NP-MRD: Showing NP-Card for 12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione (NP0250324)

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Record Information

Version

2.0

Created at

2022-09-07 13:06:59 UTC

Updated at

2022-09-07 13:06:59 UTC

NP-MRD ID

NP0250324

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione

Description

12-Benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-24-methyl-9-(propan-2-yl)-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]Triaconta-10,13,22,25-tetraene-2,8,20-trione belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. 12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione is found in Prosuberites laughlini. 12-Benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-24-methyl-9-(propan-2-yl)-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]Triaconta-10,13,22,25-tetraene-2,8,20-trione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231519462D          

 51 55  0  0  0  0            999 V2000
    5.4345   -1.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1096   -1.3089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8578   -1.6565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0365   -0.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7116   -0.0130    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3997   -0.4682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3495   -1.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1379   -0.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8260   -0.5552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7758   -1.3787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4638   -1.8339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4136   -2.6574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6753   -3.0256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9873   -2.5704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0375   -1.7469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1882    0.7235    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.9730    0.9776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5856    0.4249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1454    1.7844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8603    2.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6897    3.0033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0906    3.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5329    2.3371    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8236    3.1091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5563    3.4884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3003    3.7469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4863    3.6127    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0639    4.3213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4665    5.0415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2390    4.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8166    5.0185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8365    3.5897    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0191    3.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7070    4.4651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5137    3.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6910    2.9885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4945    2.1872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9746    1.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8258    2.2855    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2288    1.7160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4042    1.6922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4236    0.9144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9581    0.2332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4621   -0.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0177   -0.0685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2152    0.6822    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2883   -0.1396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7928   -0.7992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5910    4.5190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0677    5.1568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4050    4.6533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 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
 35 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 42 46  1  0  0  0  0
 46 47  1  0  0  0  0
  4 47  1  0  0  0  0
 47 48  2  0  0  0  0
 26 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
M  END

     RDKit          3D

102106  0  0  0  0  0  0  0  0999 V2000
   -3.9495    3.4771    1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5406    2.6985   -0.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8401    2.0017   -0.6277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5195    1.6474    0.1183 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1704    0.9545   -1.0993 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7225   -0.3472   -1.2706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5979   -0.5187   -1.8777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3635   -1.6193   -0.8473 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8705   -1.5988   -1.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4460   -2.8743   -0.6074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5786   -3.9147   -1.5042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1314   -5.1397   -1.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5666   -5.3379    0.1541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4430   -4.3086    1.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8863   -3.0941    0.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0170   -1.9006    0.5288 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9759   -2.7044    1.0115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1946   -2.1536    1.8628 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6776   -4.0663    0.6738 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8125   -4.5408   -0.7203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1833   -5.9426   -0.6036 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5246   -5.9332    0.7580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6745   -4.4951    0.9956 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7541   -3.7156    1.4175 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3921   -2.5554    0.7017 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4690   -3.2617   -0.1474 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1873   -2.3799   -1.0876 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3065   -3.9291    0.7374 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9622   -1.6226    1.6384 N   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9389    0.9685   -0.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9862    1.7459    1.2708 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2431    3.1004    1.2485 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1741    4.0955    0.1822 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5076    4.5477   -0.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0307    5.2149   -1.6428 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2338    3.9866   -2.1355 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532    3.7615   -0.9683 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0177    3.3215   -0.9301 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7774    2.2007   -1.5194 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1695    3.9431   -0.3190 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0525    5.3934   -0.0068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0093    5.4977    1.4744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2443    4.1196    2.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6536    3.2820    0.8893 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3659    2.0770    0.9271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9425    1.2247    1.8012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0398    3.7076    1.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7217    2.9468    1.9899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2870    3.3263   -1.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5599    2.8485   -0.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6508    1.4746   -1.5706 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.0378   -2.4671   -1.5198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1127   -1.3903   -2.0700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3447   -0.8071   -0.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2560   -3.8173   -2.5312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2332   -5.9517   -1.8467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0058   -6.2883    0.4729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7904   -4.4877    2.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8350   -2.3496    1.4578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6791   -1.3950    1.2108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3609   -4.7485    1.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2083   -4.0146   -1.4670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8586   -4.7424   -1.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5157   -6.1405   -1.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9575   -6.7347   -0.5678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1436   -6.3777    1.5180 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1930   -2.1566   -0.6221 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9724    3.1902   -2.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0416    3.8879   -1.0518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9588    5.9887   -0.3480 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7997    6.2078    1.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9629    4.1991    2.8318 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7005    3.6801    2.4466 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
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 48101  1  0
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 27 78  1  6
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 29 82  1  0
M  END


  Mrv1533004231519462D          

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    9.5856    0.4249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1454    1.7844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8603    2.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6897    3.0033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0906    3.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5329    2.3371    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8236    3.1091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5563    3.4884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3003    3.7469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4863    3.6127    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0639    4.3213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4665    5.0415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2390    4.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8166    5.0185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8365    3.5897    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0191    3.7013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7070    4.4651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5137    3.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6910    2.9885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4945    2.1872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9746    1.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8258    2.2855    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2288    1.7160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4042    1.6922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4236    0.9144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9581    0.2332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4621   -0.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0177   -0.0685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2152    0.6822    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2883   -0.1396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7928   -0.7992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5910    4.5190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0677    5.1568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4050    4.6533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 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
 35 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 42 46  1  0  0  0  0
 46 47  1  0  0  0  0
  4 47  1  0  0  0  0
 47 48  2  0  0  0  0
 26 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0250324

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1NC(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C(=O)C(NC(=O)C(C)NC(=O)C2CCCN2C(=O)C2CCCN2C1=O)C(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C36H51N7O8/c1-20(2)28-35(50)43-18-10-15-27(43)34(49)41-16-8-13-25(41)32(47)37-21(3)30(45)40-29(22(4)44)36(51)42-17-9-14-26(42)33(48)38-24(31(46)39-28)19-23-11-6-5-7-12-23/h5-7,11-12,20-22,24-29,44H,8-10,13-19H2,1-4H3,(H,37,47)(H,38,48)(H,39,46)(H,40,45)

> <INCHI_KEY>
ZLFKJRJBRWMMMG-UHFFFAOYSA-N

> <FORMULA>
C36H51N7O8

> <MOLECULAR_WEIGHT>
709.845

> <EXACT_MASS>
709.37991163

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
102

> <JCHEM_AVERAGE_POLARIZABILITY>
74.53354575120349

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
12-benzyl-21-(1-hydroxyethyl)-24-methyl-9-(propan-2-yl)-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triacontane-2,8,11,14,20,23,26-heptone

> <ALOGPS_LOGP>
0.75

> <JCHEM_LOGP>
-1.0241496013333333

> <ALOGPS_LOGS>
-3.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.081708675865015

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.531593148855062

> <JCHEM_PKA_STRONGEST_BASIC>
-2.937307027174053

> <JCHEM_POLAR_SURFACE_AREA>
197.56

> <JCHEM_REFRACTIVITY>
183.7262

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.30e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-benzyl-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triacontane-2,8,11,14,20,23,26-heptone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      10.144  -3.328   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.405  -2.443   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.801  -3.092   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.268  -0.909   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      12.528  -0.024   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      13.813  -0.874   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      13.719  -2.411   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      15.191  -0.187   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.475  -1.036   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.381  -2.574   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.666  -3.423   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.572  -4.960   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.194  -5.648   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.910  -4.798   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.003  -3.261   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      15.285   1.351   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      16.750   1.825   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      17.893   0.793   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      17.071   3.331   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.406   4.099   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.087   5.606   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.969   5.631   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      15.928   4.363   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0      16.471   5.804   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      17.838   6.512   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      15.494   6.994   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0      13.974   6.744   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      13.186   8.066   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      13.937   9.411   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      11.646   8.045   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.858   9.368   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0      10.895   6.701   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       9.369   6.909   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       8.786   8.335   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.426   5.692   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.890   5.578   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.523   4.083   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.419   3.410   0.000  0.00  0.00           C+0
HETATM   39  N   UNK     0       9.008   4.266   0.000  0.00  0.00           N+0
HETATM   40  C   UNK     0       7.894   3.203   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       6.354   3.159   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.257   1.707   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.389   0.435   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       8.329  -0.784   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.366  -0.128   0.000  0.00  0.00           C+0
HETATM   46  N   UNK     0       9.735   1.273   0.000  0.00  0.00           N+0
HETATM   47  C   UNK     0       9.872  -0.261   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       8.946  -1.492   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      16.037   8.436   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      15.060   9.626   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      17.556   8.686   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   47                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16    8   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   19   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   49                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   39                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   35   40                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   46                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   42   47                                                  
CONECT   47   46    4   48                                                  
CONECT   48   47                                                            
CONECT   49   26   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₅₁N₇O₈

Average Mass

709.8450 Da

Monoisotopic Mass

709.37991 Da

IUPAC Name

12-benzyl-21-(1-hydroxyethyl)-24-methyl-9-(propan-2-yl)-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triacontane-2,8,11,14,20,23,26-heptone

Traditional Name

12-benzyl-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triacontane-2,8,11,14,20,23,26-heptone

CAS Registry Number

Not Available

SMILES

CC(C)C1NC(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C(=O)C(NC(=O)C(C)NC(=O)C2CCCN2C(=O)C2CCCN2C1=O)C(C)O

InChI Identifier

InChI=1S/C36H51N7O8/c1-20(2)28-35(50)43-18-10-15-27(43)34(49)41-16-8-13-25(41)32(47)37-21(3)30(45)40-29(22(4)44)36(51)42-17-9-14-26(42)33(48)38-24(31(46)39-28)19-23-11-6-5-7-12-23/h5-7,11-12,20-22,24-29,44H,8-10,13-19H2,1-4H3,(H,37,47)(H,38,48)(H,39,46)(H,40,45)

InChI Key

ZLFKJRJBRWMMMG-UHFFFAOYSA-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
Prosuberites laughlini	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
Macrolactam
Alpha-amino acid or derivatives
Monocyclic benzene moiety
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Secondary alcohol
Carboxamide group
Lactam
Propargyl-type 1,3-dipolar organic compound
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Polyol
Organic nitrogen compound
Hydrocarbon derivative
Organonitrogen compound
Organic oxide
Organooxygen compound
Carbonyl group
Organic oxygen compound
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	0.75	ALOGPS
logP	-1	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	11.53	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	197.56 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	183.73 m³·mol⁻¹	ChemAxon
Polarizability	74.53 Å³	ChemAxon
Number of Rings	5	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

75033262

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione (NP0250324)

MOL for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

3D MOL for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

3D SDF for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

3D-SDF for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

PDB for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

3D PDB for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

SMILES for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

INCHI for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

Structure for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)

3D Structure for NP0250324 (12-benzyl-11,14,23,26-tetrahydroxy-21-(1-hydroxyethyl)-9-isopropyl-24-methyl-1,7,10,13,19,22,25-heptaazatetracyclo[25.3.0.0³,⁷.0¹⁵,¹⁹]triaconta-10,13,22,25-tetraene-2,8,20-trione)