NP-MRD: Showing NP-Card for methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate (NP0251093)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 14:10:46 UTC

Updated at

2022-09-07 14:10:46 UTC

NP-MRD ID

NP0251093

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate

Description

Methyl (2R)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-1,2,3,4,5a,6,11,11a-octahydrotetracene-1-carboxylate belongs to the class of organic compounds known as anthracyclines. These are polyketides containing a tetracenequinone ring structure with a sugar attached by glycosidic linkage. Based on a literature review very few articles have been published on methyl (2R)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-1,2,3,4,5a,6,11,11a-octahydrotetracene-1-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072216102D          

 54 60  0  0  1  0            999 V2000
    1.0488   -2.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3309   -3.5692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8612   -4.4877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 18 24  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 13 27  1  0  0  0  0
 11 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
  8 30  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 37 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 34 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  2  0  0  0  0
 31 49  1  0  0  0  0
 49 50  1  0  0  0  0
  3 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
 51 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END

     RDKit          3D

104110  0  0  0  0  0  0  0  0999 V2000
   -2.2543   -4.2638   -2.0674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6834   -4.0173   -1.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7962   -2.6897   -0.9137 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0054   -2.6379    0.2116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3141   -1.5694   -1.8528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9892   -0.3722   -0.9566 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9358   -0.6573   -0.1228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8437    0.1690   -0.2151 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5056    0.7045    1.1544 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9522    0.4029    1.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7582    0.9209    0.2641 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1010    0.7573    0.5763 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8077    1.9222    0.6756 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5555    2.1352    1.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8326    1.3676    2.0790 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5533    1.1057    0.7988 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3298   -0.0442    0.9358 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6557    0.1453    0.6209 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.5538   -0.0585    1.7977 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9993   -0.2357    1.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1615    0.4191    0.0207 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2578   -0.1929   -1.0040 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.8539   -1.2652   -1.6671 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0399   -0.5833   -0.5042 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4812    0.7796   -0.2535 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1159    0.3174   -1.5334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7311    1.9285   -0.3946 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3394    0.1755   -0.9592 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3936   -0.7560   -1.5000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2075   -0.6293   -0.7049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2048   -0.0670   -0.1276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2994    1.1334    0.4480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2619    2.0629    0.2550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4200    1.5858    1.2891 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8494    2.9177    0.7558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1651    3.9124    1.0516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0145    3.0985   -0.0808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1081    4.0989   -1.0124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1093    5.0127   -1.2426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2941    4.1527   -1.7411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3268    3.2716   -1.5618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2167    2.2708   -0.6212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0640    2.1934    0.1092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8503    1.1883    1.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8756    0.7630    1.7493 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5199    0.6126    1.4766 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3405   -0.6925    0.8067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3265   -1.6799    0.9341 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2820   -1.0183    0.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2182   -2.3556   -0.5822 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8122   -3.4072    0.2891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8187   -4.0382   -0.1125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2903   -3.7161    1.5343 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8768   -4.7274    2.3483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0632   -3.9435   -3.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6132   -3.6556   -1.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9850   -5.3452   -1.9576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0322   -4.8345   -0.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3172   -4.0564   -2.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4548   -2.3333    1.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1686   -1.2917   -2.4818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4338   -1.9532   -2.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7896    0.5178   -1.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0389    0.9795   -0.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6153    1.8020    1.2301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1254    0.2395    1.9591 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1225   -0.7000    1.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2606    0.8989    2.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4886    2.0013    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1793    2.8402    0.4893 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8034    3.2364    1.9979 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9233    1.9524    2.8350 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5186    1.9777    2.7354 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6725    0.4238    2.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1173    1.9850    0.4713 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7570    1.2295    0.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5144    0.8871    2.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2783   -0.9033    2.4439 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1988   -1.3207    1.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7146    0.1774    2.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2101    0.2126   -0.3032 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9564    1.5022    0.0593 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0675    0.5801   -1.7940 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8775   -2.0801   -1.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8924   -0.0636    0.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3916   -0.7481   -1.3987 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0597    0.8530   -1.7639 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3685    0.3867   -2.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0230    0.8835   -1.7516 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0170   -0.2086   -2.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9266   -1.6035   -2.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0053   -1.2318   -0.7285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9717    2.6717    1.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9975    1.8265    2.3132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2395    5.0417   -0.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3633    4.9484   -2.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2246    3.3656   -2.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9881    1.5483   -0.4298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5957    0.3747    2.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2242   -1.5855    0.4743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7724   -2.3447   -1.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7710   -5.1075    1.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1925   -4.3072    3.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1750   -5.5763    2.4676 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 16 25  1  0
 25 26  1  0
 25 27  1  0
 11 28  1  0
 28 29  1  0
 28 30  1  0
  6 31  1  0
 31 32  2  0
 32 33  1  0
 32 34  1  0
 34 46  1  0
 46 47  1  0
 47 48  1  0
 47 49  2  0
 49 50  1  0
 50 51  1  0
 51 52  2  0
 51 53  1  0
 53 54  1  0
 46 44  1  0
 44 45  2  0
 44 43  1  0
 43 42  2  0
 42 41  1  0
 41 40  2  0
 40 38  1  0
 38 39  1  0
 38 37  2  0
 37 35  1  0
 35 36  2  0
 50  3  1  0
 37 43  1  0
 30  8  1  0
 49 31  1  0
 27 13  1  0
 35 34  1  0
 24 18  1  0
  1 55  1  0
  1 56  1  0
  1 57  1  0
  2 58  1  0
  2 59  1  0
  4 60  1  0
  5 61  1  0
  5 62  1  0
  6 63  1  6
  8 64  1  6
  9 65  1  0
  9 66  1  0
 10 67  1  0
 10 68  1  0
 11 69  1  6
 13 70  1  6
 14 71  1  0
 14 72  1  0
 15 73  1  0
 15 74  1  0
 16 75  1  6
 18 76  1  6
 19 77  1  0
 19 78  1  0
 20 79  1  0
 20 80  1  0
 21 81  1  0
 21 82  1  0
 22 83  1  6
 23 84  1  0
 25 85  1  1
 26 86  1  0
 26 87  1  0
 26 88  1  0
 28 89  1  6
 29 90  1  0
 29 91  1  0
 29 92  1  0
 33 93  1  0
 34 94  1  1
 46 99  1  1
 48100  1  0
 50101  1  6
 54102  1  0
 54103  1  0
 54104  1  0
 42 98  1  0
 41 97  1  0
 40 96  1  0
 39 95  1  0
M  END


  Mrv1652309072216102D          

 54 60  0  0  1  0            999 V2000
    1.0488   -2.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3309   -3.5692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8612   -4.4877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 18 24  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 13 27  1  0  0  0  0
 11 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
  8 30  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 37 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 34 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  2  0  0  0  0
 31 49  1  0  0  0  0
 49 50  1  0  0  0  0
  3 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
 51 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0251093

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@]1(O)CC(OC2CCC(OC3CCC(OC4CCCC(O)O4)C(C)O3)C(C)O2)C2=C(O)C3C(C(O)=C2C1C(=O)OC)C(=O)C1=CC=CC(O)=C1C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C39H50O15/c1-5-39(47)16-23(53-27-15-13-22(18(3)50-27)52-26-14-12-21(17(2)49-26)51-25-11-7-10-24(41)54-25)29-30(33(39)38(46)48-4)37(45)31-32(36(29)44)35(43)28-19(34(31)42)8-6-9-20(28)40/h6,8-9,17-18,21-27,31-33,40-41,44-45,47H,5,7,10-16H2,1-4H3/t17?,18?,21?,22?,23?,24?,25?,26?,27?,31?,32?,33?,39-/m1/s1

> <INCHI_KEY>
ALQQOCVROWFXHV-VCPKBVRNSA-N

> <FORMULA>
C39H50O15

> <MOLECULAR_WEIGHT>
758.814

> <EXACT_MASS>
758.31497091

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
79.82068311672703

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2R)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-1,2,3,4,5a,6,11,11a-octahydrotetracene-1-carboxylate

> <JCHEM_LOGP>
2.1999849506666656

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.2333312501034

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.548465637497333

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1881564832451383

> <JCHEM_POLAR_SURFACE_AREA>
216.96999999999997

> <JCHEM_REFRACTIVITY>
189.83810000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2R)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1H-tetracene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       1.958  -5.215   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.484  -6.663   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.474  -8.377   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   8.470   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   50                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   31                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   30                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   28                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   18                                                       
CONECT   25   16   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   13                                                       
CONECT   28   11   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    8                                                       
CONECT   31    6   32   49                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   46                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   43                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   37   44                                                  
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   34   47                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   31   50                                                  
CONECT   50   49    3   51                                                  
CONECT   51   50   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51   54                                                       
CONECT   54   53                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  120    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2R)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-1,2,3,4,5a,6,11,11a-octahydrotetracene-1-carboxylic acid	Generator

Chemical Formula

C₃₉H₅₀O₁₅

Average Mass

758.8140 Da

Monoisotopic Mass

758.31497 Da

IUPAC Name

methyl (2R)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-1,2,3,4,5a,6,11,11a-octahydrotetracene-1-carboxylate

Traditional Name

methyl (2R)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1H-tetracene-1-carboxylate

CAS Registry Number

Not Available

SMILES

CC[C@@]1(O)CC(OC2CCC(OC3CCC(OC4CCCC(O)O4)C(C)O3)C(C)O2)C2=C(O)C3C(C(O)=C2C1C(=O)OC)C(=O)C1=CC=CC(O)=C1C3=O

InChI Identifier

InChI=1S/C39H50O15/c1-5-39(47)16-23(53-27-15-13-22(18(3)50-27)52-26-14-12-21(17(2)49-26)51-25-11-7-10-24(41)54-25)29-30(33(39)38(46)48-4)37(45)31-32(36(29)44)35(43)28-19(34(31)42)8-6-9-20(28)40/h6,8-9,17-18,21-27,31-33,40-41,44-45,47H,5,7,10-16H2,1-4H3/t17?,18?,21?,22?,23?,24?,25?,26?,27?,31?,32?,33?,39-/m1/s1

InChI Key

ALQQOCVROWFXHV-VCPKBVRNSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracyclines. These are polyketides containing a tetracenequinone ring structure with a sugar attached by glycosidic linkage.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Anthracyclines

Sub Class

Not Available

Direct Parent

Anthracyclines

Alternative Parents

Substituents

Anthracycline
Tetracenequinone
Anthracene carboxylic acid or derivatives
Anthracene carboxylic acid
1,4-anthraquinone
9,10-anthraquinone
Tetralin
Naphthalene
Aryl alkyl ketone
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Oxane
Vinylogous acid
Methyl ester
Tertiary alcohol
Cyclic alcohol
Ketone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Enol
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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
logP	2.2	ChemAxon
pKa (Strongest Acidic)	6.55	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	216.97 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	189.84 m³·mol⁻¹	ChemAxon
Polarizability	79.82 Å³	ChemAxon
Number of Rings	7	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

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

163107180

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate (NP0251093)

MOL for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

3D MOL for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

3D SDF for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

3D-SDF for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

PDB for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

3D PDB for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

SMILES for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

INCHI for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

Structure for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)

3D Structure for NP0251093 (methyl (2r)-2-ethyl-2,5,7,12-tetrahydroxy-4-{[5-({5-[(6-hydroxyoxan-2-yl)oxy]-6-methyloxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-6,11-dioxo-3,4,5a,11a-tetrahydro-1h-tetracene-1-carboxylate)