NP-MRD: Showing NP-Card for (+)-Alstomacroline (NP0066719)

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Record Information

Version

2.0

Created at

2022-04-28 10:58:21 UTC

Updated at

2022-04-28 10:58:21 UTC

NP-MRD ID

NP0066719

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Alstomacroline

Description

Methyl (1R,9R,10S,12S,13E,16S,17R,18S)-13-ethylidene-18-hydroxy-8-{[(1R,12R,13R,16R,17R,18R)-16-hydroxy-3,16,20-trimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0²,¹⁰.0⁴,⁹.0¹³,¹⁸]Icosa-2(10),4,6,8-tetraen-17-yl]methyl}-8,15-diazahexacyclo[14.2.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵.0¹²,¹⁷]Nonadeca-2,4,6-triene-17-carboxylate belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids. (+)-Alstomacroline is found in Alstonia macrophylla . Based on a literature review very few articles have been published on methyl (1R,9R,10S,12S,13E,16S,17R,18S)-13-ethylidene-18-hydroxy-8-{[(1R,12R,13R,16R,17R,18R)-16-hydroxy-3,16,20-trimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0²,¹⁰.0⁴,⁹.0¹³,¹⁸]Icosa-2(10),4,6,8-tetraen-17-yl]methyl}-8,15-diazahexacyclo[14.2.1.0¹,⁹.0²,⁷.0¹⁰,¹⁵.0¹²,¹⁷]Nonadeca-2,4,6-triene-17-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282212582D          

 51 61  0  0  1  0            999 V2000
    7.2013   -3.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2841   -4.0574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6147   -4.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8624   -4.2009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7796   -3.3801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4490   -2.8979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9672   -3.1143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6328   -3.9303    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1286   -4.5779    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8362   -5.5190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5604   -5.9400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3468   -5.6908    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9559   -6.2472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7786   -7.0529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9921   -7.3022    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3830   -6.7458    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5589   -6.7830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0024   -7.3921    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1077   -7.5059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0294   -8.1264    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    4.6488   -8.7727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0397   -8.2163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3222   -8.6236    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4880   -9.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3078   -9.5239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6379  -10.2800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1482  -10.9439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3284  -10.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9982  -10.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5367   -8.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7574   -6.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3023   -4.9292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2609   -5.5935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6298   -3.7528    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1581   -3.0256    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6683   -2.5225    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5022   -2.3695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6040   -3.2829    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8133   -4.1693    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4771   -4.4528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0586   -3.8335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2318   -4.1280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8371   -4.8824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3447   -3.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3293   -3.5175    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3572   -4.4244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8275   -4.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3726   -4.9640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705   -4.7722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0055   -5.5965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 20 19  1  6  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 25 30  2  0  0  0  0
 24 31  1  0  0  0  0
 19 32  1  0  0  0  0
 12 33  1  1  0  0  0
 12 34  1  6  0  0  0
  8 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
  7 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  1  0  0  0
 35 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 42 45  1  0  0  0  0
 36 45  1  0  0  0  0
 39 46  1  0  0  0  0
  7 46  1  0  0  0  0
 46 47  1  6  0  0  0
 39 48  1  6  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END

     RDKit          3D

101111  0  0  0  0  0  0  0  0999 V2000
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   -3.8760   -1.6094    1.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0070   -0.6246    2.9640 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8776   -3.1219    1.0781 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2339    0.7484    1.0935 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0952    0.5999    2.7953 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.2912   -0.9592   -2.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1943    1.3345    0.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2302    1.7073    1.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
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 13 12  1  0
 12 10  1  0
 10 11  2  0
  9 10  1  1
  9 14  1  0
 14 15  1  0
 16 15  1  6
 16 50  1  0
 50 51  1  0
 16 49  1  0
 49  6  1  0
  6  7  1  0
  7  8  1  0
  8  3  1  0
  3  4  1  0
  4  5  1  0
  3  2  2  0
  2  1  1  0
 49 23  1  0
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 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 47  1  0
 47 48  1  0
 47 40  1  0
 40 39  1  0
 39 30  1  0
 30 29  2  0
 29 37  1  0
 37 38  1  0
 37 36  1  0
 36 35  2  0
 35 34  1  0
 34 33  2  0
 33 32  1  0
 32 31  2  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 44 46  1  1
 23 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  2  0
 50  9  1  0
  5  6  1  0
 44 25  1  0
 17 22  1  0
  8  9  1  0
 41 26  1  0
  5 14  1  0
 29 28  1  0
 31 36  1  0
 16 17  1  0
 31 30  1  0
 13 62  1  0
 13 63  1  0
 13 64  1  0
 14 65  1  6
 15 66  1  0
 15 67  1  0
 50100  1  6
 51101  1  0
 49 99  1  1
  6 58  1  6
  7 59  1  0
  7 60  1  0
  8 61  1  1
  4 56  1  0
  4 57  1  0
  2 55  1  0
  1 52  1  0
  1 53  1  0
  1 54  1  0
 24 72  1  0
 24 73  1  0
 25 74  1  6
 26 75  1  1
 27 76  1  0
 27 77  1  0
 28 78  1  1
 48 96  1  0
 48 97  1  0
 48 98  1  0
 40 88  1  1
 39 86  1  0
 39 87  1  0
 38 83  1  0
 38 84  1  0
 38 85  1  0
 35 82  1  0
 34 81  1  0
 33 80  1  0
 32 79  1  0
 41 89  1  1
 42 90  1  0
 42 91  1  0
 45 92  1  0
 45 93  1  0
 45 94  1  0
 46 95  1  0
 21 71  1  0
 20 70  1  0
 19 69  1  0
 18 68  1  0
M  END


  Mrv1652304282212582D          

 51 61  0  0  1  0            999 V2000
    7.2013   -3.2366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2841   -4.0574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6147   -4.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8624   -4.2009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7796   -3.3801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4490   -2.8979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9672   -3.1143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6328   -3.9303    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1286   -4.5779    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8362   -5.5190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5604   -5.9400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3468   -5.6908    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9559   -6.2472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7786   -7.0529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9921   -7.3022    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3830   -6.7458    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5589   -6.7830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0024   -7.3921    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1077   -7.5059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0294   -8.1264    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4729   -8.7355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6488   -8.7727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0397   -8.2163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3222   -8.6236    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4880   -9.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3078   -9.5239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6379  -10.2800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1482  -10.9439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3284  -10.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9982  -10.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5367   -8.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7574   -6.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3023   -4.9292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2609   -5.5935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6298   -3.7528    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1581   -3.0256    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6683   -2.5225    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5022   -2.3695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6040   -3.2829    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8133   -4.1693    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4771   -4.4528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0586   -3.8335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2318   -4.1280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8371   -4.8824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3447   -3.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3293   -3.5175    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3572   -4.4244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8275   -4.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3726   -4.9640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705   -4.7722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0055   -5.5965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 20 19  1  6  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 25 30  2  0  0  0  0
 24 31  1  0  0  0  0
 19 32  1  0  0  0  0
 12 33  1  1  0  0  0
 12 34  1  6  0  0  0
  8 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
  7 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  1  0  0  0
 35 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 42 45  1  0  0  0  0
 36 45  1  0  0  0  0
 39 46  1  0  0  0  0
  7 46  1  0  0  0  0
 46 47  1  6  0  0  0
 39 48  1  6  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066719

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]12[C@@H]3C[C@]4([C@@H]1O)[C@H]([C@@H]1C[C@H]2\C(CN31)=C/C)N(C[C@H]1[C@@H]2C[C@H]3N(C)[C@H](CC5=C3N(C)C3=CC=CC=C53)[C@@H]2CO[C@@]1(C)O)C1=CC=CC=C41

> <INCHI_IDENTIFIER>
InChI=1S/C42H50N4O5/c1-6-22-19-45-34-17-28(22)42(39(48)50-5)35(45)18-41(38(42)47)27-12-8-10-14-31(27)46(37(34)41)20-29-24-15-33-36-25(23-11-7-9-13-30(23)44(36)4)16-32(43(33)3)26(24)21-51-40(29,2)49/h6-14,24,26,28-29,32-35,37-38,47,49H,15-21H2,1-5H3/b22-6-/t24-,26-,28+,29+,32-,33-,34+,35+,37+,38+,40-,41-,42-/m1/s1

> <INCHI_KEY>
KWWPTZADUTXZJC-GHZLNBJGSA-N

> <FORMULA>
C42H50N4O5

> <MOLECULAR_WEIGHT>
690.885

> <EXACT_MASS>
690.378120726

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
76.40054069638904

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1R,9R,10S,12S,13E,16S,17R,18S)-13-ethylidene-18-hydroxy-8-{[(1R,12R,13R,16R,17R,18R)-16-hydroxy-3,16,20-trimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0^{2,10}.0^{4,9}.0^{13,18}]icosa-2(10),4,6,8-tetraen-17-yl]methyl}-8,15-diazahexacyclo[14.2.1.0^{1,9}.0^{2,7}.0^{10,15}.0^{12,17}]nonadeca-2,4,6-triene-17-carboxylate

> <ALOGPS_LOGP>
4.30

> <JCHEM_LOGP>
3.9024676256666653

> <ALOGPS_LOGS>
-4.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
11

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
13.852608268124627

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.021102386601406

> <JCHEM_PKA_STRONGEST_BASIC>
7.5400915528449755

> <JCHEM_POLAR_SURFACE_AREA>
90.64

> <JCHEM_REFRACTIVITY>
196.0911

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,9R,10S,12S,13E,16S,17R,18S)-13-ethylidene-18-hydroxy-8-{[(1R,12R,13R,16R,17R,18R)-16-hydroxy-3,16,20-trimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0^{2,10}.0^{4,9}.0^{13,18}]icosa-2(10),4,6,8-tetraen-17-yl]methyl}-8,15-diazahexacyclo[14.2.1.0^{1,9}.0^{2,7}.0^{10,15}.0^{12,17}]nonadeca-2,4,6-triene-17-carboxylate

> <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      13.442  -6.042   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.597  -7.574   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.347  -8.474   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.943  -7.842   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.788  -6.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.038  -5.409   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.272  -5.813   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.648  -7.337   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       9.573  -8.545   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       9.028 -10.302   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.379 -11.088   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.847 -10.623   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.984 -11.661   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      12.653 -13.165   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.185 -13.631   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.048 -12.592   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.510 -12.662   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.471 -13.799   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       9.534 -14.011   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      11.255 -15.169   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.216 -16.306   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.678 -16.376   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.541 -15.337   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       6.202 -16.097   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       6.511 -17.606   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.041 -17.778   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.657 -19.189   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.743 -20.429   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.213 -20.257   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.597 -18.845   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.735 -15.465   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.747 -12.958   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.764  -9.201   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      13.554 -10.441   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       6.776  -7.005   0.000  0.00  0.00           C+0
HETATM   36  N   UNK     0       5.895  -5.648   0.000  0.00  0.00           N+0
HETATM   37  C   UNK     0       6.848  -4.709   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.404  -4.423   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.728  -6.128   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.252  -7.783   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.491  -8.312   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.843  -7.156   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.299  -7.706   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.563  -9.114   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.377  -5.747   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       8.081  -6.566   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       8.133  -8.259   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       7.145  -7.892   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       8.162  -9.266   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       5.545  -8.908   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       5.610 -10.447   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   38   46                                             
CONECT    8    7    9   35                                                  
CONECT    9    8    4   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   33   34                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   11   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20   32                                                  
CONECT   20   19   15   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   26                                                  
CONECT   23   22   18   24                                                  
CONECT   24   23   25   31                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   22   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25                                                       
CONECT   31   24                                                            
CONECT   32   19                                                            
CONECT   33   12                                                            
CONECT   34   12                                                            
CONECT   35    8   36   41                                                  
CONECT   36   35   37   45                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37    7                                                       
CONECT   39   37   40   46   48                                             
CONECT   40   39   41   42                                                  
CONECT   41   40   35                                                       
CONECT   42   40   43   45                                                  
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   42   36                                                       
CONECT   46   39    7   47                                                  
CONECT   47   46                                                            
CONECT   48   39   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   51                                                       
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  122    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1R,9R,10S,12S,13E,16S,17R,18S)-13-ethylidene-18-hydroxy-8-{[(1R,12R,13R,16R,17R,18R)-16-hydroxy-3,16,20-trimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0,.0,.0,]icosa-2(10),4,6,8-tetraen-17-yl]methyl}-8,15-diazahexacyclo[14.2.1.0,.0,.0,.0,]nonadeca-2,4,6-triene-17-carboxylic acid	Generator

Chemical Formula

C₄₂H₅₀N₄O₅

Average Mass

690.8850 Da

Monoisotopic Mass

690.37812 Da

IUPAC Name

methyl (1R,9R,10S,12S,13E,16S,17R,18S)-13-ethylidene-18-hydroxy-8-{[(1R,12R,13R,16R,17R,18R)-16-hydroxy-3,16,20-trimethyl-15-oxa-3,20-diazapentacyclo[10.7.1.0^{2,10}.0^{4,9}.0^{13,18}]icosa-2(10),4,6,8-tetraen-17-yl]methyl}-8,15-diazahexacyclo[14.2.1.0^{1,9}.0^{2,7}.0^{10,15}.0^{12,17}]nonadeca-2,4,6-triene-17-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]12[C@@H]3C[C@]4([C@@H]1O)[C@H]([C@@H]1C[C@H]2\C(CN31)=C/C)N(C[C@H]1[C@@H]2C[C@H]3N(C)[C@H](CC5=C3N(C)C3=CC=CC=C53)[C@@H]2CO[C@@]1(C)O)C1=CC=CC=C41

InChI Identifier

InChI=1S/C42H50N4O5/c1-6-22-19-45-34-17-28(22)42(39(48)50-5)35(45)18-41(38(42)47)27-12-8-10-14-31(27)46(37(34)41)20-29-24-15-33-36-25(23-11-7-9-13-30(23)44(36)4)16-32(43(33)3)26(24)21-51-40(29,2)49/h6-14,24,26,28-29,32-35,37-38,47,49H,15-21H2,1-5H3/b22-6-/t24-,26-,28+,29+,32-,33-,34+,35+,37+,38+,40-,41-,42-/m1/s1

InChI Key

KWWPTZADUTXZJC-GHZLNBJGSA-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
Alstonia macrophylla	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macroline alkaloids. These are alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Macroline alkaloids

Sub Class

Not Available

Direct Parent

Macroline alkaloids

Alternative Parents

Substituents

Macroline skeleton
Corynanthean skeleton
Pyridoindole
Beta-carboline
N-alkylindole
3-alkylindole
Quinolizidine
Piperidinecarboxylic acid
Indole or derivatives
Indole
Dialkylarylamine
Tertiary aliphatic/aromatic amine
Quinuclidine
Aralkylamine
Beta-hydroxy acid
Azepane
Benzenoid
Substituted pyrrole
Piperidine
Oxane
N-methylpyrrole
Hydroxy acid
Heteroaromatic compound
Methyl ester
Pyrrole
Cyclic alcohol
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Hemiacetal
Carboxylic acid ester
Amino acid or derivatives
Oxacycle
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.3	ALOGPS
logP	3.9	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	12.02	ChemAxon
pKa (Strongest Basic)	7.54	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	90.64 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	196.09 m³·mol⁻¹	ChemAxon
Polarizability	76.4 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

163036972

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Alstomacroline (NP0066719)

MOL for NP0066719 ((+)-Alstomacroline)

3D MOL for NP0066719 ((+)-Alstomacroline)

3D SDF for NP0066719 ((+)-Alstomacroline)

3D-SDF for NP0066719 ((+)-Alstomacroline)

PDB for NP0066719 ((+)-Alstomacroline)

3D PDB for NP0066719 ((+)-Alstomacroline)

SMILES for NP0066719 ((+)-Alstomacroline)

INCHI for NP0066719 ((+)-Alstomacroline)

Structure for NP0066719 ((+)-Alstomacroline)

3D Structure for NP0066719 ((+)-Alstomacroline)