NP-MRD: Showing NP-Card for Okaramine Q (NP0003188)

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Record Information

Version

2.0

Created at

2020-12-09 00:31:39 UTC

Updated at

2021-07-15 16:45:45 UTC

NP-MRD ID

NP0003188

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Okaramine Q

Provided By

NPAtlas

Description

(4R,5S,14S,16R,19Z)-14,16-dihydroxy-5,6,6,21,21-pentamethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]Hentriaconta-1(31),8,10,12,19,22(30),24,26,28-nonaene-2,17-dione belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. Okaramine Q is found in Penicillium. Based on a literature review very few articles have been published on (4R,5S,14S,16R,19Z)-14,16-dihydroxy-5,6,6,21,21-pentamethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0³,¹⁶.0⁴,⁷.0⁴,¹⁴.0⁸,¹³.0²²,³⁰.0²⁴,²⁹]Hentriaconta-1(31),8,10,12,19,22(30),24,26,28-nonaene-2,17-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117463D          

 72 79  0  0  0  0            999 V2000
    2.6246   -2.8873    2.1088 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5046   -1.9531    1.3645 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7964   -2.2999   -0.0814 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2832   -2.6886   -0.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9826   -3.3551   -0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.9521   -0.5062 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3742    0.3021   -1.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1731    0.6909   -2.4587 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0649    2.0238   -2.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1591    2.9996   -1.8665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3636    2.6387   -0.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4685    1.3141   -0.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6875    0.6043    1.1218 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0045    0.4126    1.4241 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8765    1.2779    2.1700 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4861    0.7219    1.9560 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0921    0.0939    3.1298 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5460    1.7898    1.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7894    3.0145    1.6833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6839    1.4309    0.9397 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5835    2.5038    1.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8889    2.6588    1.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0829    1.8516    0.9214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2233    2.8101    0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    1.2169    2.2421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    0.8128   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1579    0.6482   -0.8277 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0215   -0.3369   -1.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8747   -0.8622   -2.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4619   -1.8719   -3.5250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1770   -2.3694   -3.4028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3160   -1.8511   -2.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7426   -0.8344   -1.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.1218   -0.6260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7699   -0.4724   -0.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7790    0.1399    0.3150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -0.7265    0.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2344   -1.8335   -0.2338 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6163   -0.3359    0.9374 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9651   -0.7083    0.8185 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8332   -2.7620    3.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8977   -3.9648    1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5529   -2.7510    1.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4541   -1.7526    1.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4214   -3.7576   -0.0689 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5698   -2.3634   -1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8319   -2.0419    0.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845   -2.9258   -1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -3.7732   -0.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5583   -4.2252   -1.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0996   -0.0816   -3.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9071    2.3242   -3.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0860    4.0618   -2.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    3.3785    0.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122    0.6656    2.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8294    2.3621    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614    1.0322    3.2009 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1018    0.0642    3.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0065    3.4079    1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1161    3.7247    1.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1792    2.3779    0.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0914    3.7576    1.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2540    3.0123   -0.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6231    1.0180    2.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1468    1.9470    2.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0716    0.2683    2.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0791    1.1647   -0.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8601   -0.4804   -2.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1242   -2.3113   -4.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8976   -3.1686   -4.0750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3285   -2.2579   -2.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4537   -1.4464   -0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  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  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 23 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
 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
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 40 39  1  6  0  0  0
 40  2  1  0  0  0  0
 40  6  1  0  0  0  0
 12  7  1  0  0  0  0
 40 13  1  0  0  0  0
 39 16  1  0  0  0  0
 36 20  1  0  0  0  0
 34 26  2  0  0  0  0
 33 28  1  0  0  0  0
  1 41  1  0  0  0  0
  1 42  1  0  0  0  0
  1 43  1  0  0  0  0
  2 44  1  1  0  0  0
  4 45  1  0  0  0  0
  4 46  1  0  0  0  0
  4 47  1  0  0  0  0
  5 48  1  0  0  0  0
  5 49  1  0  0  0  0
  5 50  1  0  0  0  0
  8 51  1  0  0  0  0
  9 52  1  0  0  0  0
 10 53  1  0  0  0  0
 11 54  1  0  0  0  0
 14 55  1  0  0  0  0
 15 56  1  0  0  0  0
 15 57  1  0  0  0  0
 17 58  1  0  0  0  0
 21 59  1  0  0  0  0
 22 60  1  0  0  0  0
 24 61  1  0  0  0  0
 24 62  1  0  0  0  0
 24 63  1  0  0  0  0
 25 64  1  0  0  0  0
 25 65  1  0  0  0  0
 25 66  1  0  0  0  0
 27 67  1  0  0  0  0
 29 68  1  0  0  0  0
 30 69  1  0  0  0  0
 31 70  1  0  0  0  0
 32 71  1  0  0  0  0
 35 72  1  0  0  0  0
M  END

     RDKit          3D

 72 79  0  0  0  0  0  0  0  0999 V2000
    2.6246   -2.8873    2.1088 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5046   -1.9531    1.3645 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7964   -2.2999   -0.0814 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2832   -2.6886   -0.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9826   -3.3551   -0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.9521   -0.5062 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3742    0.3021   -1.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1731    0.6909   -2.4587 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0649    2.0238   -2.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1591    2.9996   -1.8665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3636    2.6387   -0.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4685    1.3141   -0.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6875    0.6043    1.1218 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0045    0.4126    1.4241 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8765    1.2779    2.1700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861    0.7219    1.9560 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0921    0.0939    3.1298 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5460    1.7898    1.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7894    3.0145    1.6833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6839    1.4309    0.9397 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5835    2.5038    1.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8889    2.6588    1.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0829    1.8516    0.9214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2233    2.8101    0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    1.2169    2.2421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    0.8128   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1579    0.6482   -0.8277 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0215   -0.3369   -1.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8747   -0.8622   -2.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4619   -1.8719   -3.5250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1770   -2.3694   -3.4028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3160   -1.8511   -2.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7426   -0.8344   -1.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.1218   -0.6260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7699   -0.4724   -0.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7790    0.1399    0.3150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -0.7265    0.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2344   -1.8335   -0.2338 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6163   -0.3359    0.9374 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9651   -0.7083    0.8185 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8332   -2.7620    3.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8977   -3.9648    1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5529   -2.7510    1.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4541   -1.7526    1.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4214   -3.7576   -0.0689 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5698   -2.3634   -1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8319   -2.0419    0.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845   -2.9258   -1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -3.7732   -0.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5583   -4.2252   -1.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0996   -0.0816   -3.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9071    2.3242   -3.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0860    4.0618   -2.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    3.3785    0.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122    0.6656    2.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8294    2.3621    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614    1.0322    3.2009 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1018    0.0642    3.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0065    3.4079    1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1161    3.7247    1.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1792    2.3779    0.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0914    3.7576    1.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2540    3.0123   -0.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6231    1.0180    2.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1468    1.9470    2.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0716    0.2683    2.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0791    1.1647   -0.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8601   -0.4804   -2.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1242   -2.3113   -4.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8976   -3.1686   -4.0750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3285   -2.2579   -2.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4537   -1.4464   -0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  1
  3  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  6
 23 25  1  0
 23 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 33 34  1  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  2  0
 37 39  1  0
 40 39  1  6
 40  2  1  0
 40  6  1  0
 12  7  1  0
 40 13  1  0
 39 16  1  0
 36 20  1  0
 34 26  2  0
 33 28  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  2 44  1  1
  4 45  1  0
  4 46  1  0
  4 47  1  0
  5 48  1  0
  5 49  1  0
  5 50  1  0
  8 51  1  0
  9 52  1  0
 10 53  1  0
 11 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 17 58  1  0
 21 59  1  0
 22 60  1  0
 24 61  1  0
 24 62  1  0
 24 63  1  0
 25 64  1  0
 25 65  1  0
 25 66  1  0
 27 67  1  0
 29 68  1  0
 30 69  1  0
 31 70  1  0
 32 71  1  0
 35 72  1  0
M  END


  Mrv1652306242117463D          

 72 79  0  0  0  0            999 V2000
    2.6246   -2.8873    2.1088 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5046   -1.9531    1.3645 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7964   -2.2999   -0.0814 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2832   -2.6886   -0.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9826   -3.3551   -0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.9521   -0.5062 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3742    0.3021   -1.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1731    0.6909   -2.4587 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0649    2.0238   -2.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1591    2.9996   -1.8665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3636    2.6387   -0.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4685    1.3141   -0.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6875    0.6043    1.1218 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0045    0.4126    1.4241 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8765    1.2779    2.1700 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4861    0.7219    1.9560 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0921    0.0939    3.1298 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5460    1.7898    1.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7894    3.0145    1.6833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6839    1.4309    0.9397 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5835    2.5038    1.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8889    2.6588    1.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0829    1.8516    0.9214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2233    2.8101    0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    1.2169    2.2421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    0.8128   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1579    0.6482   -0.8277 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0215   -0.3369   -1.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8747   -0.8622   -2.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4619   -1.8719   -3.5250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1770   -2.3694   -3.4028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3160   -1.8511   -2.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7426   -0.8344   -1.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.1218   -0.6260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7699   -0.4724   -0.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7790    0.1399    0.3150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -0.7265    0.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2344   -1.8335   -0.2338 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6163   -0.3359    0.9374 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9651   -0.7083    0.8185 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8332   -2.7620    3.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8977   -3.9648    1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5529   -2.7510    1.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4541   -1.7526    1.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4214   -3.7576   -0.0689 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5698   -2.3634   -1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8319   -2.0419    0.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845   -2.9258   -1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -3.7732   -0.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5583   -4.2252   -1.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0996   -0.0816   -3.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9071    2.3242   -3.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0860    4.0618   -2.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    3.3785    0.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122    0.6656    2.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8294    2.3621    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614    1.0322    3.2009 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1018    0.0642    3.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0065    3.4079    1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1161    3.7247    1.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1792    2.3779    0.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0914    3.7576    1.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2540    3.0123   -0.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6231    1.0180    2.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1468    1.9470    2.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0716    0.2683    2.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0791    1.1647   -0.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8601   -0.4804   -2.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1242   -2.3113   -4.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8976   -3.1686   -4.0750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3285   -2.2579   -2.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4537   -1.4464   -0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  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  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 23 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
 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
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 40 39  1  6  0  0  0
 40  2  1  0  0  0  0
 40  6  1  0  0  0  0
 12  7  1  0  0  0  0
 40 13  1  0  0  0  0
 39 16  1  0  0  0  0
 36 20  1  0  0  0  0
 34 26  2  0  0  0  0
 33 28  1  0  0  0  0
  1 41  1  0  0  0  0
  1 42  1  0  0  0  0
  1 43  1  0  0  0  0
  2 44  1  1  0  0  0
  4 45  1  0  0  0  0
  4 46  1  0  0  0  0
  4 47  1  0  0  0  0
  5 48  1  0  0  0  0
  5 49  1  0  0  0  0
  5 50  1  0  0  0  0
  8 51  1  0  0  0  0
  9 52  1  0  0  0  0
 10 53  1  0  0  0  0
 11 54  1  0  0  0  0
 14 55  1  0  0  0  0
 15 56  1  0  0  0  0
 15 57  1  0  0  0  0
 17 58  1  0  0  0  0
 21 59  1  0  0  0  0
 22 60  1  0  0  0  0
 24 61  1  0  0  0  0
 24 62  1  0  0  0  0
 24 63  1  0  0  0  0
 25 64  1  0  0  0  0
 25 65  1  0  0  0  0
 25 66  1  0  0  0  0
 27 67  1  0  0  0  0
 29 68  1  0  0  0  0
 30 69  1  0  0  0  0
 31 70  1  0  0  0  0
 32 71  1  0  0  0  0
 35 72  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0003188

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]12N(C(=O)\C3=C([H])\C4=C(N([H])C5=C([H])C([H])=C([H])C([H])=C45)C(\C([H])=C([H])/N3C1=O)(C([H])([H])[H])C([H])([H])[H])[C@@]13N(C4=C([H])C([H])=C([H])C([H])=C4[C@@]1(O[H])C2([H])[H])C(C([H])([H])[H])(C([H])([H])[H])[C@]3([H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C32H32N4O4/c1-18-29(4,5)35-23-13-9-7-11-21(23)30(39)17-31(40)27(38)34-15-14-28(2,3)25-20(19-10-6-8-12-22(19)33-25)16-24(34)26(37)36(31)32(18,30)35/h6-16,18,33,39-40H,17H2,1-5H3/b15-14-,24-16-/t18-,30-,31+,32+/m0/s1

> <INCHI_KEY>
WVQBDUCUXOANIV-AOXFNKRKSA-N

> <FORMULA>
C32H32N4O4

> <MOLECULAR_WEIGHT>
536.632

> <EXACT_MASS>
536.242355526

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
58.79331586742163

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1Z,4R,5S,14S,16R,19Z)-14,16-dihydroxy-5,6,6,21,21-pentamethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0^{3,16}.0^{4,7}.0^{4,14}.0^{8,13}.0^{22,30}.0^{24,29}]hentriaconta-1(31),8,10,12,19,22(30),24,26,28-nonaene-2,17-dione

> <ALOGPS_LOGP>
4.04

> <JCHEM_LOGP>
4.424706651000001

> <ALOGPS_LOGS>
-4.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.88720436099953

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.954457515352068

> <JCHEM_PKA_STRONGEST_BASIC>
-0.2755245423801681

> <JCHEM_POLAR_SURFACE_AREA>
100.11

> <JCHEM_REFRACTIVITY>
151.77620000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.31e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1Z,4R,5S,14S,16R,19Z)-14,16-dihydroxy-5,6,6,21,21-pentamethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0^{3,16}.0^{4,7}.0^{4,14}.0^{8,13}.0^{22,30}.0^{24,29}]hentriaconta-1(31),8,10,12,19,22(30),24,26,28-nonaene-2,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 72 79  0  0  0  0  0  0  0  0999 V2000
    2.6246   -2.8873    2.1088 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5046   -1.9531    1.3645 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7964   -2.2999   -0.0814 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2832   -2.6886   -0.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9826   -3.3551   -0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.9521   -0.5062 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3742    0.3021   -1.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1731    0.6909   -2.4587 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0649    2.0238   -2.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1591    2.9996   -1.8665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3636    2.6387   -0.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4685    1.3141   -0.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6875    0.6043    1.1218 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0045    0.4126    1.4241 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8765    1.2779    2.1700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861    0.7219    1.9560 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0921    0.0939    3.1298 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5460    1.7898    1.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7894    3.0145    1.6833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6839    1.4309    0.9397 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5835    2.5038    1.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8889    2.6588    1.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0829    1.8516    0.9214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2233    2.8101    0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    1.2169    2.2421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    0.8128   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1579    0.6482   -0.8277 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0215   -0.3369   -1.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8747   -0.8622   -2.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4619   -1.8719   -3.5250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1770   -2.3694   -3.4028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3160   -1.8511   -2.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7426   -0.8344   -1.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.1218   -0.6260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7699   -0.4724   -0.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7790    0.1399    0.3150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -0.7265    0.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2344   -1.8335   -0.2338 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6163   -0.3359    0.9374 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9651   -0.7083    0.8185 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8332   -2.7620    3.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8977   -3.9648    1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5529   -2.7510    1.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4541   -1.7526    1.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4214   -3.7576   -0.0689 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5698   -2.3634   -1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8319   -2.0419    0.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845   -2.9258   -1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -3.7732   -0.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5583   -4.2252   -1.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0996   -0.0816   -3.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9071    2.3242   -3.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0860    4.0618   -2.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    3.3785    0.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122    0.6656    2.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8294    2.3621    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614    1.0322    3.2009 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1018    0.0642    3.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0065    3.4079    1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1161    3.7247    1.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1792    2.3779    0.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0914    3.7576    1.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2540    3.0123   -0.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6231    1.0180    2.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1468    1.9470    2.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0716    0.2683    2.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0791    1.1647   -0.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8601   -0.4804   -2.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1242   -2.3113   -4.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8976   -3.1686   -4.0750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3285   -2.2579   -2.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4537   -1.4464   -0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  1
  3  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  6
 23 25  1  0
 23 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 33 34  1  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  2  0
 37 39  1  0
 40 39  1  6
 40  2  1  0
 40  6  1  0
 12  7  1  0
 40 13  1  0
 39 16  1  0
 36 20  1  0
 34 26  2  0
 33 28  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  2 44  1  1
  4 45  1  0
  4 46  1  0
  4 47  1  0
  5 48  1  0
  5 49  1  0
  5 50  1  0
  8 51  1  0
  9 52  1  0
 10 53  1  0
 11 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 17 58  1  0
 21 59  1  0
 22 60  1  0
 24 61  1  0
 24 62  1  0
 24 63  1  0
 25 64  1  0
 25 65  1  0
 25 66  1  0
 27 67  1  0
 29 68  1  0
 30 69  1  0
 31 70  1  0
 32 71  1  0
 35 72  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       2.625  -2.887   2.109  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.505  -1.953   1.365  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.796  -2.300  -0.081  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.283  -2.689  -0.227  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.983  -3.355  -0.724  0.00  0.00           C+0
HETATM    6  N   UNK     0       3.527  -0.952  -0.506  0.00  0.00           N+0
HETATM    7  C   UNK     0       3.374   0.302  -1.157  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.173   0.691  -2.459  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.065   2.024  -2.822  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.159   3.000  -1.867  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.364   2.639  -0.534  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.469   1.314  -0.191  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.688   0.604   1.122  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.005   0.413   1.424  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.877   1.278   2.170  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.486   0.722   1.956  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.092   0.094   3.130  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.546   1.790   1.535  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.789   3.014   1.683  0.00  0.00           O+0
HETATM   20  N   UNK     0      -0.684   1.431   0.940  0.00  0.00           N+0
HETATM   21  C   UNK     0      -1.583   2.504   1.110  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.889   2.659   1.102  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.083   1.852   0.921  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.223   2.810   0.547  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.554   1.217   2.242  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.034   0.813  -0.114  0.00  0.00           C+0
HETATM   27  N   UNK     0      -5.158   0.648  -0.828  0.00  0.00           N+0
HETATM   28  C   UNK     0      -5.021  -0.337  -1.759  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.875  -0.862  -2.705  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.462  -1.872  -3.525  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.177  -2.369  -3.403  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.316  -1.851  -2.460  0.00  0.00           C+0
HETATM   33  C   UNK     0      -3.743  -0.834  -1.639  0.00  0.00           C+0
HETATM   34  C   UNK     0      -3.143  -0.122  -0.626  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.770  -0.472  -0.310  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.779   0.140   0.315  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.380  -0.727   0.325  0.00  0.00           C+0
HETATM   38  O   UNK     0       0.234  -1.833  -0.234  0.00  0.00           O+0
HETATM   39  N   UNK     0       1.616  -0.336   0.937  0.00  0.00           N+0
HETATM   40  C   UNK     0       2.965  -0.708   0.819  0.00  0.00           C+0
HETATM   41  H   UNK     0       2.833  -2.762   3.213  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.898  -3.965   1.914  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.553  -2.751   1.992  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.454  -1.753   1.934  0.00  0.00           H+0
HETATM   45  H   UNK     0       5.421  -3.758  -0.069  0.00  0.00           H+0
HETATM   46  H   UNK     0       5.570  -2.363  -1.265  0.00  0.00           H+0
HETATM   47  H   UNK     0       5.832  -2.042   0.467  0.00  0.00           H+0
HETATM   48  H   UNK     0       2.485  -2.926  -1.642  0.00  0.00           H+0
HETATM   49  H   UNK     0       2.181  -3.773  -0.083  0.00  0.00           H+0
HETATM   50  H   UNK     0       3.558  -4.225  -1.100  0.00  0.00           H+0
HETATM   51  H   UNK     0       3.100  -0.082  -3.225  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.907   2.324  -3.845  0.00  0.00           H+0
HETATM   53  H   UNK     0       3.086   4.062  -2.064  0.00  0.00           H+0
HETATM   54  H   UNK     0       3.444   3.378   0.252  0.00  0.00           H+0
HETATM   55  H   UNK     0       5.212   0.666   2.346  0.00  0.00           H+0
HETATM   56  H   UNK     0       2.829   2.362   2.045  0.00  0.00           H+0
HETATM   57  H   UNK     0       3.261   1.032   3.201  0.00  0.00           H+0
HETATM   58  H   UNK     0       0.102   0.064   3.148  0.00  0.00           H+0
HETATM   59  H   UNK     0      -1.006   3.408   1.293  0.00  0.00           H+0
HETATM   60  H   UNK     0      -3.116   3.725   1.292  0.00  0.00           H+0
HETATM   61  H   UNK     0      -6.179   2.378   0.879  0.00  0.00           H+0
HETATM   62  H   UNK     0      -5.091   3.758   1.113  0.00  0.00           H+0
HETATM   63  H   UNK     0      -5.254   3.012  -0.524  0.00  0.00           H+0
HETATM   64  H   UNK     0      -3.623   1.018   2.812  0.00  0.00           H+0
HETATM   65  H   UNK     0      -5.147   1.947   2.828  0.00  0.00           H+0
HETATM   66  H   UNK     0      -5.072   0.268   2.074  0.00  0.00           H+0
HETATM   67  H   UNK     0      -6.079   1.165  -0.753  0.00  0.00           H+0
HETATM   68  H   UNK     0      -6.860  -0.480  -2.798  0.00  0.00           H+0
HETATM   69  H   UNK     0      -6.124  -2.311  -4.291  0.00  0.00           H+0
HETATM   70  H   UNK     0      -3.898  -3.169  -4.075  0.00  0.00           H+0
HETATM   71  H   UNK     0      -2.329  -2.258  -2.391  0.00  0.00           H+0
HETATM   72  H   UNK     0      -1.454  -1.446  -0.650  0.00  0.00           H+0
CONECT    1    2   41   42   43                                             
CONECT    2    1    3   40   44                                             
CONECT    3    2    4    5    6                                             
CONECT    4    3   45   46   47                                             
CONECT    5    3   48   49   50                                             
CONECT    6    3    7   40                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9   51                                                  
CONECT    9    8   10   52                                                  
CONECT   10    9   11   53                                                  
CONECT   11   10   12   54                                                  
CONECT   12   11   13    7                                                  
CONECT   13   12   14   15   40                                             
CONECT   14   13   55                                                       
CONECT   15   13   16   56   57                                             
CONECT   16   15   17   18   39                                             
CONECT   17   16   58                                                       
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   36                                                  
CONECT   21   20   22   59                                                  
CONECT   22   21   23   60                                                  
CONECT   23   22   24   25   26                                             
CONECT   24   23   61   62   63                                             
CONECT   25   23   64   65   66                                             
CONECT   26   23   27   34                                                  
CONECT   27   26   28   67                                                  
CONECT   28   27   29   33                                                  
CONECT   29   28   30   68                                                  
CONECT   30   29   31   69                                                  
CONECT   31   30   32   70                                                  
CONECT   32   31   33   71                                                  
CONECT   33   32   34   28                                                  
CONECT   34   33   35   26                                                  
CONECT   35   34   36   72                                                  
CONECT   36   35   37   20                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   16                                                  
CONECT   40   39    2    6   13                                             
CONECT   41    1                                                            
CONECT   42    1                                                            
CONECT   43    1                                                            
CONECT   44    2                                                            
CONECT   45    4                                                            
CONECT   46    4                                                            
CONECT   47    4                                                            
CONECT   48    5                                                            
CONECT   49    5                                                            
CONECT   50    5                                                            
CONECT   51    8                                                            
CONECT   52    9                                                            
CONECT   53   10                                                            
CONECT   54   11                                                            
CONECT   55   14                                                            
CONECT   56   15                                                            
CONECT   57   15                                                            
CONECT   58   17                                                            
CONECT   59   21                                                            
CONECT   60   22                                                            
CONECT   61   24                                                            
CONECT   62   24                                                            
CONECT   63   24                                                            
CONECT   64   25                                                            
CONECT   65   25                                                            
CONECT   66   25                                                            
CONECT   67   27                                                            
CONECT   68   29                                                            
CONECT   69   30                                                            
CONECT   70   31                                                            
CONECT   71   32                                                            
CONECT   72   35                                                            
MASTER        0    0    0    0    0    0    0    0   72    0  158    0
END

RDKit          3D

72 79  0  0  0  0  0  0  0  0999 V2000
    2.6246   -2.8873    2.1088 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5046   -1.9531    1.3645 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7964   -2.2999   -0.0814 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2832   -2.6886   -0.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9826   -3.3551   -0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266   -0.9521   -0.5062 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3742    0.3021   -1.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1731    0.6909   -2.4587 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0649    2.0238   -2.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1591    2.9996   -1.8665 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3636    2.6387   -0.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4685    1.3141   -0.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6875    0.6043    1.1218 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0045    0.4126    1.4241 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8765    1.2779    2.1700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861    0.7219    1.9560 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0921    0.0939    3.1298 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5460    1.7898    1.5354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7894    3.0145    1.6833 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6839    1.4309    0.9397 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5835    2.5038    1.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8889    2.6588    1.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0829    1.8516    0.9214 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2233    2.8101    0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    1.2169    2.2421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0340    0.8128   -0.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1579    0.6482   -0.8277 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0215   -0.3369   -1.7585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8747   -0.8622   -2.7048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4619   -1.8719   -3.5250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1770   -2.3694   -3.4028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3160   -1.8511   -2.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7426   -0.8344   -1.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427   -0.1218   -0.6260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7699   -0.4724   -0.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7790    0.1399    0.3150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3802   -0.7265    0.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2344   -1.8335   -0.2338 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6163   -0.3359    0.9374 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9651   -0.7083    0.8185 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8332   -2.7620    3.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8977   -3.9648    1.9144 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5529   -2.7510    1.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4541   -1.7526    1.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4214   -3.7576   -0.0689 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5698   -2.3634   -1.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8319   -2.0419    0.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4845   -2.9258   -1.6421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -3.7732   -0.0832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5583   -4.2252   -1.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0996   -0.0816   -3.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9071    2.3242   -3.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0860    4.0618   -2.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    3.3785    0.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122    0.6656    2.3462 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8294    2.3621    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2614    1.0322    3.2009 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1018    0.0642    3.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0065    3.4079    1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1161    3.7247    1.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1792    2.3779    0.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0914    3.7576    1.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2540    3.0123   -0.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6231    1.0180    2.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1468    1.9470    2.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0716    0.2683    2.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0791    1.1647   -0.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8601   -0.4804   -2.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1242   -2.3113   -4.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8976   -3.1686   -4.0750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3285   -2.2579   -2.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4537   -1.4464   -0.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  1
  3  5  1  0
  3  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  6
 23 25  1  0
 23 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 33 34  1  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 37 38  2  0
 37 39  1  0
 40 39  1  6
 40  2  1  0
 40  6  1  0
 12  7  1  0
 40 13  1  0
 39 16  1  0
 36 20  1  0
 34 26  2  0
 33 28  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  2 44  1  1
  4 45  1  0
  4 46  1  0
  4 47  1  0
  5 48  1  0
  5 49  1  0
  5 50  1  0
  8 51  1  0
  9 52  1  0
 10 53  1  0
 11 54  1  0
 14 55  1  0
 15 56  1  0
 15 57  1  0
 17 58  1  0
 21 59  1  0
 22 60  1  0
 24 61  1  0
 24 62  1  0
 24 63  1  0
 25 64  1  0
 25 65  1  0
 25 66  1  0
 27 67  1  0
 29 68  1  0
 30 69  1  0
 31 70  1  0
 32 71  1  0
 35 72  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₃₂H₃₂N₄O₄

Average Mass

536.6320 Da

Monoisotopic Mass

536.24236 Da

IUPAC Name

(1Z,4R,5S,14S,16R,19Z)-14,16-dihydroxy-5,6,6,21,21-pentamethyl-3,7,18,23-tetraazaoctacyclo[16.13.0.0^{3,16}.0^{4,7}.0^{4,14}.0^{8,13}.0^{22,30}.0^{24,29}]hentriaconta-1(31),8,10,12,19,22(30),24,26,28-nonaene-2,17-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1C(C)(C)N2C3=CC=CC=C3[C@@]3(O)C[C@]4(O)N(C(=O)\C5=C\C6=C(NC7=CC=CC=C67)C(C)(C)\C=C/N5C4=O)[C@@]123

InChI Identifier

InChI=1S/C32H32N4O4/c1-18-29(4,5)35-23-13-9-7-11-21(23)30(39)17-31(40)27(38)34-15-14-28(2,3)25-20(19-10-6-8-12-22(19)33-25)16-24(34)26(37)36(31)32(18,30)35/h6-16,18,33,39-40H,17H2,1-5H3/b15-14-,24-16-/t18-,30-,31+,32+/m0/s1

InChI Key

WVQBDUCUXOANIV-AOXFNKRKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Penicillium	NPAtlas	10705454

Species Where Detected

Species Name	Source	Reference
Penicillium simplicissimum	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrroloindoles. Pyrroloindoles are compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyrroloindoles

Direct Parent

Pyrroloindoles

Alternative Parents

Substituents

Pyrroloindole
Benzazepine
Alpha-amino acid or derivatives
Indole
Dioxopiperazine
Dialkylarylamine
2,5-dioxopiperazine
Azepine
N-alkylpiperazine
1,4-diazinane
Benzenoid
Piperazine
Heteroaromatic compound
Tertiary carboxylic acid amide
Pyrrole
Pyrrolidine
Tertiary alcohol
Carboxamide group
Azetidine
Lactam
Azacycle
Alkanolamine
Carboxylic acid derivative
Alcohol
Organonitrogen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Amine
Organic oxygen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.04	ALOGPS
logP	4.42	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	10.95	ChemAxon
pKa (Strongest Basic)	-0.28	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	100.11 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	151.78 m³·mol⁻¹	ChemAxon
Polarizability	58.79 Å³	ChemAxon
Number of Rings	8	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

NPAtlas ID

NPA016640

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78438266

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101007612

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Okaramine Q (NP0003188)

MOL for NP0003188 (Okaramine Q)

3D MOL for NP0003188 (Okaramine Q)

3D SDF for NP0003188 (Okaramine Q)

3D-SDF for NP0003188 (Okaramine Q)

PDB for NP0003188 (Okaramine Q)

3D PDB for NP0003188 (Okaramine Q)

SMILES for NP0003188 (Okaramine Q)

INCHI for NP0003188 (Okaramine Q)

Structure for NP0003188 (Okaramine Q)

3D Structure for NP0003188 (Okaramine Q)