NP-MRD: Showing NP-Card for 2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid (NP0252564)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 16:07:11 UTC

Updated at

2022-09-07 16:07:11 UTC

NP-MRD ID

NP0252564

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid

Description

133705-26-7, Also known as nannochelin C, belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. 2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid is found in Nannocystis exedens. 133705-26-7 Is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191514512D          

 53 54  0  0  0  0            999 V2000
    7.1447   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  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
    2.8579   -6.6000    0.0000 N   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
    3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -7.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -7.2336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -7.9480    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3316   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1566   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5691   -9.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3941   -9.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066  -10.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6316  -10.0914    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0441   -9.3770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0441  -10.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8691  -10.8059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6316  -11.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066  -11.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3941  -12.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5691  -12.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1566  -12.9493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5691  -13.6638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3941  -13.6638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066  -12.9493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -9.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -9.3770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3316  -10.0914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 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
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 27 25  1  4  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 18 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 12 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
  7 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
  2 44  1  0  0  0  0
 44 45  2  0  0  0  0
 46 44  1  4  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
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 48 53  1  0  0  0  0
M  END

     RDKit          3D

 97 98  0  0  0  0  0  0  0  0999 V2000
    3.2016    0.4033    2.3652 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9978   -0.1313    2.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1142    0.0701    3.3387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3103   -0.2006    3.1954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9627    0.1794    4.4572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0834    0.4292    2.1112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5122   -0.0144    2.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8289   -0.7208    3.1958 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5001    0.3265    1.2646 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8625   -0.1225    1.4085 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0104   -1.6058    1.2674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6112   -2.1460   -0.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3107   -1.7103   -1.2643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7437   -2.0002   -1.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7015   -1.4671   -0.5532 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1562   -2.1488    0.5250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3138   -0.1574   -0.7736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1551    0.1207    0.1099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9368    0.6336   -1.8899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2952    1.7824   -2.3230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2267    2.7651   -1.8579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6915    3.6937   -2.8269 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5417    4.7158   -2.5282 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9896    4.8865   -1.2380 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5816    4.0289   -0.2509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7028    2.9877   -0.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4184    0.3078    2.7228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7214    0.9753    3.5239 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7206   -0.0160    3.0967 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5783   -1.6874    3.1999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3658   -2.4583    2.2506 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1088   -2.2851    4.3519 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7981   -0.7712    1.0167 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0311   -0.6867    0.0889 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7191   -1.9885    0.2918 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0575   -2.2403   -0.2016 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6029   -1.9441   -1.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7875   -0.4431   -1.7188 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6956    0.1376   -0.7752 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1498    0.5535    0.4084 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1043    0.3137   -0.9502 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6404    0.8565    0.0747 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8718   -0.0384   -2.0860 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0874    0.0443   -2.4268 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3365    0.5098   -1.9114 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5625    1.0072   -0.6732 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7874    1.4927   -0.2446 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8802    1.5015   -1.0578 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6730    0.9924   -2.3375 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4726    0.5166   -2.7626 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3365   -0.5405   -1.2178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3180    0.2548   -1.2743 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6863   -1.1810   -2.3380 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4715   -0.6457    4.1875 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2844    1.1134    3.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5579   -0.4028    5.1205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9981    1.5491    2.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7562    0.0996    1.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2275    0.9118    0.4517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5117    0.4277    0.6614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2014   -2.0261    1.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9192   -2.0051    1.6990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6877   -3.2690    0.0209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5146   -1.9674   -0.2039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7731   -2.2354   -2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0711   -0.6221   -1.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0818   -1.8545   -2.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9065   -3.1548   -1.3650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7711   -3.0268    0.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1186    0.1265   -2.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7286    2.0778   -3.2816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3582    3.5853   -3.8543 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8934    5.4167   -3.2698 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6611    5.6838   -0.9740 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9153    4.1323    0.7741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3599    2.3772    0.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1746    0.5836    3.7732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0874   -3.2703    4.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0552   -1.2812    0.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5900    0.1810    0.3748 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7656   -2.1232    1.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9787   -2.8203    0.0337 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2535   -3.3704    0.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7753   -1.8055    0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6387   -2.4370   -1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0663   -2.3518   -2.4034 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8665    0.1016   -1.8159 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2830   -0.3672   -2.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8558    0.6272    1.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2109   -0.5108   -2.9009 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2020   -0.4147   -3.5166 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8036    1.0367    0.0584 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.8911    1.8920    0.7713 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.8425    1.8670   -0.7574 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.5346    0.9910   -3.0067 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3323    0.1287   -3.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6031   -0.7287   -3.2477 H   0  0  0  0  0  0  0  0  0  0  0  0
 40 39  1  0
 39 38  1  0
 38 37  1  0
 37 36  1  0
 36 35  1  0
 35 34  1  0
 34 33  1  0
 33  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 10 27  1  0
 27 29  1  0
 27 28  2  0
  4 30  1  0
 30 32  1  0
 30 31  2  0
 34 51  1  0
 51 53  1  0
 51 52  2  0
 39 41  1  0
 41 42  2  0
 41 43  1  0
 43 44  2  0
 44 45  1  0
 45 46  2  0
 46 47  1  0
 47 48  2  0
 48 49  1  0
 49 50  2  0
 26 21  1  0
 50 45  1  0
 40 89  1  0
 38 87  1  0
 38 88  1  0
 37 85  1  0
 37 86  1  0
 36 83  1  0
 36 84  1  0
 35 81  1  0
 35 82  1  0
 34 80  1  1
 33 79  1  0
  3 54  1  0
  3 55  1  0
  5 56  1  0
  6 57  1  0
  6 58  1  0
  9 59  1  0
 10 60  1  6
 11 61  1  0
 11 62  1  0
 12 63  1  0
 12 64  1  0
 13 65  1  0
 13 66  1  0
 14 67  1  0
 14 68  1  0
 16 69  1  0
 19 70  1  0
 20 71  1  0
 22 72  1  0
 23 73  1  0
 24 74  1  0
 25 75  1  0
 26 76  1  0
 29 77  1  0
 32 78  1  0
 53 97  1  0
 43 90  1  0
 44 91  1  0
 46 92  1  0
 47 93  1  0
 48 94  1  0
 49 95  1  0
 50 96  1  0
M  END


  Mrv1533004191514512D          

 53 54  0  0  0  0            999 V2000
    7.1447   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  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
    2.8579   -6.6000    0.0000 N   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
    3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -7.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184   -7.2336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -7.9480    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3316   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1566   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5691   -9.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3941   -9.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066  -10.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6316  -10.0914    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0441   -9.3770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0441  -10.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8691  -10.8059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6316  -11.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066  -11.5204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3941  -12.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5691  -12.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1566  -12.9493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5691  -13.6638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3941  -13.6638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8066  -12.9493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809   -9.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -9.3770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3316  -10.0914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 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
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 27 25  1  4  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 18 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 12 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
  7 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
  2 44  1  0  0  0  0
 44 45  2  0  0  0  0
 46 44  1  4  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
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 48 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252564

> <DATABASE_NAME>
NP-MRD

> <SMILES>
ON(CCCCC(NC(=O)CC(O)(CC(=O)NC(CCCCN(O)C(=O)C=CC1=CC=CC=C1)C(O)=O)C(O)=O)C(O)=O)C(=O)C=CC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C36H44N4O13/c41-29(37-27(33(45)46)15-7-9-21-39(52)31(43)19-17-25-11-3-1-4-12-25)23-36(51,35(49)50)24-30(42)38-28(34(47)48)16-8-10-22-40(53)32(44)20-18-26-13-5-2-6-14-26/h1-6,11-14,17-20,27-28,51-53H,7-10,15-16,21-24H2,(H,37,41)(H,38,42)(H,45,46)(H,47,48)(H,49,50)

> <INCHI_KEY>
NJZHNIXLUZOOST-UHFFFAOYSA-N

> <FORMULA>
C36H44N4O13

> <MOLECULAR_WEIGHT>
740.763

> <EXACT_MASS>
740.290487493

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
75.07795517218392

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[3-carboxy-3-({[1-carboxy-5-(N-hydroxy-3-phenylprop-2-enamido)pentyl]carbamoyl}methyl)-3-hydroxypropanamido]-6-(N-hydroxy-3-phenylprop-2-enamido)hexanoic acid

> <ALOGPS_LOGP>
0.89

> <JCHEM_LOGP>
1.6906668766666648

> <ALOGPS_LOGS>
-4.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
3.4930717789018897

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.980182706883337

> <JCHEM_PKA_STRONGEST_BASIC>
-4.152985703945814

> <JCHEM_POLAR_SURFACE_AREA>
271.40999999999997

> <JCHEM_REFRACTIVITY>
188.09230000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
23

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.45e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[3-carboxy-3-({[1-carboxy-5-(N-hydroxy-3-phenylprop-2-enamido)pentyl]carbamoyl}methyl)-3-hydroxypropanamido]-6-(N-hydroxy-3-phenylprop-2-enamido)hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  O   UNK     0      13.337 -13.860   0.000  0.00  0.00           O+0
HETATM    2  N   UNK     0      13.337 -12.320   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       5.335 -12.320   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.668 -14.630   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.541 -16.170   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.461 -16.170   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.691 -14.836   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.461 -13.503   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       0.151 -14.836   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0      -0.619 -16.170   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.159 -16.170   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.929 -17.504   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.469 -17.504   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.239 -18.837   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      -6.779 -18.837   0.000  0.00  0.00           N+0
HETATM   24  O   UNK     0      -7.549 -17.504   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -7.549 -20.171   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -9.089 -20.171   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -6.779 -21.505   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.239 -21.505   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.469 -22.838   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.929 -22.838   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.159 -24.172   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.929 -25.506   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.469 -25.506   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -5.239 -24.172   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.151 -17.504   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       1.691 -17.504   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -0.619 -18.837   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       4.001 -17.710   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       5.335 -18.480   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       2.667 -18.480   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      14.670 -10.010   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      20.005 -11.550   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      21.339 -12.320   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   44                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   41                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14   38                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   35                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   29                                                       
CONECT   35   18   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   12   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41    7   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
CONECT   44    2   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   53                                                  
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   48                                                       
MASTER        0    0    0    0    0    0    0    0   53    0  108    0
END

View in JSmol

Synonyms

Value	Source
Nannochelin C	MeSH

Chemical Formula

C₃₆H₄₄N₄O₁₃

Average Mass

740.7630 Da

Monoisotopic Mass

740.29049 Da

IUPAC Name

2-[3-carboxy-3-({[1-carboxy-5-(N-hydroxy-3-phenylprop-2-enamido)pentyl]carbamoyl}methyl)-3-hydroxypropanamido]-6-(N-hydroxy-3-phenylprop-2-enamido)hexanoic acid

Traditional Name

2-[3-carboxy-3-({[1-carboxy-5-(N-hydroxy-3-phenylprop-2-enamido)pentyl]carbamoyl}methyl)-3-hydroxypropanamido]-6-(N-hydroxy-3-phenylprop-2-enamido)hexanoic acid

CAS Registry Number

Not Available

SMILES

ON(CCCCC(NC(=O)CC(O)(CC(=O)NC(CCCCN(O)C(=O)C=CC1=CC=CC=C1)C(O)=O)C(O)=O)C(O)=O)C(=O)C=CC1=CC=CC=C1

InChI Identifier

InChI=1S/C36H44N4O13/c41-29(37-27(33(45)46)15-7-9-21-39(52)31(43)19-17-25-11-3-1-4-12-25)23-36(51,35(49)50)24-30(42)38-28(34(47)48)16-8-10-22-40(53)32(44)20-18-26-13-5-2-6-14-26/h1-6,11-14,17-20,27-28,51-53H,7-10,15-16,21-24H2,(H,37,41)(H,38,42)(H,45,46)(H,47,48)(H,49,50)

InChI Key

NJZHNIXLUZOOST-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
Nannocystis exedens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids. N-acyl-alpha amino acids are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids

Alternative Parents

Substituents

N-acyl-alpha-amino acid
Cinnamic acid or derivatives
Tricarboxylic acid or derivatives
Styrene
Alpha-hydroxy acid
Monocyclic benzene moiety
Fatty amide
Hydroxy acid
N-acyl-amine
Benzenoid
Fatty acyl
Tertiary alcohol
Hydroxamic acid
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid
Organonitrogen compound
Organic oxygen compound
Carbonyl group
Organic oxide
Organic nitrogen compound
Organooxygen compound
Hydrocarbon derivative
Alcohol
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
logP	0.89	ALOGPS
logP	1.69	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	2.98	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	271.41 Å²	ChemAxon
Rotatable Bond Count	23	ChemAxon
Refractivity	188.09 m³·mol⁻¹	ChemAxon
Polarizability	75.08 Å³	ChemAxon
Number of Rings	2	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

71341110

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid (NP0252564)

MOL for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

3D MOL for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

3D SDF for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

3D-SDF for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

PDB for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

3D PDB for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

SMILES for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

INCHI for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

Structure for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)

3D Structure for NP0252564 (2-{[3-carboxy-3-({[1-carboxy-5-(n-hydroxy-3-phenylprop-2-enamido)pentyl]-c-hydroxycarbonimidoyl}methyl)-1,3-dihydroxypropylidene]amino}-6-(n-hydroxy-3-phenylprop-2-enamido)hexanoic acid)