NP-MRD: Showing NP-Card for (-)-Demethylnorpleiomutine (NP0075924)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 21:07:53 UTC

Updated at

2022-04-28 21:07:53 UTC

NP-MRD ID

NP0075924

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Demethylnorpleiomutine

Description

(1S,9R,16S,18R,21S)-6-[(15S,17S,19R)-15-ethyl-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]Nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸.0¹⁶,²¹]Henicosa-3(8),4,6-triene-18-carboxylic acid belongs to the class of organic compounds known as aspidofractine alkaloids. These are alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond. (-)-Demethylnorpleiomutine is found in Kopsia dasyrachis. Based on a literature review very few articles have been published on (1S,9R,16S,18R,21S)-6-[(15S,17S,19R)-15-ethyl-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]Nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸.0¹⁶,²¹]Henicosa-3(8),4,6-triene-18-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282223072D          

 45 55  0  0  1  0            999 V2000
    8.3161   -3.3958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9078   -2.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7058   -2.0210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9120   -1.7960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3203   -2.3709    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5223   -3.1708    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9306   -3.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1369   -3.5207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9349   -2.7208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5266   -2.1459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3246   -1.3460    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9163   -0.7711    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7100   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7143    0.0288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3060    0.6037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1040    1.4035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3102    1.6285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7185    1.0536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9205    0.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8394    1.1527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0933    2.0737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9080    2.3764    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4505    1.6774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8128    2.0860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622    1.6652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8765    1.0419    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6514    0.1748    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8187    0.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1996    0.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3151    1.4408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3212   -0.3372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8777    0.2921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4395    2.5557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3664    2.6425    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5986    3.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4003    3.6289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0291    4.0311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3461   -1.5228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2053   -2.3357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4309   -2.6202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7973   -2.0918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9381   -1.2789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7125   -0.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5037   -1.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3017   -0.4212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 13  1  0  0  0  0
 12 14  1  6  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 20 18  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 17 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
 25 26  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 27 31  1  0  0  0  0
 31 32  1  0  0  0  0
 20 32  1  0  0  0  0
 25 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 11 38  1  0  0  0  0
 38 39  1  0  0  0  0
  9 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 38 43  2  0  0  0  0
  4 44  1  1  0  0  0
 44 45  1  0  0  0  0
M  END

     RDKit          3D

 91101  0  0  0  0  0  0  0  0999 V2000
   -5.2488   -2.4983    1.3976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9293   -2.2572    0.7561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9576   -1.7452   -0.6403 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6565   -2.6770   -1.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1255   -2.4623   -1.6990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5313   -1.0217   -1.7417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9299   -0.2889   -0.6475 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4401    1.0401   -0.5170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7848    1.8751    0.5118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3536    1.5585    0.7335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7996    0.5077    0.1026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5029    0.3494    0.4078 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2197    1.3425    1.2702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0500    1.7083    1.9400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0859    2.7997    2.7734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2204    3.5572    2.9851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3964    3.2055    2.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3442    2.1153    1.4973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7075   -0.7270   -0.1599 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4749   -0.2423   -0.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5518    0.5338   -1.9567 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5960    0.9844   -2.6021 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8386    0.6316   -2.0667 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9621   -0.1413   -0.9318 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7801   -0.5526   -0.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3892   -0.3123   -0.6931 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8133   -1.6129   -1.3155 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6090   -2.5720   -0.1609 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0667   -1.7928    0.9881 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3365   -2.2528    1.3725 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2388   -1.2941    2.0591 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7043    0.1070    2.1770 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0417    0.4657    0.8877 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0548    0.3485   -0.2288 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4382    0.7175   -1.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9837    0.8923   -1.3576 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1621    0.9806   -2.5369 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8120    2.1078   -0.4587 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4437    3.3026   -1.0863 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3865    3.9558   -0.5340 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0386    3.7899   -2.3368 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5218    1.8878    0.8585 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8512   -0.4364    0.7043 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4870   -1.6051   -1.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5166   -0.3604   -0.8102 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6012   -3.5209    1.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0598   -2.5601    2.5108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0050   -1.7292    1.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3046   -1.6430    1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4061   -3.2589    0.7061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5090   -3.7169   -1.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1907   -2.6838   -2.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4630   -2.9095   -2.6777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7183   -2.9767   -0.9202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2600   -0.5938   -2.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6336   -0.9675   -1.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5358    0.9948   -0.3589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2963    1.5623   -1.5078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9670    2.9578    0.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2939    1.6382    1.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1476    1.1200    1.7852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1510    3.0478    3.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2135    4.4044    3.6445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3093    3.7502    2.4449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3906   -1.3566    0.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5524    0.7683   -2.3139 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4989    1.5852   -3.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8597   -1.1559    0.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1537   -1.8492   -2.1770 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8439   -1.6676   -1.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1989   -3.5016   -0.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5283   -2.7829    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1862   -3.1250    2.0796 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8369   -2.7458    0.4849 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2123   -1.2579    1.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4950   -1.6178    3.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9765    0.1492    3.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5653    0.7922    2.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5705   -0.6060   -0.2896 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8391    1.1186   -0.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7170    0.0170   -2.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8369    1.7197   -1.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4221    1.2275   -3.4920 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7362    2.3258   -0.2782 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4344    4.6119   -2.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3410    2.6082    1.0289 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8025    1.9953    1.7150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0450   -0.0379    1.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0879   -2.6604   -1.0218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4782   -1.3172   -2.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2796   -0.0648   -1.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 45  1  0
 11 12  1  0
 12 19  1  0
 19 44  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 37  1  0
 36 37  1  6
 36 35  1  0
 35 34  1  0
 34 33  1  0
 33 32  1  1
 32 31  1  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 27  1  0
 26 27  1  6
 26 43  1  0
 26 24  1  0
 24 25  2  0
 33 42  1  0
 42 38  1  0
 38 39  1  0
 39 41  1  0
 39 40  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 45  3  1  0
 25 20  1  0
 18 13  1  0
 44  3  1  0
 24 23  1  0
 45  7  1  0
 26 36  1  0
 18 10  1  0
 38 36  1  0
 43 33  1  0
 43 29  1  0
  1 46  1  0
  1 47  1  0
  1 48  1  0
  2 49  1  0
  2 50  1  0
  4 51  1  0
  4 52  1  0
  5 53  1  0
  5 54  1  0
  6 55  1  0
  6 56  1  0
  8 57  1  0
  8 58  1  0
  9 59  1  0
  9 60  1  0
 45 91  1  6
 19 65  1  1
 44 89  1  0
 44 90  1  0
 21 66  1  0
 22 67  1  0
 37 83  1  0
 35 81  1  0
 35 82  1  0
 34 79  1  0
 34 80  1  0
 32 77  1  0
 32 78  1  0
 31 75  1  0
 31 76  1  0
 30 73  1  0
 30 74  1  0
 28 71  1  0
 28 72  1  0
 27 69  1  0
 27 70  1  0
 43 88  1  1
 25 68  1  0
 42 86  1  0
 42 87  1  0
 38 84  1  1
 41 85  1  0
 14 61  1  0
 15 62  1  0
 16 63  1  0
 17 64  1  0
M  END


  Mrv1652304282223072D          

 45 55  0  0  1  0            999 V2000
    8.3161   -3.3958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9078   -2.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7058   -2.0210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9120   -1.7960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3203   -2.3709    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5223   -3.1708    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9306   -3.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1369   -3.5207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9349   -2.7208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5266   -2.1459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3246   -1.3460    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9163   -0.7711    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7100   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7143    0.0288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3060    0.6037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1040    1.4035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3102    1.6285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7185    1.0536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9205    0.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8394    1.1527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0933    2.0737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9080    2.3764    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4505    1.6774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8128    2.0860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1622    1.6652    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8765    1.0419    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6514    0.1748    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8187    0.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1996    0.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3151    1.4408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3212   -0.3372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8777    0.2921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4395    2.5557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3664    2.6425    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5986    3.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4003    3.6289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0291    4.0311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3461   -1.5228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2053   -2.3357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4309   -2.6202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7973   -2.0918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9381   -1.2789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7125   -0.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5037   -1.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3017   -0.4212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 13  1  0  0  0  0
 12 14  1  6  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 20 18  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 17 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
 25 26  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 27 31  1  0  0  0  0
 31 32  1  0  0  0  0
 20 32  1  0  0  0  0
 25 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 11 38  1  0  0  0  0
 38 39  1  0  0  0  0
  9 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 38 43  2  0  0  0  0
  4 44  1  1  0  0  0
 44 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0075924

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@]12CCCN3CCC4=C([C@@H]13)N([C@@H](C2)C1=CC=C2N[C@]35CC[C@@]6(CCCN7CC[C@]3([C@H]67)C2=C1)C[C@H]5C(O)=O)C1=CC=CC=C41

> <INCHI_IDENTIFIER>
InChI=1S/C39H46N4O2/c1-2-36-12-5-17-41-19-11-26-25-7-3-4-8-30(25)43(32(26)33(36)41)31(23-36)24-9-10-29-27(21-24)38-16-20-42-18-6-13-37(35(38)42)14-15-39(38,40-29)28(22-37)34(44)45/h3-4,7-10,21,28,31,33,35,40H,2,5-6,11-20,22-23H2,1H3,(H,44,45)/t28-,31-,33-,35-,36-,37-,38+,39-/m0/s1

> <INCHI_KEY>
YKJPOSKZESOFGR-AQFJFXQZSA-N

> <FORMULA>
C39H46N4O2

> <MOLECULAR_WEIGHT>
602.823

> <EXACT_MASS>
602.362076737

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
68.54943034603006

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,9R,16S,18R,21S)-6-[(15S,17S,19R)-15-ethyl-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.1^{9,12}.0^{1,9}.0^{3,8}.0^{16,21}]henicosa-3,5,7-triene-18-carboxylic acid

> <ALOGPS_LOGP>
5.94

> <JCHEM_LOGP>
3.01194784141857

> <ALOGPS_LOGS>
-5.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
11

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
18.099045095834043

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9834567609858644

> <JCHEM_PKA_STRONGEST_BASIC>
10.27411283042382

> <JCHEM_POLAR_SURFACE_AREA>
60.739999999999995

> <JCHEM_REFRACTIVITY>
177.81449999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.96e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,9R,16S,18R,21S)-6-[(15S,17S,19R)-15-ethyl-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.1^{9,12}.0^{1,9}.0^{3,8}.0^{16,21}]henicosa-3,5,7-triene-18-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      15.523  -6.339   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.628  -5.266   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.251  -3.773   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.769  -3.353   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.665  -4.426   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      14.042  -5.919   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      12.937  -6.992   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.456  -6.572   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.078  -5.079   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.183  -4.006   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      11.806  -2.513   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      12.910  -1.439   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.392  -1.859   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.533   0.054   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.638   1.127   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.261   2.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.779   3.040   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.675   1.967   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.052   0.474   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.033   2.152   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.507   3.871   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      11.028   4.436   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       8.308   3.131   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.117   3.894   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.903   3.108   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.236   1.945   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       6.816   0.326   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       5.261   0.079   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.106   1.133   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.321   2.689   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.066  -0.629   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.105   0.545   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.420   4.771   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.151   4.933   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.584   6.411   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      10.080   6.774   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       7.521   7.525   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       9.979  -2.843   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.717  -4.360   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.271  -4.891   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.088  -3.905   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       7.351  -2.387   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.797  -1.856   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      15.874  -2.279   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      15.497  -0.786   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   13   44                                             
CONECT    5    4    6   10                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   39                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10   12   38                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12    4                                                       
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   14                                                       
CONECT   20   18   21   26   32                                             
CONECT   21   20   22   23   34                                             
CONECT   22   21   17                                                       
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   30   33                                             
CONECT   26   25   20   27                                                  
CONECT   27   26   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25                                                       
CONECT   31   27   32                                                       
CONECT   32   31   20                                                       
CONECT   33   25   34                                                       
CONECT   34   33   21   35                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   11   39   43                                                  
CONECT   39   38    9   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   38                                                       
CONECT   44    4   45                                                       
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  110    0
END

View in JSmol

Synonyms

Value	Source
(1S,9R,16S,18R,21S)-6-[(15S,17S,19R)-15-Ethyl-1,11-diazapentacyclo[9.6.2.0,.0,.0,]nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.1,.0,.0,.0,]henicosa-3(8),4,6-triene-18-carboxylate	Generator

Chemical Formula

C₃₉H₄₆N₄O₂

Average Mass

602.8230 Da

Monoisotopic Mass

602.36208 Da

IUPAC Name

(1S,9R,16S,18R,21S)-6-[(15S,17S,19R)-15-ethyl-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.1^{9,12}.0^{1,9}.0^{3,8}.0^{16,21}]henicosa-3,5,7-triene-18-carboxylic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CC[C@@]12CCCN3CCC4=C([C@@H]13)N([C@@H](C2)C1=CC=C2N[C@]35CC[C@@]6(CCCN7CC[C@]3([C@H]67)C2=C1)C[C@H]5C(O)=O)C1=CC=CC=C41

InChI Identifier

InChI=1S/C39H46N4O2/c1-2-36-12-5-17-41-19-11-26-25-7-3-4-8-30(25)43(32(26)33(36)41)31(23-36)24-9-10-29-27(21-24)38-16-20-42-18-6-13-37(35(38)42)14-15-39(38,40-29)28(22-37)34(44)45/h3-4,7-10,21,28,31,33,35,40H,2,5-6,11-20,22-23H2,1H3,(H,44,45)/t28-,31-,33-,35-,36-,37-,38+,39-/m0/s1

InChI Key

YKJPOSKZESOFGR-AQFJFXQZSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Kopsia dasyrachis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aspidofractine alkaloids. These are alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aspidofractine alkaloids

Sub Class

Not Available

Direct Parent

Aspidofractine alkaloids

Alternative Parents

Substituents

Aspidofractine skeleton
Eburna alkaloid
Aspidosperma alkaloid
Indolo[3,2-1de][1,5]naphthyridine
Quinoline-6-carboxylic acid
Pyridoindole
Carbazole
Beta-carboline
Diazanaphthalene
Quinolidine
3-alkylindole
Naphthyridine
Azaspirodecane
Indolizidine
Dihydroindole
Indole or derivatives
Indole
Aralkylamine
Secondary aliphatic/aromatic amine
Benzenoid
N-alkylpyrrolidine
Piperidine
Heteroaromatic compound
Pyrrolidine
Pyrrole
Amino acid
Tertiary aliphatic amine
Tertiary amine
Amino acid or derivatives
Azacycle
Organoheterocyclic compound
Secondary amine
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	5.94	ALOGPS
logP	3.01	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	3.98	ChemAxon
pKa (Strongest Basic)	10.27	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	60.74 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	177.81 m³·mol⁻¹	ChemAxon
Polarizability	68.55 Å³	ChemAxon
Number of Rings	11	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	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

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

162992548

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Demethylnorpleiomutine (NP0075924)

MOL for NP0075924 ((-)-Demethylnorpleiomutine)

3D MOL for NP0075924 ((-)-Demethylnorpleiomutine)

3D SDF for NP0075924 ((-)-Demethylnorpleiomutine)

3D-SDF for NP0075924 ((-)-Demethylnorpleiomutine)

PDB for NP0075924 ((-)-Demethylnorpleiomutine)

3D PDB for NP0075924 ((-)-Demethylnorpleiomutine)

SMILES for NP0075924 ((-)-Demethylnorpleiomutine)

INCHI for NP0075924 ((-)-Demethylnorpleiomutine)

Structure for NP0075924 ((-)-Demethylnorpleiomutine)

3D Structure for NP0075924 ((-)-Demethylnorpleiomutine)