NP-MRD: Showing NP-Card for (1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione (NP0265481)

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Record Information

Version

2.0

Created at

2022-09-08 09:28:44 UTC

Updated at

2022-09-08 09:28:44 UTC

NP-MRD ID

NP0265481

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione

Description

(-)-Asperginulin A belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. Based on a literature review very few articles have been published on (-)-asperginulin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082211282D          

 52 60  0  0  1  0            999 V2000
    5.1622    5.2950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5055    4.7732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5238    3.8340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7669    3.5566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3934    3.0383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8837    3.1039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4359    3.7169    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1895    3.3812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9432    3.7166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6106    3.2315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5242    2.4110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7704    2.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1031    2.5607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2961    2.3894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0468    1.5291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1398    1.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4253    1.9932    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6082    1.6954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860    2.4902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8423    1.1366    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4722    0.3993    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0591   -0.1805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7919    0.1985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6579    1.0125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5344    0.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1480    0.3078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7349    0.7694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0807    0.8935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2147    1.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5181    2.0866    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7268    2.8847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0418    3.3011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5224    3.1031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5291    3.9834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5267    4.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1709    3.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8921    2.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9704    2.1626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8371    2.9603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9808    3.5155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7991    4.5045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8601    4.0578    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6418    4.8533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0869    5.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079    6.2808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8838    6.3190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4387    5.6243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8177    4.8915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1093    2.5232    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9006    1.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2284    0.7578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1050    1.5067    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  2  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  6  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  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  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  2  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 35 48  1  0  0  0  0
 43 48  1  0  0  0  0
 33 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
 27 52  1  0  0  0  0
 52 30  1  1  0  0  0
 20 52  1  0  0  0  0
M  END

     RDKit          3D

 94102  0  0  0  0  0  0  0  0999 V2000
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   -5.5111    1.0799    0.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3970    1.8893    0.7811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1621    2.9892    1.5828 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7658    0.5426    3.7404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3557    0.4592    5.0666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5986   -0.6070    5.4723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2344   -1.5988    4.5952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6571   -1.4880    3.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4193   -0.4314    2.8385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9647   -0.0971    1.5783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7445   -0.9453    0.4599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1654   -0.7648   -0.6919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5644    0.4323   -1.1256 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9586    0.6279   -2.2631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4875    1.9336   -2.3982 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7829   -0.4120   -3.2596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8580   -0.3113   -4.6917 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7707   -1.4490   -5.2151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4934   -2.4875   -4.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4638   -1.6275   -2.9639 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0777   -1.8452   -1.7066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5715   -2.9559   -1.3986 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5616   -0.8812   -4.7955 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.4224    0.4938   -0.2590 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7474   -0.3946    0.8188 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5796   -0.0386    2.1651 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0388    1.2486    2.6830 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0702    1.1885    4.1956 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6493    1.4496    2.1840 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9271    2.4843    2.5334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0029   -1.0951    2.8612 N   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9454   -3.3404    2.2433 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3135   -4.1702    1.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1525   -3.7233   -0.0908 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6366   -2.4796   -0.3478 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2725   -1.6638    0.7107 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -1.0818   -1.3764 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2058   -1.4302   -2.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.1402   -0.2097    0.5045 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 54  1  0
 15 67  1  0
 19 68  1  0
 21 69  1  1
 22 70  1  0
 22 71  1  0
 23 72  1  0
 23 73  1  0
 27 74  1  1
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 34 79  1  0
 42 89  1  0
 44 90  1  0
 45 91  1  0
 46 92  1  0
 47 93  1  0
 38 80  1  0
 38 81  1  0
 38 82  1  0
 39 83  1  0
 39 84  1  0
 39 85  1  0
 40 86  1  0
 41 87  1  0
 41 88  1  0
 51 94  1  0
 12 66  1  0
 11 65  1  0
 10 64  1  0
  9 63  1  0
  7 62  1  0
M  END


  Mrv1652309082211282D          

 52 60  0  0  1  0            999 V2000
    5.1622    5.2950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5055    4.7732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5238    3.8340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7669    3.5566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3934    3.0383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8837    3.1039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4359    3.7169    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1895    3.3812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9432    3.7166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6106    3.2315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5242    2.4110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7704    2.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1031    2.5607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2961    2.3894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0468    1.5291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1398    1.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4253    1.9932    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6082    1.6954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860    2.4902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8423    1.1366    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4722    0.3993    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0591   -0.1805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7919    0.1985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6579    1.0125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5344    0.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1480    0.3078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7349    0.7694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0807    0.8935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2147    1.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5181    2.0866    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7268    2.8847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0418    3.3011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5224    3.1031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5291    3.9834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5267    4.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1709    3.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8921    2.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9704    2.1626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8371    2.9603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9808    3.5155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7991    4.5045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8601    4.0578    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6418    4.8533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0869    5.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079    6.2808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8838    6.3190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4387    5.6243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8177    4.8915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1093    2.5232    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9006    1.7251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2284    0.7578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1050    1.5067    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  2  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  6  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  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  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  2  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 35 48  1  0  0  0  0
 43 48  1  0  0  0  0
 33 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
 27 52  1  0  0  0  0
 52 30  1  1  0  0  0
 20 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0265481

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(C=C)C1=C(C=C2N=C(O)[C@]34[C@H](CCN3C2=O)[C@H]2CCN3C(=O)\C(=C\C5=C(NC6=CC=CC=C56)C(C)(C)C=C)N=C(O)[C@]423)C2=CC=CC=C2N1

> <INCHI_IDENTIFIER>
InChI=1S/C42H42N6O4/c1-7-39(3,4)33-25(23-13-9-11-15-29(23)43-33)21-31-35(49)47-19-17-27-28-18-20-48-36(50)32(46-38(52)42(28,48)41(27,47)37(51)45-31)22-26-24-14-10-12-16-30(24)44-34(26)40(5,6)8-2/h7-16,21-22,27-28,43-44H,1-2,17-20H2,3-6H3,(H,45,51)(H,46,52)/b31-21-,32-22?/t27-,28-,41+,42+/m1/s1

> <INCHI_KEY>
QQFNACLTCVRIER-HGHCUTENSA-N

> <FORMULA>
C42H42N6O4

> <MOLECULAR_WEIGHT>
694.836

> <EXACT_MASS>
694.326753856

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
73.87670093321888

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,5Z,10R,11R)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0^{1,14}.0^{2,7}.0^{2,10}]octadeca-3,17-diene-6,15-dione

> <JCHEM_LOGP>
5.922654856

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.050957257223494

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3094535565589225

> <JCHEM_PKA_STRONGEST_BASIC>
1.1647175369662008

> <JCHEM_POLAR_SURFACE_AREA>
137.38

> <JCHEM_REFRACTIVITY>
202.43560000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5Z,10R,11R)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0^{1,14}.0^{2,7}.0^{2,10}]octadeca-3,17-diene-6,15-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       9.636   9.884   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.410   8.910   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.445   7.157   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.032   6.639   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.201   5.671   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.116   5.794   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      10.147   6.938   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      11.554   6.312   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.961   6.938   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.206   6.032   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.045   4.501   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.638   3.875   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.392   4.780   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.886   4.460   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.421   2.854   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.728   2.893   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       6.394   3.721   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.869   3.165   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.827   4.648   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.439   2.122   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.748   0.745   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.844  -0.337   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.212   0.370   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       4.961   1.890   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       6.598   1.809   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.743   0.574   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.372   1.436   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.151   1.668   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.401   3.187   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       0.967   3.895   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       1.357   5.385   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -0.078   6.162   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.842   5.792   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.854   7.436   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.716   7.690   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.919   6.728   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.399   5.559   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.545   4.037   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.163   5.526   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.698   6.562   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.358   8.408   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0       7.206   7.574   0.000  0.00  0.00           N+0
HETATM   43  C   UNK     0       6.798   9.060   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.629  10.356   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.921  11.724   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       5.383  11.795   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.552  10.499   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       5.260   9.131   0.000  0.00  0.00           C+0
HETATM   49  N   UNK     0       3.937   4.710   0.000  0.00  0.00           N+0
HETATM   50  C   UNK     0       3.548   3.220   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       4.160   1.415   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       2.063   2.813   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13    6   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   24   52                                             
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24   16   26                                                  
CONECT   26   25                                                            
CONECT   27   21   28   52                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   52                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   49                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   48                                                  
CONECT   36   35   37   42                                                  
CONECT   37   36   38   39   40                                             
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   37   41                                                       
CONECT   41   40                                                            
CONECT   42   36   43                                                       
CONECT   43   42   44   48                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   35   43                                                  
CONECT   49   33   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50   27   30   20                                             
MASTER        0    0    0    0    0    0    0    0   52    0  120    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₄₂N₆O₄

Average Mass

694.8360 Da

Monoisotopic Mass

694.32675 Da

IUPAC Name

(1R,2R,5Z,10R,11R)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0^{1,14}.0^{2,7}.0^{2,10}]octadeca-3,17-diene-6,15-dione

Traditional Name

(1R,2R,5Z,10R,11R)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0^{1,14}.0^{2,7}.0^{2,10}]octadeca-3,17-diene-6,15-dione

CAS Registry Number

Not Available

SMILES

CC(C)(C=C)C1=C(C=C2N=C(O)[C@]34[C@H](CCN3C2=O)[C@H]2CCN3C(=O)\C(=C\C5=C(NC6=CC=CC=C56)C(C)(C)C=C)N=C(O)[C@]423)C2=CC=CC=C2N1

InChI Identifier

InChI=1S/C42H42N6O4/c1-7-39(3,4)33-25(23-13-9-11-15-29(23)43-33)21-31-35(49)47-19-17-27-28-18-20-48-36(50)32(46-38(52)42(28,48)41(27,47)37(51)45-31)22-26-24-14-10-12-16-30(24)44-34(26)40(5,6)8-2/h7-16,21-22,27-28,43-44H,1-2,17-20H2,3-6H3,(H,45,51)(H,46,52)/b31-21-,32-22?/t27-,28-,41+,42+/m1/s1

InChI Key

QQFNACLTCVRIER-HGHCUTENSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Indole or derivatives
Indole
2,5-dioxopiperazine
Dioxopiperazine
N-alkylpiperazine
Azepane
Benzenoid
Substituted pyrrole
Piperazine
1,4-diazinane
Heteroaromatic compound
Tertiary carboxylic acid amide
Pyrrolidine
Pyrrole
Secondary carboxylic acid amide
Lactam
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	5.92	ChemAxon
pKa (Strongest Acidic)	3.31	ChemAxon
pKa (Strongest Basic)	1.16	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	137.38 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	202.44 m³·mol⁻¹	ChemAxon
Polarizability	73.88 Å³	ChemAxon
Number of Rings	9	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

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

146683283

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione (NP0265481)

MOL for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

3D MOL for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

3D SDF for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

3D-SDF for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

PDB for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

3D PDB for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

SMILES for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

INCHI for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

Structure for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)

3D Structure for NP0265481 ((1r,2r,5z,10r,11r)-3,18-dihydroxy-5,16-bis({[2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl]methylidene})-4,7,14,17-tetraazapentacyclo[9.7.0.0¹,¹⁴.0²,⁷.0²,¹⁰]octadeca-3,17-diene-6,15-dione)