Da

Monoisotopic Mass

747.32548 Da

IUPAC Name

[(1R,2R,3R,4S,5S,7R,9S,10R,11S,13S,15R)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0^{3,7}.0^{11,13}]pentadecan-1-yl]methyl pyridine-3-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

CCCC(=O)O[C@H]1[C@@H](C)C[C@@]2(O)[C@H]1[C@@H](OC(=O)C1=CC=CC=C1)[C@]1(COC(=O)C3=CC=CN=C3)[C@@H](C[C@H]3[C@@H]([C@H]1[C@](C)(OC(C)=O)C2=O)C3(C)C)OC(C)=O

InChI Identifier

InChI=1S/C41H49NO12/c1-8-13-29(45)52-32-22(2)19-41(49)31(32)34(53-36(47)25-14-10-9-11-15-25)40(21-50-35(46)26-16-12-17-42-20-26)28(51-23(3)43)18-27-30(38(27,5)6)33(40)39(7,37(41)48)54-24(4)44/h9-12,14-17,20,22,27-28,30-34,49H,8,13,18-19,21H2,1-7H3/t22-,27-,28+,30-,31+,32-,33-,34+,39-,40+,41+/m0/s1

InChI Key

ZBBKIZHIJNBDOS-HUCZTCEXSA-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
Euphorbia prolifera	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
Aromatic monoterpenoid
Benzoate ester
Carane monoterpenoid
Monoterpenoid
Benzoic acid or derivatives
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
Benzoyl
Fatty acid ester
Alpha-acyloxy ketone
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Pyridine
Tertiary alcohol
Heteroaromatic compound
Cyclic alcohol
Carboxylic acid ester
Ketone
Organoheterocyclic compound
Azacycle
Alcohol
Organonitrogen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organic nitrogen 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	4.16	ALOGPS
logP	4.89	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	12.58	ChemAxon
pKa (Strongest Basic)	3.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	181.69 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	189.72 m³·mol⁻¹	ChemAxon
Polarizability	77.09 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

28505389

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

60168064

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate (NP0149233)

MOL for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

3D MOL for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

3D SDF for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

3D-SDF for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

PDB for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

3D PDB for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

SMILES for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

INCHI for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

Structure for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)

3D Structure for NP0149233 ([(1r,2r,3r,4s,5s,7r,9s,10r,11s,13s,15r)-9,15-bis(acetyloxy)-2-(benzoyloxy)-4-(butanoyloxy)-7-hydroxy-5,9,12,12-tetramethyl-8-oxotetracyclo[8.5.0.0³,⁷.0¹¹,¹³]pentadecan-1-yl]methyl pyridine-3-carboxylate)