NP-MRD: Showing NP-Card for 2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid (NP0267676)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 12:31:40 UTC

Updated at

2022-09-08 12:31:40 UTC

NP-MRD ID

NP0267676

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082214312D          

 42 44  0  0  0  0            999 V2000
   -1.5610   -5.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610   -6.0382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8465   -6.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -6.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -5.2132    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824   -4.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824   -3.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2969   -3.5632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -3.5632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2969   -5.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2969   -6.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0114   -4.8007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259   -5.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -4.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -3.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1548   -3.5632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1548   -5.2132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1548   -6.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8693   -6.4507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -6.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -7.2757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259   -6.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0114   -6.4507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824   -6.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824   -7.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3949   -7.1325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8646   -8.0510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6771   -8.1942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592   -8.9695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7717   -9.1128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020   -8.4808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1145   -8.6240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0539   -9.8880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5236  -10.5200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8057  -11.2952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111  -10.3767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1808  -11.0087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.6015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -9.4582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -7.6882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8465   -7.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610   -7.6882    0.0000 N   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  2  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  2  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  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  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 29 38  1  0  0  0  0
 38 39  1  0  0  0  0
 25 40  1  0  0  0  0
 40 41  1  0  0  0  0
  3 41  1  0  0  0  0
 41 42  2  0  0  0  0
M  END

     RDKit          3D

 82 84  0  0  0  0  0  0  0  0999 V2000
    1.9049   -0.8146    4.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2630   -0.3115    3.2800 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5950    0.0680    2.2859 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2165    0.7908    1.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9941   -0.0628   -0.1122 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0522    0.7830   -1.2188 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1578   -1.0308   -0.1666 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4060   -0.5018   -0.1500 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8545    0.2697   -1.1606 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2195    1.6737   -0.7178 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1269    1.7182    0.4676 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4038    1.2716    0.2634 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6692    2.4334   -1.7842 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7694    1.9495   -2.4330 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9134    2.7150   -3.6151 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6758    0.5236   -2.8481 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9918    0.0529   -3.0653 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0416   -0.3904   -1.8621 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9179   -0.9937   -0.9754 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6838   -0.7634   -0.1708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2582   -0.5697    0.9143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6688   -0.8014    0.7576 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1589   -1.9612    0.0925 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6470   -3.2190    0.6966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8755   -3.0915    1.7070 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9187   -4.4855    0.2797 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6533   -1.9260   -0.0515 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0916   -3.2855   -0.5645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0448   -0.8982   -0.8295 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8132    0.0969   -0.3806 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.2767   -0.0007   -0.8711 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.1010   -0.9196   -0.0435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4220   -0.8192   -0.5376 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7863    1.2896   -0.7249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3408    1.9486    0.4091 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.2122    3.0397    0.6000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8962    2.4573    0.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8738    3.7417   -0.2710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3065    1.4489   -0.7741 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9542    1.4888   -0.8615 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1533   -0.1623    2.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7651    0.0023    3.1139 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5771   -0.2277    4.4600 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3015    0.8186    1.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8545    1.8052    0.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6526    1.6673   -1.0593 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0950   -1.7423    0.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0057   -1.7236   -1.0566 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0900    0.3728   -1.9504 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2654    2.1566   -0.4023 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1544    2.7616    0.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775    1.1050    1.2735 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7856    0.7562    1.0388 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7339    2.1115   -1.8877 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4081    3.5558   -3.3939 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921    0.4780   -3.8558 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3628   -0.3330   -2.2191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5812   -1.2382   -2.4511 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9494   -1.9720   -1.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1717   -0.6039   -1.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9138   -1.8741   -0.2052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2998   -0.0946    1.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7627   -1.8987   -0.9702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7055   -5.3260    0.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0376   -1.8856    0.9984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0797   -3.2419   -1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4008   -3.7083   -1.3195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1942   -4.0316    0.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9345    0.0378    0.7191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3466   -0.2708   -1.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1698   -0.6319    1.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8492   -1.9756   -0.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0543   -1.0382    0.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3529    1.3639    1.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9245    2.8272    1.2631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3028    2.3369    1.1569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0448    3.6914   -1.2515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7875    1.7929   -1.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6061    2.3155   -1.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2931   -1.2613    4.7494 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1642    0.4595    4.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5809   -0.0890    4.9675 H   0  0  0  0  0  0  0  0  0  0  0  0
 43 42  1  0
 42 41  1  0
 41 21  2  0
 21 20  1  0
 20  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 18  1  0
 18 19  1  0
 18 16  1  0
 16 17  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 10  1  0
 10 11  1  0
 11 12  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
 21 22  1  0
 22 23  1  0
 23 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 30 39  1  0
 39 40  1  0
 39 37  1  0
 37 38  1  0
 37 35  1  0
 35 36  1  0
 35 34  1  0
 34 31  1  0
 31 32  1  0
 32 33  1  0
 23 24  1  0
 24 26  1  0
 24 25  2  0
  3 41  1  0
 31 30  1  0
 10  9  1  0
 43 80  1  0
 43 81  1  0
 43 82  1  0
 20 60  1  0
 20 61  1  0
  6 46  1  0
  7 47  1  0
  7 48  1  0
  9 49  1  6
 18 58  1  6
 19 59  1  0
 16 56  1  6
 17 57  1  0
 14 54  1  1
 15 55  1  0
 10 50  1  1
 11 51  1  0
 11 52  1  0
 12 53  1  0
  4 44  1  0
  4 45  1  0
  2  1  1  0
 22 62  1  0
 23 63  1  6
 27 65  1  1
 28 66  1  0
 28 67  1  0
 28 68  1  0
 30 69  1  1
 39 78  1  6
 40 79  1  0
 37 76  1  1
 38 77  1  0
 35 74  1  1
 36 75  1  0
 31 70  1  6
 32 71  1  0
 32 72  1  0
 33 73  1  0
 26 64  1  0
M  END


  Mrv1652309082214312D          

 42 44  0  0  0  0            999 V2000
   -1.5610   -5.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610   -6.0382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8465   -6.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -6.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -5.2132    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824   -4.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824   -3.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2969   -3.5632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -3.5632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2969   -5.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2969   -6.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0114   -4.8007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259   -5.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -4.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -3.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1548   -3.5632    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1548   -5.2132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1548   -6.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8693   -6.4507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -6.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4403   -7.2757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7259   -6.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0114   -6.4507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824   -6.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824   -7.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3949   -7.1325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8646   -8.0510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6771   -8.1942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592   -8.9695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7717   -9.1128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020   -8.4808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1145   -8.6240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0539   -9.8880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5236  -10.5200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8057  -11.2952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111  -10.3767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1808  -11.0087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.6015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -9.4582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320   -7.6882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8465   -7.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610   -7.6882    0.0000 N   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  2  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  2  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  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  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 29 38  1  0  0  0  0
 38 39  1  0  0  0  0
 25 40  1  0  0  0  0
 40 41  1  0  0  0  0
  3 41  1  0  0  0  0
 41 42  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0267676

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(CC(O)(COC2C(O)C(O)C(O)OC2CO)CC1=N)NC(C(C)OC1C(O)C(O)C(O)OC1CO)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H40N2O16/c1-8(40-20-12(6-28)42-23(36)17(32)15(20)30)13(21(33)34)26-10-4-24(37,3-9(25)18(10)38-2)7-39-19-11(5-27)41-22(35)16(31)14(19)29/h8,11-17,19-20,22-23,25-32,35-37H,3-7H2,1-2H3,(H,33,34)

> <INCHI_KEY>
SUDPAXYVXUDIJO-UHFFFAOYSA-N

> <FORMULA>
C24H40N2O16

> <MOLECULAR_WEIGHT>
612.582

> <EXACT_MASS>
612.237783216

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
59.167998936562505

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
12

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid

> <JCHEM_LOGP>
-8.780099813413512

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.016142167135255

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6678372766663214

> <JCHEM_PKA_STRONGEST_BASIC>
9.334749110819192

> <JCHEM_POLAR_SURFACE_AREA>
301.4

> <JCHEM_REFRACTIVITY>
146.03109999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.914  -9.731   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.914 -11.271   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.580 -12.041   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.246 -11.271   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      -0.246  -9.731   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       1.087  -8.961   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.087  -7.421   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.421  -6.651   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      -0.246  -6.651   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.421  -9.731   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.421 -11.271   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.755  -8.961   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.088  -9.731   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.422  -8.961   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.422  -7.421   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.756  -6.651   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       7.756  -9.731   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.756 -11.271   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.089 -12.041   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.422 -12.041   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.422 -13.581   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.088 -11.271   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.755 -12.041   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.087 -12.041   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.087 -13.581   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.604 -13.314   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.614 -15.029   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.131 -15.296   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.657 -16.743   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.174 -17.010   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.164 -15.831   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.680 -16.098   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       5.701 -18.458   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.711 -19.637   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.237 -21.084   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.194 -19.370   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.204 -20.550   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       2.667 -17.923   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       1.151 -17.655   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -0.246 -14.351   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -1.580 -13.581   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0      -2.914 -14.351   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   41                                                  
CONECT    4    3    5   24                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    6   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   13   23                                                  
CONECT   23   22                                                            
CONECT   24    4   25                                                       
CONECT   25   24   26   27   40                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   38                                                  
CONECT   30   29   31   33                                                  
CONECT   31   30   32                                                       
CONECT   32   31                                                            
CONECT   33   30   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   29   39                                                  
CONECT   39   38                                                            
CONECT   40   25   41                                                       
CONECT   41   40    3   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₄₀N₂O₁₆

Average Mass

612.5820 Da

Monoisotopic Mass

612.23778 Da

IUPAC Name

2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid

Traditional Name

2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid

CAS Registry Number

Not Available

SMILES

COC1=C(CC(O)(COC2C(O)C(O)C(O)OC2CO)CC1=N)NC(C(C)OC1C(O)C(O)C(O)OC1CO)C(O)=O

InChI Identifier

InChI=1S/C24H40N2O16/c1-8(40-20-12(6-28)42-23(36)17(32)15(20)30)13(21(33)34)26-10-4-24(37,3-9(25)18(10)38-2)7-39-19-11(5-27)41-22(35)16(31)14(19)29/h8,11-17,19-20,22-23,25-32,35-37H,3-7H2,1-2H3,(H,33,34)

InChI Key

SUDPAXYVXUDIJO-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

Classification

Not classified

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	-8.8	ChemAxon
pKa (Strongest Acidic)	3.67	ChemAxon
pKa (Strongest Basic)	9.33	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	12	ChemAxon
Polar Surface Area	301.4 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	146.03 m³·mol⁻¹	ChemAxon
Polarizability	59.17 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid (NP0267676)

MOL for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

3D MOL for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

3D SDF for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

3D-SDF for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

PDB for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

3D PDB for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

SMILES for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

INCHI for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

Structure for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)

3D Structure for NP0267676 (2-{[5-hydroxy-3-imino-2-methoxy-5-({[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}methyl)cyclohex-1-en-1-yl]amino}-3-{[4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}butanoic acid)