NP-MRD: Showing NP-Card for [(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate (NP0172766)

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Record Information

Version

2.0

Created at

2022-09-03 09:46:03 UTC

Updated at

2022-09-03 09:46:03 UTC

NP-MRD ID

NP0172766

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

Description

Meehanine D belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. [(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate is found in Meehania urticifolia. Based on a literature review very few articles have been published on Meehanine D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032211462D          

 56 60  0  0  1  0            999 V2000
    5.6543    3.8884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9912    4.3793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0848    5.1990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2346    4.0505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5715    4.5413    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3337    3.7514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5089    3.7335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2370    4.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4651    4.9806    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7506    4.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7506    3.7431    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4651    3.3306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4651    2.5056    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1796    2.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7506    2.0931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7506    1.2681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0362    2.5056    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6783    2.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0362    3.3306    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6783    3.7431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3928    3.3306    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3928    2.5056    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1073    2.0931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1073    1.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8217    0.8556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8217    0.0306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1073   -0.3819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5362   -0.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5362   -1.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2507   -1.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9651   -1.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9651   -0.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2507    0.0306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8217    2.5056    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5362    2.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8217    3.3306    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5362    3.7431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1073    3.7431    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1073    4.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4472    5.8054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1525    6.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8758    5.8365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1346    7.0582    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8400    7.4861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5632    7.0892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5811    6.2644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3044    5.8675    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0097    6.2954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9918    7.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7330    5.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4384    6.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1616    5.9295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1795    5.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4742    4.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7509    5.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3223    5.0427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  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  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  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  1  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 23 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 21 38  1  0  0  0  0
 38 39  1  1  0  0  0
  9 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 43 44  1  4  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 50 55  1  0  0  0  0
 47 56  1  0  0  0  0
  5 56  1  0  0  0  0
M  END

     RDKit          3D

107111  0  0  0  0  0  0  0  0999 V2000
   -5.5666    2.0728    4.6565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1763    0.8823    3.8807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4843   -0.2496    4.2843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4843    0.9830    2.7285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0515   -0.0715    1.8955 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4956   -0.1952    2.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7772    0.6241    0.9917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9600   -0.2383    0.0948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6856    0.2040   -1.2070 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5234    0.7892   -1.3662 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5525    2.0943   -0.9528 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6825    2.9020   -2.1012 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4598    4.2408   -1.7893 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0248    4.5285   -1.5905 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2890    4.7647   -0.6663 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5930    5.0589   -1.0519 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3858    3.8138    0.5207 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1462    3.6746    1.1389 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7282    2.4599   -0.0767 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0650    1.5139    0.8572 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3639    1.1173    0.6697 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4189   -0.2332    0.3284 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6874   -0.6026   -0.1008 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0847   -1.9880    0.4051 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3824   -2.2651   -0.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0909   -3.4200    0.1488 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5677   -4.3035    0.8533 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4358   -3.6257   -0.4060 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0501   -2.6800   -1.1857 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3326   -2.9153   -1.6963 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0130   -4.0861   -1.4382 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3858   -5.0298   -0.6531 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1199   -4.7934   -0.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7637    0.3744    0.2356 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0249    1.2849   -0.8162 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6299    1.0541    1.5573 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3694    0.4445    2.5686 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1914    1.2551    1.9316 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9319    2.4915    2.5037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6831    0.6729   -2.0709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1247   -0.2853   -3.1362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0897   -0.4566   -4.1286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1935   -0.8884   -3.2382 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4354   -1.1080   -2.6610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2963    0.1102   -2.5051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0849    0.1542   -1.2548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4996   -0.5986   -0.1577 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0211   -1.8226    0.2481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4824   -2.4002    1.3028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0949   -2.6388   -0.2761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6414   -2.5032   -1.5137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7295   -3.2721   -1.9348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2637   -4.1957   -1.0744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7548   -4.3829    0.1913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6874   -3.6008    0.5532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3653    0.0014    0.4992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6799    1.8467    5.7350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7146    2.8007    4.5624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4515    2.5723    4.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4087   -0.9668    2.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2913   -1.2736    1.8698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2637    0.0512    3.0624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3544    1.3980    0.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0192    1.2230    1.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3460   -1.2956    0.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0735   -0.4219    0.5727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4266    2.4172   -0.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7485    4.8171   -2.7084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5457    3.9692   -2.4156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1767    5.5970   -1.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3700    4.2369   -0.5860 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7841    5.6869   -0.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6806    6.0569   -1.1223 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1589    4.2103    1.1783 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2505    3.2564    2.0166 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5983    2.6507   -0.7604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8183    1.6616   -0.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6347   -0.6947   -1.2081 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0802   -2.0302    1.5205 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3792   -2.7738    0.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5310   -1.7518   -1.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8006   -2.1612   -2.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0040   -4.2335   -1.8505 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9113   -5.9565   -0.4423 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6199   -5.5344    0.4688 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7246   -0.2221    0.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5358    2.0305   -0.4356 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0648    2.0878    1.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6575    1.1586    3.2214 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8979    0.4171    2.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4879    2.3518    3.3806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5872    0.9760   -1.5371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2423    1.5939   -2.5862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5791   -1.3417   -3.9851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4363   -1.7488   -1.7426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0175   -1.7875   -3.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6999    1.0590   -2.6341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0140    0.1457   -3.3540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9824    1.2466   -0.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.1848   -5.1234    0.8744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3209   -3.7875    1.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2610    1.0900    0.1047 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
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  9  8  1  0
  8  7  1  0
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  5 56  1  0
 56 47  1  0
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 53103  1  0
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 38 90  1  1
 39 91  1  0
 17 74  1  1
 18 75  1  0
 15 72  1  1
 16 73  1  0
M  END


  Mrv1652309032211462D          

 56 60  0  0  1  0            999 V2000
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    4.2346    4.0505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5715    4.5413    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3337    3.7514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5089    3.7335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2370    4.5124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4651    4.9806    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7506    4.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2507   -1.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9651   -1.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9651   -0.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2507    0.0306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8217    2.5056    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5362    2.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8217    3.3306    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5362    3.7431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1073    3.7431    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1073    4.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4472    5.8054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1525    6.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8758    5.8365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1346    7.0582    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8400    7.4861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5632    7.0892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5811    6.2644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3044    5.8675    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0097    6.2954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9918    7.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7330    5.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4384    6.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1616    5.9295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1795    5.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4742    4.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7509    5.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3223    5.0427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  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  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  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  1  0  0  0
 21 20  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 23 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 21 38  1  0  0  0  0
 38 39  1  1  0  0  0
  9 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 43 44  1  4  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 50 55  1  0  0  0  0
 47 56  1  0  0  0  0
  5 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0172766

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@@H](ON2CCC[C@H](CN(CCCN=C(O)C2)C(=O)C2=CC=CC=C2)OC(C)=O)[C@H](O[C@@H]2O[C@H](COC(=O)C3=CC=CC=C3)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C38H51N3O15/c1-22-29(44)32(47)34(55-37-33(48)31(46)30(45)27(54-37)21-51-36(50)25-13-7-4-8-14-25)38(52-22)56-41-18-9-15-26(53-23(2)42)19-40(17-10-16-39-28(43)20-41)35(49)24-11-5-3-6-12-24/h3-8,11-14,22,26-27,29-34,37-38,44-48H,9-10,15-21H2,1-2H3,(H,39,43)/t22-,26+,27+,29-,30+,31-,32+,33+,34+,37-,38-/m0/s1

> <INCHI_KEY>
KUILDRCWBSIATI-RPSBCHAMSA-N

> <FORMULA>
C38H51N3O15

> <MOLECULAR_WEIGHT>
789.832

> <EXACT_MASS>
789.332017954

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
107

> <JCHEM_AVERAGE_POLARIZABILITY>
78.7863538861865

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3S,4S,5R,6S)-6-{[(2S,3R,4R,5R,6S)-2-{[(10R)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

> <ALOGPS_LOGP>
0.90

> <JCHEM_LOGP>
-1.1673279133465935

> <ALOGPS_LOGS>
-3.27

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.100905868820163

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.6159890101787604

> <JCHEM_PKA_STRONGEST_BASIC>
5.5048204071111435

> <JCHEM_POLAR_SURFACE_AREA>
246.81

> <JCHEM_REFRACTIVITY>
193.10039999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.24e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4S,5R,6S)-6-{[(2S,3R,4R,5R,6S)-2-{[(10R)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      10.555   7.258   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.317   8.175   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.492   9.705   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.905   7.561   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.667   8.477   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.223   7.003   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.683   6.969   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.176   8.423   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       2.735   9.297   0.000  0.00  0.00           N+0
HETATM   10  O   UNK     0       1.401   8.527   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.401   6.987   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.735   6.217   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.735   4.677   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.069   3.907   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.401   3.907   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.401   2.367   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.068   4.677   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.266   3.907   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.068   6.217   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.266   6.987   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -2.600   6.217   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.600   4.677   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -3.934   3.907   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.934   2.367   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.267   1.597   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.267   0.057   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -3.934  -0.713   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -6.601  -0.713   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -6.601  -2.253   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -7.935  -3.023   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -9.268  -2.253   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -9.268  -0.713   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -7.935   0.057   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -5.267   4.677   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -6.601   3.907   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -5.267   6.217   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -6.601   6.987   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -3.934   6.987   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -3.934   8.527   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       2.701  10.837   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.018  11.636   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       5.368  10.895   0.000  0.00  0.00           O+0
HETATM   43  N   UNK     0       3.985  13.175   0.000  0.00  0.00           N+0
HETATM   44  C   UNK     0       5.301  13.974   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.651  13.233   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       6.685  11.694   0.000  0.00  0.00           C+0
HETATM   47  N   UNK     0       8.035  10.953   0.000  0.00  0.00           N+0
HETATM   48  C   UNK     0       9.352  11.751   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       9.318  13.291   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      10.702  11.011   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      12.018  11.809   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      13.368  11.068   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      13.402   9.529   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      12.085   8.730   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      10.735   9.471   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       8.068   9.413   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   56                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   40                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   11   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   38                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   34                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   28                                                       
CONECT   34   23   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   21   39                                                  
CONECT   39   38                                                            
CONECT   40    9   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48   56                                                  
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   51   55                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   50                                                       
CONECT   56   47    5                                                       
MASTER        0    0    0    0    0    0    0    0   56    0  120    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₅₁N₃O₁₅

Average Mass

789.8320 Da

Monoisotopic Mass

789.33202 Da

IUPAC Name

[(2R,3S,4S,5R,6S)-6-{[(2S,3R,4R,5R,6S)-2-{[(10R)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@@H](ON2CCC[C@H](CN(CCCN=C(O)C2)C(=O)C2=CC=CC=C2)OC(C)=O)[C@H](O[C@@H]2O[C@H](COC(=O)C3=CC=CC=C3)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C38H51N3O15/c1-22-29(44)32(47)34(55-37-33(48)31(46)30(45)27(54-37)21-51-36(50)25-13-7-4-8-14-25)38(52-22)56-41-18-9-15-26(53-23(2)42)19-40(17-10-16-39-28(43)20-41)35(49)24-11-5-3-6-12-24/h3-8,11-14,22,26-27,29-34,37-38,44-48H,9-10,15-21H2,1-2H3,(H,39,43)/t22-,26+,27+,29-,30+,31-,32+,33+,34+,37-,38-/m0/s1

InChI Key

KUILDRCWBSIATI-RPSBCHAMSA-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
Meehania urticifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolactams

Sub Class

Not Available

Direct Parent

Macrolactams

Alternative Parents

Substituents

Macrolactam
O-glycosyl compound
Glycosyl compound
Disaccharide
Benzoate ester
Alpha-amino acid or derivatives
Benzoic acid or derivatives
Benzamide
Benzoyl
Benzenoid
Oxane
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Tertiary carboxylic acid amide
Secondary carboxylic acid amide
Secondary alcohol
Lactam
Carboxylic acid ester
Carboxamide group
Oxacycle
Azacycle
N-organohydroxylamine
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	0.9	ALOGPS
logP	-1.2	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	2.62	ChemAxon
pKa (Strongest Basic)	5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	246.81 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	193.1 m³·mol⁻¹	ChemAxon
Polarizability	78.79 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00047504

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

101481715

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate (NP0172766)

MOL for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D MOL for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D SDF for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D-SDF for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

PDB for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D PDB for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

SMILES for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

INCHI for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

Structure for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)

3D Structure for NP0172766 ([(2r,3s,4s,5r,6s)-6-{[(2s,3r,4r,5r,6s)-2-{[(10r)-10-(acetyloxy)-8-benzoyl-3-hydroxy-1,4,8-triazacyclotridec-3-en-1-yl]oxy}-4,5-dihydroxy-6-methyloxan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate)