NP-MRD: Showing NP-Card for (2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol (NP0177758)

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Record Information

Version

2.0

Created at

2022-09-03 15:38:44 UTC

Updated at

2022-09-03 15:38:44 UTC

NP-MRD ID

NP0177758

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol

Description

Inosamycin D belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines. (2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol is found in Streptomyces hygroscopicus. Based on a literature review very few articles have been published on Inosamycin D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032217382D          

 42 45  0  0  1  0            999 V2000
   -5.6091   -1.7116    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -1.7116    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4656   -1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -1.7116    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0367   -1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -0.4741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7512   -0.0616    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4656   -0.4741    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.1759    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0367    2.0009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    0.7634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6078    1.1759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -0.0616    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6078   -0.4741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -1.2991    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2752   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.5687    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5052   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1696   -3.9898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1953   -2.5687    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2897   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1101   -3.1499    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4457   -2.3962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2662   -2.3099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6017   -1.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1168   -0.8888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7511   -2.9774    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5716   -2.8911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4155   -3.7311    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9005   -4.3985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5951   -3.8173    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2595   -4.5710    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -1.7840    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8443   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -2.5366    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0367   -2.9491    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -2.9491    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4656   -3.7741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -2.5366    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8946   -2.9491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  1  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  1  0  0  0
 22 35  1  0  0  0  0
 17 35  1  0  0  0  0
 35 36  1  6  0  0  0
  5 37  1  0  0  0  0
 37 38  1  6  0  0  0
 37 39  1  0  0  0  0
 39 40  1  1  0  0  0
 39 41  1  0  0  0  0
  3 41  1  0  0  0  0
 41 42  1  6  0  0  0
M  END

     RDKit          3D

 86 89  0  0  0  0  0  0  0  0999 V2000
   -7.8166   -0.2012   -1.7630 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9608   -1.1387   -2.4259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6800   -1.3956   -1.6619 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9955   -0.2052   -1.5270 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0043   -0.2281   -0.5712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9419    0.5961   -0.9220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7809    1.6354   -0.0441 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0052    2.9897   -0.6833 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3226    3.0847   -1.2818 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7369    4.0553    0.3167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6328    3.5906    1.7470 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8775    3.2628    2.2891 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6067    2.4958    1.9136 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4059    3.1005    2.2766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4528    1.6782    0.6482 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8549    0.4557    0.8461 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3575    0.3524    0.2190 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4046   -0.6959   -0.6625 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7381   -0.7761   -1.0774 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9343   -2.1233   -1.7230 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6615   -3.1547   -0.8264 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4756   -0.6738    0.2436 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6672   -0.0061    0.1345 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7832   -0.7538    0.4585 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5287   -0.9803   -0.7266 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7632   -1.4704   -0.3321 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4385   -2.2624   -1.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6573   -1.5126   -2.5613 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6279   -0.2543   -0.0503 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8276    0.4814   -1.2175 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8688    0.5703    0.9668 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.7416    0.7689    2.0472 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6699   -0.1833    1.5060 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0082    0.7158    2.4276 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5187    0.0493    1.1503 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0196    1.1962    1.7127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5471   -1.6070   -0.1910 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8667   -2.1752   -1.3398 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6580   -2.5290    0.2018 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7463   -2.6644    1.5813 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9675   -1.8965   -0.2624 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.0074   -2.8168   -0.2402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8078   -0.3154   -2.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5507    0.7867   -1.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5169   -2.1142   -2.4780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7389   -0.8382   -3.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0884   -2.1633   -2.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4426    0.2055    0.3533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5540    1.5511    0.7473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2774    3.0360   -1.5433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3516    2.5013   -2.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5204    4.0576   -1.5332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5052    4.8504    0.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7558    4.5373    0.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2858    4.4627    2.3395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6346    3.5912    1.7411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9277    1.8545    2.7483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2374    3.9344    1.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7629    2.2867   -0.0019 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5613    1.3171   -0.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9206    0.0614   -1.7597 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2553   -2.2785   -2.5854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9690   -2.2289   -2.1512 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4993   -3.6622   -0.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6970   -1.7071    0.6174 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4905   -1.7936    0.7735 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7323   -2.0946    0.5653 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8686   -3.1913   -1.6671 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4115   -2.6196   -1.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4693   -1.7149   -3.0583 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6247   -0.5758    0.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7065    1.4554   -1.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5494    1.4980    0.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4732    1.5080    2.6239 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1193   -0.9865    2.1664 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5818    0.7859    3.2847 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8113    1.6391    1.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1456   -0.6825    1.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0435    1.1075    2.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8152   -1.5718    0.6401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7352   -3.1838   -1.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0359   -1.6085   -1.5304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5752   -3.4957   -0.3300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6806   -2.9185    1.7900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1888   -1.0073    0.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7648   -3.6499    0.2153 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  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 22 35  1  0
 35 36  1  0
  5 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41  3  1  0
 15  7  1  0
 35 17  1  0
 33 24  1  0
  1 43  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  3 47  1  6
  5 48  1  1
  7 49  1  1
  8 50  1  6
  9 51  1  0
  9 52  1  0
 10 53  1  0
 10 54  1  0
 11 55  1  1
 12 56  1  0
 13 57  1  1
 14 58  1  0
 15 59  1  6
 17 60  1  6
 19 61  1  6
 20 62  1  0
 20 63  1  0
 21 64  1  0
 22 65  1  1
 24 66  1  1
 26 67  1  1
 27 68  1  0
 27 69  1  0
 28 70  1  0
 29 71  1  1
 30 72  1  0
 31 73  1  6
 32 74  1  0
 33 75  1  1
 34 76  1  0
 34 77  1  0
 35 78  1  1
 36 79  1  0
 37 80  1  1
 38 81  1  0
 38 82  1  0
 39 83  1  6
 40 84  1  0
 41 85  1  1
 42 86  1  0
M  END


  Mrv1652309032217382D          

 42 45  0  0  1  0            999 V2000
   -5.6091   -1.7116    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -1.7116    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4656   -1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -1.7116    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0367   -1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -0.4741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7512   -0.0616    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4656   -0.4741    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.1759    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0367    2.0009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    0.7634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6078    1.1759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -0.0616    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6078   -0.4741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -1.2991    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2752   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.5687    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5052   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1696   -3.9898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1953   -2.5687    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2897   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1101   -3.1499    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4457   -2.3962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2662   -2.3099    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6017   -1.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1168   -0.8888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7511   -2.9774    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5716   -2.8911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4155   -3.7311    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9005   -4.3985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5951   -3.8173    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2595   -4.5710    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -1.7840    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8443   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -2.5366    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0367   -2.9491    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -2.9491    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4656   -3.7741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -2.5366    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8946   -2.9491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  1  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  1  0  0  0
 22 35  1  0  0  0  0
 17 35  1  0  0  0  0
 35 36  1  6  0  0  0
  5 37  1  0  0  0  0
 37 38  1  6  0  0  0
 37 39  1  0  0  0  0
 39 40  1  1  0  0  0
 39 41  1  0  0  0  0
  3 41  1  0  0  0  0
 41 42  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0177758

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](O)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H44N4O15/c24-2-7-13(32)15(34)10(26)21(37-7)40-18-5(25)1-6(30)12(31)20(18)42-23-17(36)19(9(4-29)39-23)41-22-11(27)16(35)14(33)8(3-28)38-22/h5-23,28-36H,1-4,24-27H2/t5-,6+,7+,8-,9+,10+,11+,12-,13+,14+,15+,16+,17+,18+,19+,20+,21+,22+,23-/m0/s1

> <INCHI_KEY>
ZMRHISCREAEQQW-YDGLARFFSA-N

> <FORMULA>
C23H44N4O15

> <MOLECULAR_WEIGHT>
616.618

> <EXACT_MASS>
616.280316733

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
59.542916475765665

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4R,5R,6R)-5-amino-6-{[(1R,2R,3S,4R,6S)-6-amino-2-{[(2S,3R,4S,5R)-4-{[(2R,3R,4R,5S,6S)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol

> <JCHEM_LOGP>
-8.201414152666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
4

> <JCHEM_PKA>
12.752620793051268

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.175563441178676

> <JCHEM_PKA_STRONGEST_BASIC>
9.281165981185978

> <JCHEM_POLAR_SURFACE_AREA>
341.53

> <JCHEM_REFRACTIVITY>
132.58530000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4R,5R,6R)-5-amino-6-{[(1R,2R,3S,4R,6S)-6-amino-2-{[(2S,3R,4S,5R)-4-{[(2R,3R,4R,5S,6S)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  N   UNK     0     -10.470  -3.195   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      -9.137  -2.425   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.803  -3.195   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -6.469  -2.425   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -5.136  -3.195   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.802  -2.425   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -3.802  -0.885   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.136  -0.115   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -6.469  -0.885   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -5.136   1.425   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.802   2.195   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.802   3.735   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.468   1.425   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.134   2.195   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.468  -0.115   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.134  -0.885   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.134  -2.425   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.380  -3.330   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.904  -4.795   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.810  -6.041   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.183  -7.448   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.364  -4.795   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.541  -6.041   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.072  -5.880   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.699  -4.473   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.230  -4.312   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.857  -2.905   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.951  -1.659   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.135  -5.558   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.667  -5.397   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.509  -6.965   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.414  -8.211   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.977  -7.126   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0       2.351  -8.532   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0       0.111  -3.330   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       1.576  -2.854   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -5.136  -4.735   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      -3.802  -5.505   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      -6.469  -5.505   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -6.469  -7.045   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -7.803  -4.735   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -9.137  -5.505   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   41                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   37                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   15                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    7   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   35                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   35                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   24   34                                                  
CONECT   34   33                                                            
CONECT   35   22   17   36                                                  
CONECT   36   35                                                            
CONECT   37    5   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39    3   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

View in JSmol

Synonyms

Value	Source
Inosamycin b	MeSH
Inosamycin a	MeSH
Inosamycin C	MeSH
Inosamycins	MeSH

Chemical Formula

C₂₃H₄₄N₄O₁₅

Average Mass

616.6180 Da

Monoisotopic Mass

616.28032 Da

IUPAC Name

(2R,3S,4R,5R,6R)-5-amino-6-{[(1R,2R,3S,4R,6S)-6-amino-2-{[(2S,3R,4S,5R)-4-{[(2R,3R,4R,5S,6S)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol

Traditional Name

CAS Registry Number

Not Available

SMILES

NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](O)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C23H44N4O15/c24-2-7-13(32)15(34)10(26)21(37-7)40-18-5(25)1-6(30)12(31)20(18)42-23-17(36)19(9(4-29)39-23)41-22-11(27)16(35)14(33)8(3-28)38-22/h5-23,28-36H,1-4,24-27H2/t5-,6+,7+,8-,9+,10+,11+,12-,13+,14+,15+,16+,17+,18+,19+,20+,21+,22+,23-/m0/s1

InChI Key

ZMRHISCREAEQQW-YDGLARFFSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces hygroscopicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Aminocyclitol glycosides

Alternative Parents

Substituents

Amino cyclitol glycoside
O-glycosyl compound
Glycosyl compound
Disaccharide
Aminocyclitol or derivatives
Cyclohexylamine
Cyclohexanol
Oxane
Cyclitol or derivatives
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
1,2-aminoalcohol
Oxacycle
Organoheterocyclic compound
Acetal
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Primary amine
Primary alcohol
Organonitrogen compound
Primary aliphatic amine
Amine
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	-8.2	ChemAxon
pKa (Strongest Acidic)	12.18	ChemAxon
pKa (Strongest Basic)	9.28	ChemAxon
Physiological Charge	4	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	341.53 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	132.59 m³·mol⁻¹	ChemAxon
Polarizability	59.54 Å³	ChemAxon
Number of Rings	4	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00017722

Chemspider ID

57261480

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13423461

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol (NP0177758)

MOL for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

3D MOL for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

3D SDF for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

3D-SDF for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

PDB for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

3D PDB for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

SMILES for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

INCHI for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

Structure for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)

3D Structure for NP0177758 ((2r,3s,4r,5r,6r)-5-amino-6-{[(1r,2r,3s,4r,6s)-6-amino-2-{[(2s,3r,4s,5r)-4-{[(2r,3r,4r,5s,6s)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3,4-dihydroxycyclohexyl]oxy}-2-(aminomethyl)oxane-3,4-diol)