NP-MRD: Showing NP-Card for 8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone (NP0325480)

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Record Information

Version

2.0

Created at

2022-09-12 06:15:54 UTC

Updated at

2022-09-12 06:15:54 UTC

NP-MRD ID

NP0325480

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone

Description

8,14,18,21-Tetrahydroxy-19-(1-hydroxyethyl)-4-methyl-13-(2-methylpropyl)-3,16-bis(propan-2-yl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]Hexacosa-17,20-diene-2,5,12,15-tetrone belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. 8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone is found in Streptomyces solisilvae. Based on a literature review very few articles have been published on 8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-4-methyl-13-(2-methylpropyl)-3,16-bis(propan-2-yl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]Hexacosa-17,20-diene-2,5,12,15-tetrone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122208152D          

 48 50  0  0  0  0            999 V2000
    3.6533   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6533   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3677   -4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8862   -3.0590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0448   -3.0546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -2.5559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -2.9684    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6533   -1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -1.7309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2574   -2.0690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3480   -2.5559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.0625   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -4.2059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.0625   -6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -5.0309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7954   -5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5099   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -5.4434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -4.2059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -3.7934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  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
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 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
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 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
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 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 33 34  1  4  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 34 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 40 41  1  4  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 41 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
  5 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END

     RDKit          3D

102104  0  0  0  0  0  0  0  0999 V2000
    5.1618   -2.2988   -1.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8381   -2.9541   -1.6478 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7854   -3.8774   -0.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6120   -2.2150   -1.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1545   -1.1223   -0.9903 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6531   -1.5417    0.3334 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4302   -1.2381    1.3134 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0954   -2.5059   -0.1276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9142   -2.7460   -1.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1041   -2.0826    0.9440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7840   -0.1682   -0.6327 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6703    1.8868    0.3190 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5715    1.6650    1.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1066    1.6223    2.1514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2400    2.4479    1.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3085    1.8858   -0.2234 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3494    2.9478   -1.2435 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0885    3.9687   -1.3940 C   0  0  1  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
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 20 21  1  0
 20 22  1  0
 19 17  1  0
 17 18  1  0
 17 15  1  0
 15 16  2  0
 15 14  1  0
 14 13  1  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  2  0
 34 35  1  0
 35 36  1  0
 35 37  1  0
 41 42  1  0
 42 43  1  0
 42 44  1  0
  6  5  1  0
 25 30  1  0
  8 14  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  2 52  1  0
  3 53  1  0
  3 54  1  0
  3 55  1  0
  4 56  1  0
  4 57  1  0
  5 58  1  6
 48102  1  0
 41 94  1  1
 39 93  1  0
 34 87  1  6
 32 86  1  0
 30 85  1  6
 29 83  1  0
 29 84  1  0
 28 81  1  0
 28 82  1  0
 27 79  1  0
 27 80  1  0
 26 78  1  0
 19 70  1  1
 20 71  1  0
 21 72  1  0
 21 73  1  0
 21 74  1  0
 22 75  1  0
 22 76  1  0
 22 77  1  0
 18 67  1  0
 18 68  1  0
 18 69  1  0
 14 66  1  6
 13 64  1  0
 13 65  1  0
 11 62  1  1
 12 63  1  0
 10 60  1  0
 10 61  1  0
  9 59  1  0
 35 88  1  6
 36 89  1  0
 36 90  1  0
 36 91  1  0
 37 92  1  0
 42 95  1  0
 43 96  1  0
 43 97  1  0
 43 98  1  0
 44 99  1  0
 44100  1  0
 44101  1  0
M  END


  Mrv1652309122208152D          

 48 50  0  0  0  0            999 V2000
    3.6533   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6533   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3677   -4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8862   -3.0590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0448   -3.0546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -2.5559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -2.9684    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9388   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6533   -1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -1.7309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2574   -2.0690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6836   -0.9772    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -2.5559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.7309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -3.7934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -4.2059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -5.0309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -6.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -5.0309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -5.4434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -6.2684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -6.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -6.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2243   -5.4434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5099   -4.2059    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -3.7934    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  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  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
 20 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 33 34  1  4  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 34 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 40 41  1  4  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 41 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
  5 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325480

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC1N(O)C(=O)C(N=C(O)C(N=C(O)C2CCCNN2C(=O)C(C(C)C)N(C)C(=O)C2CC(O)CNN2C1=O)C(C)O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C31H54N8O9/c1-15(2)12-22-29(45)38-21(13-19(41)14-33-38)28(44)36(8)25(17(5)6)31(47)37-20(10-9-11-32-37)26(42)35-24(18(7)40)27(43)34-23(16(3)4)30(46)39(22)48/h15-25,32-33,40-41,48H,9-14H2,1-8H3,(H,34,43)(H,35,42)

> <INCHI_KEY>
DMXYJHVUOOQCBE-UHFFFAOYSA-N

> <FORMULA>
C31H54N8O9

> <MOLECULAR_WEIGHT>
682.82

> <EXACT_MASS>
682.401375351

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
102

> <JCHEM_AVERAGE_POLARIZABILITY>
70.95658589710492

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-4-methyl-13-(2-methylpropyl)-3,16-bis(propan-2-yl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0^{6,11}]hexacosa-17,20-diene-2,5,12,15-tetrone

> <JCHEM_LOGP>
-1.9953815273381186

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.264243963609101

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9254347877153726

> <JCHEM_PKA_STRONGEST_BASIC>
4.85105303603126

> <JCHEM_POLAR_SURFACE_AREA>
231.17

> <JCHEM_REFRACTIVITY>
193.6423000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0^{6,11}]hexacosa-17,20-diene-2,5,12,15-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       6.819  -5.541   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.819  -7.081   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.153  -7.851   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.486  -7.851   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.152  -7.081   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.521  -5.710   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.684  -5.702   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       2.818  -4.771   0.000  0.00  0.00           N+0
HETATM    9  N   UNK     0       4.152  -5.541   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       5.486  -4.771   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.486  -3.231   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.819  -2.461   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.152  -2.461   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.818  -3.231   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.485  -2.461   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.485  -0.921   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       0.151  -3.231   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       0.151  -4.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.183  -2.461   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.183  -0.921   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.516  -0.151   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.151  -0.151   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.347  -3.862   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.143  -1.824   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0      -2.516  -4.771   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0      -2.516  -3.231   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0      -3.850  -2.461   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.184  -3.231   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.184  -4.771   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.850  -5.541   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.850  -7.081   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -5.184  -7.851   0.000  0.00  0.00           O+0
HETATM   33  N   UNK     0      -2.516  -7.851   0.000  0.00  0.00           N+0
HETATM   34  C   UNK     0      -2.516  -9.391   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -3.850 -10.161   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.850 -11.701   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -5.184  -9.391   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.183 -10.161   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -1.183 -11.701   0.000  0.00  0.00           O+0
HETATM   40  N   UNK     0       0.151  -9.391   0.000  0.00  0.00           N+0
HETATM   41  C   UNK     0       1.485 -10.161   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.485 -11.701   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.818 -12.471   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.151 -12.471   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.818  -9.391   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       4.152 -10.161   0.000  0.00  0.00           O+0
HETATM   47  N   UNK     0       2.818  -7.851   0.000  0.00  0.00           N+0
HETATM   48  O   UNK     0       1.485  -7.081   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   47                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   23                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   19   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25   31                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   38                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   34   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42   45                                                  
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   41   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45    5   48                                                  
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₅₄N₈O₉

Average Mass

682.8200 Da

Monoisotopic Mass

682.40138 Da

IUPAC Name

8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-4-methyl-13-(2-methylpropyl)-3,16-bis(propan-2-yl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0^{6,11}]hexacosa-17,20-diene-2,5,12,15-tetrone

Traditional Name

8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0^{6,11}]hexacosa-17,20-diene-2,5,12,15-tetrone

CAS Registry Number

Not Available

SMILES

CC(C)CC1N(O)C(=O)C(N=C(O)C(N=C(O)C2CCCNN2C(=O)C(C(C)C)N(C)C(=O)C2CC(O)CNN2C1=O)C(C)O)C(C)C

InChI Identifier

InChI=1S/C31H54N8O9/c1-15(2)12-22-29(45)38-21(13-19(41)14-33-38)28(44)36(8)25(17(5)6)31(47)37-20(10-9-11-32-37)26(42)35-24(18(7)40)27(43)34-23(16(3)4)30(46)39(22)48/h15-25,32-33,40-41,48H,9-14H2,1-8H3,(H,34,43)(H,35,42)

InChI Key

DMXYJHVUOOQCBE-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
Streptomyces solisilvae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Macrolactam
Alpha-amino acid or derivatives
1,2-diazinane
Tertiary carboxylic acid amide
Secondary carboxylic acid amide
Secondary alcohol
Lactam
Hydroxamic acid
Carboxylic acid hydrazide
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	-2	ChemAxon
pKa (Strongest Acidic)	1.93	ChemAxon
pKa (Strongest Basic)	4.85	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	231.17 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	193.64 m³·mol⁻¹	ChemAxon
Polarizability	70.96 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162814903

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone (NP0325480)

MOL for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

3D MOL for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

3D SDF for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

3D-SDF for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

PDB for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

3D PDB for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

SMILES for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

INCHI for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

Structure for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)

3D Structure for NP0325480 (8,14,18,21-tetrahydroxy-19-(1-hydroxyethyl)-3,16-diisopropyl-4-methyl-13-(2-methylpropyl)-1,4,10,11,14,17,20,26-octaazatricyclo[20.4.0.0⁶,¹¹]hexacosa-17,20-diene-2,5,12,15-tetrone)