NP-MRD: Showing NP-Card for methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate (NP0167577)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 03:11:30 UTC

Updated at

2022-09-03 03:11:31 UTC

NP-MRD ID

NP0167577

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate

Description

Methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-7,12-dihydro-4H-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate belongs to the class of organic compounds known as naphthopyranone glycosides. Naphthopyranone glycosides are compounds containing a carbohydrate moiety glycosidically linked to a naphthopyranone moiety. Methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-7,12-dihydro-4H-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251502512D          

 64 71  0  0  0  0            999 V2000
    1.6303   -1.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3360   -1.8998    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8564   -2.5400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356   -2.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3965   -1.9164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2066   -2.0723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767   -2.8518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9366   -3.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2066   -4.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1265   -3.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5864   -3.9432    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8564   -4.7228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -4.8787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9366   -5.6582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467   -5.8141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0168   -6.5937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3965   -6.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -7.0614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5864   -6.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0463   -6.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3163   -5.3464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0168   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    0.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970    1.2018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172    0.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274    0.7341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7974   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1476    0.4223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8776   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274   -1.4486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2573   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4472   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771   -1.9164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5569   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -2.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075   -2.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8867   -2.7854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4221   -2.2535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1279   -3.0243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2585   -3.8389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0675    1.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6911    0.8177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075    1.9814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375    2.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8776    3.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075    4.1641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7974    4.3200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6877    3.2287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2278    3.8523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9578    2.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7679    2.2932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4177    1.8255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4438    1.8978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5997    2.7080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6643    1.6278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0406    2.1679    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
  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
  8 10  1  0  0  0  0
  3 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
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 31 37  1  0  0  0  0
 37 38  2  0  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 25 41  1  0  0  0  0
 41 42  2  0  0  0  0
 22 42  1  0  0  0  0
 42 43  1  0  0  0  0
 35 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 44 47  1  0  0  0  0
 47 48  1  0  0  0  0
 30 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 53 56  1  0  0  0  0
 56 57  1  0  0  0  0
 56 58  1  0  0  0  0
 58 59  1  0  0  0  0
 58 60  1  0  0  0  0
 51 60  1  0  0  0  0
 49 61  1  0  0  0  0
 61 62  2  0  0  0  0
 61 63  1  0  0  0  0
 63 64  1  0  0  0  0
M  END

     RDKit          3D

121128  0  0  0  0  0  0  0  0999 V2000
    6.9838   -0.3256    2.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1251    0.4707    2.1167 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3912   -0.2089    1.0985 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5197   -1.2441    1.8282 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3531    0.8151    0.5841 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4732    0.2454   -0.4752 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0597    0.4154   -0.1467 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7050    1.5676    0.5590 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3811    1.8756    0.8519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6209    0.9934    0.4208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2887   -0.1410   -0.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0641   -0.4161   -0.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3080   -1.5599   -1.2461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3430   -1.0867   -0.6957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0254   -2.1272   -1.3308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7372   -0.8170   -0.3857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0546    0.3101    0.2919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3621    0.5535    0.5823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4510   -0.2871    0.2348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8150    0.0840    0.5578 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.3270   -0.9120    1.3396 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7947    0.2919   -0.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9904   -0.0158   -0.3293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4750    0.8370   -1.7366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4709    1.0080   -2.7114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8779    1.2794    1.5565 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.1613    1.2944    2.2957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9377    2.5637    2.1975 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.0763    2.2943    1.3883 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2446    2.4748    2.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2705    3.7529    1.6268 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.6507    4.0157    0.3116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7729    3.5717    1.6268 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0858    4.7353    0.9303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5036    2.4426    0.9121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0944   -1.4334   -0.4508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0333   -2.3367   -0.8313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2341   -2.1838   -0.5931 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6315   -3.4956   -1.5177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3128   -3.6856   -1.7858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8643   -4.9186   -2.5207 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0971   -5.0410   -3.9866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5472   -6.0870   -1.8568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1775   -5.9900   -1.8035 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6098   -5.8613   -0.4264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4552   -2.7854   -1.3962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7270   -1.6875   -0.7563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0153    1.2607    0.7241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3332    2.2938    1.3505 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9097   -0.9923   -0.8502 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2334   -0.9125   -1.2540 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5367    0.1909   -2.2107 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1329   -0.8455    0.0078 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2418   -0.0989   -0.3456 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3510   -0.8236   -0.6513 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.4706   -0.7848    0.3558 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9783    0.6319    0.4360 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3656    0.6361    0.6985 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6454    1.1297    1.9696 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6207    1.5090   -0.7027 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6864    2.4960   -0.3074 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1936    0.8625   -1.9676 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1999    1.0617   -3.0722 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9131   -0.4920   -1.8732 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1062   -1.3571    2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5957   -0.4114    3.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9934    0.1303    2.9985 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6111    1.1687    2.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4921   -1.2245    1.4370 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9124   -2.2748    1.6007 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4732   -1.0686    2.9041 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6979    1.0035    1.4881 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.7630    0.2920 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6871    0.9527   -1.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4231    2.2703    0.8929 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1244    2.7581    1.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1235   -1.9625   -1.5631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5829    1.4644    1.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2755   -0.8054    2.3046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9857    0.0298   -2.8697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0060    1.2294   -3.7209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1468    1.8449   -2.5329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0939    1.1521    2.3351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9361    1.1968    3.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8553    0.4696    2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3822    2.8506    3.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3401    3.5302    2.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1622    1.8529    3.0390 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1047    2.2038    1.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4812    4.6383    2.2842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1335    3.3932   -0.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3321    3.5033    2.6370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7409    5.6269    0.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1313    5.0181    1.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9255    4.5264   -0.1655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4161   -4.1720   -1.7928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4347   -4.3853   -4.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8811   -6.0837   -4.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1752   -4.8747   -4.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6286   -6.7298   -2.4429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7654   -6.7992    0.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5132   -5.7020   -0.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0388   -5.0558    0.1719 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4815   -1.8629   -1.7572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6994    0.2799   -2.9417 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7375    1.1727   -1.7789 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4271   -0.0738   -2.8714 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4575   -1.8913    0.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0484   -1.9112   -0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1585   -1.1278    1.3453 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2974   -1.4425   -0.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5135    1.0690    1.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.7365    1.1325    2.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1044    0.4918    2.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1774    2.1318    2.0459 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5413    2.1230   -0.9473 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1513    3.0667    0.3840 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2471    1.3564   -2.3027 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8052    1.9874   -2.8741 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6449    1.2796   -4.0083 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8453    0.1801   -3.2488 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3  4  1  0
  3  5  1  0
  5  6  1  0
  6 50  1  0
 50 51  1  0
 51 52  1  0
 51 53  1  0
 53 54  1  0
 54 55  1  0
 55 56  1  0
 56 57  1  0
 57 58  1  0
 58 59  1  0
 57 60  1  0
 60 61  1  0
 60 62  1  0
 62 63  1  0
 62 64  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 48  1  0
 48 49  2  0
 48 17  1  0
 17 18  2  0
 18 19  1  0
 19 36  2  0
 36 37  1  0
 37 38  2  0
 37 39  1  0
 39 40  2  0
 40 46  1  0
 46 47  1  0
 47 16  2  0
 16 14  1  0
 14 15  2  0
 14 11  1  0
 11 12  2  0
 12 13  1  0
 40 41  1  0
 41 42  1  6
 41 43  1  0
 43 44  1  0
 44 45  1  0
 19 20  1  0
 20 21  1  1
 20 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 28 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33 35  1  0
 20 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 53  3  1  0
 64 55  1  0
 12  7  1  0
 44 41  1  0
 35 26  1  0
 11 10  1  0
 16 17  1  0
 47 36  1  0
  1 65  1  0
  1 66  1  0
  1 67  1  0
  2 68  1  0
  4 69  1  0
  4 70  1  0
  4 71  1  0
  5 72  1  0
  5 73  1  0
  6 74  1  6
 51104  1  6
 52105  1  0
 52106  1  0
 52107  1  0
 53108  1  1
 55109  1  6
 56110  1  0
 56111  1  0
 57112  1  1
 59113  1  0
 59114  1  0
 59115  1  0
 60116  1  6
 61117  1  0
 62118  1  6
 63119  1  0
 63120  1  0
 63121  1  0
  8 75  1  0
  9 76  1  0
 18 78  1  0
 39 96  1  0
 13 77  1  0
 42 97  1  0
 42 98  1  0
 42 99  1  0
 44100  1  6
 45101  1  0
 45102  1  0
 45103  1  0
 21 79  1  0
 26 83  1  1
 27 84  1  0
 27 85  1  0
 28 86  1  1
 30 87  1  0
 30 88  1  0
 30 89  1  0
 31 90  1  1
 32 91  1  0
 33 92  1  1
 34 93  1  0
 34 94  1  0
 34 95  1  0
 25 80  1  0
 25 81  1  0
 25 82  1  0
M  END


  Mrv1533004251502512D          

 64 71  0  0  0  0            999 V2000
    1.6303   -1.1291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3360   -1.8998    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8564   -2.5400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1356   -2.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3965   -1.9164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2066   -2.0723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767   -2.8518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9366   -3.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2066   -4.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1265   -3.3196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5864   -3.9432    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8564   -4.7228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -4.8787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9366   -5.6582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467   -5.8141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0168   -6.5937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3965   -6.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -7.0614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5864   -6.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0463   -6.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3163   -5.3464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0168   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    0.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970    1.2018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172    0.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274    0.7341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7974   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1476    0.4223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8776   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274   -1.4486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2573   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4472   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771   -1.9164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5569   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -2.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075   -2.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8867   -2.7854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4221   -2.2535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1279   -3.0243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2585   -3.8389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0675    1.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6911    0.8177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075    1.9814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375    2.7609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8776    3.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075    4.1641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7974    4.3200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6877    3.2287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2278    3.8523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9578    2.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7679    2.2932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4177    1.8255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4438    1.8978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5997    2.7080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6643    1.6278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0406    2.1679    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
  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
  8 10  1  0  0  0  0
  3 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
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 31 37  1  0  0  0  0
 37 38  2  0  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 25 41  1  0  0  0  0
 41 42  2  0  0  0  0
 22 42  1  0  0  0  0
 42 43  1  0  0  0  0
 35 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 44 47  1  0  0  0  0
 47 48  1  0  0  0  0
 30 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 53 56  1  0  0  0  0
 56 57  1  0  0  0  0
 56 58  1  0  0  0  0
 58 59  1  0  0  0  0
 58 60  1  0  0  0  0
 51 60  1  0  0  0  0
 49 61  1  0  0  0  0
 61 62  2  0  0  0  0
 61 63  1  0  0  0  0
 63 64  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0167577

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CNC1(C)CC(OC(C)C1OC1CC(OC)C(O)C(C)O1)C1=CC=C2C(=O)C3=CC(=C4C(=O)C=C(OC4=C3C(=O)C2=C1O)C1(C)OC1C)C(O)(C1CC(OC)C(O)C(C)O1)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C46H57NO17/c1-18-36(49)27(56-8)15-31(60-18)46(55,43(54)58-10)25-13-24-34(41-35(25)26(48)14-30(62-41)45(6)21(4)64-45)40(53)33-23(38(24)51)12-11-22(39(33)52)29-17-44(5,47-7)42(20(3)59-29)63-32-16-28(57-9)37(50)19(2)61-32/h11-14,18-21,27-29,31-32,36-37,42,47,49-50,52,55H,15-17H2,1-10H3

> <INCHI_KEY>
YRBLXLRNBFXANX-UHFFFAOYSA-N

> <FORMULA>
C46H57NO17

> <MOLECULAR_WEIGHT>
895.952

> <EXACT_MASS>
895.362649379

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
121

> <JCHEM_AVERAGE_POLARIZABILITY>
94.68971630616313

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-7,12-dihydro-4H-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate

> <ALOGPS_LOGP>
2.19

> <JCHEM_LOGP>
1.526327769477869

> <ALOGPS_LOGS>
-4.17

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
10.484045975565417

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.295390791926181

> <JCHEM_PKA_STRONGEST_BASIC>
9.328632945807216

> <JCHEM_POLAR_SURFACE_AREA>
247.59999999999994

> <JCHEM_REFRACTIVITY>
224.97680000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.11e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       3.043  -2.108   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       2.494  -3.546   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       3.465  -4.741   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.120  -5.490   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.473  -3.577   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.986  -3.868   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.490  -5.323   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.482  -6.488   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.986  -7.943   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.969  -6.197   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.961  -7.361   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.465  -8.816   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.978  -9.107   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.482 -10.562   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.994 -10.853   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.498 -12.308   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.473 -11.726   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.978 -13.181   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.961 -11.435   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.953 -12.599   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.457  -9.980   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.994  -2.704   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.490  -1.249   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.498  -0.085   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.010  -0.376   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.018   0.788   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.514   2.243   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      11.531   0.497   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.539   1.661   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.051   1.370   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      14.555  -0.085   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      16.067  -0.376   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      17.076   0.788   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      16.571  -1.831   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      15.563  -2.995   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      14.051  -2.704   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      13.547  -1.249   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.035  -0.958   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      11.027  -2.122   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      11.531  -3.577   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       9.514  -1.831   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       8.506  -2.995   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       9.010  -4.450   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      16.067  -4.450   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      14.722  -5.199   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      17.588  -4.207   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      17.039  -5.645   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      17.283  -7.166   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      15.059   2.534   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      16.223   1.526   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      16.067   3.699   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      15.563   5.154   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      16.571   6.318   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      16.067   7.773   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      14.555   8.064   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      18.084   6.027   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      19.092   7.191   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      18.588   4.572   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      20.100   4.281   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      17.580   3.408   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      13.895   3.543   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      14.186   5.055   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      12.440   3.039   0.000  0.00  0.00           O+0
HETATM   64  C   UNK     0      11.276   4.047   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   10                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    3   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   12                                                       
CONECT   22    6   23   42                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   41                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   38                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   49                                                  
CONECT   31   30   32   37                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   44                                                  
CONECT   36   35   37                                                       
CONECT   37   36   31   38                                                  
CONECT   38   37   28   39                                                  
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   25   42                                                  
CONECT   42   41   22   43                                                  
CONECT   43   42                                                            
CONECT   44   35   45   46   47                                             
CONECT   45   44                                                            
CONECT   46   44   47                                                       
CONECT   47   46   44   48                                                  
CONECT   48   47                                                            
CONECT   49   30   50   51   61                                             
CONECT   50   49                                                            
CONECT   51   49   52   60                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54   56                                                  
CONECT   54   53   55                                                       
CONECT   55   54                                                            
CONECT   56   53   57   58                                                  
CONECT   57   56                                                            
CONECT   58   56   59   60                                                  
CONECT   59   58                                                            
CONECT   60   58   51                                                       
CONECT   61   49   62   63                                                  
CONECT   62   61                                                            
CONECT   63   61   64                                                       
CONECT   64   63                                                            
MASTER        0    0    0    0    0    0    0    0   64    0  142    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-7,12-dihydro-4H-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetic acid	Generator

Chemical Formula

C₄₆H₅₇NO₁₇

Average Mass

895.9520 Da

Monoisotopic Mass

895.36265 Da

IUPAC Name

methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-7,12-dihydro-4H-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

CNC1(C)CC(OC(C)C1OC1CC(OC)C(O)C(C)O1)C1=CC=C2C(=O)C3=CC(=C4C(=O)C=C(OC4=C3C(=O)C2=C1O)C1(C)OC1C)C(O)(C1CC(OC)C(O)C(C)O1)C(=O)OC

InChI Identifier

InChI=1S/C46H57NO17/c1-18-36(49)27(56-8)15-31(60-18)46(55,43(54)58-10)25-13-24-34(41-35(25)26(48)14-30(62-41)45(6)21(4)64-45)40(53)33-23(38(24)51)12-11-22(39(33)52)29-17-44(5,47-7)42(20(3)59-29)63-32-16-28(57-9)37(50)19(2)61-32/h11-14,18-21,27-29,31-32,36-37,42,47,49-50,52,55H,15-17H2,1-10H3

InChI Key

YRBLXLRNBFXANX-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyranone glycosides. Naphthopyranone glycosides are compounds containing a carbohydrate moiety glycosidically linked to a naphthopyranone moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Naphthopyranones

Direct Parent

Naphthopyranone glycosides

Alternative Parents

Substituents

Naphthopyranone glycoside
9,10-anthraquinone
Anthraquinone
Anthracene
O-glycosyl compound
Chromone
Glycosyl compound
Benzopyran
1-benzopyran
Aryl ketone
Aralkylamine
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Oxane
Benzenoid
Monosaccharide
Pyran
Methyl ester
Tertiary alcohol
Heteroaromatic compound
Vinylogous acid
Amino acid or derivatives
Carboxylic acid ester
Ketone
Secondary alcohol
Acetal
Secondary amine
Carboxylic acid derivative
Dialkyl ether
Secondary aliphatic amine
Oxirane
Ether
Oxacycle
Monocarboxylic acid or derivatives
Alcohol
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Amine
Organic oxide
Aromatic 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	2.19	ALOGPS
logP	1.53	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	7.3	ChemAxon
pKa (Strongest Basic)	9.33	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	247.6 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	224.98 m³·mol⁻¹	ChemAxon
Polarizability	94.69 Å³	ChemAxon
Number of Rings	8	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

195569

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate (NP0167577)

MOL for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

3D MOL for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

3D SDF for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

3D-SDF for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

PDB for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

3D PDB for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

SMILES for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

INCHI for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

Structure for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)

3D Structure for NP0167577 (methyl 2-[2-(2,3-dimethyloxiran-2-yl)-11-hydroxy-10-{5-[(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy]-4,6-dimethyl-4-(methylamino)oxan-2-yl}-4,7,12-trioxo-1-oxatetraphen-5-yl]-2-hydroxy-2-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)acetate)