NP-MRD: Showing NP-Card for 4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0234630)

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Record Information

Version

2.0

Created at

2022-09-06 16:46:48 UTC

Updated at

2022-09-06 16:46:48 UTC

NP-MRD ID

NP0234630

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Description

4-{[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 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. 4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate is found in Pedicularis striata. 4-{[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004161508442D          

 55 59  0  0  0  0            999 V2000
    9.2188   -3.3863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5543   -4.1400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0694   -4.8074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4050   -5.5611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9201   -6.2285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0996   -6.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6146   -6.8097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7942   -6.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3092   -7.3909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4888   -7.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0038   -7.9721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1834   -7.8859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6984   -8.5533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0340   -9.3070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5491   -9.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8846  -10.7281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3997  -11.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7353  -12.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5792  -11.3093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0943  -11.9767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2437  -10.5556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4232  -10.4694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7286   -9.8882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3930   -9.1345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8478   -7.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0273   -7.0460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5424   -7.7134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8780   -8.4671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7219   -7.6272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2370   -8.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4165   -8.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0684   -8.8758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8889   -8.7896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2244   -8.0359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0449   -7.9497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7395   -7.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0751   -6.6148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5902   -5.9473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0810   -7.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3327   -6.4648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9972   -5.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -5.0437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3071   -5.0437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5620   -4.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946   -3.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4466   -3.1610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3426   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5356   -3.3325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2272   -4.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4425   -4.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1532   -6.5510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6381   -5.8836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7640   -5.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2489   -4.7212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9134   -3.9675    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  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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 27  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 39  2  0  0  0  0
 31 39  1  0  0  0  0
 25 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 45 49  1  0  0  0  0
 42 49  1  0  0  0  0
 49 50  1  0  0  0  0
 40 51  1  0  0  0  0
 10 51  1  0  0  0  0
 51 52  1  0  0  0  0
  6 53  1  0  0  0  0
 53 54  2  0  0  0  0
  3 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END


  Mrv1533004161508442D          

 55 59  0  0  0  0            999 V2000
    9.2188   -3.3863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5543   -4.1400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0694   -4.8074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4050   -5.5611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9201   -6.2285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0996   -6.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6146   -6.8097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7942   -6.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3092   -7.3909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4888   -7.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0038   -7.9721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1834   -7.8859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6984   -8.5533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0340   -9.3070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5491   -9.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8846  -10.7281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3997  -11.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7353  -12.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5792  -11.3093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0943  -11.9767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2437  -10.5556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4232  -10.4694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7286   -9.8882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3930   -9.1345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8478   -7.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0273   -7.0460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5424   -7.7134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8780   -8.4671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7219   -7.6272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2370   -8.2946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4165   -8.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0684   -8.8758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8889   -8.7896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2244   -8.0359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0449   -7.9497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7395   -7.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0751   -6.6148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5902   -5.9473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0810   -7.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3327   -6.4648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9972   -5.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -5.0437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3071   -5.0437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5620   -4.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946   -3.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4466   -3.1610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3426   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5356   -3.3325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2272   -4.2590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4425   -4.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1532   -6.5510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6381   -5.8836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7640   -5.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2489   -4.7212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9134   -3.9675    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  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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 29 27  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 39  2  0  0  0  0
 31 39  1  0  0  0  0
 25 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 45 49  1  0  0  0  0
 42 49  1  0  0  0  0
 49 50  1  0  0  0  0
 40 51  1  0  0  0  0
 10 51  1  0  0  0  0
 51 52  1  0  0  0  0
  6 53  1  0  0  0  0
 53 54  2  0  0  0  0
  3 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0234630

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(CCOC2OC(COC3OC(C)C(O)C(O)C3O)C(OC(=O)C=CC3=CC=C(O)C(OC)=C3)C(OC3OCC(O)(CO)C3O)C2O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C36H48O19/c1-17-26(41)27(42)28(43)33(52-17)50-14-24-30(54-25(40)9-6-18-4-7-20(38)23(13-18)48-3)31(55-35-32(45)36(46,15-37)16-51-35)29(44)34(53-24)49-11-10-19-5-8-22(47-2)21(39)12-19/h4-9,12-13,17,24,26-35,37-39,41-46H,10-11,14-16H2,1-3H3

> <INCHI_KEY>
IBZBYLPAHLAUMG-UHFFFAOYSA-N

> <FORMULA>
C36H48O19

> <MOLECULAR_WEIGHT>
784.761

> <EXACT_MASS>
784.278979326

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
79.0648749767813

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
0.41

> <JCHEM_LOGP>
-0.16528558766666576

> <ALOGPS_LOGS>
-2.93

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.227232569787533

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.623934325052375

> <JCHEM_PKA_STRONGEST_BASIC>
-3.61218235168369

> <JCHEM_POLAR_SURFACE_AREA>
282.21

> <JCHEM_REFRACTIVITY>
184.03790000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.13e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      17.208  -6.321   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      17.835  -7.728   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      16.930  -8.974   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.556 -10.381   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.651 -11.627   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.119 -11.466   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.214 -12.711   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.682 -12.550   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      11.777 -13.796   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      10.246 -13.635   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.341 -14.881   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.809 -14.720   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.904 -15.966   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.530 -17.373   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.625 -18.619   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.251 -20.026   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.346 -21.272   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.972 -22.679   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.815 -21.111   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.909 -22.357   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.188 -19.704   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.657 -19.543   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.093 -18.458   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.467 -17.051   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.183 -13.313   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.651 -13.152   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.746 -14.398   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.372 -15.805   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.214 -14.237   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.309 -15.483   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.777 -15.322   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.128 -16.568   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.659 -16.407   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -2.286 -15.000   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -3.817 -14.839   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -1.380 -13.754   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -2.007 -12.348   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.102 -11.102   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.151 -13.915   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.088 -12.068   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       7.461 -10.661   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.367  -9.415   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       9.907  -9.415   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      10.382  -7.950   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.137  -7.045   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      10.167  -5.901   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       8.106  -5.901   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       6.600  -6.221   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       7.891  -7.950   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       6.426  -7.474   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       9.619 -12.229   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      10.525 -10.983   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      14.493 -10.059   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      15.398  -8.813   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0      14.772  -7.406   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   54                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   53                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   51                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   25                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   15   24                                                  
CONECT   24   23                                                            
CONECT   25   12   26   40                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   39                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   39                                                  
CONECT   37   36   38                                                       
CONECT   38   37                                                            
CONECT   39   36   31                                                       
CONECT   40   25   41   51                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43   49                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46   47   49                                             
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47                                                            
CONECT   49   45   42   50                                                  
CONECT   50   49                                                            
CONECT   51   40   10   52                                                  
CONECT   52   51                                                            
CONECT   53    6   54                                                       
CONECT   54   53    3   55                                                  
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  118    0
END

View in JSmol

Synonyms

Value	Source
4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₃₆H₄₈O₁₉

Average Mass

784.7610 Da

Monoisotopic Mass

784.27898 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC=C(CCOC2OC(COC3OC(C)C(O)C(O)C3O)C(OC(=O)C=CC3=CC=C(O)C(OC)=C3)C(OC3OCC(O)(CO)C3O)C2O)C=C1O

InChI Identifier

InChI=1S/C36H48O19/c1-17-26(41)27(42)28(43)33(52-17)50-14-24-30(54-25(40)9-6-18-4-7-20(38)23(13-18)48-3)31(55-35-32(45)36(46,15-37)16-51-35)29(44)34(53-24)49-11-10-19-5-8-22(47-2)21(39)12-19/h4-9,12-13,17,24,26-35,37-39,41-46H,10-11,14-16H2,1-3H3

InChI Key

IBZBYLPAHLAUMG-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Pedicularis striata	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
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Glycosyl compound
O-glycosyl compound
Methoxyphenol
Tyrosol derivative
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Styrene
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Phenol
Oxane
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Tetrahydrofuran
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Carboxylic acid ester
Polyol
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Acetal
Ether
Primary alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	0.41	ALOGPS
logP	-0.17	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	9.62	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	282.21 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	184.04 m³·mol⁻¹	ChemAxon
Polarizability	79.06 Å³	ChemAxon
Number of Rings	5	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

85131431

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0234630)

MOL for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D MOL for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D SDF for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D-SDF for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

PDB for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D PDB for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

SMILES for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

INCHI for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

Structure for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D Structure for NP0234630 (4-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)