NP-MRD: Showing NP-Card for methyl (1s,4s,5r,6s,7r,8s,10s,14s,15s,16r,18s,19r,22r,23r,25s,26s)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2e)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1⁸,¹⁵.0¹,⁵.0⁶,¹⁸.0⁷,¹⁶.0¹⁰,¹⁴.0²²,²⁶]heptacos-12-ene-4-carboxylate (NP0322751)

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Record Information

Version

2.0

Created at

2022-09-12 01:42:24 UTC

Updated at

2022-09-12 01:42:24 UTC

NP-MRD ID

NP0322751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,4s,5r,6s,7r,8s,10s,14s,15s,16r,18s,19r,22r,23r,25s,26s)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2e)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1⁸,¹⁵.0¹,⁵.0⁶,¹⁸.0⁷,¹⁶.0¹⁰,¹⁴.0²²,²⁶]heptacos-12-ene-4-carboxylate

Description

Methyl (1S,4S,5R,6S,7R,8S,10S,14S,15S,16R,18S,19R,22R,23R,25S,26S)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2E)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1⁸,¹⁵.0¹,⁵.0⁶,¹⁸.0⁷,¹⁶.0¹⁰,¹⁴.0²²,²⁶]Heptacos-12-ene-4-carboxylate belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. methyl (1s,4s,5r,6s,7r,8s,10s,14s,15s,16r,18s,19r,22r,23r,25s,26s)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2e)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1⁸,¹⁵.0¹,⁵.0⁶,¹⁸.0⁷,¹⁶.0¹⁰,¹⁴.0²²,²⁶]heptacos-12-ene-4-carboxylate is found in Melia azedarach. Based on a literature review very few articles have been published on methyl (1S,4S,5R,6S,7R,8S,10S,14S,15S,16R,18S,19R,22R,23R,25S,26S)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2E)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1⁸,¹⁵.0¹,⁵.0⁶,¹⁸.0⁷,¹⁶.0¹⁰,¹⁴.0²²,²⁶]Heptacos-12-ene-4-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122203422D          

 50 58  0  0  1  0            999 V2000
    2.7106    2.6823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5431    1.8745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1589    1.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9423    1.5844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9915    0.5177    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8124    0.4356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2939    1.1055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2056    0.7687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9570    0.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.5661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5964   -0.0172    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7639    0.7906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1480    1.3396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3647    1.0807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3155    2.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6997    2.6964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8671    3.5042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2513    4.0531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4188    4.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2021    5.1198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8180    4.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6505    3.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8131   -0.2760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6456   -1.0839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1377   -1.3427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2615   -1.6328    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5567   -2.0617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5080   -2.5961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3289   -2.6782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6607   -1.9229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4440   -1.6640    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1605   -2.0729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7708   -1.5178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9704   -2.3183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5703   -1.7214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4003   -0.7812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8079   -0.0317    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6165    0.1318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2485   -0.3985    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0392   -0.1632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5074   -0.8425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0060   -1.4976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2279   -1.2232    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3550   -2.0384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4315   -0.7659    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9633   -0.0866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6115   -0.8562    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6073   -0.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9956   -0.3073    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0448   -1.3740    0.0000 C   0  0  2  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  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 11 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 29  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  6  0  0  0
 37 36  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 39 43  1  0  0  0  0
 35 43  1  0  0  0  0
 43 44  1  1  0  0  0
 37 45  1  0  0  0  0
 33 45  1  0  0  0  0
 45 46  1  6  0  0  0
 45 47  1  0  0  0  0
 31 47  1  0  0  0  0
 47 48  1  1  0  0  0
 49 47  1  1  0  0  0
  5 49  1  0  0  0  0
 10 49  1  0  0  0  0
 50 30  1  1  0  0  0
 10 50  1  0  0  0  0
 26 50  1  0  0  0  0
M  END

     RDKit          3D

 94102  0  0  0  0  0  0  0  0999 V2000
   -0.7323   -1.1572    4.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5399   -0.1057    3.5953 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2265   -0.2654    2.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7037   -1.4292    2.3178 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4237    0.8332    1.4711 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1790    1.9255    2.0847 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4100    2.3522    3.2214 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7514    1.1200    1.1664 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7035    1.6203   -0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8400    0.5964   -0.8540 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7319   -0.5616   -1.1372 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3494   -1.2363   -0.1248 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744   -1.2766    0.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4645   -0.6076   -0.5089 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2230   -2.0419    1.3248 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5210   -2.0238    1.5710 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1695   -2.7436    2.6527 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5357   -2.6624    2.8198 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2307   -3.3081    3.8194 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5281   -4.0935    4.7236 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1571   -4.1979    4.5864 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5059   -3.5324    3.5689 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3016   -1.4356   -2.3026 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4701   -0.6768   -3.6295 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5114   -1.2111   -4.4823 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1244    0.7983   -3.3875 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2610    1.7156   -3.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0547    1.2464   -4.3994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8719    1.9870   -3.7291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6230    1.9858   -2.3888 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8418    1.5898   -1.5626 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5259    0.5452   -2.0891 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1361   -0.1715   -1.1031 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8175   -1.6315   -1.3096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6526   -0.1043   -1.1016 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9186   -0.0370    0.4104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8764    1.0565    0.7377 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2783    2.2291    0.2121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2374    2.2569   -0.7426 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.5583    2.3723   -0.2563 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4006    1.6020   -1.0512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6945    0.8729   -1.8959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2246    1.1192   -1.7162 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6469    1.4615   -2.9510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6651    0.3964    0.2040 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2803   -0.5893    1.1047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4867    1.3120   -0.1272 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6323    2.6552    0.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2616    0.5282    0.1235 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2746    0.8420   -2.1726 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1009   -1.0351    5.4353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7808   -1.1976    4.8927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5314   -2.1533    4.0667 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4716    2.6380    2.9902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0546    3.3785    3.4434 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3023    1.8137    4.1479 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7559    1.5337   -0.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3944    2.6475   -0.2402 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6203   -0.0184   -1.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5815   -2.6371    1.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1400   -1.4247    0.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1275   -2.0511    2.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2982   -3.2380    3.9411 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0032   -4.6303    5.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6141   -4.8114    5.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4374   -3.6445    3.5019 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3483   -1.9276   -2.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0637   -2.2719   -2.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4861   -0.8011   -4.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2896   -1.5106   -3.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2096    1.1245   -3.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2010    2.3491   -4.4364 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4098    2.4429   -2.6947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4362    0.4079   -4.8916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5321    1.9010   -5.1833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2344    2.9682   -2.0607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4960    2.4934   -1.6368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4665   -2.3038   -0.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7979   -1.9390   -1.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0970   -1.9113   -2.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1334   -1.0153   -1.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9282    0.2731    0.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6993   -0.9792    0.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8632    1.0727    1.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0748    3.1943   -1.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4909    1.5578   -1.0333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0814    0.1856   -2.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6138    2.4593   -3.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7182   -1.4451    1.0107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3376    3.3233   -0.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2054    2.6312    1.4965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7427    3.2939    0.5307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4850   -0.5854    0.2402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4039   -0.0775   -2.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  1
  6  7  1  0
  5  8  1  0
  8  9  1  0
 10  9  1  1
 10 50  1  0
 50 30  1  0
 30 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  1  1
 26 24  1  0
 24 25  1  0
 24 23  1  0
 23 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  1
 33 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  2  0
 42 43  1  0
 43 44  1  6
 37 45  1  0
 45 46  1  1
 45 47  1  0
 47 48  1  1
 47 49  1  0
 49  5  1  0
 11 10  1  0
 22 17  1  0
 47 31  1  0
 49 10  1  0
 26 50  1  0
 45 33  1  0
 43 35  1  0
 43 39  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  7 54  1  0
  7 55  1  0
  7 56  1  0
  9 57  1  0
  9 58  1  0
 50 94  1  6
 30 76  1  1
 28 74  1  0
 28 75  1  0
 27 71  1  0
 27 72  1  0
 27 73  1  0
 24 69  1  6
 25 70  1  0
 23 67  1  0
 23 68  1  0
 11 59  1  6
 15 60  1  0
 16 61  1  0
 18 62  1  0
 19 63  1  0
 20 64  1  0
 21 65  1  0
 22 66  1  0
 31 77  1  1
 34 78  1  0
 34 79  1  0
 34 80  1  0
 35 81  1  6
 36 82  1  0
 36 83  1  0
 37 84  1  1
 39 85  1  6
 41 86  1  0
 42 87  1  0
 44 88  1  0
 46 89  1  0
 48 90  1  0
 48 91  1  0
 48 92  1  0
 49 93  1  1
M  END


  Mrv1652309122203422D          

 50 58  0  0  1  0            999 V2000
    2.7106    2.6823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5431    1.8745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1589    1.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9423    1.5844    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9915    0.5177    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8124    0.4356    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2939    1.1055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2056    0.7687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9570    0.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.5661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5964   -0.0172    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7639    0.7906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1480    1.3396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3647    1.0807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3155    2.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6997    2.6964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8671    3.5042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2513    4.0531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4188    4.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2021    5.1198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8180    4.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6505    3.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8131   -0.2760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6456   -1.0839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1377   -1.3427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2615   -1.6328    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5567   -2.0617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5080   -2.5961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3289   -2.6782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6607   -1.9229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4440   -1.6640    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1605   -2.0729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7708   -1.5178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9704   -2.3183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5703   -1.7214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4003   -0.7812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8079   -0.0317    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6165    0.1318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2485   -0.3985    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0392   -0.1632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5074   -0.8425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0060   -1.4976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2279   -1.2232    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3550   -2.0384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4315   -0.7659    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9633   -0.0866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6115   -0.8562    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6073   -0.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9956   -0.3073    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0448   -1.3740    0.0000 C   0  0  2  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  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 11 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30 29  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  6  0  0  0
 37 36  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 39 43  1  0  0  0  0
 35 43  1  0  0  0  0
 43 44  1  1  0  0  0
 37 45  1  0  0  0  0
 33 45  1  0  0  0  0
 45 46  1  6  0  0  0
 45 47  1  0  0  0  0
 31 47  1  0  0  0  0
 47 48  1  1  0  0  0
 49 47  1  1  0  0  0
  5 49  1  0  0  0  0
 10 49  1  0  0  0  0
 50 30  1  1  0  0  0
 10 50  1  0  0  0  0
 26 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322751

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]1(OC)OC[C@@]23[C@H]4[C@@H](OC[C@]4(C)[C@H](O)C[C@@H]2OC(=O)\C=C\C2=CC=CC=C2)[C@H]2O[C@]4(C)[C@H]5C[C@H](O[C@@H]6OC=C[C@]56O)[C@]4(O)[C@@]2(C)[C@H]13

> <INCHI_IDENTIFIER>
InChI=1S/C37H44O13/c1-31-17-46-25-26(31)34(22(16-21(31)38)48-24(39)12-11-19-9-7-6-8-10-19)18-47-36(44-5,29(40)43-4)28(34)32(2)27(25)50-33(3)20-15-23(37(32,33)42)49-30-35(20,41)13-14-45-30/h6-14,20-23,25-28,30,38,41-42H,15-18H2,1-5H3/b12-11+/t20-,21-,22+,23+,25-,26+,27-,28+,30+,31-,32-,33-,34+,35+,36+,37+/m1/s1

> <INCHI_KEY>
UPZJANQVCYBAES-SBZMTXNHSA-N

> <FORMULA>
C37H44O13

> <MOLECULAR_WEIGHT>
696.746

> <EXACT_MASS>
696.278191477

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
69.76752675468342

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,4S,5R,6S,7R,8S,10S,14S,15S,16R,18S,19R,22R,23R,25S,26S)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2E)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1^{8,15}.0^{1,5}.0^{6,18}.0^{7,16}.0^{10,14}.0^{22,26}]heptacos-12-ene-4-carboxylate

> <JCHEM_LOGP>
1.5532070359999988

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.651954573998346

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.038311181632274

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9996932642557033

> <JCHEM_POLAR_SURFACE_AREA>
168.67

> <JCHEM_REFRACTIVITY>
171.09020000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4S,5R,6S,7R,8S,10S,14S,15S,16R,18S,19R,22R,23R,25S,26S)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2E)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1^{8,15}.0^{1,5}.0^{6,18}.0^{7,16}.0^{10,14}.0^{22,26}]heptacos-12-ene-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       5.060   5.007   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.747   3.499   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.897   2.474   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.359   2.958   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.584   0.966   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.116   0.813   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.015   2.064   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.117   1.435   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.653   0.210   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.130  -1.057   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.980  -0.032   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.293   1.476   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.143   2.501   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.681   2.017   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.456   4.009   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.306   5.033   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.619   6.541   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.469   7.566   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.782   9.074   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.244   9.557   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.394   8.532   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.081   7.024   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.518  -0.515   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.205  -2.023   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.257  -2.506   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.355  -3.048   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.039  -3.848   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.815  -4.846   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.347  -4.999   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.967  -3.589   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.429  -3.106   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.766  -3.869   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       8.906  -2.833   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.278  -4.328   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.398  -3.213   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.081  -1.458   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.975  -0.059   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      10.484   0.246   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      11.664  -0.744   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      13.140  -0.305   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      14.014  -1.573   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      13.078  -2.796   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      11.626  -2.283   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      11.863  -3.805   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       8.272  -1.430   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       7.398  -0.162   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       6.741  -1.598   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       6.734  -0.058   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       5.592  -0.574   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       3.817  -2.565   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    8   49                                             
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   49   50                                             
CONECT   11   10   12   23                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   11   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28   50                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   50                                                  
CONECT   31   30   32   47                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35   45                                             
CONECT   34   33                                                            
CONECT   35   33   36   43                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   45                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   43                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   39   35   44                                             
CONECT   44   43                                                            
CONECT   45   37   33   46   47                                             
CONECT   46   45                                                            
CONECT   47   45   31   48   49                                             
CONECT   48   47                                                            
CONECT   49   47    5   10                                                  
CONECT   50   30   10   26                                                  
MASTER        0    0    0    0    0    0    0    0   50    0  116    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,4S,5R,6S,7R,8S,10S,14S,15S,16R,18S,19R,22R,23R,25S,26S)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2E)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1,.0,.0,.0,.0,.0,]heptacos-12-ene-4-carboxylic acid	Generator

Chemical Formula

C₃₇H₄₄O₁₃

Average Mass

696.7460 Da

Monoisotopic Mass

696.27819 Da

IUPAC Name

methyl (1S,4S,5R,6S,7R,8S,10S,14S,15S,16R,18S,19R,22R,23R,25S,26S)-7,14,23-trihydroxy-4-methoxy-6,16,22-trimethyl-25-{[(2E)-3-phenylprop-2-enoyl]oxy}-3,9,11,17,20-pentaoxaoctacyclo[17.6.1.1^{8,15}.0^{1,5}.0^{6,18}.0^{7,16}.0^{10,14}.0^{22,26}]heptacos-12-ene-4-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]1(OC)OC[C@@]23[C@H]4[C@@H](OC[C@]4(C)[C@H](O)C[C@@H]2OC(=O)\C=C\C2=CC=CC=C2)[C@H]2O[C@]4(C)[C@H]5C[C@H](O[C@@H]6OC=C[C@]56O)[C@]4(O)[C@@]2(C)[C@H]13

InChI Identifier

InChI=1S/C37H44O13/c1-31-17-46-25-26(31)34(22(16-21(31)38)48-24(39)12-11-19-9-7-6-8-10-19)18-47-36(44-5,29(40)43-4)28(34)32(2)27(25)50-33(3)20-15-23(37(32,33)42)49-30-35(20,41)13-14-45-30/h6-14,20-23,25-28,30,38,41-42H,15-18H2,1-5H3/b12-11+/t20-,21-,22+,23+,25-,26+,27-,28+,30+,31-,32-,33-,34+,35+,36+,37+/m1/s1

InChI Key

UPZJANQVCYBAES-SBZMTXNHSA-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
Melia azedarach	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Cinnamic acid or derivatives
Cinnamic acid ester
Furopyran
Styrene
Ketal
Fatty acid ester
Oxepane
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Oxane
Fatty acyl
Pyran
Benzenoid
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Methyl ester
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Furan
Dihydrofuran
Secondary alcohol
Carboxylic acid ester
Polyol
Acetal
Carboxylic acid derivative
Oxacycle
Dialkyl ether
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Organic oxide
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.55	ChemAxon
pKa (Strongest Acidic)	12.04	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	168.67 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	171.09 m³·mol⁻¹	ChemAxon
Polarizability	69.77 Å³	ChemAxon
Number of Rings	9	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

162861916

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]