NP-MRD: Showing NP-Card for 2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione (NP0309019)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-11 03:16:39 UTC

Updated at

2022-09-11 03:16:40 UTC

NP-MRD ID

NP0309019

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione

Description

2-{[4-(Dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxy-2H,5H,10H-benzo[b]fluorene-5,10-dione 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-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione is found in Micromonospora echinospora. Based on a literature review very few articles have been published on 2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxy-2H,5H,10H-benzo[b]fluorene-5,10-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112205162D          

 37 41  0  0  0  0            999 V2000
    0.5024   -1.9967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4358   -2.8190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1146   -3.2878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5350   -3.8749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2632   -3.6665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8428   -4.2536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6410   -4.0452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2206   -4.6323    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0189   -4.4239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0020   -5.4278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8597   -3.2497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6579   -3.0413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8766   -2.2458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2801   -2.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4987   -1.8671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4818   -2.8710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585   -2.5379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2799   -2.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7574   -3.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5769   -3.2287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1960   -2.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0334   -1.8747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9778   -2.9471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5969   -2.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4343   -1.5930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3787   -2.6654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5413   -3.4742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9222   -4.0195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0848   -4.8283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1404   -3.7559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5213   -4.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6839   -5.1099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7395   -4.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0205   -4.4422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4136   -3.8834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5922   -3.9606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2483   -4.7105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  5 16  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 20 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 19 35  1  0  0  0  0
 35 36  2  0  0  0  0
  3 36  1  0  0  0  0
 36 37  1  0  0  0  0
M  END

     RDKit          3D

 68 72  0  0  0  0  0  0  0  0999 V2000
   -1.3426   -3.0421    1.5656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6661   -2.3789    0.3847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1419   -0.9991    0.7225 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0763   -0.1036    1.1289 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1118    0.2044    0.2948 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3906   -0.0786    1.0457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6066    0.5931    0.5378 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6070   -0.4188    0.2381 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0062   -1.1497    1.4168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3120   -1.2499   -0.8784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4299    1.6117   -0.5131 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0777    2.8207   -0.1999 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0647    3.1533   -1.1109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0092    1.9233   -0.8848 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6728    1.4326   -2.2843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0693    1.5653    0.0525 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7240   -1.2332    1.9426 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012   -1.0143    1.9886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6870   -0.5169    0.8308 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9677   -0.2149    0.6204 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1523   -0.2673    1.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9561   -0.6804    2.6369 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4814    0.1230    1.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5660    0.0485    1.8584 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4661   -0.3829    3.1469 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8526    0.4265    1.4165 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9786    0.8583    0.1416 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8721    0.9377   -0.7403 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1105    1.3875   -2.0074 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6103    0.5719   -0.3218 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4683    0.6528   -1.2274 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5777    1.0507   -2.4062 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1459    0.2543   -0.7408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9454    0.2274   -1.3414 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9563   -0.2597   -0.3865 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6462   -0.4955   -0.4010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0157   -0.2270   -1.6051 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7257   -2.3181    2.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1851   -3.6815    1.1847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6719   -3.7442    2.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2191   -3.0008    0.1305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3105   -2.3675   -0.5130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1035   -0.3276   -0.6708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1753    0.1490    2.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5066   -1.2024    1.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0634    1.1301    1.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4162   -2.0817    1.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7684   -0.5049    2.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0919   -1.3749    1.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7185   -2.1594   -0.6344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8516   -0.7570   -1.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2994   -1.6550   -1.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9319    1.2544   -1.4514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5036    4.1090   -0.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8681    2.4213   -1.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6631    3.3464   -2.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8860    3.0488   -0.9845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8547    0.3661   -2.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3787    1.9641   -2.9888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6626    1.7784   -2.5452 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2097   -1.6097    2.8210 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5341   -1.2148    2.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7789   -0.6948    3.7260 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6784    0.3563    2.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9564    1.1628   -0.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5711    1.5337   -2.7734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7369    0.5178   -2.3657 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3550    0.4262   -2.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  1
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 14 16  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
  3 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 33 31  1  0
 31 32  2  0
 31 30  1  0
 30 28  2  0
 28 29  1  0
 28 27  1  0
 27 26  2  0
 26 24  1  0
 24 25  1  0
 24 23  2  0
 23 21  1  0
 21 22  2  0
 36  3  1  0
 23 30  1  0
 16  5  1  0
 35 19  1  0
 21 20  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  2 41  1  0
  2 42  1  0
  5 43  1  6
  6 44  1  0
  6 45  1  0
  7 46  1  1
 11 53  1  6
 13 54  1  0
 13 55  1  0
 13 56  1  0
 14 57  1  6
 15 58  1  0
 15 59  1  0
 15 60  1  0
  9 47  1  0
  9 48  1  0
  9 49  1  0
 10 50  1  0
 10 51  1  0
 10 52  1  0
 17 61  1  0
 18 62  1  0
 34 67  1  0
 37 68  1  0
 29 66  1  0
 27 65  1  0
 26 64  1  0
 25 63  1  0
M  END


  Mrv1652309112205162D          

 37 41  0  0  0  0            999 V2000
    0.5024   -1.9967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4358   -2.8190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1146   -3.2878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5350   -3.8749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2632   -3.6665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8428   -4.2536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6410   -4.0452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2206   -4.6323    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0189   -4.4239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0020   -5.4278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8597   -3.2497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6579   -3.0413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8766   -2.2458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2801   -2.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4987   -1.8671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4818   -2.8710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4585   -2.5379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2799   -2.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7574   -3.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5769   -3.2287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1960   -2.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0334   -1.8747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9778   -2.9471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5969   -2.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4343   -1.5930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3787   -2.6654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5413   -3.4742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9222   -4.0195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0848   -4.8283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1404   -3.7559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5213   -4.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6839   -5.1099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7395   -4.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0205   -4.4422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4136   -3.8834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5922   -3.9606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2483   -4.7105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  5 16  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 20 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 19 35  1  0  0  0  0
 35 36  2  0  0  0  0
  3 36  1  0  0  0  0
 36 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0309019

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1(OC2CC(C(OC)C(C)O2)N(C)C)C=CC2=C3C(=CC2=C1O)C(=O)C1=C(O)C=CC(O)=C1C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H31NO8/c1-6-28(37-20-12-17(29(3)4)26(35-5)13(2)36-20)10-9-14-15(27(28)34)11-16-21(14)25(33)23-19(31)8-7-18(30)22(23)24(16)32/h7-11,13,17,20,26,30-31,34H,6,12H2,1-5H3

> <INCHI_KEY>
UXGXZONKJVEYNM-UHFFFAOYSA-N

> <FORMULA>
C28H31NO8

> <MOLECULAR_WEIGHT>
509.555

> <EXACT_MASS>
509.204966962

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
53.56074609394085

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxy-2H,5H,10H-benzo[b]fluorene-5,10-dione

> <JCHEM_LOGP>
0.858927721774047

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.510780638489905

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.2183127682949655

> <JCHEM_PKA_STRONGEST_BASIC>
10.46157322542583

> <JCHEM_POLAR_SURFACE_AREA>
125.76

> <JCHEM_REFRACTIVITY>
139.22449999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       0.938  -3.727   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.814  -5.262   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.081  -6.137   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.999  -7.233   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.491  -6.844   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.573  -7.940   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.063  -7.551   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -4.145  -8.647   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      -5.635  -8.258   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.737 -10.132   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.471  -6.066   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.961  -5.677   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -5.370  -4.192   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.390  -4.970   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.798  -3.485   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.899  -5.359   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.723  -4.737   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.256  -4.593   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.147  -5.849   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.677  -6.027   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.833  -5.009   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.529  -3.499   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.292  -5.501   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.448  -4.483   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.144  -2.974   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      11.907  -4.975   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.210  -6.485   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.055  -7.503   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      11.358  -9.013   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.595  -7.011   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.440  -8.029   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.743  -9.539   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.980  -7.537   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.638  -8.292   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.505  -7.249   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.972  -7.393   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.330  -8.793   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17   36                                             
CONECT    4    3    5                                                       
CONECT    5    4    6   16                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    5                                                       
CONECT   17    3   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   35                                                  
CONECT   20   19   21   33                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   30                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   23   31                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   20   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   19   36                                                  
CONECT   36   35    3   37                                                  
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₁NO₈

Average Mass

509.5550 Da

Monoisotopic Mass

509.20497 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCC1(OC2CC(C(OC)C(C)O2)N(C)C)C=CC2=C3C(=CC2=C1O)C(=O)C1=C(O)C=CC(O)=C1C3=O

InChI Identifier

InChI=1S/C28H31NO8/c1-6-28(37-20-12-17(29(3)4)26(35-5)13(2)36-20)10-9-14-15(27(28)34)11-16-21(14)25(33)23-19(31)8-7-18(30)22(23)24(16)32/h7-11,13,17,20,26,30-31,34H,6,12H2,1-5H3

InChI Key

UXGXZONKJVEYNM-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Micromonospora echinospora	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
Naphthoquinone
Hexose monosaccharide
O-glycosyl compound
Glycosyl compound
Tetralin
Naphthalene
Aryl ketone
Quinone
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Oxane
Monosaccharide
Vinylogous acid
Tertiary aliphatic amine
Tertiary amine
Ketone
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Enol
Dialkyl ether
Acetal
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162815551

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione (NP0309019)

MOL for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

3D MOL for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

3D SDF for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

3D-SDF for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

PDB for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

3D PDB for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

SMILES for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

INCHI for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

Structure for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)

3D Structure for NP0309019 (2-{[4-(dimethylamino)-5-methoxy-6-methyloxan-2-yl]oxy}-2-ethyl-1,6,9-trihydroxybenzo[b]fluorene-5,10-dione)