NP-MRD: Showing NP-Card for 2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol (NP0164850)

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Record Information

Version

2.0

Created at

2022-09-02 23:48:45 UTC

Updated at

2022-09-02 23:48:45 UTC

NP-MRD ID

NP0164850

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

Description

2-{[5-({3,4-Dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. 2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol is found in Eriobotrya japonica. 2-{[5-({3,4-Dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181503022D          

 57 60  0  0  0  0            999 V2000
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020  -13.5020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -13.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -14.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -16.9125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -18.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -18.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270  -12.0730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9520  -12.0730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -16.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -17.3250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -16.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -14.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  2  0  0  0  0
  9 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 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
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 34 42  1  0  0  0  0
 42 43  1  0  0  0  0
 32 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 28 46  1  0  0  0  0
 46 47  1  0  0  0  0
 26 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  7 50  1  0  0  0  0
 50 51  1  0  0  0  0
  4 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  1  0  0  0  0
 54 55  1  0  0  0  0
 54 56  1  0  0  0  0
  2 56  1  0  0  0  0
 56 57  1  0  0  0  0
M  END

     RDKit          3D

123126  0  0  0  0  0  0  0  0999 V2000
   -0.8868   -2.0033    5.1651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9298   -1.9219    3.8418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8557   -1.0186    3.1688 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2604   -1.4223    3.6562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6761    0.3899    3.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4234    1.0838    3.2561 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7688    0.3991    3.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5723    0.9844    4.6357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2514    2.3625    5.0954 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7795    0.2589    5.1408 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0611    1.0069    4.8074 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1964    0.2018    5.3526 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1240   -0.2535    4.5396 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0725    0.0138    3.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2695   -1.0640    5.0729 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8156   -1.0330    1.7824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0828   -2.2378    1.1942 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2903   -2.1227    0.5183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6749   -3.2649   -0.1376 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1719   -2.8451   -1.5184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2488   -1.9806   -1.2693 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8359   -1.4934   -2.4312 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.1710   -1.9604   -2.3924 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8177   -1.5901   -3.5672 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9754   -1.9449   -4.7514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0702   -0.1018   -3.4604 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.9614    0.1119   -2.4197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8206    0.6846   -3.2464 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.3714    1.1595   -4.4797 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7496   -0.0039   -2.4717 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5246    0.3119   -3.1054 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7179   -4.3884   -0.1636 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7155   -5.0692    1.0451 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3321   -3.9123   -0.4991 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4652   -4.9962   -0.2245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9674   -2.7069    0.3121 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5332   -1.7268   -0.5781 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7876   -1.3590   -0.4020 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9162   -0.0144   -0.0497 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3736    0.8160   -1.0360 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1622    2.1956   -0.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3285    0.7940   -2.2244 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4324    1.4672   -1.8825 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7765    2.6152   -2.4647 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7981    3.6271   -1.4721 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7771    4.8839   -2.0662 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0881    5.9348   -1.0244 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7281    4.9883   -3.2290 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0371    5.0868   -4.4593 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7387    3.8776   -3.2549 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3738    3.8441   -4.5046 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1956    2.5209   -2.9795 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9421    1.9143   -1.9433 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4274   -0.6078   -2.6675 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2708   -0.8095   -3.7587 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6778   -1.6170   -1.5687 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4925   -2.8774   -2.1347 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2062   -2.6679    5.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5316   -1.4118    5.7927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2468   -2.5670    3.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2860   -1.1238    4.7249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4005   -2.5028    3.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0383   -0.8230    3.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6550    0.3248    4.7794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5918    1.0066    3.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4965    2.1221    3.6758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4104    1.1635    2.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0194   -0.5906    3.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0073    2.7348    5.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2364    2.3453    5.5390 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2323    3.0143    4.2017 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6656    0.1806    6.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8420   -0.7285    4.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1687    1.1218    3.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9820    1.9876    5.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2600   -0.0087    6.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1198   -0.3107    2.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8721   -0.5354    2.5473 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2187    1.1089    2.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2258   -0.5262    4.9787 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0949   -1.2951    6.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3709   -2.0161    4.5081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2487   -2.9873    1.9932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6104   -3.6470    0.3749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3663   -2.2067   -1.9598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4410   -3.6921   -2.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2974   -1.9124   -3.2956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7995   -2.0938   -3.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2081   -1.1743   -4.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6579   -2.0785   -5.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4992   -2.9362   -4.5864 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


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M  END
> <DATABASE_ID>
NP0164850

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OCC2OC(OC(C)(CCC=C(C)CCC=C(C)C)C=C)C(OC3OC(C)C(OC4OC(C)C(O)C(O)C4O)C(O)C3O)C(O)C2O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C39H66O18/c1-9-39(8,15-11-14-18(4)13-10-12-17(2)3)57-38-34(28(45)25(42)22(54-38)16-50-35-30(47)26(43)23(40)19(5)51-35)56-37-32(49)29(46)33(21(7)53-37)55-36-31(48)27(44)24(41)20(6)52-36/h9,12,14,19-38,40-49H,1,10-11,13,15-16H2,2-8H3

> <INCHI_KEY>
RTDSIIMUYUALQO-UHFFFAOYSA-N

> <FORMULA>
C39H66O18

> <MOLECULAR_WEIGHT>
822.939

> <EXACT_MASS>
822.424915285

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
123

> <JCHEM_AVERAGE_POLARIZABILITY>
85.83250294049321

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

> <ALOGPS_LOGP>
0.81

> <JCHEM_LOGP>
0.3645940449999982

> <ALOGPS_LOGS>
-2.69

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.18513899070713

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.7516220958282

> <JCHEM_PKA_STRONGEST_BASIC>
-3.64896557544842

> <JCHEM_POLAR_SURFACE_AREA>
276.14

> <JCHEM_REFRACTIVITY>
199.03130000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.69e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335 -13.860   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.001 -14.630   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -4.001 -16.170   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.667 -16.940   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.667 -18.480   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334 -19.250   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.334 -20.790   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.000 -21.560   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.000 -23.100   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.334 -23.870   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.564 -25.204   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667 -24.640   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667 -26.180   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001 -26.950   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.001 -28.490   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.667 -29.260   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.335 -29.260   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.335 -30.800   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.668 -31.570   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.668 -33.110   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -8.002 -33.880   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.335 -33.880   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.104 -22.536   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.644 -22.536   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.334 -20.790   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.667 -21.560   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.667 -23.100   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.334 -23.870   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       1.334 -25.410   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.000 -26.180   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.667 -26.180   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.667 -27.720   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.001 -28.490   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.335 -27.720   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.668 -28.490   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.002 -27.720   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.668 -30.030   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       8.002 -30.800   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       5.335 -30.800   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       5.335 -32.340   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       4.001 -30.030   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       2.667 -30.800   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       4.001 -25.410   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       5.335 -26.180   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       4.001 -23.870   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       5.335 -23.100   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       1.334 -19.250   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       2.667 -18.480   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       0.000 -18.480   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       0.000 -16.940   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      -5.335 -16.940   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -5.335 -18.480   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      -6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      -8.002 -16.940   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0      -6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      -8.002 -13.860   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   56                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   52                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   50                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   26                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13   24                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   11   25                                                       
CONECT   25   24                                                            
CONECT   26    9   27   48                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   46                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   44                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   42                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   34   43                                                  
CONECT   43   42                                                            
CONECT   44   32   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   28   47                                                  
CONECT   47   46                                                            
CONECT   48   26   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48    7   51                                                  
CONECT   51   50                                                            
CONECT   52    4   53   54                                                  
CONECT   53   52                                                            
CONECT   54   52   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54    2   57                                                  
CONECT   57   56                                                            
MASTER        0    0    0    0    0    0    0    0   57    0  120    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₆₆O₁₈

Average Mass

822.9390 Da

Monoisotopic Mass

822.42492 Da

IUPAC Name

2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

Traditional Name

2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC1OC(OCC2OC(OC(C)(CCC=C(C)CCC=C(C)C)C=C)C(OC3OC(C)C(OC4OC(C)C(O)C(O)C4O)C(O)C3O)C(O)C2O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C39H66O18/c1-9-39(8,15-11-14-18(4)13-10-12-17(2)3)57-38-34(28(45)25(42)22(54-38)16-50-35-30(47)26(43)23(40)19(5)51-35)56-37-32(49)29(46)33(21(7)53-37)55-36-31(48)27(44)24(41)20(6)52-36/h9,12,14,19-38,40-49H,1,10-11,13,15-16H2,2-8H3

InChI Key

RTDSIIMUYUALQO-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
Eriobotrya japonica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Fatty acyl glycoside
Sesquiterpenoid
Farsesane sesquiterpenoid
Alkyl glycoside
O-glycosyl compound
Glycosyl compound
Oxane
Fatty acyl
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Alcohol
Hydrocarbon derivative
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	0.81	ALOGPS
logP	0.36	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	11.75	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	276.14 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	199.03 m³·mol⁻¹	ChemAxon
Polarizability	85.83 Å³	ChemAxon
Number of Rings	4	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol (NP0164850)

MOL for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

3D MOL for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

3D SDF for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

3D-SDF for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

PDB for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

3D PDB for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

SMILES for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

INCHI for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

Structure for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)

3D Structure for NP0164850 (2-{[5-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,4-dihydroxy-6-[(3,7,11-trimethyldodeca-1,6,10-trien-3-yl)oxy]oxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol)