NP-MRD: Showing NP-Card for 4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate (NP0143460)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-01 22:13:00 UTC

Updated at

2022-09-01 22:13:00 UTC

NP-MRD ID

NP0143460

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate

Description

4-(Acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate belongs to the class of organic compounds known as lappaconitine-type diterpenoid alkaloids. These are c18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lappaconitine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position. 4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate is found in Delphinium elatum. Based on a literature review very few articles have been published on 4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022200132D          

 51 58  0  0  0  0            999 V2000
   -0.5402    1.7053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5654    0.8198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -0.0965    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6588   -0.8063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2975   -1.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1083   -1.9440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4165   -2.7563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1087   -3.5916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2034   -2.9329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7245   -2.2933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5389   -2.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323   -3.1959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3112   -3.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4967   -3.7040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9756   -4.3436    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1868   -5.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8857   -5.6313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4936   -5.5884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8540   -5.0673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1092   -5.5126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1519   -4.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4814   -3.7391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0658   -2.4074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7386   -2.6387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2651   -1.9996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0518   -2.7238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1291   -3.6581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0555   -1.1386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4024   -1.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3127   -0.3021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5563    0.1723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4317    0.3063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3214    0.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3008    0.9141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7448   -0.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2286   -0.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3558    0.6674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429    0.0078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6610   -0.5791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4363   -0.1751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9818    0.4764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3846   -1.4246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5644   -2.1314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8378   -1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -2.4040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3108   -1.0284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9548   -1.7699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8046   -2.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6783   -2.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4442   -2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1157   -3.1631    0.0000 O   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  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 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  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  2  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
  3 35  1  0  0  0  0
 28 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 39 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 28 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 36 46  1  0  0  0  0
 46 47  1  0  0  0  0
 42 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  2  0  0  0  0
M  END

     RDKit          3D

 99106  0  0  0  0  0  0  0  0999 V2000
    0.0188    3.1787   -2.5180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9631    2.4888   -1.6456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5173    1.3598   -0.9129 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5642    0.7865   -0.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2163   -0.2322    0.8361 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8925   -1.4461    0.4599 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2675   -1.3569    0.3079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9454   -0.3331    0.4641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9798   -2.5893   -0.0802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3236   -3.8016   -0.1178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9463   -4.9807   -0.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3016   -4.9309   -0.7044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9571   -3.7339   -0.6697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3268   -2.5511   -0.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0406   -1.3062   -0.3873 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9720   -0.8303    0.5604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0266   -1.1598    1.7795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9046    0.1361   -0.0899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0047    0.7597   -1.1333 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4324    2.0317   -0.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9784   -0.2802   -1.3868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1813   -0.2356   -2.3551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5241    0.0250    2.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9163    1.3014    2.6779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3632    1.7084    2.0024 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1417    2.9852    1.4984 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7090    3.9385    2.3172 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9835    0.8444    1.0214 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7881    1.2794   -0.4637 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5098    0.1683   -1.1744 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3561    0.1897   -2.5459 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5975   -0.9438   -0.5934 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1392   -2.1407   -0.8304 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5866   -2.9619   -1.7538 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3132   -0.5174    0.7963 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8853   -0.2124   -0.8487 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0626   -1.4997   -1.4435 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0366    0.6650   -1.1015 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8816    1.1681    0.0260 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2129    0.7194   -0.2459 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0974    1.7492   -0.4243 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6571    0.6873    1.3901 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3800    1.0408    2.1612 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4378    0.8334    1.1314 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8317    1.9181    0.3171 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9104   -0.5060    0.6215 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2952   -0.7954    1.1373 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1457   -1.2944    0.1230 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9326   -2.3885    0.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8441   -2.9251   -0.6799 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9582   -2.9976    1.5065 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8516    3.6782   -1.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3418    2.5822   -3.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5416    4.0452   -2.9983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4697    3.2625   -1.0300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7878    2.1166   -2.3292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2817    0.3878   -0.9549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2134    1.5589    0.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2621   -3.7919    0.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4340   -5.9217   -0.4510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8130   -5.8725   -0.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0129   -3.6858   -0.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6944   -0.4447   -0.6467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3738    0.8299    0.5973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5853    0.9636   -2.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8284    1.7565    0.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2909    2.6356   -0.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8791    2.6125   -1.3193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5953    0.0146    2.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0591   -0.8020    2.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7159    2.0887    2.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8303    1.2667    3.7853 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0668    1.8731    2.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2390    3.8771    3.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7890    3.8502    2.4898 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4752    4.9606    1.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2551    2.2865   -0.6072 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2043    0.1136   -3.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3070   -0.8595   -1.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2129   -3.9031   -1.7809 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5823   -2.5917   -2.7897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4124   -3.3159   -1.3983 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4288   -1.2251    1.6004 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6335   -1.4253   -2.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6878    0.1017   -1.8489 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6992    1.5083   -1.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0454    2.2768    0.0052 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0909    2.3448    0.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7899    2.4616   -1.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1046    1.3392   -0.5488 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5466    0.7721    2.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4627    2.0391    2.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3308    0.2919    2.9800 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8522    2.7097    0.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3040   -1.3002    0.9882 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3581   -1.3726    2.0463 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4069   -3.8729   -1.0463 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8749   -3.0247   -0.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8605   -2.2083   -1.5437 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
  4  5  1  0
  5 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 25 28  1  0
 28 35  1  0
 35 32  1  0
 32 33  1  0
 33 34  1  0
 32 30  1  0
 30 31  1  6
 30 29  1  0
 30 36  1  0
 36 37  1  6
 36 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 39 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  6
 44 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  1  0
 49 51  2  0
  5  6  1  6
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 29  3  1  0
 46 36  1  0
 14  9  1  0
 21 15  1  0
 35  5  1  0
 47 42  1  0
 29 28  1  0
 28 44  1  1
  1 52  1  0
  1 53  1  0
  1 54  1  0
  2 55  1  0
  2 56  1  0
  4 57  1  0
  4 58  1  0
 23 69  1  0
 23 70  1  0
 24 71  1  0
 24 72  1  0
 25 73  1  1
 27 74  1  0
 27 75  1  0
 27 76  1  0
 35 83  1  1
 32 79  1  6
 34 80  1  0
 34 81  1  0
 34 82  1  0
 31 78  1  0
 29 77  1  1
 37 84  1  0
 38 85  1  0
 38 86  1  0
 39 87  1  1
 41 88  1  0
 41 89  1  0
 41 90  1  0
 42 91  1  1
 43 92  1  0
 43 93  1  0
 45 94  1  0
 46 95  1  6
 47 96  1  1
 50 97  1  0
 50 98  1  0
 50 99  1  0
 10 59  1  0
 11 60  1  0
 12 61  1  0
 13 62  1  0
 18 63  1  0
 18 64  1  0
 19 65  1  6
 20 66  1  0
 20 67  1  0
 20 68  1  0
M  END


  Mrv1652309022200132D          

 51 58  0  0  0  0            999 V2000
   -0.5402    1.7053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5654    0.8198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -0.0965    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6588   -0.8063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2975   -1.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1083   -1.9440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4165   -2.7563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1087   -3.5916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2034   -2.9329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7245   -2.2933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5389   -2.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8323   -3.1959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3112   -3.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4967   -3.7040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9756   -4.3436    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1868   -5.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8857   -5.6313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4936   -5.5884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8540   -5.0673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1092   -5.5126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1519   -4.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4814   -3.7391    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0658   -2.4074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7386   -2.6387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2651   -1.9996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0518   -2.7238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1291   -3.6581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0555   -1.1386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4024   -1.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3127   -0.3021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5563    0.1723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4317    0.3063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3214    0.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3008    0.9141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7448   -0.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2286   -0.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3558    0.6674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0429    0.0078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6610   -0.5791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4363   -0.1751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9818    0.4764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3846   -1.4246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5644   -2.1314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8378   -1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -2.4040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3108   -1.0284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9548   -1.7699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8046   -2.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6783   -2.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4442   -2.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1157   -3.1631    0.0000 O   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  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 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  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  2  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
  3 35  1  0  0  0  0
 28 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 39 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 28 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 36 46  1  0  0  0  0
 46 47  1  0  0  0  0
 42 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0143460

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1CC2(CCC(OC)C34C2C(OC)C(O)(C13)C1(O)CC(OC)C2CC4(O)C1C2OC(C)=O)OC(=O)C1=CC=CC=C1N1C(=O)CC(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C37H48N2O12/c1-7-38-17-33(51-31(43)20-10-8-9-11-22(20)39-25(41)14-18(2)30(39)42)13-12-24(48-5)36-28(33)29(49-6)37(46,32(36)38)35(45)16-23(47-4)21-15-34(36,44)27(35)26(21)50-19(3)40/h8-11,18,21,23-24,26-29,32,44-46H,7,12-17H2,1-6H3

> <INCHI_KEY>
QRQAYVQOURYHFI-UHFFFAOYSA-N

> <FORMULA>
C37H48N2O12

> <MOLECULAR_WEIGHT>
712.793

> <EXACT_MASS>
712.320724994

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
72.75083213779638

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate

> <ALOGPS_LOGP>
1.28

> <JCHEM_LOGP>
-0.7190475673333341

> <ALOGPS_LOGS>
-3.11

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.595675238533346

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.174482525979768

> <JCHEM_PKA_STRONGEST_BASIC>
8.656455294422017

> <JCHEM_POLAR_SURFACE_AREA>
181.6

> <JCHEM_REFRACTIVITY>
176.3563

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.55e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.008   3.183   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.055   1.530   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -0.182  -0.180   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -1.230  -1.505   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.555  -2.953   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.069  -3.629   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.644  -5.145   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.070  -6.704   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -4.113  -5.475   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.086  -4.281   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.606  -4.526   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -7.154  -5.966   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.181  -7.160   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.661  -6.914   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -3.688  -8.108   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -4.082  -9.597   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -5.387 -10.512   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.788 -10.432   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.594  -9.459   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.204 -10.290   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.150  -8.023   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.899  -6.980   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.123  -4.494   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.379  -4.926   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.361  -3.733   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.830  -5.084   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.974  -6.828   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.970  -2.125   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.751  -2.251   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.584  -0.564   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -1.039   0.322   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -2.672   0.572   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.467   0.070   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.428   1.706   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       1.390  -0.301   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.160  -0.366   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       4.398   1.246   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       5.680   0.015   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.834  -1.081   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       8.281  -0.327   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       9.299   0.889   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.318  -2.659   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.787  -3.979   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.431  -2.924   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       2.984  -4.488   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       4.314  -1.920   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       5.516  -3.304   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       7.102  -4.176   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       8.733  -4.518   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      10.163  -3.806   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       9.549  -5.904   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   35                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   23   29                                             
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16   21                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   15   22                                                  
CONECT   22   21                                                            
CONECT   23    5   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29   35   44                                             
CONECT   29   28    5   30                                                  
CONECT   30   29   31   33                                                  
CONECT   31   30   32                                                       
CONECT   32   31                                                            
CONECT   33   30   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33    3   28                                                  
CONECT   36   33   37   38   46                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40   42                                                  
CONECT   40   39   41                                                       
CONECT   41   40                                                            
CONECT   42   39   43   47                                                  
CONECT   43   42   44                                                       
CONECT   44   43   28   45   46                                             
CONECT   45   44                                                            
CONECT   46   44   36   47                                                  
CONECT   47   46   42   48                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  116    0
END

View in JSmol

Synonyms

Value	Source
4-(Acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1,.0,.0,.0,]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoic acid	Generator

Chemical Formula

C₃₇H₄₈N₂O₁₂

Average Mass

712.7930 Da

Monoisotopic Mass

712.32072 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCN1CC2(CCC(OC)C34C2C(OC)C(O)(C13)C1(O)CC(OC)C2CC4(O)C1C2OC(C)=O)OC(=O)C1=CC=CC=C1N1C(=O)CC(C)C1=O

InChI Identifier

InChI=1S/C37H48N2O12/c1-7-38-17-33(51-31(43)20-10-8-9-11-22(20)39-25(41)14-18(2)30(39)42)13-12-24(48-5)36-28(33)29(49-6)37(46,32(36)38)35(45)16-23(47-4)21-15-34(36,44)27(35)26(21)50-19(3)40/h8-11,18,21,23-24,26-29,32,44-46H,7,12-17H2,1-6H3

InChI Key

QRQAYVQOURYHFI-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
Delphinium elatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lappaconitine-type diterpenoid alkaloids. These are c18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lappaconitine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Lappaconitine-type diterpenoid alkaloids

Alternative Parents

Substituents

Lappaconitine-type diterpenoid alkaloid
Acylaminobenzoic acid or derivatives
1-phenylpyrrolidine
Quinolidine
Benzoate ester
Benzoic acid or derivatives
Alkaloid or derivatives
Benzoyl
Azepane
Dicarboxylic acid or derivatives
Carboxylic acid imide, n-substituted
Piperidine
Pyrrolidone
2-pyrrolidone
Benzenoid
Monocyclic benzene moiety
Dicarboximide
Pyrrolidine
Pyrrole
Cyclic alcohol
Tertiary alcohol
Carboxylic acid imide
Carboxylic acid ester
Lactam
Tertiary amine
Tertiary aliphatic amine
Amino acid or derivatives
1,2-aminoalcohol
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Polyol
Dialkyl ether
Ether
Carbonyl group
Alcohol
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Amine
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organopnictogen 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	1.28	ALOGPS
logS	-3.1	ALOGPS

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

163030297

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate (NP0143460)

MOL for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

3D MOL for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

3D SDF for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

3D-SDF for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

PDB for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

3D PDB for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

SMILES for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

INCHI for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

Structure for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)

3D Structure for NP0143460 (4-(acetyloxy)-11-ethyl-2,8,9-trihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate)