NP-MRD: Showing NP-Card for (2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid (NP0287609)

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Record Information

Version

2.0

Created at

2022-09-09 16:51:27 UTC

Updated at

2022-09-09 16:51:27 UTC

NP-MRD ID

NP0287609

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid

Description

Amonabactin P 750 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. (2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid is found in Aeromonas hydrophila. Based on a literature review very few articles have been published on Amonabactin P 750.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092218512D          

 54 56  0  0  1  0            999 V2000
    0.7145   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  4  0  0  0
 22 24  2  0  0  0  0
 25 24  1  1  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
 30 29  1  4  0  0  0
 30 31  2  0  0  0  0
 31 32  1  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  2  0  0  0  0
 33 39  1  0  0  0  0
 39 40  1  0  0  0  0
 25 41  1  0  0  0  0
 41 42  1  4  0  0  0
 41 43  2  0  0  0  0
 44 43  1  1  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 46 51  1  0  0  0  0
 44 52  1  0  0  0  0
 52 53  2  0  0  0  0
 52 54  1  0  0  0  0
M  END

     RDKit          3D

100102  0  0  0  0  0  0  0  0999 V2000
   -0.7338   -1.0208    0.8869 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5788    0.0623   -0.0628 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7364    1.0261    0.0806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0574    0.3796   -0.1744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2093   -0.2141   -1.5441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6158   -0.8289   -1.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6765   -1.8303   -0.5877 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7679   -2.4575   -0.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9018   -3.4354    0.6003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9622   -2.1598   -1.1996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9996   -1.6939   -0.2759 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0509   -1.1359   -0.7679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1954   -0.9813   -2.1390 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1121   -0.6559    0.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2309   -0.0627   -0.4152 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2381    0.3943    0.3954 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1241    0.2553    1.7551 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0137   -0.3358    2.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8967   -0.4766    3.6863 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0287   -0.7801    1.4824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9154   -1.3721    2.0406 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7345    0.7494    0.0562 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9961    1.8145   -0.7896 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6319    0.3649    0.9374 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8800    1.0707    0.9992 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8713    0.3448    0.1344 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1857   -1.0407    0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0828   -2.0370    0.5448 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8199   -3.3766    0.9493 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7595   -3.7162    0.0392 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6844   -4.4713   -0.2327 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3094   -4.2505   -1.4943 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2379   -5.5782    0.5633 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6625   -5.8707    1.7975 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1676   -6.8888    2.5580 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2364   -7.6214    2.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8240   -7.3704    0.9201 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9031   -8.1185    0.4801 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3203   -6.3245    0.1177 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9438   -6.1201   -1.0559 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7369    2.4840    0.5628 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8560    3.2933    1.2477 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4186    2.9189   -0.4211 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3637    4.2629   -0.9291 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3258    5.0774   -0.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4185    6.4898   -0.4788 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5920    7.4469    0.0477 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6783    8.7880   -0.3084 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6543    9.1182   -1.2352 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4857    8.1733   -1.7687 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3720    6.8669   -1.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5998    4.3538   -2.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8561    3.3593   -3.1159 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5512    5.5835   -3.0078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3236   -1.9093    0.5757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5006   -0.7680    1.8567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5865   -0.3946   -1.0794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7752    1.4461    1.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6005    1.8528   -0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3422   -0.3457    0.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8290    1.2011   -0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0962    0.5352   -2.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5193   -1.0851   -1.6863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3868   -0.0441   -1.5164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7298   -1.2603   -2.6404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1581   -4.3862    0.3854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7837   -1.4315   -2.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3461   -3.0873   -1.7056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5829   -0.4560   -2.7155 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2911    0.0328   -1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1218    0.8608   -0.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9073    0.6074    2.4225 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6171   -0.1533    4.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7631   -1.5052    3.0155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9082    1.8118   -1.7756 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2685    1.1282    2.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8513    0.9066    0.0701 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4796    0.4234   -0.9218 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7625   -1.1438    1.4547 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6494   -2.2865   -0.4430 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6450   -8.4418    2.7231 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2949    4.5764    0.0092 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848    5.0740    0.9491 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8219    7.1975    0.7767 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0165    9.4982    0.1249 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7489   10.1484   -1.5344 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2473    8.4614   -2.4969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0522    6.1309   -1.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6996    6.1601   -3.0016 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
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 20 21  1  0
  2 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
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 31 32  1  0
 31 33  1  0
 33 34  2  0
 34 35  1  0
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 36 37  1  0
 37 38  1  0
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 39 40  1  0
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 41 42  1  0
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 43 44  1  0
 44 45  1  0
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 47 48  1  0
 48 49  2  0
 49 50  1  0
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 44 52  1  0
 52 54  1  0
 52 53  2  0
 20 14  1  0
 39 33  1  0
 51 46  1  0
  1 55  1  0
  1 56  1  0
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  4 60  1  0
  4 61  1  0
  5 62  1  0
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  6 64  1  0
  6 65  1  0
  9 66  1  0
 10 67  1  0
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 13 69  1  0
 15 70  1  0
 16 71  1  0
 17 72  1  0
 19 73  1  0
 21 74  1  0
 23 75  1  0
 25 76  1  1
 26 77  1  0
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 27 79  1  0
 27 80  1  0
 28 81  1  0
 28 82  1  0
 29 83  1  0
 29 84  1  0
 32 85  1  0
 34 86  1  0
 35 87  1  0
 36 88  1  0
 38 89  1  0
 40 90  1  0
 42 91  1  0
 44 92  1  6
 45 93  1  0
 45 94  1  0
 47 95  1  0
 48 96  1  0
 49 97  1  0
 50 98  1  0
 51 99  1  0
 54100  1  0
M  END


  Mrv1652309092218512D          

 54 56  0  0  1  0            999 V2000
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    0.7145   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  4  0  0  0
 22 24  2  0  0  0  0
 25 24  1  1  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
 30 29  1  4  0  0  0
 30 31  2  0  0  0  0
 31 32  1  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  2  0  0  0  0
 33 39  1  0  0  0  0
 39 40  1  0  0  0  0
 25 41  1  0  0  0  0
 41 42  1  4  0  0  0
 41 43  2  0  0  0  0
 44 43  1  1  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 46 51  1  0  0  0  0
 44 52  1  0  0  0  0
 52 53  2  0  0  0  0
 52 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287609

> <DATABASE_NAME>
NP-MRD

> <SMILES>
N[C@@H](CCCCN=C(O)CN=C(O)C1=CC=CC(O)=C1O)C(O)=N[C@@H](CCCCN=C(O)C1=CC=CC(O)=C1O)C(O)=N[C@@H](CC1=CC=CC=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C37H46N6O11/c38-25(14-4-6-18-39-30(46)21-41-34(50)24-13-9-17-29(45)32(24)48)35(51)42-26(36(52)43-27(37(53)54)20-22-10-2-1-3-11-22)15-5-7-19-40-33(49)23-12-8-16-28(44)31(23)47/h1-3,8-13,16-17,25-27,44-45,47-48H,4-7,14-15,18-21,38H2,(H,39,46)(H,40,49)(H,41,50)(H,42,51)(H,43,52)(H,53,54)/t25-,26-,27-/m0/s1

> <INCHI_KEY>
AQVANOYBWBHIEH-QKDODKLFSA-N

> <FORMULA>
C37H46N6O11

> <MOLECULAR_WEIGHT>
750.806

> <EXACT_MASS>
750.322456325

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
78.2326842703294

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-{[(2S)-2-{[(2S)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid

> <JCHEM_LOGP>
3.6018583322105027

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
3.5870387006885815

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0361910949814903

> <JCHEM_PKA_STRONGEST_BASIC>
9.416528187947094

> <JCHEM_POLAR_SURFACE_AREA>
307.18999999999994

> <JCHEM_REFRACTIVITY>
197.89970000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
21

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-{[(2S)-2-{[(2S)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  N   UNK     0       1.334  -2.310   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      -2.667  -9.240   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -4.001  -8.470   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -6.668  -8.470   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -5.335  -6.160   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -8.002  -6.160   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.669  -6.160   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -9.336  -3.850   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -6.668  -3.850   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.001  -3.850   0.000  0.00  0.00           O+0
HETATM   24  N   UNK     0       2.667  -6.160   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.002  -6.160   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0      10.669  -6.160   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      12.003  -8.470   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      13.337  -6.160   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.670  -3.850   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      16.004  -6.160   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      17.338  -6.930   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      14.670  -8.470   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   43  N   UNK     0       5.335  -9.240   0.000  0.00  0.00           N+0
HETATM   44  C   UNK     0       5.335 -10.780   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       6.668 -13.090   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       8.002 -15.400   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       5.335 -15.400   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0       4.001 -13.090   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0       2.667 -10.780   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   14   21                                                  
CONECT   21   20                                                            
CONECT   22    2   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   41                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   39                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   33   40                                                  
CONECT   40   39                                                            
CONECT   41   25   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45   52                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   51                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   46                                                       
CONECT   52   44   53   54                                                  
CONECT   53   52                                                            
CONECT   54   52                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  112    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₆N₆O₁₁

Average Mass

750.8060 Da

Monoisotopic Mass

750.32246 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

N[C@@H](CCCCN=C(O)CN=C(O)C1=CC=CC(O)=C1O)C(O)=N[C@@H](CCCCN=C(O)C1=CC=CC(O)=C1O)C(O)=N[C@@H](CC1=CC=CC=C1)C(O)=O

InChI Identifier

InChI=1S/C37H46N6O11/c38-25(14-4-6-18-39-30(46)21-41-34(50)24-13-9-17-29(45)32(24)48)35(51)42-26(36(52)43-27(37(53)54)20-22-10-2-1-3-11-22)15-5-7-19-40-33(49)23-12-8-16-28(44)31(23)47/h1-3,8-13,16-17,25-27,44-45,47-48H,4-7,14-15,18-21,38H2,(H,39,46)(H,40,49)(H,41,50)(H,42,51)(H,43,52)(H,53,54)/t25-,26-,27-/m0/s1

InChI Key

AQVANOYBWBHIEH-QKDODKLFSA-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
Aeromonas hydrophila	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
Phenylalanine or derivatives
Hippuric acid or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
3-phenylpropanoic-acid
Amphetamine or derivatives
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Salicylic acid or derivatives
Salicylamide
Benzoic acid or derivatives
Benzamide
Benzoyl
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Fatty acyl
Fatty amide
N-acyl-amine
Vinylogous acid
Carboxamide group
Secondary carboxylic acid amide
Amino acid or derivatives
Amino acid
Carboxylic acid
Monocarboxylic acid or derivatives
Organic nitrogen compound
Carbonyl group
Primary aliphatic amine
Organonitrogen compound
Organooxygen compound
Primary amine
Hydrocarbon derivative
Organic oxide
Amine
Organopnictogen compound
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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

78440345

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586937

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid (NP0287609)

MOL for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

3D MOL for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

3D SDF for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

3D-SDF for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

PDB for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

3D PDB for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

SMILES for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

INCHI for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

Structure for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)

3D Structure for NP0287609 ((2s)-2-{[(2s)-2-{[(2s)-2-amino-6-[(2-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyethylidene)amino]-1-hydroxyhexylidene]amino}-6-{[(2,3-dihydroxyphenyl)(hydroxy)methylidene]amino}-1-hydroxyhexylidene]amino}-3-phenylpropanoic acid)