NP-MRD: Showing NP-Card for 2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde (NP0153730)

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Record Information

Version

2.0

Created at

2022-09-02 10:26:17 UTC

Updated at

2022-09-02 10:26:17 UTC

NP-MRD ID

NP0153730

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde

Description

Cirramycin F1 belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars. 2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde is found in Streptomyces cirratus. Based on a literature review very few articles have been published on Cirramycin F1.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022212262D          

 48 51  0  0  1  0            999 V2000
    3.9069    1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8108    0.3708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4724   -0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2301    0.2044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8917   -0.2885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7956   -1.1078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6493    0.0381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3109   -0.4548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0685   -0.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2148   -1.2742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0398   -1.2841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4572   -1.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1188   -2.0936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8764   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9725   -0.9477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7301   -0.6211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8261    0.1983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3917   -1.1140    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1493   -0.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8109   -1.2803    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.5686   -0.9538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2302   -1.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1341   -2.2661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.7957   -2.7590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3765   -2.5926    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.2804   -3.4120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7149   -2.0997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2957   -1.9334    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.9573   -2.4263    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5380   -2.2599    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.4420   -3.0793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3612   -2.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0228   -2.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9267   -3.7324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5883   -4.2252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6035   -2.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5075   -3.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1691   -4.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7499   -3.8925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6538   -4.7119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0883   -3.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1843   -2.5803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5227   -2.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -2.7490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8611   -1.5946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6188   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3764   -0.9415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -1.4344    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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 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
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 20 19  1  1  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  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 20 27  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 14 30  1  0  0  0  0
 30 31  1  1  0  0  0
 12 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 32 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
  3 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END

     RDKit          3D

105108  0  0  0  0  0  0  0  0999 V2000
   -5.7075   -2.8657    1.7237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7587   -1.7631    1.3523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1193   -0.4114    1.8653 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1163    0.5361    1.4997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1207    1.0763    2.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0319    2.3516    2.3606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0683    0.2729    2.8649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8272    0.1014    1.9861 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0661   -0.6676    2.7288 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1666   -0.5347    0.6594 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9938   -2.0380    0.6553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3065    0.0500   -0.4801 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9757    0.0972    0.0660 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9044   -0.7139   -0.5666 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8953    0.1387   -1.0733 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8409   -0.5178   -1.8093 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3309   -1.1633   -3.0626 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6676   -1.4492   -0.9494 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4965   -0.6976   -0.1920 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8438   -0.8602   -0.3235 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6146    0.3078   -0.8296 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0511    1.2790    0.2232 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5740    0.8485    1.5977 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2342    1.0652    1.7869 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9291   -0.6205    1.7317 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.4385   -0.7788    1.7692 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3250   -1.4364    0.8277 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7893   -2.2865   -0.0428 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4658   -3.5708   -0.6200 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5889   -1.5472    0.4774 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9299   -0.7290    1.5667 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8147    1.4668   -0.8303 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5032    2.2684   -0.9607 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2882    3.6815   -1.2868 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0131    4.4887   -0.3918 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4606    1.5522   -2.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9537    1.6331   -2.2552 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6209    0.2895   -2.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5583    2.7423   -1.5220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8559    3.3477   -0.5885 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8783    3.3252   -1.6595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0554    2.8643   -1.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4486    1.5393   -0.8138 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9884    0.6299   -1.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5936    1.8373    0.1302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1908    1.4165    0.4965 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3942    0.1908    1.3587 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.4415   -0.7175    0.8238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1790   -3.6333    2.3934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0251   -3.5032    0.8617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5421   -2.5218    2.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7684   -2.0218    1.8098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5550   -1.7775    0.2570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1130   -0.4936    2.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6919    0.8849    3.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4576   -0.6963    3.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    1.0887    1.7716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3371   -1.0512    3.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2332   -0.3479    0.4780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6671   -2.3424    1.6565 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3743   -0.6300   -1.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5679    0.2763   -2.1481 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2177   -1.5413   -3.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1486   -2.1605   -1.6416 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9569   -1.6666   -1.1155 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5393   -0.0815   -1.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0367    0.7783   -1.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6802    2.3149    0.0677 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1564    1.3716    0.2960 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1327    1.3832    2.3871 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9913    1.9126    1.3075 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5663   -0.9212    2.7567 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8206   -1.2251    0.8197 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7720   -1.3737    2.6489 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9608    0.2085    1.8535 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4248   -2.5150    0.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7559   -3.6267   -1.6008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4616   -3.8234   -0.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8744   -2.2992    0.8558 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3569    1.7703    0.0580 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1068    2.1123   -0.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3488    4.1142   -2.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1645    0.6339   -2.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.9784    0.1235   -1.1085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7933   -0.4697   -2.3058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8851    4.4007   -2.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9435    3.5088   -1.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6757   -0.4293   -1.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1012    0.7391   -2.0384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5783    0.9218   -2.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6724    2.2493    1.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8743    0.6402    2.3018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1269   -0.0380    0.2034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1301   -1.5744    0.2465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1796   -1.0868    1.6007 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  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
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 25 27  1  0
 18 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 12 32  1  0
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 34 35  2  0
 32 36  1  0
 36 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  2  0
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 41 42  2  0
 42 43  1  0
 43 44  1  6
 43 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 47  3  1  0
 30 14  1  0
 46 43  1  0
 27 20  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  2 52  1  0
  2 53  1  0
  3 54  1  1
  7 55  1  0
  7 56  1  0
  8 57  1  6
  9 58  1  0
 10 59  1  6
 11 60  1  0
 11 61  1  0
 11 62  1  0
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 17 66  1  0
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 18 69  1  6
 20 70  1  6
 21 71  1  0
 21 72  1  0
 22 73  1  0
 22 74  1  0
 23 75  1  1
 24 76  1  0
 25 77  1  1
 26 78  1  0
 26 79  1  0
 26 80  1  0
 28 81  1  1
 29 82  1  0
 29 83  1  0
 30 84  1  1
 31 85  1  0
 32 86  1  1
 33 87  1  0
 33 88  1  0
 34 89  1  0
 36 90  1  0
 36 91  1  0
 37 92  1  6
 38 93  1  0
 38 94  1  0
 38 95  1  0
 41 96  1  0
 42 97  1  0
 44 98  1  0
 44 99  1  0
 44100  1  0
 46101  1  1
 47102  1  1
 48103  1  0
 48104  1  0
 48105  1  0
M  END


  Mrv1652309022212262D          

 48 51  0  0  1  0            999 V2000
    3.9069    1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8108    0.3708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4724   -0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2301    0.2044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8917   -0.2885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7956   -1.1078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6493    0.0381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3109   -0.4548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0685   -0.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2148   -1.2742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0398   -1.2841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4572   -1.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1188   -2.0936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8764   -1.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9725   -0.9477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7301   -0.6211    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8261    0.1983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3917   -1.1140    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1493   -0.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8109   -1.2803    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.5686   -0.9538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2302   -1.4467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1341   -2.2661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.7957   -2.7590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3765   -2.5926    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.2804   -3.4120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7149   -2.0997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2957   -1.9334    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.9573   -2.4263    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5380   -2.2599    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.4420   -3.0793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3612   -2.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0228   -2.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9267   -3.7324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5883   -4.2252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6035   -2.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5075   -3.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1691   -4.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7499   -3.8925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6538   -4.7119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0883   -3.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1843   -2.5803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5227   -2.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0298   -2.7490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8611   -1.5946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6188   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3764   -0.9415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -1.4344    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  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 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
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 20 19  1  1  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  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 20 27  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 14 30  1  0  0  0  0
 30 31  1  1  0  0  0
 12 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 32 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
  3 47  1  0  0  0  0
 47 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0153730

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1OC(=O)CC(O)C(C)C(OC2O[C@H](C)[C@@H](O[C@H]3CC[C@@H](O)[C@H](C)O3)[C@H](N)[C@H]2O)C(CC=O)CC(C)C(=O)\C=C\C2(C)OC2C1C

> <INCHI_IDENTIFIER>
InChI=1S/C35H57NO12/c1-8-26-19(4)33-35(7,48-33)13-11-23(38)17(2)15-22(12-14-37)31(18(3)25(40)16-27(41)45-26)47-34-30(42)29(36)32(21(6)44-34)46-28-10-9-24(39)20(5)43-28/h11,13-14,17-22,24-26,28-34,39-40,42H,8-10,12,15-16,36H2,1-7H3/b13-11+/t17?,18?,19?,20-,21+,22?,24+,25?,26?,28-,29+,30+,31?,32+,33?,34?,35?/m0/s1

> <INCHI_KEY>
GAYWYEZTOAUHGL-HHHNAWRGSA-N

> <FORMULA>
C35H57NO12

> <MOLECULAR_WEIGHT>
683.836

> <EXACT_MASS>
683.388076279

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
72.29638748018864

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(14E)-9-{[(3R,4R,5S,6R)-4-amino-3-hydroxy-5-{[(2S,5R,6S)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde

> <ALOGPS_LOGP>
1.73

> <JCHEM_LOGP>
2.057832309666666

> <ALOGPS_LOGS>
-3.53

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.068313052531675

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.74027869649445

> <JCHEM_PKA_STRONGEST_BASIC>
8.603161089225516

> <JCHEM_POLAR_SURFACE_AREA>
196.6

> <JCHEM_REFRACTIVITY>
173.01150000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.03e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(14E)-9-{[(3R,4R,5S,6R)-4-amino-3-hydroxy-5-{[(2S,5R,6S)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       7.293   2.222   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.114   0.692   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.349  -0.228   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.763   0.382   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.998  -0.538   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.818  -2.068   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      12.412   0.071   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.647  -0.849   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      15.061  -0.239   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      13.468  -2.378   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.008  -2.397   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.053  -2.988   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      13.288  -3.908   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      14.703  -3.299   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      14.882  -1.769   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      16.296  -1.159   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.475   0.370   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      17.531  -2.079   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      18.945  -1.470   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      20.180  -2.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.595  -1.780   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      22.830  -2.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.650  -4.230   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      23.885  -5.150   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      21.236  -4.840   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      21.057  -6.369   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      20.001  -3.920   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      17.352  -3.609   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0      18.587  -4.529   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0      15.938  -4.219   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      15.758  -5.748   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      11.874  -4.518   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.109  -5.438   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.930  -6.967   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      14.165  -7.887   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      10.460  -5.127   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.281  -6.657   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.516  -7.577   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.866  -7.266   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       8.687  -8.796   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.631  -6.346   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       7.811  -4.817   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       6.576  -3.897   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.656  -5.131   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       5.341  -2.976   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       6.755  -2.367   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.169  -1.757   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       9.404  -2.677   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   47                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   32                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   30                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   28                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   27                                                  
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   20                                                       
CONECT   28   18   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   14   31                                                  
CONECT   31   30                                                            
CONECT   32   12   33   36                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   32   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   45   46                                             
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45   43   47                                                  
CONECT   47   46    3   48                                                  
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

View in JSmol

Synonyms

Value	Source
Cirramycin F-1	MeSH

Chemical Formula

C₃₅H₅₇NO₁₂

Average Mass

683.8360 Da

Monoisotopic Mass

683.38808 Da

IUPAC Name

2-[(14E)-9-{[(3R,4R,5S,6R)-4-amino-3-hydroxy-5-{[(2S,5R,6S)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde

Traditional Name

CAS Registry Number

Not Available

SMILES

CCC1OC(=O)CC(O)C(C)C(OC2O[C@H](C)[C@@H](O[C@H]3CC[C@@H](O)[C@H](C)O3)[C@H](N)[C@H]2O)C(CC=O)CC(C)C(=O)\C=C\C2(C)OC2C1C

InChI Identifier

InChI=1S/C35H57NO12/c1-8-26-19(4)33-35(7,48-33)13-11-23(38)17(2)15-22(12-14-37)31(18(3)25(40)16-27(41)45-26)47-34-30(42)29(36)32(21(6)44-34)46-28-10-9-24(39)20(5)43-28/h11,13-14,17-22,24-26,28-34,39-40,42H,8-10,12,15-16,36H2,1-7H3/b13-11+/t17?,18?,19?,20-,21+,22?,24+,25?,26?,28-,29+,30+,31?,32+,33?,34?,35?/m0/s1

InChI Key

GAYWYEZTOAUHGL-HHHNAWRGSA-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 cirratus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Aminoglycosides

Alternative Parents

Substituents

Aminoglycoside core
Glycosyl compound
O-glycosyl compound
Monosaccharide
Oxane
Alpha-hydrogen aldehyde
1,2-aminoalcohol
Amino acid or derivatives
Carboxylic acid ester
Ketone
Lactone
Secondary alcohol
Cyclic ketone
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Alcohol
Amine
Carbonyl group
Organopnictogen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Aldehyde
Primary aliphatic amine
Primary amine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	1.73	ALOGPS
logP	2.06	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	12.74	ChemAxon
pKa (Strongest Basic)	8.6	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	196.6 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	173.01 m³·mol⁻¹	ChemAxon
Polarizability	72.3 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

C00017662

Chemspider ID

4953071

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6450466

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde (NP0153730)

MOL for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

3D MOL for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

3D SDF for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

3D-SDF for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

PDB for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

3D PDB for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

SMILES for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

INCHI for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

Structure for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)

3D Structure for NP0153730 (2-[(14e)-9-{[(3r,4r,5s,6r)-4-amino-3-hydroxy-5-{[(2s,5r,6s)-5-hydroxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-3-ethyl-7-hydroxy-2,8,12,16-tetramethyl-5,13-dioxo-4,17-dioxabicyclo[14.1.0]heptadec-14-en-10-yl]acetaldehyde)