NP-MRD: Showing NP-Card for methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate (NP0321857)

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Record Information

Version

2.0

Created at

2022-09-12 00:17:21 UTC

Updated at

2022-09-12 00:17:21 UTC

NP-MRD ID

NP0321857

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate

Description

4-(Methoxycarbonyl)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-6-yl 6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton. methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate is found in Strychnos lucida. 4-(Methoxycarbonyl)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-6-yl 6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251513182D          

 52 57  0  0  0  0            999 V2000
    6.8809    4.5695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0559    4.5695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6434    5.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0559    5.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8184    5.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059    5.9985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5809    5.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684    5.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3434    5.2840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9309    5.9985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1059    5.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6934    6.7130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1316    6.7130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5441    7.4274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1059    7.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6934    8.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9309    7.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3434    8.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3434    6.7130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684    6.7130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5809    4.5695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3260    3.7849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5413    3.5300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6608    3.7849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059    4.5695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
  8 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  5 26  1  0  0  0  0
 21 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 35 44  1  0  0  0  0
 44 45  1  0  0  0  0
 33 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 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
 30 52  1  0  0  0  0
 46 52  1  0  0  0  0
M  END

     RDKit          3D

100105  0  0  0  0  0  0  0  0999 V2000
    3.8456   -2.9917   -6.6840 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3189   -2.2715   -5.5383 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4559   -1.9154   -4.5151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2499   -2.2425   -4.6228 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8814   -1.1872   -3.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1743   -0.8575   -3.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5215   -0.1659   -2.1111 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9819   -0.6427   -0.8772 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4904    0.0795    0.1959 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1709   -0.7287    1.1019 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4897   -0.3753    1.0483 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8863    0.7631    1.6586 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2419    0.5626    2.3571 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6483    1.7315    2.9820 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9040    1.4489    2.5358 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5731    2.2312    3.4760 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9397    0.5385    3.2507 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5805    0.0742    4.4028 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5299   -0.6594    2.4390 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7281   -1.8467    3.1863 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4997   -0.5389   -0.9440 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9101   -0.8293   -2.2927 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1144    0.3999   -2.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8167    1.1176   -1.3787 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5248    0.7606   -0.9496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4810    1.7280   -0.8697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1260    2.9075   -1.2012 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8459    1.4454   -0.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6987    2.4452   -0.4120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0200    2.2846   -0.0237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5308    0.9916    0.4054 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5455    1.2164    1.3242 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7578    0.8439    0.7399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.3905   -0.1222    1.4992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4674   -0.6961    0.8776 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.0498   -1.9305    0.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1485   -2.5288   -0.4966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1592    0.2897   -0.0687 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.4818   -0.0721   -0.2004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0841    1.6370    0.6108 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.6615    1.5048    1.8739 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6646    2.0784    0.6914 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.2974    2.8278   -0.4183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3719    0.3156    1.0282 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3293    0.1187   -0.0614 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3139   -0.7082    0.6866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1928   -1.7524    1.3412 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3112   -2.8001    0.4043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5639   -1.0772    1.5180 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6431   -1.8609    0.8584 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9236    0.7567   -0.4508 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9369    1.8892   -0.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6893   -3.3700   -7.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1995   -3.8203   -6.2955 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2702   -2.3099   -7.3258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9005   -1.1071   -4.0244 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2617   -1.7052   -0.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1058   -1.7727    0.7259 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1438    1.4991    0.8339 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1936   -0.2915    3.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0216    0.3042    1.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9162    1.5485    3.9139 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3010    2.1576    1.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3174    3.1667    3.4747 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0515    1.1093    3.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7850    0.7914    5.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4309   -0.6012    2.2932 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8702   -2.5676    2.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1019   -1.3379   -0.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1713   -1.6600   -2.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1881    0.1275   -3.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7606    1.0038   -3.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8702    2.2195   -1.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3478    3.4558   -0.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9281    0.5412   -0.5230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5769    0.4672   -0.2713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2652   -1.0169    1.6011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2923   -1.7024   -0.6346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6486   -2.6591    0.8551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4050   -1.9583   -1.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6128    0.3467   -1.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0829    0.7039    0.0251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6839    2.4090    0.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7960    2.3948    2.2866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4404    2.6449    1.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2149    2.2179   -1.1876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9545    1.0021    1.7994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7588   -0.4451   -0.9176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7964   -0.0762    1.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5892   -1.2218    0.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7843   -2.1152    2.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2069   -2.4709   -0.5266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7373   -1.0461    2.6004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9793   -1.4439   -0.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2150   -2.8914    0.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4518   -2.0466    1.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5951    0.6377    0.6050 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3319    2.0720    0.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7222    1.8068   -1.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3667    2.8227   -0.6903 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
  3  5  1  0
  5  6  2  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
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  8 21  1  0
 21 51  1  0
 51 52  1  0
 51 24  1  0
 24 23  1  0
 23 22  1  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 35 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 31 44  1  0
 44 49  1  0
 49 50  1  0
 49 47  1  0
 47 48  1  0
 47 46  1  0
 46 45  1  0
 22  5  1  0
 45 28  1  0
 19 10  1  0
 22 21  1  0
 42 33  1  0
 45 44  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
  6 56  1  0
  8 57  1  1
 10 58  1  6
 12 59  1  6
 13 60  1  0
 13 61  1  0
 14 62  1  0
 15 63  1  6
 16 64  1  0
 17 65  1  1
 18 66  1  0
 19 67  1  6
 20 68  1  0
 21 69  1  1
 51 97  1  1
 52 98  1  0
 52 99  1  0
 52100  1  0
 24 73  1  6
 23 71  1  0
 23 72  1  0
 22 70  1  1
 29 74  1  0
 31 75  1  6
 33 76  1  6
 35 77  1  1
 36 78  1  0
 36 79  1  0
 37 80  1  0
 38 81  1  6
 39 82  1  0
 40 83  1  6
 41 84  1  0
 42 85  1  1
 43 86  1  0
 44 87  1  1
 49 93  1  1
 50 94  1  0
 50 95  1  0
 50 96  1  0
 47 91  1  1
 48 92  1  0
 46 89  1  0
 46 90  1  0
 45 88  1  6
M  END


  Mrv1533004251513182D          

 52 57  0  0  0  0            999 V2000
    6.8809    4.5695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0559    4.5695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6434    5.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0559    5.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8184    5.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059    5.9985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5809    5.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684    5.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3434    5.2840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9309    5.9985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1059    5.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6934    6.7130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1316    6.7130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5441    7.4274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1059    7.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6934    8.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9309    7.4274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3434    8.1419    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3434    6.7130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684    6.7130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5809    4.5695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3260    3.7849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5413    3.5300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6608    3.7849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059    4.5695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
  8 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  5 26  1  0  0  0  0
 21 26  1  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 35 44  1  0  0  0  0
 44 45  1  0  0  0  0
 33 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 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
 30 52  1  0  0  0  0
 46 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321857

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C(C)C(CC12)OC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C(C)C(O)CC12

> <INCHI_IDENTIFIER>
InChI=1S/C33H48O19/c1-10-16(36)4-12-15(9-47-30(20(10)12)51-32-26(41)24(39)22(37)18(6-34)49-32)29(44)48-17-5-13-14(28(43)45-3)8-46-31(21(13)11(17)2)52-33-27(42)25(40)23(38)19(7-35)50-33/h8-13,16-27,30-42H,4-7H2,1-3H3

> <INCHI_KEY>
RFGKYBWBAYNUAA-UHFFFAOYSA-N

> <FORMULA>
C33H48O19

> <MOLECULAR_WEIGHT>
748.728

> <EXACT_MASS>
748.278979326

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
75.08880491878136

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

> <ALOGPS_LOGP>
-1.53

> <JCHEM_LOGP>
-3.1557138600000005

> <ALOGPS_LOGS>
-2.05

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.427484925815982

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.906001714002889

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601512576

> <JCHEM_POLAR_SURFACE_AREA>
290.04999999999995

> <JCHEM_REFRACTIVITY>
166.6875

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.74e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

> <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      12.844   8.530   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.304   8.530   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.534   9.863   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      11.304  11.197   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.994   9.863   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.224  11.197   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.684  11.197   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.914   9.863   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.374   9.863   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.604  11.197   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.064  11.197   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.294  12.531   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.246  12.531   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.016  13.865   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.064  13.865   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.294  15.198   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.604  13.865   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.374  15.198   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.374  12.531   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.914  12.531   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.684   8.530   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.208   7.065   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.744   6.589   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.454   6.160   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.700   7.065   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.224   8.530   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.454   4.620   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.787   4.620   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.454   0.000   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.121  -2.310   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       7.454  -3.080   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       8.788  -2.310   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      10.122  -3.080   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.455  -2.310   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      11.455  -0.770   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      10.122  -4.620   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      11.455  -5.390   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.788  -5.390   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       8.788  -6.930   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       7.454  -4.620   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       6.121  -5.390   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       2.846  -1.941   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       0.877   0.770   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   26                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   21                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   10   20                                                  
CONECT   20   19                                                            
CONECT   21    8   22   26                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25    5   21                                                  
CONECT   27   24   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   52                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   46                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   44                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   40                                                  
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   37   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   35   45                                                  
CONECT   45   44                                                            
CONECT   46   33   47   52                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52                                                       
CONECT   52   51   30   46                                                  
MASTER        0    0    0    0    0    0    0    0   52    0  114    0
END

View in JSmol

Synonyms

Value	Source
4-(Methoxycarbonyl)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyran-6-yl 6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyran-4-carboxylic acid	Generator

Chemical Formula

C₃₃H₄₈O₁₉

Average Mass

748.7280 Da

Monoisotopic Mass

748.27898 Da

IUPAC Name

methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C(C)C(CC12)OC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C(C)C(O)CC12

InChI Identifier

InChI=1S/C33H48O19/c1-10-16(36)4-12-15(9-47-30(20(10)12)51-32-26(41)24(39)22(37)18(6-34)49-32)29(44)48-17-5-13-14(28(43)45-3)8-46-31(21(13)11(17)2)52-33-27(42)25(40)23(38)19(7-35)50-33/h8-13,16-27,30-42H,4-7H2,1-3H3

InChI Key

RFGKYBWBAYNUAA-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Strychnos lucida	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Iridoid O-glycosides

Alternative Parents

Substituents

Iridoid o-glycoside
Glycosyl compound
Iridoid-skeleton
O-glycosyl compound
Monoterpenoid
Dicarboxylic acid or derivatives
Monosaccharide
Oxane
Enoate ester
Methyl ester
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Acetal
Oxacycle
Carbonyl group
Organooxygen compound
Organic oxygen compound
Organic oxide
Alcohol
Hydrocarbon derivative
Primary alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-1.5	ALOGPS
logP	-3.2	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	290.05 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	166.69 m³·mol⁻¹	ChemAxon
Polarizability	75.09 Å³	ChemAxon
Number of Rings	6	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

85446569

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate (NP0321857)

MOL for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D MOL for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D SDF for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D-SDF for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

PDB for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D PDB for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

SMILES for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

INCHI for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

Structure for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D Structure for NP0321857 (methyl 6-(6-hydroxy-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carbonyloxy)-7-methyl-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-4-carboxylate)