NP-MRD: Showing NP-Card for (5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one (NP0204736)

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Record Information

Version

2.0

Created at

2022-09-05 00:28:18 UTC

Updated at

2022-09-05 00:28:18 UTC

NP-MRD ID

NP0204736

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one

Description

(5S)-3-methyl-5-[(1R,4R,7S,9S,10E,12S,17R,19S,20R,24R,29S,32S)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]Pentatriaconta-10,13,22-trien-14-yl]-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as azepines. These are organic compounds containing an unsaturated seven-member heterocycle with one nitrogen atom replacing a carbon atom. (5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one is found in Alexandrium ostenfeldii. Based on a literature review very few articles have been published on (5S)-3-methyl-5-[(1R,4R,7S,9S,10E,12S,17R,19S,20R,24R,29S,32S)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]Pentatriaconta-10,13,22-trien-14-yl]-2,5-dihydrofuran-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052202282D          

 50 56  0  0  1  0            999 V2000
    4.2777   -0.9679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7279   -0.3528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2682    0.2875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0935    0.0828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8159   -0.3983    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4170    0.1668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2605   -1.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4180   -1.2615    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9318   -1.9289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1724   -2.7048    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5624   -3.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9200   -3.0158    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9821   -3.8385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6243   -2.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9247   -1.8001    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5624   -1.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4003   -1.3340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6868   -2.1108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5002   -2.2483    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0896   -1.6711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8208   -2.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5597   -1.6864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6833   -2.8667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2605   -3.4561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8671   -2.9873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1642   -2.7463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4520   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3376   -2.6045    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9911   -3.4257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4083   -4.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9070   -4.7343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6341   -4.4578    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7346   -5.2766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7640   -4.2699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8699   -3.9832    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8333   -4.2505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0689   -4.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655   -3.9095    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2695   -4.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8741   -3.3594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3756   -2.6920    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7129   -1.9235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2770   -1.2226    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4408   -1.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0634   -2.0049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5181   -2.6803    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1254   -3.4059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0236   -0.8233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1654   -3.0455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8069   -4.7121    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 19 25  1  0  0  0  0
 18 26  2  0  0  0  0
 26 27  1  0  0  0  0
 28 26  1  6  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 43 42  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 41 46  1  0  0  0  0
 46 47  1  1  0  0  0
 43 48  1  0  0  0  0
  2 48  1  0  0  0  0
 41 49  1  6  0  0  0
 38 49  1  6  0  0  0
 38 50  1  0  0  0  0
 35 50  1  6  0  0  0
M  END

     RDKit          3D

109115  0  0  0  0  0  0  0  0999 V2000
    2.7090   -2.7563    3.4683 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6793   -1.4805    3.1313 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3927   -0.7635    3.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2639   -1.5414    2.4823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0163   -0.9612    1.0817 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0658   -1.4517    0.3040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2957   -1.5149    0.6431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3807   -2.7375    1.0380 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3746   -3.7659    0.9098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7549   -3.9731   -0.5431 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3054   -5.3664   -1.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0115   -2.9965   -1.4060 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1488   -3.5155   -2.8469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5285   -1.6051   -1.4195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3747   -0.8305   -0.1268 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6390   -1.0002    0.6383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5471    0.1694    0.7706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184    1.2925    1.2981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2353    2.1363    2.3978 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5572    2.7047    1.9487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5451    4.0170    2.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6720    4.9496    1.6384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2375    4.4015    2.4811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8462    5.6008    2.6665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4970    3.2627    2.6993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5353    1.5150    0.7617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6236    2.6084    1.2814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0942    0.6204   -0.3624 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7485    1.0557   -1.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0567    1.2869   -2.7333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6844    0.9042   -4.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7426    1.9045   -2.6661 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.4374    0.9847   -2.5915 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4908    1.7242   -1.7623 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1896    2.6819   -2.6758 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5351    1.9746   -2.8926 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6818    1.2956   -1.5329 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3195    2.2857   -0.6203 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3164    1.4532    0.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1052    0.0258   -0.3528 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1685   -0.6493    0.3748 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5737   -1.2663    1.5195 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0631   -1.3349    1.7141 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6534   -1.8114    0.3874 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3988   -0.6866   -0.5877 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4420    0.2459   -0.4335 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9270   -0.7592    2.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5523    0.2463   -1.6392 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4028    0.9082   -1.1682 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8373   -3.3397    3.7349 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5306    0.1821    2.5390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6441   -1.5728    3.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2424   -0.0934    1.6317 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5054    1.5239    3.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4289    1.2217   -3.6807 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5854    2.7815    0.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8325    3.1070   -1.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0943    1.5719    1.2132 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3353    1.7908   -0.1305 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2370   -2.3437    1.4348 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2567   -2.1178    2.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5099   -0.4067    2.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7129   -2.0552    0.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0424   -2.6828    0.0740 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4973   -1.0966   -1.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9597    0.0597    0.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6814   -0.8823    3.6161 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7340    0.3324    2.7498 H   0  0  0  0  0  0  0  0  0  0  0  0
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 10  9  1  0
  9  8  1  0
  8  7  2  0
  7  5  1  0
  5  6  1  0
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  2  1  2  3
  2 48  1  0
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  1 52  1  0
 48108  1  0
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 43101  1  6
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 45104  1  0
 45105  1  0
 46106  1  6
 47107  1  0
 40 99  1  0
 40100  1  0
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 39 98  1  0
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 35 92  1  1
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 32 88  1  6
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 31 85  1  0
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 31 87  1  0
 29 84  1  0
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 17 73  1  0
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 16 71  1  0
 16 72  1  0
 14 69  1  0
 14 70  1  0
 12 65  1  1
 13 66  1  0
 13 67  1  0
 13 68  1  0
 19 75  1  1
 22 77  1  0
 22 78  1  0
 22 79  1  0
 20 76  1  0
M  END


  Mrv1652309052202282D          

 50 56  0  0  1  0            999 V2000
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    3.7279   -0.3528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2682    0.2875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0935    0.0828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8159   -0.3983    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4170    0.1668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2605   -1.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4180   -1.2615    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.9318   -1.9289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1724   -2.7048    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5624   -3.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9200   -3.0158    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9821   -3.8385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6243   -2.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9247   -1.8001    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5624   -1.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4003   -1.3340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6868   -2.1108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5002   -2.2483    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0896   -1.6711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8208   -2.0533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5597   -1.6864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6833   -2.8667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2605   -3.4561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8671   -2.9873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1642   -2.7463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4520   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3376   -2.6045    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9911   -3.4257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4083   -4.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9070   -4.7343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6341   -4.4578    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7346   -5.2766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7640   -4.2699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8699   -3.9832    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8333   -4.2505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0689   -4.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1655   -3.9095    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2695   -4.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8741   -3.3594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3756   -2.6920    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7129   -1.9235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2770   -1.2226    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4408   -1.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0634   -2.0049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5181   -2.6803    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1254   -3.4059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0236   -0.8233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1654   -3.0455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8069   -4.7121    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 19 25  1  0  0  0  0
 18 26  2  0  0  0  0
 26 27  1  0  0  0  0
 28 26  1  6  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 43 42  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 41 46  1  0  0  0  0
 46 47  1  1  0  0  0
 43 48  1  0  0  0  0
  2 48  1  0  0  0  0
 41 49  1  6  0  0  0
 38 49  1  6  0  0  0
 38 50  1  0  0  0  0
 35 50  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0204736

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CN=C2[C@H](O)CCC(=C)C[C@@H]3CC[C@H](O)[C@]4(CC[C@@]5(CC[C@@H](C[C@H](O)\C(C)=C/[C@H]6C(C)=C(CC[C@]26C[C@@H]1C)[C@H]1OC(=O)C(C)=C1)O5)O4)O3

> <INCHI_IDENTIFIER>
InChI=1S/C41H59NO8/c1-23-7-9-33(43)37-39(21-26(4)27(5)22-42-37)13-12-31(35-19-25(3)38(46)47-35)28(6)32(39)18-24(2)34(44)20-30-11-14-40(48-30)15-16-41(50-40)36(45)10-8-29(17-23)49-41/h18-19,26-27,29-30,32-36,43-45H,1,7-17,20-22H2,2-6H3/b24-18-/t26-,27-,29-,30-,32-,33+,34-,35-,36-,39+,40+,41+/m0/s1

> <INCHI_KEY>
YEBJLPZBBAZOPS-IEMRVDQYSA-N

> <FORMULA>
C41H59NO8

> <MOLECULAR_WEIGHT>
693.922

> <EXACT_MASS>
693.424067864

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
109

> <JCHEM_AVERAGE_POLARIZABILITY>
76.02545396825715

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5S)-3-methyl-5-[(1R,4R,7S,9S,10Z,12S,17R,19S,20R,24R,29S,32S)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1^{1,4}.1^{4,7}.0^{12,17}.0^{17,23}]pentatriaconta-10,13,22-trien-14-yl]-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
5.9597689963333345

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.638325246935477

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.053587724491098

> <JCHEM_PKA_STRONGEST_BASIC>
5.843627446921748

> <JCHEM_POLAR_SURFACE_AREA>
127.04000000000002

> <JCHEM_REFRACTIVITY>
192.86519999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(5S)-3-methyl-5-[(1R,4R,7S,9S,10Z,12S,17R,19S,20R,24R,29S,32S)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1^{1,4}.1^{4,7}.0^{12,17}.0^{17,23}]pentatriaconta-10,13,22-trien-14-yl]-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       7.985  -1.807   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.959  -0.659   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.967   0.537   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.508   0.155   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.856  -0.743   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.978   0.311   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      11.686  -2.174   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      10.114  -2.355   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       9.206  -3.601   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.655  -5.049   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.516  -6.086   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.051  -5.629   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.167  -7.165   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.365  -4.833   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.926  -3.360   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.117  -2.229   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.681  -2.490   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.215  -3.940   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.734  -4.197   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.834  -3.119   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      20.199  -3.833   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      21.578  -3.148   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.942  -5.351   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      21.020  -6.451   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      18.419  -5.576   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      15.240  -5.126   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.777  -6.570   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.697  -4.862   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.050  -6.395   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.962  -7.610   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.893  -8.837   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.517  -8.321   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      10.705  -9.850   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.893  -7.970   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.224  -7.435   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.289  -7.934   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.729  -9.188   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.909  -7.298   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.236  -7.558   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.498  -6.271   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.434  -5.025   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       5.064  -3.591   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       4.250  -2.282   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.689  -2.364   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.985  -3.742   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.834  -5.003   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       2.101  -6.358   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       5.644  -1.537   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       5.909  -5.685   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       7.106  -8.796   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   48                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    7   16   28                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   19                                                       
CONECT   26   18   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   15   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   50                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   49   50                                             
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   46   49                                             
CONECT   42   41   43                                                       
CONECT   43   42   44   48                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   41   47                                                  
CONECT   47   46                                                            
CONECT   48   43    2                                                       
CONECT   49   41   38                                                       
CONECT   50   38   35                                                       
MASTER        0    0    0    0    0    0    0    0   50    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₅₉NO₈

Average Mass

693.9220 Da

Monoisotopic Mass

693.42407 Da

IUPAC Name

(5S)-3-methyl-5-[(1R,4R,7S,9S,10Z,12S,17R,19S,20R,24R,29S,32S)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1^{1,4}.1^{4,7}.0^{12,17}.0^{17,23}]pentatriaconta-10,13,22-trien-14-yl]-2,5-dihydrofuran-2-one

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1CN=C2[C@H](O)CCC(=C)C[C@@H]3CC[C@H](O)[C@]4(CC[C@@]5(CC[C@@H](C[C@H](O)\C(C)=C/[C@H]6C(C)=C(CC[C@]26C[C@@H]1C)[C@H]1OC(=O)C(C)=C1)O5)O4)O3

InChI Identifier

InChI=1S/C41H59NO8/c1-23-7-9-33(43)37-39(21-26(4)27(5)22-42-37)13-12-31(35-19-25(3)38(46)47-35)28(6)32(39)18-24(2)34(44)20-30-11-14-40(48-30)15-16-41(50-40)36(45)10-8-29(17-23)49-41/h18-19,26-27,29-30,32-36,43-45H,1,7-17,20-22H2,2-6H3/b24-18-/t26-,27-,29-,30-,32-,33+,34-,35-,36-,39+,40+,41+/m0/s1

InChI Key

YEBJLPZBBAZOPS-IEMRVDQYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Alexandrium ostenfeldii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azepines. These are organic compounds containing an unsaturated seven-member heterocycle with one nitrogen atom replacing a carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azepines

Sub Class

Not Available

Direct Parent

Azepines

Alternative Parents

Substituents

Ketal
Azepine
Oxane
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Dihydrofuran
Secondary alcohol
Lactone
Ketimine
Carboxylic acid ester
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
Carbonyl group
Alcohol
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	5.96	ChemAxon
pKa (Strongest Acidic)	13.05	ChemAxon
pKa (Strongest Basic)	5.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	127.04 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	192.87 m³·mol⁻¹	ChemAxon
Polarizability	76.03 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	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

163000531

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one (NP0204736)

MOL for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

3D MOL for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

3D SDF for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

3D-SDF for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

PDB for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

3D PDB for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

SMILES for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

INCHI for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

Structure for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)

3D Structure for NP0204736 ((5s)-3-methyl-5-[(1r,4r,7s,9s,10z,12s,17r,19s,20r,24r,29s,32s)-9,24,32-trihydroxy-10,13,19,20-tetramethyl-27-methylidene-33,34,35-trioxa-22-azahexacyclo[27.3.1.1¹,⁴.1⁴,⁷.0¹²,¹⁷.0¹⁷,²³]pentatriaconta-10,13,22-trien-14-yl]-5h-furan-2-one)