NP-MRD: Showing NP-Card for 1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline (NP0011905)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-01-05 21:27:02 UTC

Updated at

2021-07-15 17:10:17 UTC

NP-MRD ID

NP0011905

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline

Provided By

NPAtlas

Description

(2S,3R,4S,5S,6R)-2-[(1-hydroxy-3-methoxy-8-methylnaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. 1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline is found in Mucor. Based on a literature review very few articles have been published on (2S,3R,4S,5S,6R)-2-[(1-hydroxy-3-methoxy-8-methylnaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242121133D          

 48 50  0  0  0  0            999 V2000
   -0.3666   -0.3596   -3.9107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358   -0.5248   -2.5310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1536   -0.5289   -1.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4603   -0.3632   -2.0217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4796   -0.3657   -1.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7878   -0.1991   -1.5330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8051   -0.2018   -0.6061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5224   -0.3659    0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2206   -0.5360    1.1935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9545   -0.7119    2.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2033   -0.5328    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8772   -0.6950    0.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5836   -0.8616    1.9763 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363   -0.6970   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -0.8537    0.0831 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902    0.1482    0.4007 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4173    0.0918   -0.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    1.1576   -0.4069 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3003    1.0994   -1.5305 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0331   -0.0774   -1.5312 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9503    1.1565    0.9408 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5464    2.2850    1.6763 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5141   -0.0611    1.6905 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8997   -1.2263    1.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9999   -0.0697    1.7563 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6328    0.9091    2.6789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0497   -1.1357   -4.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6209   -0.5494   -4.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7762    0.6309   -4.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6821   -0.2352   -3.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9975   -0.0689   -2.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8161   -0.0729   -0.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3134   -0.3702    1.4577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5551   -1.6978    2.8973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9489   -0.6530    3.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3765    0.1419    3.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6737   -0.9866    2.3554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9025    1.1631    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7199    2.1079   -0.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0394    1.9359   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7783    1.1801   -2.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6900   -0.7468   -2.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0559    1.1739    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2179    2.4566    2.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255   -0.0946    2.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8901   -1.2912    0.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7197   -1.0612    2.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563    0.5569    3.5982 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  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
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14  3  1  0  0  0  0
 25 16  1  0  0  0  0
 11  5  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  4 30  1  0  0  0  0
  6 31  1  0  0  0  0
  7 32  1  0  0  0  0
  8 33  1  0  0  0  0
 10 34  1  0  0  0  0
 10 35  1  0  0  0  0
 10 36  1  0  0  0  0
 13 37  1  0  0  0  0
 16 38  1  1  0  0  0
 18 39  1  6  0  0  0
 19 40  1  0  0  0  0
 19 41  1  0  0  0  0
 20 42  1  0  0  0  0
 21 43  1  6  0  0  0
 22 44  1  0  0  0  0
 23 45  1  1  0  0  0
 24 46  1  0  0  0  0
 25 47  1  1  0  0  0
 26 48  1  0  0  0  0
M  END

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
   -0.3666   -0.3596   -3.9107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358   -0.5248   -2.5310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1536   -0.5289   -1.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4603   -0.3632   -2.0217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4796   -0.3657   -1.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7878   -0.1991   -1.5330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8051   -0.2018   -0.6061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5224   -0.3659    0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2206   -0.5360    1.1935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9545   -0.7119    2.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2033   -0.5328    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8772   -0.6950    0.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5836   -0.8616    1.9763 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363   -0.6970   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -0.8537    0.0831 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902    0.1482    0.4007 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4173    0.0918   -0.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    1.1576   -0.4069 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3003    1.0994   -1.5305 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0331   -0.0774   -1.5312 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9503    1.1565    0.9408 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5464    2.2850    1.6763 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5141   -0.0611    1.6905 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8997   -1.2263    1.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9999   -0.0697    1.7563 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6328    0.9091    2.6789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0497   -1.1357   -4.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6209   -0.5494   -4.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7762    0.6309   -4.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6821   -0.2352   -3.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9975   -0.0689   -2.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8161   -0.0729   -0.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3134   -0.3702    1.4577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5551   -1.6978    2.8973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9489   -0.6530    3.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3765    0.1419    3.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6737   -0.9866    2.3554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9025    1.1631    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7199    2.1079   -0.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0394    1.9359   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7783    1.1801   -2.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6900   -0.7468   -2.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0559    1.1739    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2179    2.4566    2.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255   -0.0946    2.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8901   -1.2912    0.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7197   -1.0612    2.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563    0.5569    3.5982 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  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
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14  3  1  0
 25 16  1  0
 11  5  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  6 31  1  0
  7 32  1  0
  8 33  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
 13 37  1  0
 16 38  1  1
 18 39  1  6
 19 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  6
 22 44  1  0
 23 45  1  1
 24 46  1  0
 25 47  1  1
 26 48  1  0
M  END


  Mrv1652306242121133D          

 48 50  0  0  0  0            999 V2000
   -0.3666   -0.3596   -3.9107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358   -0.5248   -2.5310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1536   -0.5289   -1.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4603   -0.3632   -2.0217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4796   -0.3657   -1.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7878   -0.1991   -1.5330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8051   -0.2018   -0.6061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5224   -0.3659    0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2206   -0.5360    1.1935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9545   -0.7119    2.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2033   -0.5328    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8772   -0.6950    0.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5836   -0.8616    1.9763 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363   -0.6970   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -0.8537    0.0831 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902    0.1482    0.4007 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4173    0.0918   -0.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    1.1576   -0.4069 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3003    1.0994   -1.5305 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0331   -0.0774   -1.5312 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9503    1.1565    0.9408 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5464    2.2850    1.6763 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5141   -0.0611    1.6905 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8997   -1.2263    1.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9999   -0.0697    1.7563 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6328    0.9091    2.6789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0497   -1.1357   -4.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6209   -0.5494   -4.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7762    0.6309   -4.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6821   -0.2352   -3.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9975   -0.0689   -2.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8161   -0.0729   -0.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3134   -0.3702    1.4577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5551   -1.6978    2.8973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9489   -0.6530    3.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3765    0.1419    3.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6737   -0.9866    2.3554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9025    1.1631    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7199    2.1079   -0.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0394    1.9359   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7783    1.1801   -2.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6900   -0.7468   -2.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0559    1.1739    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2179    2.4566    2.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255   -0.0946    2.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8901   -1.2912    0.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7197   -1.0612    2.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563    0.5569    3.5982 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  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
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14  3  1  0  0  0  0
 25 16  1  0  0  0  0
 11  5  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  4 30  1  0  0  0  0
  6 31  1  0  0  0  0
  7 32  1  0  0  0  0
  8 33  1  0  0  0  0
 10 34  1  0  0  0  0
 10 35  1  0  0  0  0
 10 36  1  0  0  0  0
 13 37  1  0  0  0  0
 16 38  1  1  0  0  0
 18 39  1  6  0  0  0
 19 40  1  0  0  0  0
 19 41  1  0  0  0  0
 20 42  1  0  0  0  0
 21 43  1  6  0  0  0
 22 44  1  0  0  0  0
 23 45  1  1  0  0  0
 24 46  1  0  0  0  0
 25 47  1  1  0  0  0
 26 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011905

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(O[C@]2([H])O[C@]([H])(C([H])([H])O[H])[C@@]([H])(O[H])[C@]([H])(O[H])[C@@]2([H])O[H])C(OC([H])([H])[H])=C([H])C2=C([H])C([H])=C([H])C(=C12)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H22O8/c1-8-4-3-5-9-6-10(24-2)17(14(21)12(8)9)26-18-16(23)15(22)13(20)11(7-19)25-18/h3-6,11,13,15-16,18-23H,7H2,1-2H3/t11-,13-,15+,16-,18+/m1/s1

> <INCHI_KEY>
CPJZGHWPEYNNPY-CXEWAAMLSA-N

> <FORMULA>
C18H22O8

> <MOLECULAR_WEIGHT>
366.366

> <EXACT_MASS>
366.131467668

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
36.94797524860421

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-2-[(1-hydroxy-3-methoxy-8-methylnaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
0.28

> <JCHEM_LOGP>
0.4432739596666662

> <ALOGPS_LOGS>
-1.97

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.200883677770147

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.521590703345698

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092366212878

> <JCHEM_POLAR_SURFACE_AREA>
128.84

> <JCHEM_REFRACTIVITY>
90.11880000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.95e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-2-[(1-hydroxy-3-methoxy-8-methylnaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
   -0.3666   -0.3596   -3.9107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358   -0.5248   -2.5310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1536   -0.5289   -1.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4603   -0.3632   -2.0217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4796   -0.3657   -1.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7878   -0.1991   -1.5330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8051   -0.2018   -0.6061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5224   -0.3659    0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2206   -0.5360    1.1935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9545   -0.7119    2.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2033   -0.5328    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8772   -0.6950    0.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5836   -0.8616    1.9763 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363   -0.6970   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -0.8537    0.0831 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902    0.1482    0.4007 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4173    0.0918   -0.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    1.1576   -0.4069 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3003    1.0994   -1.5305 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0331   -0.0774   -1.5312 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9503    1.1565    0.9408 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5464    2.2850    1.6763 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5141   -0.0611    1.6905 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8997   -1.2263    1.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9999   -0.0697    1.7563 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6328    0.9091    2.6789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0497   -1.1357   -4.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6209   -0.5494   -4.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7762    0.6309   -4.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6821   -0.2352   -3.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9975   -0.0689   -2.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8161   -0.0729   -0.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3134   -0.3702    1.4577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5551   -1.6978    2.8973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9489   -0.6530    3.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3765    0.1419    3.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6737   -0.9866    2.3554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9025    1.1631    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7199    2.1079   -0.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0394    1.9359   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7783    1.1801   -2.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6900   -0.7468   -2.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0559    1.1739    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2179    2.4566    2.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255   -0.0946    2.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8901   -1.2912    0.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7197   -1.0612    2.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563    0.5569    3.5982 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  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
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14  3  1  0
 25 16  1  0
 11  5  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  6 31  1  0
  7 32  1  0
  8 33  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
 13 37  1  0
 16 38  1  1
 18 39  1  6
 19 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  6
 22 44  1  0
 23 45  1  1
 24 46  1  0
 25 47  1  1
 26 48  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.367  -0.360  -3.911  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.136  -0.525  -2.531  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.154  -0.529  -1.590  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.460  -0.363  -2.022  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.480  -0.366  -1.094  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.788  -0.199  -1.533  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.805  -0.202  -0.606  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.522  -0.366   0.716  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.221  -0.536   1.194  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.954  -0.712   2.645  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.203  -0.533   0.262  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.877  -0.695   0.643  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.584  -0.862   1.976  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.836  -0.697  -0.259  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.474  -0.854   0.083  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.390   0.148   0.401  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.417   0.092  -0.542  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.301   1.158  -0.407  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.300   1.099  -1.531  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.033  -0.077  -1.531  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.950   1.157   0.941  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.546   2.285   1.676  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.514  -0.061   1.690  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.900  -1.226   1.038  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.000  -0.070   1.756  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.633   0.909   2.679  0.00  0.00           O+0
HETATM   27  H   UNK     0      -1.050  -1.136  -4.318  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.621  -0.549  -4.415  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.776   0.631  -4.170  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.682  -0.235  -3.052  0.00  0.00           H+0
HETATM   31  H   UNK     0      -4.997  -0.069  -2.595  0.00  0.00           H+0
HETATM   32  H   UNK     0      -6.816  -0.073  -0.946  0.00  0.00           H+0
HETATM   33  H   UNK     0      -6.313  -0.370   1.458  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.555  -1.698   2.897  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.949  -0.653   3.181  0.00  0.00           H+0
HETATM   36  H   UNK     0      -3.377   0.142   3.078  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.674  -0.987   2.355  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.903   1.163   0.360  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.720   2.108  -0.551  0.00  0.00           H+0
HETATM   40  H   UNK     0       5.039   1.936  -1.438  0.00  0.00           H+0
HETATM   41  H   UNK     0       3.778   1.180  -2.494  0.00  0.00           H+0
HETATM   42  H   UNK     0       4.690  -0.747  -2.173  0.00  0.00           H+0
HETATM   43  H   UNK     0       5.056   1.174   0.870  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.218   2.457   2.372  0.00  0.00           H+0
HETATM   45  H   UNK     0       3.926  -0.095   2.712  0.00  0.00           H+0
HETATM   46  H   UNK     0       4.890  -1.291   0.934  0.00  0.00           H+0
HETATM   47  H   UNK     0       1.720  -1.061   2.194  0.00  0.00           H+0
HETATM   48  H   UNK     0       1.556   0.557   3.598  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   14                                                  
CONECT    4    3    5   30                                                  
CONECT    5    4    6   11                                                  
CONECT    6    5    7   31                                                  
CONECT    7    6    8   32                                                  
CONECT    8    7    9   33                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9   34   35   36                                             
CONECT   11    9   12    5                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   37                                                       
CONECT   14   12   15    3                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25   38                                             
CONECT   17   16   18                                                       
CONECT   18   17   19   21   39                                             
CONECT   19   18   20   40   41                                             
CONECT   20   19   42                                                       
CONECT   21   18   22   23   43                                             
CONECT   22   21   44                                                       
CONECT   23   21   24   25   45                                             
CONECT   24   23   46                                                       
CONECT   25   23   26   16   47                                             
CONECT   26   25   48                                                       
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    4                                                            
CONECT   31    6                                                            
CONECT   32    7                                                            
CONECT   33    8                                                            
CONECT   34   10                                                            
CONECT   35   10                                                            
CONECT   36   10                                                            
CONECT   37   13                                                            
CONECT   38   16                                                            
CONECT   39   18                                                            
CONECT   40   19                                                            
CONECT   41   19                                                            
CONECT   42   20                                                            
CONECT   43   21                                                            
CONECT   44   22                                                            
CONECT   45   23                                                            
CONECT   46   24                                                            
CONECT   47   25                                                            
CONECT   48   26                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  100    0
END

RDKit          3D

48 50  0  0  0  0  0  0  0  0999 V2000
   -0.3666   -0.3596   -3.9107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358   -0.5248   -2.5310 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1536   -0.5289   -1.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4603   -0.3632   -2.0217 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4796   -0.3657   -1.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7878   -0.1991   -1.5330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8051   -0.2018   -0.6061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5224   -0.3659    0.7160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2206   -0.5360    1.1935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9545   -0.7119    2.6447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2033   -0.5328    0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8772   -0.6950    0.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5836   -0.8616    1.9763 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363   -0.6970   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4741   -0.8537    0.0831 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902    0.1482    0.4007 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4173    0.0918   -0.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3012    1.1576   -0.4069 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3003    1.0994   -1.5305 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0331   -0.0774   -1.5312 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9503    1.1565    0.9408 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5464    2.2850    1.6763 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5141   -0.0611    1.6905 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8997   -1.2263    1.0376 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9999   -0.0697    1.7563 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6328    0.9091    2.6789 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0497   -1.1357   -4.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6209   -0.5494   -4.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7762    0.6309   -4.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6821   -0.2352   -3.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9975   -0.0689   -2.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8161   -0.0729   -0.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3134   -0.3702    1.4577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5551   -1.6978    2.8973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9489   -0.6530    3.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3765    0.1419    3.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6737   -0.9866    2.3554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9025    1.1631    0.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7199    2.1079   -0.5505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0394    1.9359   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7783    1.1801   -2.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6900   -0.7468   -2.1732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0559    1.1739    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2179    2.4566    2.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255   -0.0946    2.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8901   -1.2912    0.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7197   -1.0612    2.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563    0.5569    3.5982 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  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
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14  3  1  0
 25 16  1  0
 11  5  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  6 31  1  0
  7 32  1  0
  8 33  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
 13 37  1  0
 16 38  1  1
 18 39  1  6
 19 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  6
 22 44  1  0
 23 45  1  1
 24 46  1  0
 25 47  1  1
 26 48  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
1-Hydroxy-3-methoxy-8-methyl-2-O-b-D-glucopyranosylnaphthaline	Generator
1-Hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline	Generator

Chemical Formula

C₁₈H₂₂O₈

Average Mass

366.3660 Da

Monoisotopic Mass

366.13147 Da

IUPAC Name

(2S,3R,4S,5S,6R)-2-[(1-hydroxy-3-methoxy-8-methylnaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2S,3R,4S,5S,6R)-2-[(1-hydroxy-3-methoxy-8-methylnaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

COC1=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(C)=CC=CC2=C1

InChI Identifier

InChI=1S/C18H22O8/c1-8-4-3-5-9-6-10(24-2)17(14(21)12(8)9)26-18-16(23)15(22)13(20)11(7-19)25-18/h3-6,11,13,15-16,18-23H,7H2,1-2H3/t11-,13-,15+,16-,18+/m1/s1

InChI Key

CPJZGHWPEYNNPY-CXEWAAMLSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Mucor	NPAtlas	23822523

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Hexose monosaccharide
1-naphthol
O-glycosyl compound
Naphthalene
Anisole
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Monosaccharide
Benzenoid
Oxane
Secondary alcohol
Acetal
Organoheterocyclic compound
Ether
Oxacycle
Polyol
Alcohol
Primary alcohol
Hydrocarbon derivative
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	0.28	ALOGPS
logP	0.44	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	9.52	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	128.84 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	90.12 m³·mol⁻¹	ChemAxon
Polarizability	36.95 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA015145

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78438088

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72708523

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline (NP0011905)

MOL for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

3D MOL for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

3D SDF for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

3D-SDF for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

PDB for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

3D PDB for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

SMILES for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

INCHI for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

Structure for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)

3D Structure for NP0011905 (1-hydroxy-3-methoxy-8-methyl-2-O-β-D-glucopyranosylnaphthaline)