NP-MRD: Showing NP-Card for 5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid (NP0208686)

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Record Information

Version

2.0

Created at

2022-09-05 05:46:58 UTC

Updated at

2022-09-05 05:46:58 UTC

NP-MRD ID

NP0208686

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid

Description

5-Amino-2-{[5-(N,3-dihydroxy-2-{[1-hydroxy-5-(N-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-N-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-C-hydroxycarbonimidoyl]ethyl}pentanimidic acid 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. Based on a literature review very few articles have been published on 5-amino-2-{[5-(N,3-dihydroxy-2-{[1-hydroxy-5-(N-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-N-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-C-hydroxycarbonimidoyl]ethyl}pentanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052207472D          

 51 51  0  0  0  0            999 V2000
   -8.5485   -4.0547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7345   -4.1887    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2115   -3.5507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5025   -2.7787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3165   -2.6448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6076   -1.8728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4216   -1.7389    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9446   -2.3769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7126   -0.9669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5267   -0.8329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3974   -3.6846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8744   -3.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1064   -4.4566    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2923   -4.5905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5243   -6.0005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7693   -3.9525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0603   -3.1806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9552   -4.0865    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6642   -4.8584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4322   -3.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182   -3.5824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3271   -4.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8502   -4.9924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5875   -5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6356   -6.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5591   -5.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0822   -6.4024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7451   -5.8983    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4541   -6.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9771   -7.3083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7911   -7.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3142   -7.8123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0231   -8.5843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6400   -6.8042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3490   -7.5762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1170   -6.1662    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6971   -6.3001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881   -7.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8022   -7.2060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2201   -5.6621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9291   -4.8901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0342   -5.7961    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5572   -5.1580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2662   -4.3861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7892   -3.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6032   -3.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8943   -4.6540    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7083   -4.7879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3712   -5.2920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6623   -6.0640    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  4  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 29 30  1  4  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 37 38  1  4  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 43 44  1  4  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 44 50  1  0  0  0  0
 50 51  2  0  0  0  0
M  END

     RDKit          3D

105105  0  0  0  0  0  0  0  0999 V2000
    8.5605    1.9467   -3.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4465    2.0612   -1.6267 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1574    0.9005   -0.8537 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1982   -0.1757   -0.8088 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5893   -0.7808   -2.0950 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6078   -1.9149   -1.8576 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7750   -1.4342   -1.2015 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.7837   -0.9520   -1.9879 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9482   -1.4232    0.1968 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0906   -1.8651    1.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9301    1.2942    0.5871 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0341    1.9641    1.1539 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9303    1.0845    1.2364 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6680    0.4108    0.8693 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7993    1.4597    0.2838 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6031    1.0610   -0.2609 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2133   -0.3572    2.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2643   -0.7621    2.7710 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0291   -0.7649    2.5545 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1004   -1.5850    3.7020 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6865   -0.4649    2.1617 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1588   -1.4439    1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7786   -1.1901    0.6653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2954   -1.1939    1.6837 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1823   -0.1960    2.7103 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2675    1.1592    2.2584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6193   -1.0073    0.9963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9289    0.1451    0.3166 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4571   -1.9819    1.0709 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7406   -1.8639    0.4390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5615   -3.0607    0.8156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9348   -3.0874    0.2365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8612   -3.0824   -1.2843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2308   -3.1121   -1.8028 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3857   -0.5859    0.8660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4387   -0.4202    2.2793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8329    0.2504    0.1552 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3388    1.1963   -0.6512 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2528    0.8822   -2.1557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9278    0.7151   -2.5108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7869    1.4391   -0.3510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4771    2.3737   -1.0806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3471    0.7701    0.5782 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7350    0.8955    0.9802 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.6061   -0.0504    0.2266 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0204    0.4225    0.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1741    1.8356   -0.3701 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1475    2.7373    0.0544 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2353    4.0250   -0.3978 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1158    2.3013    0.8922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4921    3.1359    1.5933 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1726    0.9950   -3.4468 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9811    2.7706   -3.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6097    2.1395   -3.3974 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7308    2.7809   -1.3889 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2346    0.4194   -1.2725 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8052   -0.9844   -0.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0883    0.2609   -0.2793 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7656   -1.1882   -2.6769 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1179    0.0134   -2.7041 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0458   -2.7056   -1.3155 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8934   -2.3186   -2.8651 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.4246   -0.5365   -2.8069 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.8721   -1.0127    0.6177 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2328    1.8200    2.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9772   -0.3008    0.0346 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3395    2.0314   -0.5354 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6276    2.2700    1.0749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7328    0.6760   -1.1652 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6282   -2.4197    3.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0111   -0.6062    3.0988 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5157    0.5613    1.8789 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8362   -1.4668    0.2544 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1523   -2.4960    1.6122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5332   -1.9895   -0.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8051   -0.2080    0.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3219   -2.1867    2.2417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894   -0.3646    3.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3086    1.3099    1.3444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3254    1.4728    2.1438 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2220    1.8056    3.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7167    0.2779   -0.6772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5918   -1.8556   -0.6480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0407   -3.9827    0.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6389   -3.1400    1.9384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4705   -2.1460    0.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5507   -3.9104    0.5942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3527   -2.1581   -1.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2954   -3.9388   -1.6670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8250   -3.7892   -1.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2838   -3.2665   -2.8166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5760   -0.5134    2.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8515    2.2227   -0.4911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7044    1.7825   -2.6549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8633    0.0341   -2.4466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6576    1.5190   -3.0306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9963    2.2016   -1.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7392    0.6304    2.0839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1136   -0.3231   -0.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6714   -0.9951    0.8440 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4665   -0.2350   -0.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6551    0.1921    0.9632 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3855    1.9175   -1.4793 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1415    2.2064    0.0894 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5990    4.0471   -1.3163 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
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 45100  1  0
 46101  1  0
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 47103  1  0
 47104  1  0
 49105  1  0
M  END


  Mrv1652309052207472D          

 51 51  0  0  0  0            999 V2000
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   -7.2115   -3.5507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5025   -2.7787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3165   -2.6448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6076   -1.8728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4216   -1.7389    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9446   -2.3769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7126   -0.9669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5267   -0.8329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3974   -3.6846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8744   -3.0466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2923   -4.5905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5243   -6.0005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0603   -3.1806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9552   -4.0865    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6642   -4.8584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4322   -3.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6182   -3.5824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3271   -4.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8502   -4.9924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5875   -5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6356   -6.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5591   -5.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0822   -6.4024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7451   -5.8983    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4541   -6.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9771   -7.3083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7911   -7.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3142   -7.8123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0231   -8.5843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6400   -6.8042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3490   -7.5762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1170   -6.1662    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6971   -6.3001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881   -7.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8022   -7.2060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2201   -5.6621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9291   -4.8901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0342   -5.7961    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5572   -5.1580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2662   -4.3861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7892   -3.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6032   -3.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8943   -4.6540    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7083   -4.7879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3712   -5.2920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6623   -6.0640    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  4  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 29 30  1  4  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 30 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 37 38  1  4  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 43 44  1  4  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
 44 50  1  0  0  0  0
 50 51  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0208686

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CNC(CCCN(O)C=O)C(O)=NC(CO)C(=O)N(O)CCCC(NC)C(O)=NC(CCCN)C(O)=NC(CO)C(O)=NC1CCCN(O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C29H54N10O12/c1-31-18(8-4-12-37(49)17-42)25(44)36-23(16-41)29(48)39(51)13-5-9-19(32-2)24(43)33-20(7-3-11-30)26(45)35-22(15-40)27(46)34-21-10-6-14-38(50)28(21)47/h17-23,31-32,40-41,49-51H,3-16,30H2,1-2H3,(H,33,43)(H,34,46)(H,35,45)(H,36,44)

> <INCHI_KEY>
UOBSAMDBIABJEC-UHFFFAOYSA-N

> <FORMULA>
C29H54N10O12

> <MOLECULAR_WEIGHT>
734.809

> <EXACT_MASS>
734.392267219

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
73.7704612842689

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
12

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-amino-2-{[5-(N,3-dihydroxy-2-{[1-hydroxy-5-(N-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-N-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-C-hydroxycarbonimidoyl]ethyl}pentanimidic acid

> <JCHEM_LOGP>
-11.174991010661685

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
3

> <JCHEM_PKA>
3.185048257439847

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7025154864556744

> <JCHEM_PKA_STRONGEST_BASIC>
10.22971733352033

> <JCHEM_POLAR_SURFACE_AREA>
342.5200000000001

> <JCHEM_REFRACTIVITY>
179.59969999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
5-amino-2-{[5-(N,3-dihydroxy-2-{[1-hydroxy-5-(N-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-N-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-C-hydroxycarbonimidoyl]ethyl}pentanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0     -15.957  -7.569   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0     -14.438  -7.819   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0     -13.461  -6.628   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -14.005  -5.187   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -15.524  -4.937   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -16.067  -3.496   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0     -17.587  -3.246   0.000  0.00  0.00           N+0
HETATM    8  O   UNK     0     -18.563  -4.437   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0     -18.130  -1.805   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0     -19.650  -1.555   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0     -11.942  -6.878   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0     -10.965  -5.687   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0     -11.399  -8.319   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -9.879  -8.569   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0     -10.312 -11.201   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -8.903  -7.378   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -9.446  -5.937   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0      -7.383  -7.628   0.000  0.00  0.00           N+0
HETATM   20  O   UNK     0      -6.840  -9.069   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -6.407  -6.437   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.887  -6.687   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.344  -8.128   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.320  -9.319   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0      -6.697 -10.010   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      -6.786 -11.547   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.777 -10.760   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -5.753 -11.951   0.000  0.00  0.00           O+0
HETATM   29  N   UNK     0      -3.257 -11.010   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0      -2.714 -12.451   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.691 -13.642   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.210 -13.392   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.186 -14.583   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0      -5.643 -16.024   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0      -1.195 -12.701   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.651 -14.142   0.000  0.00  0.00           O+0
HETATM   37  N   UNK     0      -0.218 -11.510   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0       1.301 -11.760   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.844 -13.201   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.364 -13.451   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.278 -10.569   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       1.734  -9.128   0.000  0.00  0.00           O+0
HETATM   43  N   UNK     0       3.797 -10.819   0.000  0.00  0.00           N+0
HETATM   44  C   UNK     0       4.773  -9.628   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.230  -8.187   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       5.206  -6.996   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       6.726  -7.246   0.000  0.00  0.00           C+0
HETATM   48  N   UNK     0       7.269  -8.687   0.000  0.00  0.00           N+0
HETATM   49  O   UNK     0       8.789  -8.937   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       6.293  -9.878   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       6.836 -11.319   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9                                                            
CONECT   11    3   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   30   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   41                                                  
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   38   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45   50                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   44   51                                                  
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  102    0
END

View in JSmol

Synonyms

Value	Source
5-Amino-2-{[5-(N,3-dihydroxy-2-{[1-hydroxy-5-(N-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-N-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-C-hydroxycarbonimidoyl]ethyl}pentanimidate	Generator

Chemical Formula

C₂₉H₅₄N₁₀O₁₂

Average Mass

734.8090 Da

Monoisotopic Mass

734.39227 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CNC(CCCN(O)C=O)C(O)=NC(CO)C(=O)N(O)CCCC(NC)C(O)=NC(CCCN)C(O)=NC(CO)C(O)=NC1CCCN(O)C1=O

InChI Identifier

InChI=1S/C29H54N10O12/c1-31-18(8-4-12-37(49)17-42)25(44)36-23(16-41)29(48)39(51)13-5-9-19(32-2)24(43)33-20(7-3-11-30)26(45)35-22(15-40)27(46)34-21-10-6-14-38(50)28(21)47/h17-23,31-32,40-41,49-51H,3-16,30H2,1-2H3,(H,33,43)(H,34,46)(H,35,45)(H,36,44)

InChI Key

UOBSAMDBIABJEC-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

Not Available

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
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Serine or derivatives
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Delta-lactam
Piperidinone
Piperidine
Fatty acyl
Fatty amide
N-acyl-amine
Lactam
Hydroxamic acid
Secondary carboxylic acid amide
Carboxamide group
Amino acid or derivatives
Azacycle
Secondary aliphatic amine
Organoheterocyclic compound
Secondary amine
Primary amine
Organic oxygen compound
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Amine
Organopnictogen compound
Primary aliphatic amine
Primary alcohol
Organooxygen compound
Organonitrogen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source

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

162998820

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid (NP0208686)

MOL for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

3D MOL for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

3D SDF for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

3D-SDF for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

PDB for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

3D PDB for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

SMILES for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

INCHI for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

Structure for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)

3D Structure for NP0208686 (5-amino-2-{[5-(n,3-dihydroxy-2-{[1-hydroxy-5-(n-hydroxyformamido)-2-(methylamino)pentylidene]amino}propanamido)-1-hydroxy-2-(methylamino)pentylidene]amino}-n-{2-hydroxy-1-[(1-hydroxy-2-oxopiperidin-3-yl)-c-hydroxycarbonimidoyl]ethyl}pentanimidic acid)