NP-MRD: Showing NP-Card for myrobotinol (NP0025216)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-06-19 17:23:58 UTC

Updated at

2021-06-29 23:50:00 UTC

NP-MRD ID

NP0025216

Secondary Accession Numbers

None

Natural Product Identification

Common Name

myrobotinol

Provided By

JEOL Database JEOL Logo

Description

(1R,6S,10R,11R,14R,16R,18R,22R,23R)-12-oxa-2,21-diazahexacyclo[12.6.2.1²,⁶.0¹¹,²¹.0¹⁸,²².0¹⁰,²³]Tricosan-16-ol belongs to the class of organic compounds known as pyridopyrimidines. Pyridopyrimidines are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. myrobotinol is found in Myrioneuron nutans (Rubiaceae). myrobotinol was first documented in 2007 (Pham, V. C., et al.). Based on a literature review very few articles have been published on (1R,6S,10R,11R,14R,16R,18R,22R,23R)-12-oxa-2,21-diazahexacyclo[12.6.2.1²,⁶.0¹¹,²¹.0¹⁸,²².0¹⁰,²³]Tricosan-16-ol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119233D          

 56 61  0  0  0  0            999 V2000
    4.1782   -1.2736    3.2378 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0080   -0.6036    2.7821 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8028   -1.1795    3.5243 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4538   -0.6603    3.0060 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1907    0.7878    3.4309 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1582    1.2353    2.8783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2457    1.0590    1.3435 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5540    1.4990    0.8228 N   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7227    0.8599    1.4402 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0363    1.4235    0.8941 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1088    1.3255   -0.6218 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8751    1.9858   -1.2488 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8833    1.8615   -2.7801 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5489    0.4556   -3.2723 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2381   -0.0492   -2.6764 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2583    0.0051   -1.1400 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5620    1.4308   -0.6507 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9396   -0.4809   -0.5205 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1629    0.1831   -1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4094   -0.3752   -0.7441 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5686   -0.1916    0.7575 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8778   -0.7881    1.2713 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3489   -0.8147    1.4746 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9364   -0.3195    0.9403 N   0  0  1  0  0  0  0  0  0  0  0  0
    4.9448   -0.8547    2.8100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1205    0.4592    3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9029   -0.9827    4.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8209   -2.2744    3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3279   -1.2829    3.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1798    0.8622    4.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9761    1.4642    3.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9244    0.6434    3.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3292    2.2854    3.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4956    1.7449    0.9255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7453    1.0541    2.5168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7080   -0.2288    1.3125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8807    0.8844    1.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1370    2.4738    1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0209    1.8195   -0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1887    0.2721   -0.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9273    3.0583   -1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1432    2.5601   -3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8562    2.1699   -3.1807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4744    0.4608   -4.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3604   -0.2357   -3.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0606   -1.0786   -3.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4158    0.5592   -3.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0507   -0.6769   -0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7650    2.0973   -1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8641   -1.5517   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2020    0.1560   -1.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4580   -1.4294   -1.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    0.8883    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392   -1.8558    1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7340   -0.3190    0.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3701   -1.8980    1.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 21  1  0  0  0  0
 24 23  1  0  0  0  0
 24 18  1  0  0  0  0
 17 12  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 23  1  0  0  0  0
  7  8  1  0  0  0  0
 16 18  1  0  0  0  0
 16 17  1  0  0  0  0
 18 19  1  0  0  0  0
  4  5  1  0  0  0  0
  4  3  1  0  0  0  0
 23 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22  2  1  0  0  0  0
  2  3  1  0  0  0  0
  5  6  1  0  0  0  0
  2  1  1  0  0  0  0
 16 15  1  0  0  0  0
  4 29  1  1  0  0  0
 12 13  1  0  0  0  0
 16 48  1  1  0  0  0
 13 14  1  0  0  0  0
 18 50  1  1  0  0  0
 14 15  1  0  0  0  0
 23 56  1  1  0  0  0
 17  8  1  0  0  0  0
 21 53  1  6  0  0  0
  6  7  1  0  0  0  0
  7 34  1  6  0  0  0
 24  7  1  0  0  0  0
 12 41  1  6  0  0  0
 19 20  1  0  0  0  0
 17 49  1  6  0  0  0
 20 51  1  0  0  0  0
 20 52  1  0  0  0  0
  5 30  1  0  0  0  0
  5 31  1  0  0  0  0
  6 32  1  0  0  0  0
  6 33  1  0  0  0  0
 13 42  1  0  0  0  0
 13 43  1  0  0  0  0
 14 44  1  0  0  0  0
 14 45  1  0  0  0  0
 15 46  1  0  0  0  0
 15 47  1  0  0  0  0
  9 35  1  0  0  0  0
  9 36  1  0  0  0  0
 10 37  1  0  0  0  0
 10 38  1  0  0  0  0
 11 39  1  0  0  0  0
 11 40  1  0  0  0  0
 22 54  1  0  0  0  0
 22 55  1  0  0  0  0
  2 26  1  6  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
  1 25  1  0  0  0  0
M  END

     RDKit          3D

 56 61  0  0  0  0  0  0  0  0999 V2000
    4.1782   -1.2736    3.2378 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0080   -0.6036    2.7821 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8028   -1.1795    3.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4538   -0.6603    3.0060 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1907    0.7878    3.4309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1582    1.2353    2.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2457    1.0590    1.3435 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5540    1.4990    0.8228 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7227    0.8599    1.4402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0363    1.4235    0.8941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1088    1.3255   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8751    1.9858   -1.2488 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8833    1.8615   -2.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5489    0.4556   -3.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2381   -0.0492   -2.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2583    0.0051   -1.1400 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5620    1.4308   -0.6507 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9396   -0.4809   -0.5205 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1629    0.1831   -1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4094   -0.3752   -0.7441 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5686   -0.1916    0.7575 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8778   -0.7881    1.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3489   -0.8147    1.4746 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9364   -0.3195    0.9403 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9448   -0.8547    2.8100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1205    0.4592    3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9029   -0.9827    4.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8209   -2.2744    3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3279   -1.2829    3.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1798    0.8622    4.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9761    1.4642    3.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9244    0.6434    3.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3292    2.2854    3.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4956    1.7449    0.9255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7453    1.0541    2.5168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7080   -0.2288    1.3125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8807    0.8844    1.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1370    2.4738    1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0209    1.8195   -0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1887    0.2721   -0.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9273    3.0583   -1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1432    2.5601   -3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8562    2.1699   -3.1807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4744    0.4608   -4.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3604   -0.2357   -3.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0606   -1.0786   -3.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4158    0.5592   -3.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0507   -0.6769   -0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7650    2.0973   -1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8641   -1.5517   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2020    0.1560   -1.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4580   -1.4294   -1.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    0.8883    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392   -1.8558    1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7340   -0.3190    0.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3701   -1.8980    1.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 21  1  0
 24 23  1  0
 24 18  1  0
 17 12  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
  4 23  1  0
  7  8  1  0
 16 18  1  0
 16 17  1  0
 18 19  1  0
  4  5  1  0
  4  3  1  0
 23 21  1  0
 21 22  1  0
 22  2  1  0
  2  3  1  0
  5  6  1  0
  2  1  1  0
 16 15  1  0
  4 29  1  1
 12 13  1  0
 16 48  1  1
 13 14  1  0
 18 50  1  1
 14 15  1  0
 23 56  1  1
 17  8  1  0
 21 53  1  6
  6  7  1  0
  7 34  1  6
 24  7  1  0
 12 41  1  6
 19 20  1  0
 17 49  1  6
 20 51  1  0
 20 52  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 22 54  1  0
 22 55  1  0
  2 26  1  6
  3 27  1  0
  3 28  1  0
  1 25  1  0
M  END


  Mrv1652306192119233D          

 56 61  0  0  0  0            999 V2000
    4.1782   -1.2736    3.2378 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0080   -0.6036    2.7821 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8028   -1.1795    3.5243 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4538   -0.6603    3.0060 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1907    0.7878    3.4309 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1582    1.2353    2.8783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2457    1.0590    1.3435 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5540    1.4990    0.8228 N   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7227    0.8599    1.4402 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0363    1.4235    0.8941 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1088    1.3255   -0.6218 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8751    1.9858   -1.2488 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8833    1.8615   -2.7801 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5489    0.4556   -3.2723 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2381   -0.0492   -2.6764 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2583    0.0051   -1.1400 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5620    1.4308   -0.6507 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9396   -0.4809   -0.5205 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1629    0.1831   -1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4094   -0.3752   -0.7441 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5686   -0.1916    0.7575 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8778   -0.7881    1.2713 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3489   -0.8147    1.4746 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9364   -0.3195    0.9403 N   0  0  1  0  0  0  0  0  0  0  0  0
    4.9448   -0.8547    2.8100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1205    0.4592    3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9029   -0.9827    4.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8209   -2.2744    3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3279   -1.2829    3.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1798    0.8622    4.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9761    1.4642    3.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9244    0.6434    3.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3292    2.2854    3.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4956    1.7449    0.9255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7453    1.0541    2.5168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7080   -0.2288    1.3125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8807    0.8844    1.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1370    2.4738    1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0209    1.8195   -0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1887    0.2721   -0.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9273    3.0583   -1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1432    2.5601   -3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8562    2.1699   -3.1807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4744    0.4608   -4.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3604   -0.2357   -3.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0606   -1.0786   -3.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4158    0.5592   -3.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0507   -0.6769   -0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7650    2.0973   -1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8641   -1.5517   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2020    0.1560   -1.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4580   -1.4294   -1.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    0.8883    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392   -1.8558    1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7340   -0.3190    0.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3701   -1.8980    1.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 21  1  0  0  0  0
 24 23  1  0  0  0  0
 24 18  1  0  0  0  0
 17 12  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 23  1  0  0  0  0
  7  8  1  0  0  0  0
 16 18  1  0  0  0  0
 16 17  1  0  0  0  0
 18 19  1  0  0  0  0
  4  5  1  0  0  0  0
  4  3  1  0  0  0  0
 23 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22  2  1  0  0  0  0
  2  3  1  0  0  0  0
  5  6  1  0  0  0  0
  2  1  1  0  0  0  0
 16 15  1  0  0  0  0
  4 29  1  1  0  0  0
 12 13  1  0  0  0  0
 16 48  1  1  0  0  0
 13 14  1  0  0  0  0
 18 50  1  1  0  0  0
 14 15  1  0  0  0  0
 23 56  1  1  0  0  0
 17  8  1  0  0  0  0
 21 53  1  6  0  0  0
  6  7  1  0  0  0  0
  7 34  1  6  0  0  0
 24  7  1  0  0  0  0
 12 41  1  6  0  0  0
 19 20  1  0  0  0  0
 17 49  1  6  0  0  0
 20 51  1  0  0  0  0
 20 52  1  0  0  0  0
  5 30  1  0  0  0  0
  5 31  1  0  0  0  0
  6 32  1  0  0  0  0
  6 33  1  0  0  0  0
 13 42  1  0  0  0  0
 13 43  1  0  0  0  0
 14 44  1  0  0  0  0
 14 45  1  0  0  0  0
 15 46  1  0  0  0  0
 15 47  1  0  0  0  0
  9 35  1  0  0  0  0
  9 36  1  0  0  0  0
 10 37  1  0  0  0  0
 10 38  1  0  0  0  0
 11 39  1  0  0  0  0
 11 40  1  0  0  0  0
 22 54  1  0  0  0  0
 22 55  1  0  0  0  0
  2 26  1  6  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
  1 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0025216

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C([H])([H])[C@@]2([H])C([H])([H])O[C@@]3([H])N4[C@@]([H])(N5C([H])([H])C([H])([H])C([H])([H])[C@]6([H])C([H])([H])C([H])([H])C([H])([H])[C@]3([H])[C@]56[H])C([H])([H])C([H])([H])[C@]([H])(C1([H])[H])[C@]24[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H32N2O2/c23-15-9-13-6-7-17-21-8-2-4-12-3-1-5-16(19(12)21)20-22(17)18(13)14(10-15)11-24-20/h12-20,23H,1-11H2/t12-,13+,14-,15+,16+,17+,18+,19+,20+/m0/s1

> <INCHI_KEY>
QGSCHHAXALLULW-UPBDHPHQSA-N

> <FORMULA>
C20H32N2O2

> <MOLECULAR_WEIGHT>
332.488

> <EXACT_MASS>
332.246378278

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
38.55980814296497

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,6S,10R,11R,14R,16R,18R,22R,23R)-12-oxa-2,21-diazahexacyclo[12.6.2.1^{2,6}.0^{11,21}.0^{18,22}.0^{10,23}]tricosan-16-ol

> <ALOGPS_LOGP>
2.42

> <JCHEM_LOGP>
2.5507606089999992

> <ALOGPS_LOGS>
-2.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.234269496627512

> <JCHEM_PKA_STRONGEST_BASIC>
6.936320041690752

> <JCHEM_POLAR_SURFACE_AREA>
35.940000000000005

> <JCHEM_REFRACTIVITY>
92.88979999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.45e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,6S,10R,11R,14R,16R,18R,22R,23R)-12-oxa-2,21-diazahexacyclo[12.6.2.1^{2,6}.0^{11,21}.0^{18,22}.0^{10,23}]tricosan-16-ol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 56 61  0  0  0  0  0  0  0  0999 V2000
    4.1782   -1.2736    3.2378 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0080   -0.6036    2.7821 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8028   -1.1795    3.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4538   -0.6603    3.0060 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1907    0.7878    3.4309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1582    1.2353    2.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2457    1.0590    1.3435 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5540    1.4990    0.8228 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7227    0.8599    1.4402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0363    1.4235    0.8941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1088    1.3255   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8751    1.9858   -1.2488 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8833    1.8615   -2.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5489    0.4556   -3.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2381   -0.0492   -2.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2583    0.0051   -1.1400 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5620    1.4308   -0.6507 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9396   -0.4809   -0.5205 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1629    0.1831   -1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4094   -0.3752   -0.7441 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5686   -0.1916    0.7575 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8778   -0.7881    1.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3489   -0.8147    1.4746 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9364   -0.3195    0.9403 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9448   -0.8547    2.8100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1205    0.4592    3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9029   -0.9827    4.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8209   -2.2744    3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3279   -1.2829    3.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1798    0.8622    4.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9761    1.4642    3.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9244    0.6434    3.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3292    2.2854    3.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4956    1.7449    0.9255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7453    1.0541    2.5168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7080   -0.2288    1.3125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8807    0.8844    1.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1370    2.4738    1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0209    1.8195   -0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1887    0.2721   -0.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9273    3.0583   -1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1432    2.5601   -3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8562    2.1699   -3.1807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4744    0.4608   -4.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3604   -0.2357   -3.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0606   -1.0786   -3.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4158    0.5592   -3.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0507   -0.6769   -0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7650    2.0973   -1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8641   -1.5517   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2020    0.1560   -1.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4580   -1.4294   -1.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    0.8883    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392   -1.8558    1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7340   -0.3190    0.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3701   -1.8980    1.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 21  1  0
 24 23  1  0
 24 18  1  0
 17 12  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
  4 23  1  0
  7  8  1  0
 16 18  1  0
 16 17  1  0
 18 19  1  0
  4  5  1  0
  4  3  1  0
 23 21  1  0
 21 22  1  0
 22  2  1  0
  2  3  1  0
  5  6  1  0
  2  1  1  0
 16 15  1  0
  4 29  1  1
 12 13  1  0
 16 48  1  1
 13 14  1  0
 18 50  1  1
 14 15  1  0
 23 56  1  1
 17  8  1  0
 21 53  1  6
  6  7  1  0
  7 34  1  6
 24  7  1  0
 12 41  1  6
 19 20  1  0
 17 49  1  6
 20 51  1  0
 20 52  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 22 54  1  0
 22 55  1  0
  2 26  1  6
  3 27  1  0
  3 28  1  0
  1 25  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  O   UNK     0       4.178  -1.274   3.238  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.008  -0.604   2.782  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.803  -1.180   3.524  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.454  -0.660   3.006  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.191   0.788   3.431  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.158   1.235   2.878  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.246   1.059   1.343  0.00  0.00           C+0
HETATM    8  N   UNK     0      -2.554   1.499   0.823  0.00  0.00           N+0
HETATM    9  C   UNK     0      -3.723   0.860   1.440  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.036   1.424   0.894  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.109   1.325  -0.622  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.875   1.986  -1.249  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.883   1.861  -2.780  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.549   0.456  -3.272  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.238  -0.049  -2.676  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.258   0.005  -1.140  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.562   1.431  -0.651  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.940  -0.481  -0.521  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.163   0.183  -1.147  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.409  -0.375  -0.744  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.569  -0.192   0.758  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.878  -0.788   1.271  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.349  -0.815   1.475  0.00  0.00           C+0
HETATM   24  N   UNK     0      -0.936  -0.320   0.940  0.00  0.00           N+0
HETATM   25  H   UNK     0       4.945  -0.855   2.810  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.120   0.459   3.024  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.903  -0.983   4.599  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.821  -2.274   3.432  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.328  -1.283   3.465  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.180   0.862   4.525  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.976   1.464   3.077  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.924   0.643   3.392  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.329   2.285   3.145  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.496   1.745   0.926  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.745   1.054   2.517  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.708  -0.229   1.313  0.00  0.00           H+0
HETATM   37  H   UNK     0      -5.881   0.884   1.339  0.00  0.00           H+0
HETATM   38  H   UNK     0      -5.137   2.474   1.197  0.00  0.00           H+0
HETATM   39  H   UNK     0      -6.021   1.819  -0.977  0.00  0.00           H+0
HETATM   40  H   UNK     0      -5.189   0.272  -0.912  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.927   3.058  -1.011  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.143   2.560  -3.192  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.856   2.170  -3.181  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.474   0.461  -4.366  0.00  0.00           H+0
HETATM   45  H   UNK     0      -4.360  -0.236  -3.018  0.00  0.00           H+0
HETATM   46  H   UNK     0      -2.061  -1.079  -3.010  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.416   0.559  -3.073  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.051  -0.677  -0.803  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.765   2.097  -1.014  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.864  -1.552  -0.759  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.202   0.156  -1.281  0.00  0.00           H+0
HETATM   52  H   UNK     0       1.458  -1.429  -1.043  0.00  0.00           H+0
HETATM   53  H   UNK     0       1.591   0.888   0.953  0.00  0.00           H+0
HETATM   54  H   UNK     0       2.939  -1.856   1.022  0.00  0.00           H+0
HETATM   55  H   UNK     0       3.734  -0.319   0.771  0.00  0.00           H+0
HETATM   56  H   UNK     0       0.370  -1.898   1.280  0.00  0.00           H+0
CONECT    1    2   25                                                       
CONECT    2   22    3    1   26                                             
CONECT    3    4    2   27   28                                             
CONECT    4   23    5    3   29                                             
CONECT    5    4    6   30   31                                             
CONECT    6    5    7   32   33                                             
CONECT    7    8    6   34   24                                             
CONECT    8    9    7   17                                                  
CONECT    9    8   10   35   36                                             
CONECT   10    9   11   37   38                                             
CONECT   11   10   12   39   40                                             
CONECT   12   17   11   13   41                                             
CONECT   13   12   14   42   43                                             
CONECT   14   13   15   44   45                                             
CONECT   15   16   14   46   47                                             
CONECT   16   18   17   15   48                                             
CONECT   17   12   16    8   49                                             
CONECT   18   24   16   19   50                                             
CONECT   19   18   20                                                       
CONECT   20   21   19   51   52                                             
CONECT   21   20   23   22   53                                             
CONECT   22   21    2   54   55                                             
CONECT   23   24    4   21   56                                             
CONECT   24   23   18    7                                                  
CONECT   25    1                                                            
CONECT   26    2                                                            
CONECT   27    3                                                            
CONECT   28    3                                                            
CONECT   29    4                                                            
CONECT   30    5                                                            
CONECT   31    5                                                            
CONECT   32    6                                                            
CONECT   33    6                                                            
CONECT   34    7                                                            
CONECT   35    9                                                            
CONECT   36    9                                                            
CONECT   37   10                                                            
CONECT   38   10                                                            
CONECT   39   11                                                            
CONECT   40   11                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
CONECT   43   13                                                            
CONECT   44   14                                                            
CONECT   45   14                                                            
CONECT   46   15                                                            
CONECT   47   15                                                            
CONECT   48   16                                                            
CONECT   49   17                                                            
CONECT   50   18                                                            
CONECT   51   20                                                            
CONECT   52   20                                                            
CONECT   53   21                                                            
CONECT   54   22                                                            
CONECT   55   22                                                            
CONECT   56   23                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  122    0
END

RDKit          3D

56 61  0  0  0  0  0  0  0  0999 V2000
    4.1782   -1.2736    3.2378 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0080   -0.6036    2.7821 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8028   -1.1795    3.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4538   -0.6603    3.0060 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1907    0.7878    3.4309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1582    1.2353    2.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2457    1.0590    1.3435 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5540    1.4990    0.8228 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7227    0.8599    1.4402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0363    1.4235    0.8941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1088    1.3255   -0.6218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8751    1.9858   -1.2488 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8833    1.8615   -2.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5489    0.4556   -3.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2381   -0.0492   -2.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2583    0.0051   -1.1400 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5620    1.4308   -0.6507 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9396   -0.4809   -0.5205 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1629    0.1831   -1.1467 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4094   -0.3752   -0.7441 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5686   -0.1916    0.7575 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8778   -0.7881    1.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3489   -0.8147    1.4746 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9364   -0.3195    0.9403 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9448   -0.8547    2.8100 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1205    0.4592    3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9029   -0.9827    4.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8209   -2.2744    3.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3279   -1.2829    3.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1798    0.8622    4.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9761    1.4642    3.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9244    0.6434    3.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3292    2.2854    3.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4956    1.7449    0.9255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7453    1.0541    2.5168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7080   -0.2288    1.3125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8807    0.8844    1.3389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1370    2.4738    1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0209    1.8195   -0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1887    0.2721   -0.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9273    3.0583   -1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1432    2.5601   -3.1917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8562    2.1699   -3.1807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4744    0.4608   -4.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3604   -0.2357   -3.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0606   -1.0786   -3.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4158    0.5592   -3.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0507   -0.6769   -0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7650    2.0973   -1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8641   -1.5517   -0.7588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2020    0.1560   -1.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4580   -1.4294   -1.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5911    0.8883    0.9526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9392   -1.8558    1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7340   -0.3190    0.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3701   -1.8980    1.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 21  1  0
 24 23  1  0
 24 18  1  0
 17 12  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
  4 23  1  0
  7  8  1  0
 16 18  1  0
 16 17  1  0
 18 19  1  0
  4  5  1  0
  4  3  1  0
 23 21  1  0
 21 22  1  0
 22  2  1  0
  2  3  1  0
  5  6  1  0
  2  1  1  0
 16 15  1  0
  4 29  1  1
 12 13  1  0
 16 48  1  1
 13 14  1  0
 18 50  1  1
 14 15  1  0
 23 56  1  1
 17  8  1  0
 21 53  1  6
  6  7  1  0
  7 34  1  6
 24  7  1  0
 12 41  1  6
 19 20  1  0
 17 49  1  6
 20 51  1  0
 20 52  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 22 54  1  0
 22 55  1  0
  2 26  1  6
  3 27  1  0
  3 28  1  0
  1 25  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂N₂O₂

Average Mass

332.4880 Da

Monoisotopic Mass

332.24638 Da

IUPAC Name

(1R,6S,10R,11R,14R,16R,18R,22R,23R)-12-oxa-2,21-diazahexacyclo[12.6.2.1^{2,6}.0^{11,21}.0^{18,22}.0^{10,23}]tricosan-16-ol

Traditional Name

(1R,6S,10R,11R,14R,16R,18R,22R,23R)-12-oxa-2,21-diazahexacyclo[12.6.2.1^{2,6}.0^{11,21}.0^{18,22}.0^{10,23}]tricosan-16-ol

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])C([H])([H])[C@@]2([H])C([H])([H])O[C@@]3([H])N4[C@@]([H])(N5C([H])([H])C([H])([H])C([H])([H])[C@]6([H])C([H])([H])C([H])([H])C([H])([H])[C@]3([H])[C@]56[H])C([H])([H])C([H])([H])[C@]([H])(C1([H])[H])[C@]24[H]

InChI Identifier

InChI=1S/C20H32N2O2/c23-15-9-13-6-7-17-21-8-2-4-12-3-1-5-16(19(12)21)20-22(17)18(13)14(10-15)11-24-20/h12-20,23H,1-11H2/t12-,13+,14-,15+,16+,17+,18+,19+,20+/m0/s1

InChI Key

QGSCHHAXALLULW-UPBDHPHQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Myrioneuron nutans (Rubiaceae)	JEOL database	Pham, V. C., et al, J. Org. Chem. 72, 9826 (2007)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyridopyrimidines. Pyridopyrimidines are compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridopyrimidines

Sub Class

Not Available

Direct Parent

Pyridopyrimidines

Alternative Parents

Substituents

Pyridopyrimidine
Quinolidine
1,3-oxazinane
1,3-diazinane
Oxazinane
Piperidine
Pyridine
Pyrimidine
Cyclic alcohol
Hemiaminal
Secondary alcohol
Aminal
Azacycle
Oxacycle
Alcohol
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organopnictogen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.42	ALOGPS
logP	2.55	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	15.23	ChemAxon
pKa (Strongest Basic)	6.94	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	35.94 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	92.89 m³·mol⁻¹	ChemAxon
Polarizability	38.56 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	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

28284765

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24179289

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pham, V. C., et al. (2007). Pham, V. C., et al, J. Org. Chem. 72, 9826 (2007). J. Org. Chem..

Showing NP-Card for myrobotinol (NP0025216)

MOL for NP0025216 (myrobotinol)

3D MOL for NP0025216 (myrobotinol)

3D SDF for NP0025216 (myrobotinol)

3D-SDF for NP0025216 (myrobotinol)

PDB for NP0025216 (myrobotinol)

3D PDB for NP0025216 (myrobotinol)

SMILES for NP0025216 (myrobotinol)

INCHI for NP0025216 (myrobotinol)

Structure for NP0025216 (myrobotinol)

3D Structure for NP0025216 (myrobotinol)